SYMPAZAN®  is indicated for the adjunctive treatment of seizures associated with Lennox-Gastaut Syndrome (LGS) in patients 2 years of age or older.

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A daily dose of SYMPAZAN®  greater than 5 mg should be administered in divided doses twice daily; a 5 mg daily dose can be administered as a single dose. Dose patients according to body weight. Individualize dosing within each body weight group, based on clinical efficacy and tolerability. Each dose in Table 1 (e.g., 5 to 20 mg in 30 kg or less weight group) has been shown to be effective, although effectiveness increases with increasing dose [see Clinical Studies (14)]. Do not proceed with dose escalation more rapidly than weekly, because serum concentrations of clobazam and its active metabolite require 5 and 9 days, respectively, to reach steady-state.

<div class="scrollingtable"><table> <colgroup> <col width="213"/> <col width="213"/> <col width="278"/> </colgroup> <tbody class="Headless"> <tr class="First"> <td align="center" class="Lrule Rrule Toprule" colspan="3"><span class="Bold">Table 1: Recommended Total Daily Dosing by Weight Group</span></td> </tr> <tr> <td class="Lrule Rrule Toprule"></td><td align="center" class="Lrule Rrule Toprule"><span class="Bold">30 kg </span><span class="Bold">or Less </span><span class="Bold">Body Weight</span></td><td align="center" class="Lrule Rrule Toprule"><span class="Bold">Greater than </span><span class="Bold">30 kg Body Weight</span></td> </tr> <tr> <td class="Lrule Rrule Toprule">Starting Dose      </td><td align="center" class="Lrule Rrule Toprule">5 mg</td><td align="center" class="Lrule Rrule Toprule">10 mg</td> </tr> <tr> <td class="Lrule Rrule Toprule">Starting Day 7     </td><td align="center" class="Lrule Rrule Toprule">10 mg</td><td align="center" class="Lrule Rrule Toprule">20 mg</td> </tr> <tr class="Last"> <td class="Lrule Rrule Toprule">Starting Day 14     </td><td align="center" class="Lrule Rrule Toprule">20 mg</td><td align="center" class="Lrule Rrule Toprule">40 mg</td> </tr> </tbody> </table></div>

To reduce the risk of withdrawal reactions, increased seizure frequency, and status epilepticus, use a gradual taper to discontinue SYMPAZAN or reduce the dosage. Taper by decreasing the total daily dosage by 5-10 mg/day on a weekly basis until discontinued. If a patient develops withdrawal reactions, consider pausing the taper or increasing the dosage to the previous tapered dosage level. Subsequently decrease the dosage more slowly [see Warnings and Precautions (5.3) and Drug Abuse and Dependence (9.3)].

Instruct patients and/or caregivers to read the “Instructions for Use” carefully for complete directions on how to properly dose and administer SYMPAZAN® oral films.

Apply SYMPAZAN®  on top of the tongue where it adheres and dissolves.

SYMPAZAN® oral film can be taken with or without food [see Clinical Pharmacology (12.3)]. Do not administer with liquids. As the film dissolves, saliva should be swallowed in a normal manner, but the patient should refrain from chewing, spitting or talking.

Only one oral film should be taken at a time; if a second film is needed to complete the dosage, it should not be taken until the first film has completely dissolved.

Plasma concentrations at any given dose are generally higher in geriatric patients [see Clinical Pharmacology (12.3)]. Therefore, the starting dosage should generally be 5 mg/day for all geriatric patients. Then proceed slowly with dose escalation; titrate according to weight, but to half the dosage presented in Table 1, as tolerated. If necessary and based upon clinical response, an additional titration to the maximum dosage (20 mg/day or 40 mg/day, depending on weight) may be started on day 21 [see Use in Specific Populations (8.5)].

In CYP2C19 poor metabolizers, levels of N-desmethylclobazam, clobazam's active metabolite, will be increased [see Clinical Pharmacology (12.5)]. Therefore, the starting dosage should be 5 mg/day in patients known to be CYP2C19 poor metabolizers. Then proceed slowly with dose escalation; titrate according to weight, but to half the dosage presented in Table 1, as tolerated. If necessary and based upon clinical response, an additional titration to the maximum dosage (20 mg/day or 40 mg/day, depending on weight) may be started on day 21 [see Use in Specific Populations (8.6)].

SYMPAZAN®  is hepatically metabolized; however, there are limited data to characterize the effect of hepatic impairment on the pharmacokinetics of SYMPAZAN®. For patients with mild to moderate hepatic impairment (Child-Pugh score 5-9), the starting dosage should be 5 mg/day (regardless of weight). Then proceed slowly with dosing escalations; titrate patients according to weight, but to half the dosage presented in Table 1, as tolerated. If necessary and based upon clinical response, an additional titration to the maximum dosage (20 mg/day or 40 mg/day, depending on weight) may be started on day 21. There is inadequate information about metabolism of clobazam in patients with severe hepatic impairment. Therefore, no dosing recommendation can be given for those patients [see Use in Specific Populations (8.8), Clinical Pharmacology (12 .3)].

SYMPAZAN® Oral Film: Thin, white, rectangular, orally dissolving film strips:

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SYMPAZAN® is contraindicated in patients with a history of hypersensitivity to the drug or its ingredients. Hypersensitivity reactions have included serious dermatological reactions [see Warnings and Precautions (5.6)].

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Concomitant use of benzodiazepines, including SYMPAZAN®, and opioids may result in profound sedation, respiratory depression, coma, and death. Because of these risks, reserve concomitant prescribing of benzodiazepines and opioids in patients for whom alternative treatment options are inadequate.

Observational studies have demonstrated that concomitant use of opioid analgesics and benzodiazepines increases the risk of drug-related mortality compared to use of opioids alone. If a decision is made to prescribe SYMPAZAN® concomitantly with opioids, prescribe the lowest effective dosages and minimum durations of concomitant use, and follow patients closely for signs and symptoms of respiratory depression and sedation. Advise both patients and caregivers about the risks of respiratory depression and sedation when SYMPAZAN®  is used with opioids [see Drug Interactions (7.1)].

The use of benzodiazepines, including SYMPAZAN, exposes users to the risks of abuse, misuse, and addiction, which can lead to overdose or death. Abuse and misuse of benzodiazepines often (but not always) involve the use of doses greater than the maximum recommended dosage and commonly involve concomitant use of other medications, alcohol, and/or illicit substances, which is associated with an increased frequency of serious adverse outcomes, including respiratory depression, overdose, or death [see Drug Abuse and Dependence (9.2)].

Before prescribing SYMPAZAN and throughout treatment, assess each patient’s risk for abuse, misuse, and addiction (e.g., using a standardized screening tool). Use of SYMPAZAN, particularly in patients at elevated risk, necessitates counseling about the risks and proper use of SYMPAZAN along with monitoring for signs and symptoms of abuse, misuse, and addiction. Prescribe the lowest effective dosage; avoid or minimize concomitant use of CNS depressants and other substances associated with abuse, misuse, and addiction (e.g., opioid analgesics, stimulants); and advise patients on the proper disposal of unused drug. If a substance use disorder is suspected, evaluate the patient and institute (or refer them for) early treatment, as appropriate.

To reduce the risk of withdrawal reactions, use a gradual taper to discontinue SYMPAZAN or reduce the dosage [see Dosage and Administration (2.2)].

Patients at an increased risk of withdrawal adverse reactions after benzodiazepine discontinuation or rapid dosage reduction include those who take higher dosages, and those who have had longer durations of use.

Acute Withdrawal Reactions The continued use of benzodiazepines, including SYMPAZAN, may lead to clinically significant physical dependence. Abrupt discontinuation or rapid dosage reduction of SYMPAZAN after continued use, or administration of flumazenil (a benzodiazepine antagonist) may precipitate acute withdrawal reactions, which can be life-threatening (e.g., seizures) [see Drug Abuse and Dependence (9.3)].

Protracted Withdrawal Syndrome In some cases, benzodiazepine users have developed a protracted withdrawal syndrome with withdrawal symptoms lasting weeks to more than 12 months [see Drug Abuse and Dependence (9.3)].

Since SYMPAZAN® has a central nervous system (CNS) depressant effect, patients or their caregivers should be cautioned against simultaneous use with other CNS depressant drugs or alcohol, and cautioned that the effects of other CNS depressant drugs or alcohol may be potentiated [see Drug Interactions (7.2)].

SYMPAZAN® causes somnolence and sedation. In clinical trials, somnolence or sedation was reported at all effective doses and was dose-related [see Adverse Reactions (6.1)].

In general, somnolence and sedation begin within the first month of treatment and may diminish with continued treatment. Prescribers should monitor patients for somnolence and sedation, particularly with concomitant use of other central nervous system depressants. Prescribers should caution patients against engaging in hazardous activities requiring mental alertness, such as operating dangerous machinery or motor vehicles, until the effect of SYMPAZAN® is known.

Serious skin reactions, including Stevens-Johnson Syndrome (SJS) and toxic epidermal necrolysis (TEN), have been reported with clobazam in both children and adults during the post-marketing period. Patients should be closely monitored for signs or symptoms of SJS/TEN, especially during the first 8 weeks of treatment initiation or when re-introducing therapy. SYMPAZAN® should be discontinued at the first sign of rash, unless the rash is clearly not drug-related. If signs or symptoms suggest SJS/TEN, use of this drug should not be resumed and alternative therapy should be considered [see Contraindications (4)].

Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS), also known as multiorgan hypersensitivity, has been reported in patients taking antiepileptic drugs, including clobazam. These events can be fatal or life-threatening, particularly if diagnosis and treatment do not occur as early as possible. DRESS typically, although not exclusively, presents with fever, rash, lymphadenopathy, and/or facial swelling, in association with other organ system involvement, such as hepatitis, nephritis, hematological abnormalities, myocarditis, or myositis, sometimes resembling an acute viral infection. Eosinophilia is often present. Because this disorder is variable in its expression, other organ systems not noted here may be involved. It is important to note that early manifestations of hypersensitivity, such as fever or lymphadenopathy, may be present even though rash is not evident. If such signs or symptoms are present, the patient should be evaluated immediately. SYMPAZAN should be discontinued if an alternative etiology for the signs or symptoms cannot be established [see Contraindications (4)].

Antiepileptic drugs (AEDs), including SYMPAZAN®, increase the risk of suicidal thoughts or behavior in patients taking these drugs for any indication. Patients treated with any AED for any indication should be monitored for the emergence or worsening of depression, suicidal thoughts or behavior, and/or any unusual changes in mood or behavior.

Pooled analyses of 199 placebo-controlled clinical trials (mono- and adjunctive therapy) of 11 different AEDs showed that patients randomized to one of the AEDs had approximately twice the risk (adjusted relative risk 1.8, 95% confidence interval [CI]: 1.2, 2.7) of suicidal thinking or behavior compared to patients randomized to placebo. In these trials, which had a median treatment duration of 12 weeks, the estimated incidence rate of suicidal behavior or ideation among 27,863 AED-treated patients was 0.43%, compared to 0.24% among 16,029 placebo-treated patients, representing an increase of approximately one case of suicidal thinking or behavior for every 530 patients treated. There were four suicides in drug-treated patients in the trials and none in placebo-treated patients, but the number is too small to allow any conclusion about drug effect on suicide.

The increased risk of suicidal thoughts or behavior with AEDs was observed as early as one week after starting drug treatment with AEDs and persisted for the duration of treatment assessed. Because most trials included in the analysis did not extend beyond 24 weeks, the risk of suicidal thoughts or behavior beyond 24 weeks could not be assessed.

The risk of suicidal thoughts or behavior was generally consistent among drugs in the data analyzed. The finding of increased risk with AEDs of varying mechanisms of action and across a range of indications suggests that the risk applies to all AEDs used for any indication. The risk did not vary substantially by age (5-100 years) in the clinical trials analyzed. Table 2 shows absolute and relative risk by indication for all evaluated AEDs.

<div class="scrollingtable"><table> <colgroup> <col width="121"/> <col width="144"/> <col width="144"/> <col width="192"/> <col width="138"/> </colgroup> <tbody class="Headless"> <tr class="First"> <td align="center" class="Lrule Rrule Toprule" colspan="5"><span class="Bold">Table 2</span><span class="Bold">: </span><span class="Bold">Risk by Indication for Antiepileptic Drugs in the Pooled Analysis</span></td> </tr> <tr> <td class="Lrule Rrule Toprule"> <br/> <span class="Bold">Indication</span></td><td align="center" class="Lrule Rrule Toprule"><span class="Bold">Placebo </span><span class="Bold">Patients </span> <br/> <span class="Bold">with </span> <br/> <span class="Bold">Events per 1000</span> <br/> <span class="Bold">Patients</span></td><td align="center" class="Lrule Rrule Toprule"> <br/> <span class="Bold">Drug Patients with Events per 1000</span> <br/> <span class="Bold">Patients</span></td><td align="center" class="Lrule Rrule Toprule"><span class="Bold">Relative Risk: Incidence</span> <br/> <span class="Bold">of Drug</span> <br/> <span class="Bold">Events in Drug</span> <br/> <span class="Bold">Patients/Incidence</span> <br/> <span class="Bold">in Placebo Patients</span></td><td align="center" class="Lrule Rrule Toprule"><span class="Bold">Risk Difference:</span> <br/> <span class="Bold">Additional</span> <br/> <span class="Bold">Drug Patients with Events</span> <br/> <span class="Bold">per 1000 Patients</span></td> </tr> <tr> <td class="Lrule Rrule Toprule">Epilepsy</td><td align="center" class="Lrule Rrule Toprule">1.0</td><td align="center" class="Lrule Rrule Toprule">3.4</td><td align="center" class="Lrule Rrule Toprule">3.5</td><td align="center" class="Lrule Rrule Toprule">2.4</td> </tr> <tr> <td class="Lrule Rrule Toprule">Psychiatric</td><td align="center" class="Lrule Rrule Toprule">5.7</td><td align="center" class="Lrule Rrule Toprule">8.5</td><td align="center" class="Lrule Rrule Toprule">1.5</td><td align="center" class="Lrule Rrule Toprule">2.9</td> </tr> <tr> <td class="Lrule Rrule Toprule">Other</td><td align="center" class="Lrule Rrule Toprule">1.0</td><td align="center" class="Lrule Rrule Toprule">1.8</td><td align="center" class="Lrule Rrule Toprule">1.9</td><td align="center" class="Lrule Rrule Toprule">0.9</td> </tr> <tr class="Last"> <td class="Lrule Rrule Toprule">Total</td><td align="center" class="Lrule Rrule Toprule">2.4</td><td align="center" class="Lrule Rrule Toprule">4.3</td><td align="center" class="Lrule Rrule Toprule">1.8</td><td align="center" class="Lrule Rrule Toprule">1.9</td> </tr> </tbody> </table></div>

The relative risk for suicidal thoughts or behavior was higher in clinical trials for epilepsy than in clinical trials for psychiatric or other conditions, but the absolute risk differences were similar for the epilepsy and psychiatric indications.

Anyone considering prescribing SYMPAZAN® or any other AED must balance the risk of suicidal thoughts or behavior with the risk of untreated illness. Epilepsy and many other illnesses for which AEDs are prescribed are themselves associated with morbidity and mortality and an increased risk of suicidal thoughts and behavior. Should suicidal thoughts and behavior emerge during treatment, the prescriber needs to consider whether the emergence of these symptoms in any given patient may be related to the illness being treated.

Use of SYMPAZAN late in pregnancy can result in sedation (respiratory depression, lethargy, hypotonia) and/or withdrawal symptoms (hyperreflexia, irritability, restlessness, tremors, inconsolable crying, and feeding difficulties) in the neonate [see Use in Specific Populations (8.1)]. Monitor neonates exposed to SYMPAZAN during pregnancy or labor for signs of sedation and monitor neonates exposed to SYMPAZAN during pregnancy for signs of withdrawal; manage these neonates accordingly.

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The following adverse events have been reported in clinical trials of patients treated with clobazam, the active ingredient of SYMPAZAN®.

During its development for the adjunctive treatment of seizures associated with LGS, clobazam was administered to 333 healthy volunteers and 300 patients with a current or prior diagnosis of LGS, including 197 patients treated for 12 months or more. The conditions and duration of exposure varied greatly and included single- and multiple-dose clinical pharmacology studies in healthy volunteers and two double-blind studies in patients with LGS (Study 1 and 2) [see Clinical Studies (14)]. Only Study 1 included a placebo group, allowing comparison of adverse reaction rates on clobazam at several doses to placebo.

Adverse Reactions Leading to Discontinuation in an LGS Placebo Controlled Clinical Trial (Study 1) The adverse reactions associated with clobazam treatment discontinuation in ≥1% of patients in decreasing order of frequency included lethargy, somnolence, ataxia, aggression, fatigue, and insomnia.

Most Common Adverse Reactions in an LGS Placebo Controlled Clinical Trial (Study 1) Table 3 lists the adverse reactions that occurred in ≥5% of clobazam-treated patients (at any dose), and at a rate greater than placebo-treated patients, in the randomized, double-blind, placebo-controlled, parallel group clinical study of adjunctive AED therapy for 15 weeks (Study 1).

<div class="scrollingtable"><table> <colgroup> <col width="143"/> <col width="2"/> <col width="70"/> <col width="80"/> <col width="90"/> <col width="76"/> <col width="90"/> <col width="156"/> </colgroup> <tbody class="Headless"> <tr class="First"> <td align="center" class="Lrule Rrule Toprule" colspan="8"><span class="Bold">Table 3: </span><span class="Bold">Adverse Reactions Reported for ≥5% of Patients and More Frequently than Placebo in Any Treatment Group</span></td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="2"></td><td align="center" class="Lrule Rrule Toprule"></td><td align="center" class="Lrule Rrule Toprule" colspan="4"><span class="Bold">Clobazam Dose Level</span></td><td align="center" class="Lrule Rrule Toprule"><span class="Bold">All </span> <br/> <span class="Bold">Clobazam</span> <br/> <span class="Bold">N=179</span> <br/>%</td> </tr> <tr> <td class="Lrule Rrule" colspan="2"></td><td align="center" class="Lrule Rrule"><span class="Bold">Placebo</span> <br/> <span class="Bold">N=59</span> <br/>%</td><td align="center" class="Lrule Rrule Toprule" valign="bottom"><span class="Bold">Low</span><span class="Bold"><span class="Sup">a</span></span> <br/> <span class="Bold">N=58</span> <br/>%</td><td align="center" class="Lrule Rrule Toprule" colspan="2" valign="bottom"><span class="Bold">Medium</span><span class="Bold"><span class="Sup">b</span></span> <br/> <span class="Bold">N=62</span> <br/>%</td><td align="center" class="Lrule Rrule Toprule" valign="bottom"><span class="Bold">High</span><span class="Bold"><span class="Sup">c</span></span> <br/> <span class="Bold">N=59</span> <br/>%</td><td class="Lrule Rrule"></td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="8"><span class="Bold">Gastrointestinal Disorders</span></td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="2">Vomiting</td><td align="center" class="Lrule Rrule Toprule">  5</td><td align="center" class="Lrule Rrule Toprule">  9</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  5</td><td align="center" class="Lrule Rrule Toprule">  7</td><td align="center" class="Lrule Rrule Toprule">  7</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="2">Constipation</td><td align="center" class="Lrule Rrule Toprule">  0</td><td align="center" class="Lrule Rrule Toprule">  2</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  2</td><td align="center" class="Lrule Rrule Toprule">  10</td><td align="center" class="Lrule Rrule Toprule">  5</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="2">Dysphagia</td><td align="center" class="Lrule Rrule Toprule">  0</td><td align="center" class="Lrule Rrule Toprule">  0</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  0</td><td align="center" class="Lrule Rrule Toprule">  5</td><td align="center" class="Lrule Rrule Toprule">  2</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="8"><span class="Bold">General Disorders and Administration Site Conditions</span></td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="2">Pyrexia</td><td align="center" class="Lrule Rrule Toprule">  3</td><td align="center" class="Lrule Rrule Toprule">  17</td><td align="center" class="Lrule Rrule Toprule">  10</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  12</td><td align="center" class="Lrule Rrule Toprule">  13</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="2">Irritability</td><td align="center" class="Lrule Rrule Toprule">  5</td><td align="center" class="Lrule Rrule Toprule">  3</td><td align="center" class="Lrule Rrule Toprule">  11</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  5</td><td align="center" class="Lrule Rrule Toprule">  7</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="2">Fatigue</td><td align="center" class="Lrule Rrule Toprule">  2</td><td align="center" class="Lrule Rrule Toprule">  5</td><td align="center" class="Lrule Rrule Toprule">  5</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  3</td><td align="center" class="Lrule Rrule Toprule">  5</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="8"><span class="Bold">Infections and Infestations</span></td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="2">Upper respiratory tract infection</td><td align="center" class="Lrule Rrule Toprule">  10</td><td align="center" class="Lrule Rrule Toprule">  10</td><td align="center" class="Lrule Rrule Toprule">  13</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  14</td><td align="center" class="Lrule Rrule Toprule">  12</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="2">Pneumonia</td><td align="center" class="Lrule Rrule Toprule">  2</td><td align="center" class="Lrule Rrule Toprule">  3</td><td align="center" class="Lrule Rrule Toprule">  3</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  7</td><td align="center" class="Lrule Rrule Toprule">  4</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="2">Urinary tract infection</td><td align="center" class="Lrule Rrule Toprule">  0</td><td align="center" class="Lrule Rrule Toprule">  2</td><td align="center" class="Lrule Rrule Toprule">  5</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  5</td><td align="center" class="Lrule Rrule Toprule">  4</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="2">Bronchitis</td><td align="center" class="Lrule Rrule Toprule">  0</td><td align="center" class="Lrule Rrule Toprule">  2</td><td align="center" class="Lrule Rrule Toprule">  0</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  5</td><td align="center" class="Lrule Rrule Toprule">  2</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="8"><span class="Bold">Metabolism and Nutrition Disorders</span></td> </tr> <tr> <td class="Lrule Rrule Toprule">Decreased appetite</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  3</td><td align="center" class="Lrule Rrule Toprule">  3</td><td align="center" class="Lrule Rrule Toprule">  0</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  7</td><td align="center" class="Lrule Rrule Toprule">  3</td> </tr> <tr> <td class="Lrule Rrule Toprule">Increased appetite</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  0</td><td align="center" class="Lrule Rrule Toprule">  2</td><td align="center" class="Lrule Rrule Toprule">  3</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  5</td><td align="center" class="Lrule Rrule Toprule">  3</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="8"><span class="Bold">Nervous System Disorders</span></td> </tr> <tr> <td class="Lrule Rrule Toprule">Somnolence or Sedation</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  15</td><td align="center" class="Lrule Rrule Toprule">  17</td><td align="center" class="Lrule Rrule Toprule">  27</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  32</td><td align="center" class="Lrule Rrule Toprule">  26</td> </tr> <tr> <td class="Lrule Rrule Toprule">Somnolence</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  12</td><td align="center" class="Lrule Rrule Toprule">  16</td><td align="center" class="Lrule Rrule Toprule">  24</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  25</td><td align="center" class="Lrule Rrule Toprule">  22</td> </tr> <tr> <td class="Lrule Rrule Toprule">Sedation</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  3</td><td align="center" class="Lrule Rrule Toprule">  2</td><td align="center" class="Lrule Rrule Toprule">  3</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  9</td><td align="center" class="Lrule Rrule Toprule">  5</td> </tr> <tr> <td class="Lrule Rrule Toprule">Lethargy</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  5</td><td align="center" class="Lrule Rrule Toprule">  10</td><td align="center" class="Lrule Rrule Toprule">  5</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  15</td><td align="center" class="Lrule Rrule Toprule">  10</td> </tr> <tr> <td class="Lrule Rrule Toprule">Drooling</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  3</td><td align="center" class="Lrule Rrule Toprule">  0</td><td align="center" class="Lrule Rrule Toprule">  13</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  14</td><td align="center" class="Lrule Rrule Toprule">  9</td> </tr> <tr> <td class="Lrule Rrule Toprule">Ataxia</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  3</td><td align="center" class="Lrule Rrule Toprule">  3</td><td align="center" class="Lrule Rrule Toprule">  2</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  10</td><td align="center" class="Lrule Rrule Toprule">  5</td> </tr> <tr> <td class="Lrule Rrule Toprule">Psychomotor hyperactivity</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  3</td><td align="center" class="Lrule Rrule Toprule">  3</td><td align="center" class="Lrule Rrule Toprule">  3</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  5</td><td align="center" class="Lrule Rrule Toprule">  4</td> </tr> <tr> <td class="Lrule Rrule Toprule">Dysarthria</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  0</td><td align="center" class="Lrule Rrule Toprule">  2</td><td align="center" class="Lrule Rrule Toprule">  2</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  5</td><td align="center" class="Lrule Rrule Toprule">  3</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="8"><span class="Bold">Psychiatric Disorders</span></td> </tr> <tr> <td class="Lrule Rrule Toprule">Aggression</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  5</td><td align="center" class="Lrule Rrule Toprule">  3</td><td align="center" class="Lrule Rrule Toprule">  8</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  14</td><td align="center" class="Lrule Rrule Toprule">  8</td> </tr> <tr> <td class="Lrule Rrule Toprule">Insomnia</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  2</td><td align="center" class="Lrule Rrule Toprule">  2</td><td align="center" class="Lrule Rrule Toprule">  5</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  7</td><td align="center" class="Lrule Rrule Toprule">  5</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="8"><span class="Bold">Respiratory Disorders</span></td> </tr> <tr class="Last"> <td class="Lrule Rrule Toprule">Cough</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  0</td><td align="center" class="Lrule Rrule Toprule">  3</td><td align="center" class="Lrule Rrule Toprule">  5</td><td align="center" class="Lrule Rrule Toprule" colspan="2">  7</td><td align="center" class="Lrule Rrule Toprule">  5</td> </tr> </tbody> </table></div>

a Maximum daily dose of 5 mg for ≤30 kg body weight; 10 mg for >30 kg body weight b Maximum daily dose of 10 mg for ≤30 kg body weight; 20 mg for >30 kg body weight c Maximum daily dose of 20 mg for ≤30 kg body weight; 40 mg for >30 kg body weight

The following adverse reactions have been identified during post-approval use of clobazam tablets. These reactions are reported voluntarily from a population of uncertain size; therefore, it is not possible to estimate their frequency or establish a causal relationship to drug exposure. Adverse reactions are categorized by system organ class.

Blood Disorders: Anemia, eosinophilia, leukopenia, thrombocytopenia Eye Disorders: Diplopia, vision blurred Gastrointestinal Disorders: Abdominal distention General Disorders and Administration Site Conditions: Hypothermia Investigations: Hepatic enzyme increased Musculoskeletal: Muscle spasms Psychiatric Disorders: Agitation, anxiety, apathy, confusional state, depression, delirium, delusion, hallucination Renal and Urinary Disorders: Urinary retention Respiratory Disorders: Aspiration, respiratory depression Skin and Subcutaneous Tissue Disorders: Rash, urticaria, angioedema, and facial and lip edema

The concomitant use of benzodiazepines and opioids increases the risk of respiratory depression because of actions at different receptor sites in the CNS that control respiration. Benzodiazepines interact at GABAA sites, and opioids interact primarily at mu receptors. When benzodiazepines and opioids are combined, the potential for benzodiazepines to significantly worsen opioid-related respiratory depression exists. Limit dosage and duration of concomitant use of benzodiazepines and opioids, and follow patients closely for respiratory depression and sedation [see Warnings and Precautions (5.1)].

Concomitant use of SYMPAZAN® with other CNS depressants may increase the risk of sedation and somnolence [see Warnings and Precautions (5.4)].

Alcohol, as a CNS depressant, will interact with SYMPAZAN® in a similar way and also increases clobazam's maximum plasma exposure by approximately 50%. Therefore, caution patients or their caregivers against simultaneous use with other CNS depressant drugs or alcohol, and caution that the effects of other CNS depressant drugs or alcohol may be potentiated [see Warnings and Precautions (5.4)].

Hormonal Contraceptives

SYMPAZAN® is a weak CYP3A4 inducer. As some hormonal contraceptives are metabolized by CYP3A4, their effectiveness may be diminished when given with SYMPAZAN®. Additional non-hormonal forms of contraception are recommended when using SYMPAZAN® [see Clinical Pharmacology (12.3), Patient Counseling Information (17)].

Drugs Metabolized by CYP2D6

SYMPAZAN® inhibits CYP2D6. Dose adjustment of drugs metabolized by CYP2D6 may be necessary [see Clinical Pharmacology (12.3)].

Strong and Moderate Inhibitors of CYP2C19 Coadministration with strong or moderate inhibitors of CYP2C19 may result in increased exposure to N-desmethylclobazam, the active metabolite of clobazam. This may increase the risk of dose-related adverse reactions. Dosage adjustment of SYMPAZAN® may be necessary when co-administered with strong CYP2C19 inhibitors (e.g., fluconazole, fluvoxamine, ticlopidine) or moderate CYP2C19 inhibitors (e.g., omeprazole) [see Clinical Pharmacology (12.3)].

Effect of Cannabidiol on SYMPAZAN®

Coadministration of cannabidiol, a CYP3A4 and CYP2C19 substrate and a CYP2C19 inhibitor, with clobazam may increase the risk of clobazam-related adverse reactions [see Warnings and Precautions (5.4, 5.5), Clinical Pharmacology (12.3)]. Consider a reduction in dosage of cannabidiol or clobazam if adverse reactions known to occur with SYMPAZAN are experienced.

Pregnancy Exposure Registry

There is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to AEDs, such as SYMPAZAN®, during pregnancy. Healthcare providers are encouraged to recommend that pregnant women taking SYMPAZAN® enroll in the North American Antiepileptic Drug (NAAED) Pregnancy Registry by calling 1-888-233-2334 or online at http://www.aedpregnancyregistry.org/

Risk Summary

Neonates born to mothers using benzodiazepines late in pregnancy have been reported to experience symptoms of sedation and/or neonatal withdrawal [see Warnings and Precautions (5.9) and Clinical Considerations]. Available data from published observational studies of pregnant women exposed to benzodiazepines do not report a clear association with benzodiazepines and major birth defects (see Data). Administration of clobazam to pregnant rats and rabbits during the period of organogenesis or to rats throughout pregnancy and lactation resulted in developmental toxicity, including increased incidences of fetal malformations and mortality, at plasma exposures for clobazam and its major active metabolite, N-desmethylclobazam, below those expected at therapeutic doses in patients [see Animal Data].

Data for other benzodiazepines suggest the possibility of long-term effects on neurobehavioral and immunological function in animals following prenatal exposure to benzodiazepines at clinically relevant doses.

The background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2%-4% and 15% -20%, respectively.

Clinical Considerations

Fetal/Neonatal Adverse Reactions

Benzodiazepines cross the placenta and may produce respiratory depression, hypotonia, and sedation in neonates. Monitor neonates exposed to SYMPAZAN during pregnancy or labor for signs of sedation, respiratory depression, hypotonia, and feeding problems. Monitor neonates exposed to SYMPAZAN during pregnancy for signs of withdrawal. Manage these neonates accordingly [see Warnings and Precautions (5.9)].

Data

Human Data

Published data from observational studies on the use of benzodiazepines during pregnancy do not report a clear association with benzodiazepines and major birth defects. Although early studies reported an increased risk of congenital malformations with diazepam and chlordiazepoxide, there was no consistent pattern noted. In addition, the majority of more recent case-control and cohort studies of benzodiazepine use during pregnancy, which were adjusted for confounding exposures to alcohol, tobacco and other medications, have not confirmed these findings.

Animal Data

In a study in which clobazam (0, 150, 450, or 750 mg/kg/day) was orally administered to pregnant rats throughout the period of organogenesis, embryofetal mortality and incidences of fetal skeletal variations were increased at all doses. The low-effect dose for embryofetal developmental toxicity in rats (150 mg/kg/day) was associated with plasma exposures (AUC) for clobazam and its major active metabolite, N-desmethylclobazam, lower than those in humans at the maximum recommended human dose (MRHD) of 40 mg/day.

Oral administration of clobazam (0, 10, 30, or 75 mg/kg/day) to pregnant rabbits throughout the period of organogenesis resulted in decreased fetal body weights, and increased incidences of fetal malformations (visceral and skeletal) at the mid and high doses, and an increase in embryofetal mortality at the high dose. Incidences of fetal variations were increased at all doses. The highest dose tested was associated with maternal toxicity (ataxia and decreased activity). The low effect dose for embryofetal developmental toxicity in rabbits (10 mg/kg/day) was associated with plasma exposures for clobazam and N-desmethylclobazam lower than those in humans at the MRHD.

Oral administration of clobazam (0, 50, 350, or 750 mg/kg/day) to rats throughout pregnancy and lactation resulted in increased embryofetal mortality at the high dose, decreased pup survival at the mid and high doses and alterations in offspring behavior (locomotor activity) at all doses. The low-effect dose for adverse effects on preand postnatal development in rats (50 mg/kg/day) was associated with plasma exposures for clobazam and N-desmethylclobazam lower than those in humans at the MRHD.

Risk Summary

SYMPAZAN® is excreted in human milk (see Data). There are reports of sedation, poor feeding and poor weight gain in infants exposed to benzodiazepines through breast milk. There are no data on the effects of clobazam on milk production.

The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for SYMPAZAN® and any potential adverse effects on the breastfed infant from SYMPAZAN® or from the underlying maternal condition.

Clinical Considerations

Adverse reactions such as somnolence and difficulty feeding have been reported in infants during breastfeeding in postmarketing experience with clobazam. Infants exposed to SYMPAZAN through breast milk should be monitored for sedation, poor feeding and poor weight gain.

Data

Scientific literature on clobazam use during lactation is limited. After short-term administration, clobazam and N-desmethylclobazam are transferred into breast milk.

Administration of clobazam to rats prior to and during mating and early gestation resulted in adverse effects on fertility and early embryonic development at plasma exposures for clobazam and its major active metabolite, N-desmethylclobazam, below those in humans at the MRHD [see Nonclinical Toxicology (13.1)].

Safety and effectiveness for the adjunctive treatment of seizures associated with Lennox-Gastaut syndrome in pediatric patients 2 years of age and older have been established in two adequate and well-controlled studies [see Clinical Studies (14)].

Safety and effectiveness in patients less than 2 years of age have not been established.

Juvenile Animal Data

In a study in which clobazam (0, 4, 36, or 120 mg/kg/day) was orally administered to rats during the juvenile period of development (postnatal days 14 to 48), adverse effects on growth (decreased bone density and bone length) and behavior (altered motor activity and auditory startle response; learning deficit) were observed at the high dose. The effect on bone density, but not on behavior, was reversible when drug was discontinued. The no-effect level for juvenile toxicity (36 mg/kg/day) was associated with plasma exposures (AUC) to clobazam and its major active metabolite, N-desmethylclobazam, less than those expected at therapeutic doses in pediatric patients.

Clinical studies of clobazam did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. However, elderly subjects appear to eliminate clobazam more slowly than younger subjects based on population pharmacokinetic analysis. For these reasons, dosage modification is recommended [see Dosage and Administration (2.4), Clinical Pharmacology (12.3)].

Concentrations of clobazam's active metabolite, N-desmethylclobazam, are higher in CYP2C19 poor metabolizers than in extensive metabolizers. For this reason, dosage modification is recommended [see Dosage and Administration (2.5), Clinical Pharmacology (12.3)].

The pharmacokinetics of clobazam were evaluated in patients with mild and moderate renal impairment. There were no significant differences in systemic exposure (AUC and Cmax) between patients with mild or moderate renal impairment and healthy subjects. No dose adjustment is required for patients with mild and moderate renal impairment. There is essentially no experience with SYMPAZAN® in patients with severe renal impairment or ESRD. It is not known if clobazam or its active metabolite, N-desmethyl-clobazam, is dialyzable [see Clinical Pharmacology (12.3)].

SYMPAZAN® is hepatically metabolized; however, there are limited data to characterize the effect of hepatic impairment on the pharmacokinetics of clobazam. For this reason, dosage adjustment is recommended in patients with mild to moderate hepatic impairment (Child-Pugh score 5-9) [see Dosage and Administration (2.6)]. There is inadequate information about metabolism of SYMPAZAN® in patients with severe hepatic impairment [see Clinical Pharmacology (12.3)].

SYMPAZAN® contains clobazam, a Schedule IV controlled substance.

SYMPAZAN is a benzodiazepine and a CNS depressant with a potential for abuse and addiction. Abuse is the intentional, non-therapeutic use of a drug, even once, for its desirable psychological or physiological effects. Misuse is the intentional use, for therapeutic purposes, of a drug by an individual in a way other than prescribed by a health care provider or for whom it was not prescribed. Drug addiction is a cluster of behavioral, cognitive, and physiological phenomena that may include a strong desire to take the drug, difficulties in controlling drug use (e.g., continuing drug use despite harmful consequences, giving a higher priority to drug use than other activities and obligations), and possible tolerance or physical dependence. Even taking benzodiazepines as prescribed may put patients at risk for abuse and misuse of their medication. Abuse and misuse of benzodiazepines may lead to addiction.

Abuse and misuse of benzodiazepines often (but not always) involve the use of doses greater than the maximum recommended dosage and commonly involve concomitant use of other medications, alcohol, and/or illicit substances, which is associated with an increased frequency of serious adverse outcomes, including respiratory depression, overdose, or death. Benzodiazepines are often sought by individuals who abuse drugs and other substances, and by individuals with addictive disorders [see Warnings and Precautions (5.2)].

The following adverse reactions have occurred with benzodiazepine abuse and/or misuse: abdominal pain, amnesia, anorexia, anxiety, aggression, ataxia, blurred vision, confusion, depression, disinhibition, disorientation, dizziness, euphoria, impaired concentration and memory, indigestion, irritability, muscle pain, slurred speech, tremors, and vertigo.

The following severe adverse reactions have occurred with benzodiazepine abuse and/or misuse: delirium, paranoia, suicidal ideation and behavior, seizures, coma, breathing difficulty, and death. Death is more often associated with polysubstance use (especially benzodiazepines with other CNS depressants such as opioids and alcohol). The World Health Organization epidemiology database contains reports of drug abuse, misuse, and overdoses associated with clobazam.

Physical Dependence

SYMPAZAN may produce physical dependence from continued therapy. Physical dependence is a state that develops as a result of physiological adaptation in response to repeated drug use, manifested by withdrawal signs and symptoms after abrupt discontinuation or a significant dose reduction of a drug. Abrupt discontinuation or rapid dosage reduction of benzodiazepines or administration of flumazenil, a benzodiazepine antagonist, may precipitate acute withdrawal reactions, including seizures, which can be life-threatening. Patients at an increased risk of withdrawal adverse reactions after benzodiazepine discontinuation or rapid dosage reduction include those who take higher dosages (i.e., higher and/or more frequent doses) and those who have had longer durations of use [see Warnings and Precautions (5.3)].

To reduce the risk of withdrawal reactions, use a gradual taper to discontinue SYMPAZAN or reduce the dosage [see Dosage and Administration (2.2) and Warnings and Precautions (5.3)].

Acute Withdrawal Signs and Symptoms

Acute withdrawal signs and symptoms associated with benzodiazepines have included abnormal involuntary movements, anxiety, blurred vision, depersonalization, depression, derealization, dizziness, fatigue, gastrointestinal adverse reactions (e.g., nausea, vomiting, diarrhea, weight loss, decreased appetite), headache, hyperacusis, hypertension, irritability, insomnia, memory impairment, muscle pain and stiffness, panic attacks, photophobia, restlessness, tachycardia, and tremor. More severe acute withdrawal signs and symptoms, including life-threatening reactions, have included catatonia, convulsions, delirium tremens, depression, hallucinations, mania, psychosis, seizures, and suicidality.

Protracted Withdrawal Syndrome

Protracted withdrawal syndrome associated with benzodiazepines is characterized by anxiety, cognitive impairment, depression, insomnia, formication, motor symptoms (e.g., weakness, tremor, muscle twitches), paresthesia, and tinnitus that persists beyond 4 to 6 weeks after initial benzodiazepine withdrawal. Protracted withdrawal symptoms may last weeks to more than 12 months. As a result, there may be difficulty in differentiating withdrawal symptoms from potential re-emergence or continuation of symptoms for which the benzodiazepine was being used.

Tolerance

Tolerance to SYMPAZAN may develop from continued therapy. Tolerance is a physiological state characterized by a reduced response to a drug after repeated administration (i.e., a higher dose of a drug is required to produce the same effect that was once obtained at a lower dose). Tolerance to the therapeutic effect of SYMPAZAN may develop; however, little tolerance develops to the amnestic reactions and other cognitive impairments caused by benzodiazepines.

Overdosage of benzodiazepines is characterized by central nervous system depression ranging from drowsiness to coma. In mild to moderate cases, symptoms can include drowsiness, confusion, dysarthria, lethargy, hypnotic state, diminished reflexes, ataxia, and hypotonia. Rarely, paradoxical or disinhibitory reactions (including agitation, irritability, impulsivity, violent behavior, confusion, restlessness, excitement, and talkativeness) may occur. In severe overdosage cases, patients may develop respiratory depression and coma. Overdosage of benzodiazepines in combination with other CNS depressants (including alcohol and opioids) may be fatal [see Warnings and Precautions (5.2)]. Markedly abnormal (lowered or elevated) blood pressure, heart rate, or respiratory rate raise the concern that additional drugs and/or alcohol are involved in the overdosage.

In managing benzodiazepine overdosage, employ general supportive measures, including intravenous fluids and airway maintenance. Flumazenil, a specific benzodiazepine receptor antagonist indicated for the complete or partial reversal of the sedative effects of benzodiazepines in the management of benzodiazepine overdosage, can lead to withdrawal and adverse reactions, including seizures, particularly in the context of mixed overdosage with drugs that increase seizure risk (e.g., tricyclic and tetracyclic antidepressants) and in patients with long-term benzodiazepine use and physical dependency. The risk of withdrawal seizures with flumazenil use may be increased in patients with epilepsy. Flumazenil is contraindicated in patients who have received a benzodiazepine for control of a potentially life-threatening condition (e.g., status epilepticus). If the decision is made to use flumazenil, it should be used as an adjunct to, not as a substitute for, supportive management of benzodiazepine overdosage. See the flumazenil injection Prescribing Information.

Consider contacting the Poison Help line (1-800-222-1222) or a medical toxicologist for additional overdosage management recommendations.

SYMPAZAN® contains clobazam, a benzodiazepine derivative, which is chemically known as 7-Chloro-1-methyl-5-phenyl-1H-1,5 benzodiazepine-2,4(3H,5H)-dione with a molecular formula of C16H13ClN2O2, molecular weight of 300.74, and it has the following structural formula:

{ "type": "p", "children": [], "text": "SYMPAZAN® contains clobazam, a benzodiazepine derivative, which is chemically known as 7-Chloro-1-methyl-5-phenyl-1H-1,5 benzodiazepine-2,4(3H,5H)-dione with a molecular formula of C16H13ClN2O2, molecular weight of 300.74, and it has the following structural formula:" }

Clobazam is a white or almost white, crystalline powder with a slightly bitter taste. It is slightly soluble in water and sparingly soluble in ethanol.

{ "type": "p", "children": [], "text": "Clobazam is a white or almost white, crystalline powder with a slightly bitter taste. It is slightly soluble in water and sparingly soluble in ethanol." }

Each SYMPAZAN® Oral Film contains 5 mg, 10 mg or 20 mg of clobazam and the following inactive ingredients: artificial cooling flavor, citric acid, glycerol monooleate, hypromellose, maltitol, natural and artificial bitter masker, natural raspberry type flavor, polyethylene oxide, purified water, sodium phosphate dibasic, and sucralose.

{ "type": "p", "children": [], "text": "Each SYMPAZAN® Oral Film contains 5 mg, 10 mg or 20 mg of clobazam and the following inactive ingredients: artificial cooling flavor, citric acid, glycerol monooleate, hypromellose, maltitol, natural and artificial bitter masker, natural raspberry type flavor, polyethylene oxide, purified water, sodium phosphate dibasic, and sucralose." }

The exact mechanism of action for clobazam, a 1,5-benzodiazepine, is not fully understood but is thought to involve potentiation of GABAergic neurotransmission resulting from binding at the benzodiazepine site of the GABAA receptor.

Effects on Electrocardiogram The effect of clobazam 20 mg and 80 mg administered twice daily on QTc interval was evaluated in a randomized, evaluator-blinded, placebo-, and active-controlled (moxifloxacin 400 mg) parallel thorough QT study in 280 healthy subjects. In a study with demonstrated ability to detect small effects, the upper bound of the one-sided 95% confidence interval for the largest placebo adjusted, baseline-corrected QTc based on the Fridericia correction method was below 10 ms, the threshold for regulatory concern. Thus, at a dose two times the maximum recommended dose, clobazam did not prolong the QTc interval to any clinically relevant extent.

SYMPAZAN® Oral Films at single doses of 10 mg and 20 mg clobazam have been shown to be bioequivalent (Cmax and AUC) to clobazam tablets at equivalent doses. Following single-dose administration of SYMPAZAN®, peak plasma levels (Cmax) and the area under the curve (AUC) of clobazam are dose-proportional over the dose range of 10-20 mg. Based on a population pharmacokinetic analysis with clobazam tablets, the pharmacokinetics of clobazam are linear from 5-160 mg/day. Clobazam is converted to N-desmethylclobazam which has about 1/5 the activity of clobazam. The estimated mean elimination half-lives (t1/2) of clobazam and N-desmethylclobazam were 36-42 hours and 71-82 hours, respectively.

Absorption

The time to peak concentrations (Tmax) of SYMPAZAN® clobazam oral film under fasted conditions ranged from 0.33 to 4.0 hours after single-dose administration. The administration of clobazam tablets with food does not affect absorption. Although not studied, the oral bioavailability of SYMPAZAN® oral film is unlikely to be affected under fed conditions.

Distribution

Clobazam is lipophilic and distributes rapidly throughout the body. The apparent volume of distribution at steady state was approximately 100 L. The in vitro plasma protein binding of clobazam and N-desmethylclobazam is approximately 80-90% and 70%, respectively.

Metabolism and Excretion

Clobazam is extensively metabolized in the liver, with approximately 2% of the dose recovered in urine and 1% in feces as unchanged drug. The major metabolic pathway of clobazam involves N-demethylation, primarily by CYP3A4 and to a lesser extent by CYP2C19 and CYP2B6. N-desmethylclobazam, an active metabolite, is the major circulating metabolite in humans, and at therapeutic doses, plasma concentrations are 3-5 times higher than those of the parent compound. Based on animal and in vitro receptor binding data, estimates of the relative potency of N-desmethylclobazam compared to parent compound range from 1/5 to equal potency. N-desmethylclobazam is extensively metabolized, mainly by CYP2C19. N-desmethylclobazam and its metabolites comprise ~94% of the total drug-related components in urine. Following a single oral dose of radiolabeled drug, approximately 11% of the dose was excreted in the feces and approximately 82% was excreted in the urine.

The polymorphic CYP2C19 is the major contributor to the metabolism of the pharmacologically active N-desmethylclobazam [see Clinical Pharmacology (12.5)]. In CYP2C19 poor metabolizers, levels of N-desmethylclobazam were 5-fold higher in plasma and 2- to 3-fold higher in the urine than in CYP2C19 extensive metabolizers.

Pharmacokinetics in Specific Populations

Age Population pharmacokinetic analyses showed that the clearance of clobazam is lower in elderly subjects compared to other age groups (ages less than 64). Dosing should be adjusted in the elderly [see Dosage and Administration (2.4)].

Sex Population pharmacokinetic analyses showed no difference in the clearance of clobazam between women and men.

Race Population pharmacokinetic analyses including Caucasian (75%), African American (15%), and Asian (9%) subjects showed that there is no evidence of clinically significant effect of race on the clearance of clobazam.

Renal Impairment The effect of renal impairment on the pharmacokinetics of clobazam was evaluated in patients with mild (creatinine clearance [CLCR] >50 to 80 mL/min; N=6) and moderate (CLCR=30 to 50 mL/min; N=6) renal dysfunction, with matching healthy controls (N=6), following administration of multiple doses of clobazam 20 mg/day. There were insignificant changes in Cmax (3-24%) and AUC (≤13%) for clobazam or N-desmethylclobazam in patients with mild or moderate renal impairment compared to patients with normal renal function. Patients with severe renal impairment or ESRD were not included in this study.

Hepatic Impairment There are limited data to characterize the effect of hepatic impairment on the pharmacokinetics of clobazam. In a small study, the pharmacokinetics of a 20 mg single oral dose of clobazam in 9 patients with liver impairment were compared to healthy controls (N=6). The Cmax and the mean plasma clearance of clobazam, as well as the Cmax of N-desmethylclobazam, showed no significant change compared to the healthy controls. The AUC values of N-desmethylclobazam in these patients were not available. Adjust dosage in patients with hepatic impairment [see Dosage and Administration (2.6)].

Drug Interaction Studies

In vitro studies:Clobazam did not inhibit CYP1A2, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP3A4, UGT1A1, UGT1A4, UGT1A6, or UGT2B4 in vitro. N-desmethylclobazam showed weak inhibition of CYP2C9, UGT1A4, UGT1A6 and UGT2B4.

Clobazam and N-desmethylclobazam did not significantly increase CYP1A2 or CYP2C19 activities, but did induce CYP3A4 activity in a concentration-dependent manner. Clobazam and N-desmethylclobazam also increased UGT1A1 mRNA but at concentrations much higher than therapeutic levels. The potential for clobazam or N-desmethylclobazam to induce CYP2B6 and CYP2C8 has not been evaluated.

Clobazam and N-desmethylclobazam do not inhibit P-glycoprotein (P-gp), but are P-gp substrates.

In vivo studies:

Potential for Clobazam to Affect Other Drugs The effect of repeated 40 mg once-daily doses of clobazam on the pharmacokinetic profiles of single-dose dextromethorphan (CYP2D6 substrate), midazolam (CYP3A4 substrate), caffeine (CYP1A2 substrate), and tolbutamide (CYP2C9 substrate), was studied when these probe substrates were given as a drug cocktail (N=18).

Clobazam increased AUC and Cmax of dextromethorphan by 90% and 59%, respectively, reflecting its inhibition of CYP2D6 in vivo. Drugs metabolized by CYP2D6 may require dose adjustment when used with clobazam.

Clobazam decreased the AUC and Cmax of midazolam by 27% and 24%, respectively, and increased the AUC and Cmax of the metabolite 1-hydroxymidazolam by 4-fold and 2-fold, respectively. This level of induction does not call for dosage adjustment of drugs that are primarily metabolized by CYP3A4 when used concomitantly with clobazam. Some hormonal contraceptives are metabolized by CYP3A4 and their effectiveness may be diminished when given with SYMPAZAN®[see Drug Interactions (7.3)]. Repeated clobazam doses had no effect on caffeine and tolbutamide.

A population pharmacokinetic analysis indicated clobazam did not affect the exposure of valproic acid (a CYP2C9/2C19 substrate) or lamotrigine (a UGT substrate).

Potential for Other Drugs to Affect SYMPAZAN® Co-administration of ketoconazole (a strong CYP3A4 inhibitor) 400 mg once-daily for 5 days increased clobazam AUC by 54%, with an insignificant effect on clobazam Cmax. There was no significant change in AUC and Cmax of N-desmethylclobazam (N=18).

Strong (e.g., fluconazole, fluvoxamine, ticlopidine) and moderate (e.g., omeprazole) inhibitors of CYP2C19 may result in up to a 5-fold increase in exposure to N-desmethylclobazam, the active metabolite of clobazam, based on extrapolation from pharmacogenomic data [see Clinical Pharmacology (12.5)]. Dosage adjustment of SYMPAZAN® may be necessary when co-administered with strong or moderate CYP2C19 inhibitors [see Drug Interactions (7.4)].

Coadministration of cannabidiol (a CYP3A4 and CYP2C19 substrate; an inhibitor of CYP2C19) produced a 3-fold increase in plasma concentrations of N-desmethylclobazam, the active metabolite of clobazam (a substrate of CYP2C19). This may increase the risk of clobazam-related adverse reactions [see Warnings and Precautions (5.4, 5.5), Drug Interactions (7.4)].

The effects of concomitant antiepileptic drugs that are CYP3A4 inducers (phenobarbital, phenytoin, and carbamazepine), CYP2C19 inducers (valproic acid, phenobarbital, phenytoin, and carbamazepine), and CYP2C19 inhibitors (felbamate and oxcarbazepine) were evaluated using data from clinical trials. Results of population pharmacokinetic analysis show that these concomitant antiepileptic drugs did not significantly alter the pharmacokinetics of clobazam or N-desmethylclobazam at steady-state.

Alcohol has been reported to increase the maximum plasma exposure of clobazam by approximately 50%. Alcohol may have additive CNS depressant effects when taken with SYMPAZAN®[see Warnings and Precautions (5.4), Drug Interactions (7.2)].

The polymorphic CYP2C19 is the main enzyme that metabolizes the pharmacologically active N-desmethyl-clobazam. Compared to CYP2C19 extensive metabolizers, N-desmethylclobazam AUC and Cmax are approximately 3-5 times higher in poor metabolizers (e.g., subjects with *2/*2 genotype) and 2 times higher in intermediate metabolizers (e.g., subjects with *1/*2 genotype). The prevalence of CYP2C19 poor metabolism differs depending on racial/ethnic background. Dosage in patients who are known CYP2C19 poor metabolizers may need to be adjusted [see Dosage and Administration (2.5)].

The systemic exposure of clobazam is similar for both CYP2C19 poor and extensive metabolizers.

Carcinogenesis In mice, oral administration of clobazam (0, 6, 12, or 24 mg/kg/day) for 2 years did not result in an increase in tumors. The highest dose tested was approximately 3 times the maximum recommended human dose (MRHD) of 40 mg/day, based on body surface area (mg/m2).

In rats, oral administration of clobazam for 2 years resulted in increases in tumors of the thyroid gland (follicular cell adenoma and carcinoma) and liver (hepatocellular adenoma) at the mid and high doses. The low dose, not associated with an increase in tumors, was associated with plasma exposures (AUC) for clobazam and its major active metabolite, N-desmethylclobazam, less than that in humans at the MRHD.

Mutagenesis Clobazam and the major active metabolite, N-desmethylclobazam, were negative for genotoxicity, based on data from a battery of in vitro (bacteria reverse mutation, mammalian clastogenicity) and in vivo (mouse micronucleus) assays.

Impairment of Fertility In a fertility study in which clobazam (50, 350, or 750 mg/kg/day, corresponding to 12, 84, and 181 times the oral Maximum Recommended Human Dose, MRHD, of 40mg/day based on mg/m2 body surface) was orally administered to male and female rats prior to and during mating and continuing in females to gestation day 6, increases in abnormal sperm and pre-implantation loss were observed at the highest dose tested.  The no-effect level for fertility and early embryonic development in rats was associated with plasma exposures (AUC) for clobazam and its major active metabolite, N-desmethylclobazam, less than those in humans at the maximum recommended human dose of 40 mg/day.

The efficacy of SYMPAZAN® is based upon bioavailability studies comparing clobazam tablets to SYMPAZAN®[see Clinical Pharmacology (12.3)].

The effectiveness of clobazam for the adjunctive treatment of seizures associated with Lennox-Gastaut Syndrome was established in two multicenter controlled studies (Study 1 and Study 2). Both studies were similar in terms of disease characteristics and concomitant AED treatments. The most common concomitant AED treatments at baseline included: valproate, lamotrigine, levetiracetam, and topiramate.

Study 1 Study 1 (N=238) was a randomized, double-blind, placebo-controlled study consisting of a 4-week baseline period followed by a 3-week titration period and 12-week maintenance period. Patients age 2-54 years with a current or prior diagnosis of LGS were stratified into 2 weight groups (12.5 kg to ≤30 kg or >30 kg) and then randomized to placebo or one of three target maintenance doses of clobazam according to Table 4.

<div class="scrollingtable"><table> <colgroup> <col width="176"/> <col width="253"/> <col width="253"/> </colgroup> <tbody class="Headless"> <tr class="First"> <td align="center" class="Lrule Rrule Toprule" colspan="3"><span class="Bold">Table 4: Study 1 Total Daily Dose</span></td> </tr> <tr> <td class="Lrule Rrule Toprule"></td><td align="center" class="Lrule Rrule Toprule"><span class="Bold">≤30 kg Body Weight</span></td><td align="center" class="Lrule Rrule Toprule"><span class="Bold">&gt;30 kg Body Weight</span></td> </tr> <tr> <td class="Lrule Rrule Toprule">  Low Dose</td><td align="center" class="Lrule Rrule Toprule">  5 mg daily</td><td align="center" class="Lrule Rrule Toprule">  10 mg daily</td> </tr> <tr> <td class="Lrule Rrule Toprule">  Medium Dose</td><td align="center" class="Lrule Rrule Toprule">  10 mg daily</td><td align="center" class="Lrule Rrule Toprule">  20 mg daily</td> </tr> <tr class="Last"> <td class="Lrule Rrule Toprule">  High Dose</td><td align="center" class="Lrule Rrule Toprule">  20 mg daily</td><td align="center" class="Lrule Rrule Toprule">  40 mg daily</td> </tr> </tbody> </table></div>

Doses above 5 mg/day were administered in two divided doses.

The primary efficacy measure was the percent reduction in the weekly frequency of drop seizures (atonic, tonic, or myoclonic), also known as drop attacks, from the 4-week baseline period to 12-week maintenance period.

The pre-dosing baseline mean weekly drop seizure frequency was 98, 100, 61, and 105 for the placebo, low-, medium-, and high-dose groups, respectively. Figure 1 presents the mean percent reduction in weekly drop seizures from this baseline. All dose groups of clobazam were statistically superior (p≤0.05) to the placebo group. This effect appeared to be dose dependent.

                    Figure 1: Mean Percent Reduction from Baseline in Weekly Drop Seizure Frequency (Study 1)

Figure 2 shows changes from baseline in weekly drop seizure frequency by category for patients treated with clobazam and placebo in Study 1. Patients in whom the seizure frequency increased are shown at left as "worse." Patients in whom the seizure frequency decreased are shown in five categories.

                          Figure 2: Drop Seizure Response by Category for Clobazam and Placebo (Study 1)

There was no evidence that tolerance to the therapeutic effect of clobazam developed during the 3-month maintenance period.

Study 2 Study 2 (N=68) was a randomized, double-blind comparison study of high- and low-dose clobazam, consisting of a 4-week baseline period followed by a 3-week titration period and 4-week maintenance period. Patients age 2-25 years with a current or prior diagnosis of LGS were stratified by weight, then randomized to either a low or high dose of clobazam, and then entered a 3-week titration period.

The primary efficacy measure was the percent reduction in the weekly frequency of drop seizures (atonic, tonic, or myoclonic), also known as drop attacks, from the 4-week baseline period to the 4-week maintenance period.

A statistically significantly greater reduction in seizure frequency was observed in the high-dose group compared to the low-dose group (median percent reduction of 93% vs 29%; p<0.05).

Each SYMPAZAN® oral film is a white rectangular film that contains 5 mg, 10 mg or 20 mg of clobazam and printed in black ink either "C5,” "C10" or "C20" on the strip according to their respective strengths and each film is packaged in a pouch (sachet).

{ "type": "p", "children": [], "text": "Each SYMPAZAN® oral film is a white rectangular film that contains 5 mg, 10 mg or 20 mg of clobazam and printed in black ink either \"C5,” \"C10\" or \"C20\" on the strip according to their respective strengths and each film is packaged in a pouch (sachet)." }

NDC 10094-205-60: 5 mg oral film, Package of 60

{ "type": "p", "children": [], "text": "NDC 10094-205-60: 5 mg oral film, Package of 60" }

NDC 10094-210-60: 10 mg oral film, Package of 60

{ "type": "p", "children": [], "text": "NDC 10094-210-60: 10 mg oral film, Package of 60" }

NDC 10094-220-60: 20 mg oral film, Package of 60

{ "type": "p", "children": [], "text": "NDC 10094-220-60: 20 mg oral film, Package of 60" }

Store SYMPAZAN® oral film pouches (sachets) at 20°C to 25°C (68°F to 77°F); Excursions permitted to 15°C to 30°C (59°F to 86°F) [See USP controlled room temperature].

{ "type": "p", "children": [], "text": "Store SYMPAZAN® oral film pouches (sachets) at 20°C to 25°C (68°F to 77°F); Excursions permitted to 15°C to 30°C (59°F to 86°F) [See USP controlled room temperature]." }

Advise the patient to read the FDA-approved patient labeling (Medication Guide and Instructions for Use).

{ "type": "p", "children": [], "text": "Advise the patient to read the FDA-approved patient labeling (Medication Guide and Instructions for Use)." }

Risks from Concomitant Use with Opioids

{ "type": "p", "children": [], "text": "\nRisks from Concomitant Use with Opioids\n" }

Inform patients and caregivers that potentially fatal additive effects may occur if SYMPAZAN® is used with opioids and not to use such drugs concomitantly unless supervised by a healthcare provider [see Warnings and Precautions (5.1), Drug Interactions (7.1)].

{ "type": "p", "children": [], "text": "Inform patients and caregivers that potentially fatal additive effects may occur if SYMPAZAN® is used with opioids and not to use such drugs concomitantly unless supervised by a healthcare provider [see Warnings and Precautions (5.1), Drug Interactions (7.1)].\n" }

Abuse, Misuse, and Addiction

{ "type": "p", "children": [], "text": "\nAbuse, Misuse, and Addiction \n" }

Inform patients that the use of SYMPAZAN, even at recommended dosages, exposes users to risks of abuse, misuse, and addiction, which can lead to overdose and death, especially when used in combination with other medications (e.g., opioid analgesics), alcohol, and/or illicit substances. Inform patients about the signs and symptoms of benzodiazepine abuse, misuse, and addiction; to seek medical help if they develop these signs and/or symptoms; and on the proper disposal of unused drug [see Warnings and Precautions (5.2) and Drug Abuse and Dependence (9.2)].

{ "type": "p", "children": [], "text": "Inform patients that the use of SYMPAZAN, even at recommended dosages, exposes users to risks of abuse, misuse, and addiction, which can lead to overdose and death, especially when used in combination with other medications (e.g., opioid analgesics), alcohol, and/or illicit substances. Inform patients about the signs and symptoms of benzodiazepine abuse, misuse, and addiction; to seek medical help if they develop these signs and/or symptoms; and on the proper disposal of unused drug [see Warnings and Precautions (5.2) and Drug Abuse and Dependence (9.2)].\n" }

Withdrawal Reactions

{ "type": "p", "children": [], "text": "\nWithdrawal Reactions\n" }

Advise patients or caregivers that abrupt withdrawal of AEDs may increase their risk of seizure. Inform patients that the continued use of SYMPAZAN may lead to clinically significant physical dependence and that abrupt discontinuation or rapid dosage reduction of SYMPAZAN may precipitate acute withdrawal reactions, which can be life-threatening. Inform patients that in some cases, patients taking benzodiazepines have developed a protracted withdrawal syndrome with withdrawal symptoms lasting weeks to more than 12 months. Instruct patients that discontinuation or dosage reduction of SYMPAZAN may require a slow taper [see Warnings and Precautions (5.3) and Drug Abuse and Dependence (9.3)].

{ "type": "p", "children": [], "text": "Advise patients or caregivers that abrupt withdrawal of AEDs may increase their risk of seizure. Inform patients that the continued use of SYMPAZAN may lead to clinically significant physical dependence and that abrupt discontinuation or rapid dosage reduction of SYMPAZAN may precipitate acute withdrawal reactions, which can be life-threatening. Inform patients that in some cases, patients taking benzodiazepines have developed a protracted withdrawal syndrome with withdrawal symptoms lasting weeks to more than 12 months. Instruct patients that discontinuation or dosage reduction of SYMPAZAN may require a slow taper [see Warnings and Precautions (5.3) and Drug Abuse and Dependence (9.3)].\n" }

Somnolence or Sedation Advise patients or caregivers to check with their healthcare provider before SYMPAZAN® is taken with other CNS depressants such as other benzodiazepines, opioids, tricyclic antidepressants, sedating antihistamines, or alcohol [see Warnings and Precautions (5.4, 5.5)].

{ "type": "p", "children": [], "text": "\nSomnolence or Sedation\nAdvise patients or caregivers to check with their healthcare provider before SYMPAZAN® is taken with other CNS depressants such as other benzodiazepines, opioids, tricyclic antidepressants, sedating antihistamines, or alcohol [see Warnings and Precautions (5.4, 5.5)].\n" }

If applicable, caution patients about operating hazardous machinery, including automobiles, until they are reasonably certain that SYMPAZAN® does not affect them adversely (e.g., impair judgment, thinking or motor skills).

{ "type": "p", "children": [], "text": "If applicable, caution patients about operating hazardous machinery, including automobiles, until they are reasonably certain that SYMPAZAN® does not affect them adversely (e.g., impair judgment, thinking or motor skills)." }

Hypersensitivity

{ "type": "p", "children": [], "text": "\nHypersensitivity\n" }

Inform patients or caregivers that SYMPAZAN® is contraindicated in patients with a history of hypersensitivity to the drug or its ingredients [see Warnings and Precautions (5.6)].

{ "type": "p", "children": [], "text": "Inform patients or caregivers that SYMPAZAN® is contraindicated in patients with a history of hypersensitivity to the drug or its ingredients [see Warnings and Precautions (5.6)].\n" }

Interactions with Hormonal Contraceptives Counsel women to also use non-hormonal methods of contraception when SYMPAZAN® is used with hormonal contraceptives and to continue these alternative methods for 28 days after discontinuing SYMPAZAN® to ensure contraceptive reliability [see Drug Interactions (7.3), Clinical Pharmacology (12.3)].

{ "type": "p", "children": [], "text": "\nInteractions with Hormonal Contraceptives\nCounsel women to also use non-hormonal methods of contraception when SYMPAZAN® is used with hormonal contraceptives and to continue these alternative methods for 28 days after discontinuing SYMPAZAN® to ensure contraceptive reliability [see Drug Interactions (7.3), Clinical Pharmacology (12.3)].\n" }

Serious Dermatological Reactions Advise patients or caregivers that serious skin reactions have been reported in patients taking clobazam.  Serious skin reactions, including SJS/TEN, may need to be treated in a hospital and may be life-threatening. If a skin reaction occurs while taking SYMPAZAN®, patients or caregivers should consult with healthcare providers immediately [see Warnings and Precautions (5.6)].

{ "type": "p", "children": [], "text": "\nSerious Dermatological Reactions\nAdvise patients or caregivers that serious skin reactions have been reported in patients taking clobazam.  Serious skin reactions, including SJS/TEN, may need to be treated in a hospital and may be life-threatening. If a skin reaction occurs while taking SYMPAZAN®, patients or caregivers should consult with healthcare providers immediately [see Warnings and Precautions (5.6)].\n" }

DRESS/Multiorgan Hypersensitivity 

{ "type": "p", "children": [], "text": "\nDRESS/Multiorgan Hypersensitivity \n" }

Instruct patients and caregivers that a fever or rash associated with signs of other organ system involvement (e.g., lymphadenopathy, hepatic dysfunction) may be drug-related and should be reported to their healthcare provider immediately. SYMPAZAN should be discontinued immediately if a serious hypersensitivity reaction is suspected [see Warnings and Precautions (5.7)].

{ "type": "p", "children": [], "text": "Instruct patients and caregivers that a fever or rash associated with signs of other organ system involvement (e.g., lymphadenopathy, hepatic dysfunction) may be drug-related and should be reported to their healthcare provider immediately. SYMPAZAN should be discontinued immediately if a serious hypersensitivity reaction is suspected [see Warnings and Precautions (5.7)]." }

Suicidal Thinking and Behavior Counsel patients, their caregivers, and their families that AEDs, including SYMPAZAN®, may increase the risk of suicidal thoughts and behavior and advise them of the need to be alert for the emergence or worsening of symptoms of depression, any unusual changes in mood or behavior, or the emergence of suicidal thoughts, behavior, or thoughts of self-harm. Patients should report behaviors of concern immediately to healthcare providers [see Warnings and Precautions (5.8)].

{ "type": "p", "children": [], "text": "\nSuicidal Thinking and Behavior\nCounsel patients, their caregivers, and their families that AEDs, including SYMPAZAN®, may increase the risk of suicidal thoughts and behavior and advise them of the need to be alert for the emergence or worsening of symptoms of depression, any unusual changes in mood or behavior, or the emergence of suicidal thoughts, behavior, or thoughts of self-harm. Patients should report behaviors of concern immediately to healthcare providers [see Warnings and Precautions (5.8)].\n" }

Pregnancy

{ "type": "p", "children": [], "text": "\nPregnancy\n" }

Advise pregnant females that the use of SYMPAZAN® late in pregnancy can result in in sedation (respiratory depression, lethargy, hypotonia) and/or withdrawal symptoms (hyperreflexia, irritability, restlessness, tremors, inconsolable crying, and feeding difficulties) in newborns [see Warnings and Precautions (5.9) and Use in Specific Populations (8.1)]. Instruct patients to notify their healthcare provider if they are pregnant.

{ "type": "p", "children": [], "text": "Advise pregnant females that the use of SYMPAZAN® late in pregnancy can result in in sedation (respiratory depression, lethargy, hypotonia) and/or withdrawal symptoms (hyperreflexia, irritability, restlessness, tremors, inconsolable crying, and feeding difficulties) in newborns [see Warnings and Precautions (5.9) and Use in Specific Populations (8.1)]. Instruct patients to notify their healthcare provider if they are pregnant." }

Encourage patients to enroll in the North American Antiepileptic Drug (NAAED) Pregnancy Registry if they become pregnant while taking SYMPAZAN. The registry is collecting information about the safety of antiepileptic drugs during pregnancy [see Use in Specific Populations (8.1)].

{ "type": "p", "children": [], "text": "Encourage patients to enroll in the North American Antiepileptic Drug (NAAED) Pregnancy Registry if they become pregnant while taking SYMPAZAN. The registry is collecting information about the safety of antiepileptic drugs during pregnancy [see Use in Specific Populations (8.1)].\n" }

Lactation

{ "type": "p", "children": [], "text": "\nLactation\n" }

Counsel patients that clobazam, the active ingredient in SYMPAZAN®, is excreted in breast milk. Instruct patients to notify their healthcare provider if they are breast feeding or intend to breastfeed. Instruct breastfeeding patients who take SYMPAZAN to monitor their infants for excessive sedation, poor feeding and poor weight gain, and to seek medical attention if they notice these signs [see Use in Specific Populations (8.2)].

{ "type": "p", "children": [], "text": "Counsel patients that clobazam, the active ingredient in SYMPAZAN®, is excreted in breast milk. Instruct patients to notify their healthcare provider if they are breast feeding or intend to breastfeed. Instruct breastfeeding patients who take SYMPAZAN to monitor their infants for excessive sedation, poor feeding and poor weight gain, and to seek medical attention if they notice these signs [see Use in Specific Populations (8.2)].\n" }

Manufactured by: Aquestive TherapeuticsWarren, NJ 07059

{ "type": "p", "children": [], "text": "Manufactured by: Aquestive TherapeuticsWarren, NJ 07059" }

<div class="scrollingtable"><table> <colgroup> <col width="166"/> <col width="166"/> <col width="4"/> <col width="162"/> <col width="166"/> </colgroup> <tbody class="Headless"> <tr class="First"> <td align="center" class="Lrule Rrule Toprule" colspan="5"><span class="Bold"> MEDICATION GUIDE</span> <br/> <span class="Bold">SYMPAZAN</span><span class="Bold"><span class="Sup">®</span></span><span class="Bold">(SYM-pa-zan)</span><span class="Bold"> <br/>(clobazam)</span><span class="Bold"> <br/>oral film, CIV</span></td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="5"><span class="Bold">What is the most important information I should know about SYMPAZAN?</span> <br/> <ul class="Disc"> <li> <span class="Bold">SYMPAZAN is a benzodiazepine medicine. </span><span class="Bold">Taking b</span><span class="Bold">enzodiazepines </span><span class="Bold">with opioid medicines, alcohol, or other central nervous system (CNS) depressants </span><span class="Bold">(including street drugs) </span><span class="Bold">can cause severe drowsiness, breathing </span><span class="Bold">problems </span><span class="Bold">(respiratory </span><span class="Bold">depre</span><span class="Bold">ssion), </span><span class="Bold">coma, </span><span class="Bold">and </span><span class="Bold">death</span><span class="Bold">.</span> <br/>Get emergency help right away if any of the following happens:<span class="Bold"> <br/>○ </span>shallow or slowed breathing<br/>○ breathing stops (which may lead to the heart stopping)<br/>○ excessive sleepiness (sedation)<br/>Do not drive or operate heavy machinery until you know how taking SYMPAZAN with opioids affects you.</li> <li> <span class="Bold">Risk of abuse, misuse, and addiction.</span> There is a risk for abuse, misuse, and addiction with benzodiazepines, including SYMPAZAN, which can lead to overdose and serious side effects including coma and death.<br/>○ <span class="Bold">Serious side effects including coma and death have happened in people who have abused or misused benzodiazepines, including SYMPAZAN. </span>These serious side effects may also include delirium, paranoia, suicidal thoughts or actions, seizures, and difficulty breathing. <span class="Bold">Call your healthcare provider or go to the nearest hospital emergency room right away if you get any of these serious side effects.</span><span class="Bold"> <br/>○ </span><span class="Bold">You can develop an addiction even if you take SYMPAZAN as prescribed by your healthcare provider. </span> <br/>○ <span class="Bold">Take SYMPAZAN exactly as your healthcare provider prescribed.</span> <br/>○ Do not share your SYMPAZAN with other people.<br/>○ Keep SYMPAZAN in a safe place and away from children.</li> <li> <span class="Bold">Physical dependence and withdrawal reactions. </span>SYMPAZAN can cause physical dependence and withdrawal reactions.<br/>○ <span class="Bold">Do not suddenly stop taking SYMPAZAN. </span>Stopping SYMPAZAN suddenly can cause serious and life-threatening side effects, including, unusual movements, responses, or expressions, seizures, sudden and severe mental or nervous system changes, depression, seeing or hearing things that others do not see or hear, an extreme increase in activity or talking, losing touch with reality, and suicidal thoughts or actions. <span class="Bold">Call your healthcare provider or go to the nearest hospital emergency room right away if you get any of these symptoms.</span> <br/>○ <span class="Bold">Some people who suddenly stop benzodiazepines have symptoms that can last for several weeks to more than 12 months, </span>including, anxiety, trouble remembering, learning, or concentrating, depression, problems sleeping, feeling like insects are crawling under your skin, weakness, shaking, muscle twitching, burning, or prickling feeling in your hands, arms, legs or feet, and ringing in your ears.<br/>○ Physical dependence is not the same as drug addiction. Your healthcare provider can tell you more about the differences between physical dependence and drug addiction.<br/>○ Do not take more SYMPAZAN than prescribed or take SYMPAZAN for longer than prescribed.</li> <li> <span class="Bold">SYMPAZAN can make you sleepy or dizzy and can slow your thinking and motor skills. </span> <br/>○ Do not drive, operate heavy machinery, or do other dangerous activities until you know how SYMPAZAN affects you.<br/>○ Do not drink alcohol or take other drugs that may make you sleepy or dizzy while taking SYMPAZAN without first talking to your healthcare provider. When taken with alcohol or drugs that cause sleepiness or dizziness, SYMPAZAN may make your sleepiness or dizziness much worse.</li> <li> <span class="Bold">Serious skin reactions have been seen when SYMPAZAN is taken with other medicines and may require </span><span class="Bold">stopping </span><span class="Bold">its </span><span class="Bold">use. </span>Do not stop taking SYMPAZAN without first talking to your healthcare provider.<br/>○ A serious skin reaction can happen at any time during your treatment with SYMPAZAN, but is more likely to happen within the first 8 weeks of treatment. These skin reactions may need to be treated right away.<br/>○ Call your healthcare provider immediately if you have skin blisters, rash, sores in mouth, hives or any other allergic reaction.</li> <li> <span class="Bold">A serious allergic reaction that may affect your skin or other parts of your body such as your liver, kidneys, heart, or blood cells.</span>This allergic reaction can be life-threatening and can cause death, particularly if it is not treated as early as possible. Call your healthcare provider right away if you have:<p class="First First TableParagraph">○ a skin rash                                ○ fever or swollen glands that do not go away</p> <p class="TableParagraph">○ swelling of your face                ○ shortness of breath</p> <p class="TableParagraph">○ dark urine                                 ○ yellowing of the skin or whites of the eyes</p> </li> </ul> <ul class="Disc"> <li> <span class="Bold">Like </span><span class="Bold">other </span><span class="Bold">antiepileptic </span><span class="Bold">medicines, </span><span class="Bold">SYMPAZAN </span><span class="Bold">may </span><span class="Bold">cause </span><span class="Bold">suicidal </span><span class="Bold">thoughts </span><span class="Bold">or </span><span class="Bold">actions </span><span class="Bold">in </span><span class="Bold">a </span><span class="Bold">very </span><span class="Bold">small number of people, about 1 in </span><span class="Bold">500.</span> </li> </ul> <span class="Bold">Call your healthcare provider right away if you have any of these symptoms, especially if they are new, worse, or worry you:</span></td> </tr> <tr> <td class="Lrule" colspan="3"><span class="Bold">○ </span>thoughts about suicide or dying</td><td class="Rrule" colspan="2"><span class="Bold">○ </span>attempts to commit suicide</td> </tr> <tr> <td class="Lrule" colspan="3"><span class="Bold">○ </span>new or worse depression</td><td class="Rrule" colspan="2"><span class="Bold">○ </span>new or worse anxiety or irritability</td> </tr> <tr> <td class="Lrule" colspan="3"><span class="Bold">○ </span>feeling agitated or restless</td><td class="Rrule" colspan="2"><span class="Bold">○ </span>an extreme increase in activity and talking (mania)</td> </tr> <tr> <td class="Lrule" colspan="3">○ trouble sleeping (insomnia)</td><td class="Rrule" colspan="2">○ new or worse panic attacks</td> </tr> <tr> <td class="Lrule" colspan="3">○ acting aggressive, being angry or violent</td><td class="Rrule" colspan="2">○ acting on dangerous impulses</td> </tr> <tr> <td class="Lrule" colspan="3">○ other unusual changes in behavior or mood</td><td class="Rrule" colspan="2"></td> </tr> <tr> <td class="Lrule Rrule" colspan="5"><span class="Bold">How can I watch for early symptoms of suicidal thoughts and actions?</span> <br/> <ul class="Disc"> <li>Pay attention to any changes, especially sudden changes, in mood, behaviors, thoughts, or feelings.</li> <li>Keep all follow-up visits with your healthcare provider as scheduled.</li> </ul>Call your healthcare provider between visits as needed, especially if you are worried about symptoms.<br/>Stopping a seizure medicine suddenly in a patient who has epilepsy can cause seizures that will not stop (status epilepticus).<br/>Suicidal thoughts or actions can be caused by things other than medicines. If you have suicidal thoughts or actions, your healthcare provider may check for other causes.</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="5"><span class="Bold">What is SYMPAZAN?</span> <br/> <ul class="Disc"> <li>SYMPAZAN is a prescription medicine used along with other medicines to treat seizures associated with Lennox-Gastaut Syndrome in people 2 years of age or older.</li> <li> <span class="Bold">SYMPAZAN is a federally controlled substance (C-IV) because it contains clobazam that can be abused or lead to dependence. </span>Keep SYMPAZAN in a safe place to prevent misuse and abuse. Selling or giving away SYMPAZAN may harm others, and is against the law. Tell your healthcare provider if you have ever abused or been dependent on alcohol, prescription medicines or street drugs.</li> </ul>It is not known if SYMPAZAN is safe and effective in children less than 2 years old.</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="5"><span class="Bold">Do not take SYMPAZAN if you:</span> <ul class="Disc"> <li>are allergic to clobazam or any of the ingredients in SYMPAZAN.  See the end of this Medication Guide for a complete list of ingredients in SYMPAZAN.</li> </ul> </td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="5"><span class="Bold">Before you take SYMPAZAN, tell your healthcare provider about all of your medical conditions, including if you:</span> <br/> <ul class="Disc"> <li>have liver or kidney problems</li> <li>have lung problems (respiratory disease)</li> <li>have or have had depression, mood problems, or suicidal thoughts or behavior</li> <li>use birth control medicine. SYMPAZAN may cause your birth control medicine to be less effective. Talk to your healthcare provider about the best birth control method to use.</li> <li>are pregnant or plan to become pregnant. <br/>o    Taking SYMPAZAN late in pregnancy may cause your baby to have symptoms of sedation (breathing<br/>      problems, sluggishness, low muscle tone) and/or withdrawal symptoms (jitteriness, irritability,<br/>      restlessness, shaking, excessive crying, feeding problems).<br/>o    Tell your healthcare provider right away if you become pregnant or think you are pregnant during<br/>      treatment with SYMPAZAN.<br/>o    If you become pregnant while taking SYMPAZAN, talk to your healthcare provider about registering<br/>      with the North American Antiepileptic Drug Pregnancy Registry. You can register by calling 1-888-<br/>      233-2334. For more information about the registry go to http://www.aedpregnancyregistry.org. The<br/>      purpose of this registry is to collect information about the safety of antiepileptic drugs during<br/>      pregnancy.</li> <li>Are breastfeeding or plan to breastfeed. SYMPAZAN can pass into breast milk.<br/>o    Breastfeeding during treatment with SYMPAZAN may cause your baby to have sleepiness, feeding<br/>      problems, and decreased weight gain.<br/>o    Talk to your healthcare provider about the best way to feed your baby if you take SYMPAZAN.</li> </ul> <span class="Bold">Tell your healthcare provider about all the medicines you take,</span> including prescription and over-the­ counter medicines, vitamins, and herbal supplements. Taking SYMPAZAN with certain other medicines can cause side effects or affect how well SYMPAZAN or the other medicines work. Do not start or stop other medicines without talking to your healthcare provider.</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="5"><span class="Bold">How should I take SYMPAZAN?</span> <ul class="Disc"> <li>Take SYMPAZAN exactly as your healthcare provider tells you to take it.</li> <li>Your healthcare provider will tell you how much SYMPAZAN to take and when to take it.</li> <li>Place the entire SYMPAZAN oral film on top of the tongue.</li> <li>SYMPAZAN oral films can be taken with or without food.</li> <li> <span class="Bold">Do not</span> take liquids with SYMPAZAN oral films.</li> <li>Take only 1 SYMPAZAN oral film at a time.</li> <li>Read the <span class="Bold">Instructions for Use</span> at the end of this Medication Guide for information on the right way to take SYMPAZAN oral films.</li> <li>Your healthcare provider may change your dose if needed. <span class="Bold">Do not</span> change your dose of SYMPAZAN without talking to your healthcare provider.</li> <li> <span class="Bold">Do not</span> stop taking SYMPAZAN without first talking to your healthcare provider.</li> <li>Stopping SYMPAZAN suddenly can cause serious problems.</li> <li>If you take too much SYMPAZAN, call your healthcare provider or go to the nearest hospital emergency room right away.</li> </ul> </td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="5"><span class="Bold">What should I avoid while taking SYMPAZAN?</span> <br/>See <span class="Bold">“What is the most important information I should know about SYMPAZAN?”</span></td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="5"><span class="Bold">What are the possible side effects of SYMPAZAN?</span> <br/> <span class="Bold">SYMPAZAN may cause serious side effects, including: </span> <br/> <ul class="Disc"> <li> <span class="Bold">See "What is the most important information I should know about SYMPAZAN?"</span> </li> </ul> <span class="Bold">The most common side effects of SYMPAZAN include: </span></td> </tr> <tr> <td class="Lrule">● sleepiness</td><td>● drooling</td><td colspan="2">● constipation</td><td class="Rrule">● cough</td> </tr> <tr> <td class="Lrule">● pain with urination</td><td>● fever</td><td colspan="2">● acting aggressive, being angry, or violent</td><td class="Rrule">● difficulty sleeping</td> </tr> <tr> <td class="Lrule">● slurred speech</td><td>● tiredness</td><td colspan="2">● problems with breathing</td><td class="Rrule"></td> </tr> <tr> <td class="Lrule Rrule" colspan="5">These are not all the possible side effects of SYMPAZAN. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.</td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="5"><span class="Bold">How should I store SYMPAZAN?</span> <br/> <ul class="Disc"> <li>Store SYMPAZAN oral film at room temperature between 68°F to 77°F (20°C to 25°C).</li> </ul> <span class="Bold">Keep SYMPAZAN and all medicines out of the reach of children.</span></td> </tr> <tr> <td class="Lrule Rrule Toprule" colspan="5"><span class="Bold">General Information about the safe and effective use of SYMPAZAN.</span> <br/>Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use SYMPAZAN for a condition for which it was not prescribed. Do not give SYMPAZAN to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about SYMPAZAN that is written for health professionals.</td> </tr> <tr class="Last"> <td class="Lrule Rrule Toprule" colspan="5"><span class="Bold">What are the ingredients in SYMPAZAN?</span> <br/> <span class="Bold">Active ingredient: </span>clobazam<br/> <span class="Bold">Inactive ingredients: </span>artificial cooling flavor, citric acid, glycerol monooleate, hypromellose, maltitol, natural and artificial bitter masker, natural raspberry type flavor, polyethylene oxide, purified water, sodium phosphate dibasic, and sucralose.<br/> <br/>Manufactured by:<br/>Aquestive Therapeutics <br/>Warren, NJ 07059<br/> <br/>SYMPAZAN<span class="Sup">®</span> is a registered trademark of Aquestive Therapeutics<br/> <br/>For more information, go to www.SYMPAZAN.com or call the Aquestive Therapeutics Rx Patient and Caregiver Support Line at 1-833-AQUESTV (1-833-278- 3788).</td> </tr> </tbody> </table></div>

{ "type": "table", "children": [], "text": "<div class=\"scrollingtable\"><table>\n<colgroup>\n<col width=\"166\"/>\n<col width=\"166\"/>\n<col width=\"4\"/>\n<col width=\"162\"/>\n<col width=\"166\"/>\n</colgroup>\n<tbody class=\"Headless\">\n<tr class=\"First\">\n<td align=\"center\" class=\"Lrule Rrule Toprule\" colspan=\"5\"><span class=\"Bold\"> MEDICATION GUIDE</span>\n<br/>\n<span class=\"Bold\">SYMPAZAN</span><span class=\"Bold\"><span class=\"Sup\">®</span></span><span class=\"Bold\">(SYM-pa-zan)</span><span class=\"Bold\">\n<br/>(clobazam)</span><span class=\"Bold\">\n<br/>oral film, CIV</span></td>\n</tr>\n<tr>\n<td class=\"Lrule Rrule Toprule\" colspan=\"5\"><span class=\"Bold\">What is the most important information I should know about SYMPAZAN?</span>\n<br/>\n<ul class=\"Disc\">\n<li>\n<span class=\"Bold\">SYMPAZAN is a benzodiazepine medicine. </span><span class=\"Bold\">Taking b</span><span class=\"Bold\">enzodiazepines </span><span class=\"Bold\">with opioid medicines, alcohol, or other central nervous system (CNS) depressants </span><span class=\"Bold\">(including street drugs) </span><span class=\"Bold\">can cause severe drowsiness, breathing </span><span class=\"Bold\">problems </span><span class=\"Bold\">(respiratory </span><span class=\"Bold\">depre</span><span class=\"Bold\">ssion), </span><span class=\"Bold\">coma, </span><span class=\"Bold\">and </span><span class=\"Bold\">death</span><span class=\"Bold\">.</span>\n<br/>Get emergency help right away if any of the following happens:<span class=\"Bold\">\n<br/>○ </span>shallow or slowed breathing<br/>○ breathing stops (which may lead to the heart stopping)<br/>○ excessive sleepiness (sedation)<br/>Do not drive or operate heavy machinery until you know how taking SYMPAZAN with opioids affects you.</li>\n<li>\n<span class=\"Bold\">Risk of abuse, misuse, and addiction.</span> There is a risk for abuse, misuse, and addiction with benzodiazepines, including SYMPAZAN, which can lead to overdose and serious side effects including coma and death.<br/>○ <span class=\"Bold\">Serious side effects including coma and death have happened in people who have abused or misused benzodiazepines, including SYMPAZAN. </span>These serious side effects may also include delirium, paranoia, suicidal thoughts or actions, seizures, and difficulty breathing. <span class=\"Bold\">Call your healthcare provider or go to the nearest hospital emergency room right away if you get any of these serious side effects.</span><span class=\"Bold\">\n<br/>○ </span><span class=\"Bold\">You can develop an addiction even if you take SYMPAZAN as prescribed by your healthcare provider. </span>\n<br/>○ <span class=\"Bold\">Take SYMPAZAN exactly as your healthcare provider prescribed.</span>\n<br/>○ Do not share your SYMPAZAN with other people.<br/>○ Keep SYMPAZAN in a safe place and away from children.</li>\n<li>\n<span class=\"Bold\">Physical dependence and withdrawal reactions. </span>SYMPAZAN can cause physical dependence and withdrawal reactions.<br/>○ <span class=\"Bold\">Do not suddenly stop taking SYMPAZAN. </span>Stopping SYMPAZAN suddenly can cause serious and life-threatening side effects, including, unusual movements, responses, or expressions, seizures, sudden and severe mental or nervous system changes, depression, seeing or hearing things that others do not see or hear, an extreme increase in activity or talking, losing touch with reality, and suicidal thoughts or actions. <span class=\"Bold\">Call your healthcare provider or go to the nearest hospital emergency room right away if you get any of these symptoms.</span>\n<br/>○ <span class=\"Bold\">Some people who suddenly stop benzodiazepines have symptoms that can last for several weeks to more than 12 months, </span>including, anxiety, trouble remembering, learning, or concentrating, depression, problems sleeping, feeling like insects are crawling under your skin, weakness, shaking, muscle twitching, burning, or prickling feeling in your hands, arms, legs or feet, and ringing in your ears.<br/>○ Physical dependence is not the same as drug addiction. Your healthcare provider can tell you more about the differences between physical dependence and drug addiction.<br/>○ Do not take more SYMPAZAN than prescribed or take SYMPAZAN for longer than prescribed.</li>\n<li>\n<span class=\"Bold\">SYMPAZAN can make you sleepy or dizzy and can slow your thinking and motor skills. </span>\n<br/>○ Do not drive, operate heavy machinery, or do other dangerous activities until you know how SYMPAZAN affects you.<br/>○ Do not drink alcohol or take other drugs that may make you sleepy or dizzy while taking SYMPAZAN without first talking to your healthcare provider. When taken with alcohol or drugs that cause sleepiness or dizziness, SYMPAZAN may make your sleepiness or dizziness much worse.</li>\n<li>\n<span class=\"Bold\">Serious skin reactions have been seen when SYMPAZAN is taken with other medicines and may require </span><span class=\"Bold\">stopping </span><span class=\"Bold\">its </span><span class=\"Bold\">use. </span>Do not stop taking SYMPAZAN without first talking to your healthcare provider.<br/>○ A serious skin reaction can happen at any time during your treatment with SYMPAZAN, but is more likely to happen within the first 8 weeks of treatment. These skin reactions may need to be treated right away.<br/>○ Call your healthcare provider immediately if you have skin blisters, rash, sores in mouth, hives or any other allergic reaction.</li>\n<li>\n<span class=\"Bold\">A serious allergic reaction that may affect your skin or other parts of your body such as your liver, kidneys, heart, or blood cells.</span>This allergic reaction can be life-threatening and can cause death, particularly if it is not treated as early as possible. Call your healthcare provider right away if you have:<p class=\"First First TableParagraph\">○ a skin rash                                ○ fever or swollen glands that do not go away</p>\n<p class=\"TableParagraph\">○ swelling of your face                ○ shortness of breath</p>\n<p class=\"TableParagraph\">○ dark urine                                 ○ yellowing of the skin or whites of the eyes</p>\n</li>\n</ul>\n<ul class=\"Disc\">\n<li>\n<span class=\"Bold\">Like </span><span class=\"Bold\">other </span><span class=\"Bold\">antiepileptic </span><span class=\"Bold\">medicines, </span><span class=\"Bold\">SYMPAZAN </span><span class=\"Bold\">may </span><span class=\"Bold\">cause </span><span class=\"Bold\">suicidal </span><span class=\"Bold\">thoughts </span><span class=\"Bold\">or </span><span class=\"Bold\">actions </span><span class=\"Bold\">in </span><span class=\"Bold\">a </span><span class=\"Bold\">very </span><span class=\"Bold\">small number of people, about 1 in </span><span class=\"Bold\">500.</span>\n</li>\n</ul>\n<span class=\"Bold\">Call your healthcare provider right away if you have any of these symptoms, especially if they are new, worse, or worry you:</span></td>\n</tr>\n<tr>\n<td class=\"Lrule\" colspan=\"3\"><span class=\"Bold\">○ </span>thoughts about suicide or dying</td><td class=\"Rrule\" colspan=\"2\"><span class=\"Bold\">○ </span>attempts to commit suicide</td>\n</tr>\n<tr>\n<td class=\"Lrule\" colspan=\"3\"><span class=\"Bold\">○ </span>new or worse depression</td><td class=\"Rrule\" colspan=\"2\"><span class=\"Bold\">○ </span>new or worse anxiety or irritability</td>\n</tr>\n<tr>\n<td class=\"Lrule\" colspan=\"3\"><span class=\"Bold\">○ </span>feeling agitated or restless</td><td class=\"Rrule\" colspan=\"2\"><span class=\"Bold\">○ </span>an extreme increase in activity and talking (mania)</td>\n</tr>\n<tr>\n<td class=\"Lrule\" colspan=\"3\">○ trouble sleeping (insomnia)</td><td class=\"Rrule\" colspan=\"2\">○ new or worse panic attacks</td>\n</tr>\n<tr>\n<td class=\"Lrule\" colspan=\"3\">○ acting aggressive, being angry or violent</td><td class=\"Rrule\" colspan=\"2\">○ acting on dangerous impulses</td>\n</tr>\n<tr>\n<td class=\"Lrule\" colspan=\"3\">○ other unusual changes in behavior or mood</td><td class=\"Rrule\" colspan=\"2\"></td>\n</tr>\n<tr>\n<td class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">How can I watch for early symptoms of suicidal thoughts and actions?</span>\n<br/>\n<ul class=\"Disc\">\n<li>Pay attention to any changes, especially sudden changes, in mood, behaviors, thoughts, or feelings.</li>\n<li>Keep all follow-up visits with your healthcare provider as scheduled.</li>\n</ul>Call your healthcare provider between visits as needed, especially if you are worried about symptoms.<br/>Stopping a seizure medicine suddenly in a patient who has epilepsy can cause seizures that will not stop (status epilepticus).<br/>Suicidal thoughts or actions can be caused by things other than medicines. If you have suicidal thoughts or actions, your healthcare provider may check for other causes.</td>\n</tr>\n<tr>\n<td class=\"Lrule Rrule Toprule\" colspan=\"5\"><span class=\"Bold\">What is SYMPAZAN?</span>\n<br/>\n<ul class=\"Disc\">\n<li>SYMPAZAN is a prescription medicine used along with other medicines to treat seizures associated with Lennox-Gastaut Syndrome in people 2 years of age or older.</li>\n<li>\n<span class=\"Bold\">SYMPAZAN is a federally controlled substance (C-IV) because it contains clobazam that can be abused or lead to dependence. </span>Keep SYMPAZAN in a safe place to prevent misuse and abuse. Selling or giving away SYMPAZAN may harm others, and is against the law. Tell your healthcare provider if you have ever abused or been dependent on alcohol, prescription medicines or street drugs.</li>\n</ul>It is not known if SYMPAZAN is safe and effective in children less than 2 years old.</td>\n</tr>\n<tr>\n<td class=\"Lrule Rrule Toprule\" colspan=\"5\"><span class=\"Bold\">Do not take SYMPAZAN if you:</span>\n<ul class=\"Disc\">\n<li>are allergic to clobazam or any of the ingredients in SYMPAZAN.  See the end of this Medication Guide for a complete list of ingredients in SYMPAZAN.</li>\n</ul>\n</td>\n</tr>\n<tr>\n<td class=\"Lrule Rrule Toprule\" colspan=\"5\"><span class=\"Bold\">Before you take SYMPAZAN, tell your healthcare provider about all of your medical conditions, including if you:</span>\n<br/>\n<ul class=\"Disc\">\n<li>have liver or kidney problems</li>\n<li>have lung problems (respiratory disease)</li>\n<li>have or have had depression, mood problems, or suicidal thoughts or behavior</li>\n<li>use birth control medicine. SYMPAZAN may cause your birth control medicine to be less effective. Talk to your healthcare provider about the best birth control method to use.</li>\n<li>are pregnant or plan to become pregnant. <br/>o    Taking SYMPAZAN late in pregnancy may cause your baby to have symptoms of sedation (breathing<br/>      problems, sluggishness, low muscle tone) and/or withdrawal symptoms (jitteriness, irritability,<br/>      restlessness, shaking, excessive crying, feeding problems).<br/>o    Tell your healthcare provider right away if you become pregnant or think you are pregnant during<br/>      treatment with SYMPAZAN.<br/>o    If you become pregnant while taking SYMPAZAN, talk to your healthcare provider about registering<br/>      with the North American Antiepileptic Drug Pregnancy Registry. You can register by calling 1-888-<br/>      233-2334. For more information about the registry go to http://www.aedpregnancyregistry.org. The<br/>      purpose of this registry is to collect information about the safety of antiepileptic drugs during<br/>      pregnancy.</li>\n<li>Are breastfeeding or plan to breastfeed. SYMPAZAN can pass into breast milk.<br/>o    Breastfeeding during treatment with SYMPAZAN may cause your baby to have sleepiness, feeding<br/>      problems, and decreased weight gain.<br/>o    Talk to your healthcare provider about the best way to feed your baby if you take SYMPAZAN.</li>\n</ul>\n<span class=\"Bold\">Tell your healthcare provider about all the medicines you take,</span> including prescription and over-the­ counter medicines, vitamins, and herbal supplements. Taking SYMPAZAN with certain other medicines can cause side effects or affect how well SYMPAZAN or the other medicines work. Do not start or stop other medicines without talking to your healthcare provider.</td>\n</tr>\n<tr>\n<td class=\"Lrule Rrule Toprule\" colspan=\"5\"><span class=\"Bold\">How should I take SYMPAZAN?</span>\n<ul class=\"Disc\">\n<li>Take SYMPAZAN exactly as your healthcare provider tells you to take it.</li>\n<li>Your healthcare provider will tell you how much SYMPAZAN to take and when to take it.</li>\n<li>Place the entire SYMPAZAN oral film on top of the tongue.</li>\n<li>SYMPAZAN oral films can be taken with or without food.</li>\n<li>\n<span class=\"Bold\">Do not</span> take liquids with SYMPAZAN oral films.</li>\n<li>Take only 1 SYMPAZAN oral film at a time.</li>\n<li>Read the <span class=\"Bold\">Instructions for Use</span> at the end of this Medication Guide for information on the right way to take SYMPAZAN oral films.</li>\n<li>Your healthcare provider may change your dose if needed. <span class=\"Bold\">Do not</span> change your dose of SYMPAZAN without talking to your healthcare provider.</li>\n<li>\n<span class=\"Bold\">Do not</span> stop taking SYMPAZAN without first talking to your healthcare provider.</li>\n<li>Stopping SYMPAZAN suddenly can cause serious problems.</li>\n<li>If you take too much SYMPAZAN, call your healthcare provider or go to the nearest hospital emergency room right away.</li>\n</ul>\n</td>\n</tr>\n<tr>\n<td class=\"Lrule Rrule Toprule\" colspan=\"5\"><span class=\"Bold\">What should I avoid while taking SYMPAZAN?</span>\n<br/>See <span class=\"Bold\">“What is the most important information I should know about SYMPAZAN?”</span></td>\n</tr>\n<tr>\n<td class=\"Lrule Rrule Toprule\" colspan=\"5\"><span class=\"Bold\">What are the possible side effects of SYMPAZAN?</span>\n<br/>\n<span class=\"Bold\">SYMPAZAN may cause serious side effects, including: </span>\n<br/>\n<ul class=\"Disc\">\n<li>\n<span class=\"Bold\">See \"What is the most important information I should know about SYMPAZAN?\"</span>\n</li>\n</ul>\n<span class=\"Bold\">The most common side effects of SYMPAZAN include: </span></td>\n</tr>\n<tr>\n<td class=\"Lrule\">● sleepiness</td><td>● drooling</td><td colspan=\"2\">● constipation</td><td class=\"Rrule\">● cough</td>\n</tr>\n<tr>\n<td class=\"Lrule\">● pain with urination</td><td>● fever</td><td colspan=\"2\">● acting aggressive, being angry, or violent</td><td class=\"Rrule\">● difficulty sleeping</td>\n</tr>\n<tr>\n<td class=\"Lrule\">● slurred speech</td><td>● tiredness</td><td colspan=\"2\">● problems with breathing</td><td class=\"Rrule\"></td>\n</tr>\n<tr>\n<td class=\"Lrule Rrule\" colspan=\"5\">These are not all the possible side effects of SYMPAZAN. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.</td>\n</tr>\n<tr>\n<td class=\"Lrule Rrule Toprule\" colspan=\"5\"><span class=\"Bold\">How should I store SYMPAZAN?</span>\n<br/>\n<ul class=\"Disc\">\n<li>Store SYMPAZAN oral film at room temperature between 68°F to 77°F (20°C to 25°C).</li>\n</ul>\n<span class=\"Bold\">Keep SYMPAZAN and all medicines out of the reach of children.</span></td>\n</tr>\n<tr>\n<td class=\"Lrule Rrule Toprule\" colspan=\"5\"><span class=\"Bold\">General Information about the safe and effective use of SYMPAZAN.</span>\n<br/>Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use SYMPAZAN for a condition for which it was not prescribed. Do not give SYMPAZAN to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about SYMPAZAN that is written for health professionals.</td>\n</tr>\n<tr class=\"Last\">\n<td class=\"Lrule Rrule Toprule\" colspan=\"5\"><span class=\"Bold\">What are the ingredients in SYMPAZAN?</span>\n<br/>\n<span class=\"Bold\">Active ingredient: </span>clobazam<br/>\n<span class=\"Bold\">Inactive ingredients: </span>artificial cooling flavor, citric acid, glycerol monooleate, hypromellose, maltitol, natural and artificial bitter masker, natural raspberry type flavor, polyethylene oxide, purified water, sodium phosphate dibasic, and sucralose.<br/>\n<br/>Manufactured by:<br/>Aquestive Therapeutics <br/>Warren, NJ 07059<br/>\n<br/>SYMPAZAN<span class=\"Sup\">®</span> is a registered trademark of Aquestive Therapeutics<br/>\n<br/>For more information, go to www.SYMPAZAN.com or call the Aquestive Therapeutics Rx Patient and Caregiver Support Line at 1-833-AQUESTV (1-833-278- 3788).</td>\n</tr>\n</tbody>\n</table></div>" }

This Medication Guide has been approved by the U.S. Food and Drug Administration       Revised: 3/2024

{ "type": "p", "children": [], "text": "This Medication Guide has been approved by the U.S. Food and Drug Administration       Revised: 3/2024" }

Instructions for Use

{ "type": "p", "children": [], "text": "\nInstructions for Use\n" }

SYMPAZAN® (SIM-pa-zan)

{ "type": "p", "children": [], "text": "\nSYMPAZAN® (SIM-pa-zan)\n" }

(clobazam) oral film, CIV

{ "type": "p", "children": [], "text": "\n(clobazam) oral film, CIV\n" }

Read this Instructions for Use before you start using SYMPAZAN and each time you get a refill. There may be new information. The information does not take the place of talking with your healthcare provider about your medical condition or treatment.

{ "type": "p", "children": [], "text": "Read this Instructions for Use before you start using SYMPAZAN and each time you get a refill. There may be new information. The information does not take the place of talking with your healthcare provider about your medical condition or treatment." }

Important Information for Patient and Caregiver:

{ "type": "p", "children": [], "text": "\nImportant Information for Patient and Caregiver: \n" }

{ "type": "ul", "children": [ "\nDo not take SYMPAZAN until:○  you have read and understand these instructions.○ you have reviewed the steps with your healthcare provider on how to take it.○ you know the right time, how often, and the dose to take.○  you feel comfortable with how to use SYMPAZAN.", "If you are not sure about giving treatment or when to give treatment, call your healthcare provider before using SYMPAZAN.\n" ], "text": "" }

How should I store SYMPAZAN?

{ "type": "p", "children": [], "text": "\nHow should I store SYMPAZAN?\n" }

{ "type": "ul", "children": [ "Store SYMPAZAN at room temperature between 68°F to 77°F (20°C to 25°C).", "Keep SYMPAZAN in the foil pouch until you are ready to use. Use right away after opening foil pouch.", "\nKeep SYMPAZAN and all medicines out of the reach of children.\n" ], "text": "" }

How to Use SYMPAZAN:

{ "type": "p", "children": [], "text": "\nHow to Use SYMPAZAN:\n" }

{ "type": "ul", "children": [ "Take only 1 SYMPAZAN film at a time unless instructed differently by your healthcare provider. If a second film is needed to get a full dose of SYMPAZAN, do not take the second film until the first film has completely dissolved.", "\nPlace the entire SYMPAZAN oral film on top of the tongue. Check your prescription or contact your healthcare provider if you are not sure about the amount to take.", "Make sure your hands are clean and dry before handling the SYMPAZAN film.", "Check the expiration date printed on the foil pouch. Do not use SYMPAZAN if expired." ], "text": "" }

<div class="scrollingtable"><table> <colgroup> <col width="420"/> <col width="203"/> </colgroup> <tbody class="Headless"> <tr class="First"> <td><span class="Bold">Step 1. Open Pouch</span> <ul class="Disc"> <li>Fold foil pouch along solid line.</li> <li>Note where the slit is and carefully tear it to open pouch.</li> </ul> </td><td><img alt="Step 1. Open Pouch" src="/dailymed/image.cfm?name=sympazan-05.jpg&amp;setid=5e3d8fcb-aa7d-4822-88fc-4f06264c3242"/></td> </tr> <tr> <td><span class="Bold">Step 2. Remove Film</span> <ul class="Disc"> <li>Remove the SYMPAZAN from the foil pouch.</li> </ul> </td><td><img alt="Step 2. Remove Film" src="/dailymed/image.cfm?name=sympazan-06.jpg&amp;setid=5e3d8fcb-aa7d-4822-88fc-4f06264c3242"/></td> </tr> <tr> <td><span class="Bold">Step 3. </span><span class="Bold">Place on Tongue</span> <br/> <ul class="Disc"> <li>Place SYMPAZAN on top of the tongue. The film will stick to the tongue and begin to dissolve.</li> </ul> </td><td><img alt="Step 3. Place on Tongue" src="/dailymed/image.cfm?name=sympazan-07.jpg&amp;setid=5e3d8fcb-aa7d-4822-88fc-4f06264c3242"/></td> </tr> <tr class="Last"> <td><span class="Bold">Step 4. Close Mouth and Swallow Saliva Normally</span> <br/> <ul class="Disc"> <li>Close mouth.</li> <li>Swallow saliva normally as SYMPAZAN dissolves.</li> <li> <span class="Bold">Do not</span> take with liquids.</li> <li> <span class="Bold">Do not</span> chew, spit, or talk while SYMPAZAN dissolves.</li> </ul> </td><td><img alt="Step 4. Close Mouth and Swallow Saliva Normally" src="/dailymed/image.cfm?name=sympazan-08.jpg&amp;setid=5e3d8fcb-aa7d-4822-88fc-4f06264c3242"/></td> </tr> </tbody> </table></div>

{ "type": "table", "children": [], "text": "<div class=\"scrollingtable\"><table>\n<colgroup>\n<col width=\"420\"/>\n<col width=\"203\"/>\n</colgroup>\n<tbody class=\"Headless\">\n<tr class=\"First\">\n<td><span class=\"Bold\">Step 1. Open Pouch</span>\n<ul class=\"Disc\">\n<li>Fold foil pouch along solid line.</li>\n<li>Note where the slit is and carefully tear it to open pouch.</li>\n</ul>\n</td><td><img alt=\"Step 1. Open Pouch\" src=\"/dailymed/image.cfm?name=sympazan-05.jpg&amp;setid=5e3d8fcb-aa7d-4822-88fc-4f06264c3242\"/></td>\n</tr>\n<tr>\n<td><span class=\"Bold\">Step 2. Remove Film</span>\n<ul class=\"Disc\">\n<li>Remove the SYMPAZAN from the foil pouch.</li>\n</ul>\n</td><td><img alt=\"Step 2. Remove Film\" src=\"/dailymed/image.cfm?name=sympazan-06.jpg&amp;setid=5e3d8fcb-aa7d-4822-88fc-4f06264c3242\"/></td>\n</tr>\n<tr>\n<td><span class=\"Bold\">Step 3. </span><span class=\"Bold\">Place on Tongue</span>\n<br/>\n<ul class=\"Disc\">\n<li>Place SYMPAZAN on top of the tongue. The film will stick to the tongue and begin to dissolve.</li>\n</ul>\n</td><td><img alt=\"Step 3. Place on Tongue\" src=\"/dailymed/image.cfm?name=sympazan-07.jpg&amp;setid=5e3d8fcb-aa7d-4822-88fc-4f06264c3242\"/></td>\n</tr>\n<tr class=\"Last\">\n<td><span class=\"Bold\">Step 4. Close Mouth and Swallow Saliva Normally</span>\n<br/>\n<ul class=\"Disc\">\n<li>Close mouth.</li>\n<li>Swallow saliva normally as SYMPAZAN dissolves.</li>\n<li>\n<span class=\"Bold\">Do not</span> take with liquids.</li>\n<li>\n<span class=\"Bold\">Do not</span> chew, spit, or talk while SYMPAZAN dissolves.</li>\n</ul>\n</td><td><img alt=\"Step 4. Close Mouth and Swallow Saliva Normally\" src=\"/dailymed/image.cfm?name=sympazan-08.jpg&amp;setid=5e3d8fcb-aa7d-4822-88fc-4f06264c3242\"/></td>\n</tr>\n</tbody>\n</table></div>" }

{ "type": "ul", "children": [ "\nWash your hands after taking SYMPAZAN.\n", "\nThrow away the empty foil pouch in the regular trash.\n" ], "text": "" }

Manufactured by:Aquestive TherapeuticsWarren, NJ 07059

{ "type": "p", "children": [], "text": "Manufactured by:Aquestive TherapeuticsWarren, NJ 07059" }

For more information or support about SYMPAZAN: Call 1-833-AQUESTV (1-833-278-3788).

{ "type": "p", "children": [], "text": "For more information or support about SYMPAZAN: Call 1-833-AQUESTV (1-833-278-3788)." }

This Instructions for Use has been approved by the U.S. Food and Drug Administration. Revision Date: 11/2018

{ "type": "p", "children": [], "text": "This Instructions for Use has been approved by the U.S. Food and Drug Administration. Revision Date: 11/2018" }

NDC 10094-205-01Sympazan(clobazam) Oral film5 mgRx Only1 Oral films

{ "type": "p", "children": [], "text": "NDC 10094-205-01Sympazan(clobazam) Oral film5 mgRx Only1 Oral films" }

NDC 10094-205-60Sympazan(clobazam) Oral film5 mgRx Only60 Oral films

{ "type": "p", "children": [], "text": "NDC 10094-205-60Sympazan(clobazam) Oral film5 mgRx Only60 Oral films" }

NDC 10094-210-01Sympazan(clobazam) Oral film10 mgRx Only1 Oral films

{ "type": "p", "children": [], "text": "NDC 10094-210-01Sympazan(clobazam) Oral film10 mgRx Only1 Oral films" }

NDC 10094-210-60Sympazan(clobazam) Oral film10 mgRx Only60 Oral films

{ "type": "p", "children": [], "text": "NDC 10094-210-60Sympazan(clobazam) Oral film10 mgRx Only60 Oral films" }

NDC 10094-220-01Sympazan(clobazam) Oral film20 mgRx Only1 Oral films

{ "type": "p", "children": [], "text": "NDC 10094-220-01Sympazan(clobazam) Oral film20 mgRx Only1 Oral films" }

NDC 10094-220-60Sympazan(clobazam) Oral film20 mgRx Only60 Oral films

{ "type": "p", "children": [], "text": "NDC 10094-220-60Sympazan(clobazam) Oral film20 mgRx Only60 Oral films" }

Clobazam oral suspension is indicated for the adjunctive treatment of seizures associated with Lennox-Gastaut syndrome (LGS) in patients 2 years of age or older.

{ "type": "p", "children": [], "text": "Clobazam oral suspension is indicated for the adjunctive treatment of seizures associated with Lennox-Gastaut syndrome (LGS) in patients 2 years of age or older." }

A daily dose of clobazam oral suspension greater than 5 mg should be administered in divided doses twice daily; a 5 mg daily dose can be administered as a single dose. Dose patients according to body weight. Individualize dosing within each body weight group, based on clinical efficacy and tolerability. Each dose in Table 1 (e.g., 5 mg to 20 mg in ≤ 30 kg weight group) has been shown to be effective, although effectiveness increases with increasing dose [see Clinical Studies (14)]. Do not proceed with dose escalation more rapidly than weekly, because serum concentrations of clobazam and its active metabolite require 5 and 9 days, respectively, to reach steady-state.

<div class="scrollingtable"><table width="85%"> <caption> <span>Table 1: Recommended Total Daily Dosing by Weight Group</span> </caption> <col align="left" valign="top" width="34%"/> <col align="center" valign="top" width="33%"/> <col align="center" valign="top" width="33%"/> <thead> <tr class="First Last"> <th align="left" class="Lrule Rrule"></th><th align="center" class="Rrule">≤ 30 kg Body Weight</th><th align="center" class="Rrule">&gt; 30 kg Body Weight</th> </tr> </thead> <tbody> <tr class="Botrule First"> <td align="left" class="Lrule Rrule">Starting Dose</td><td align="center" class="Rrule">5 mg</td><td align="center" class="Rrule">10 mg</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Starting Day 7</td><td align="center" class="Rrule">10 mg</td><td align="center" class="Rrule">20 mg</td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule">Starting Day 14</td><td align="center" class="Rrule">20 mg</td><td align="center" class="Rrule">40 mg</td> </tr> </tbody> </table></div>

To reduce the risk of withdrawal reactions, increased seizure frequency, and status epilepticus, use a gradual taper to discontinue clobazam oral suspension or reduce the dosage. Taper by decreasing the total daily dose by 5 mg/day to 10 mg/day on a weekly basis until discontinued. If a patient develops withdrawal reactions, consider pausing the taper or increasing the dosage to the previous tapered dosage level. Subsequently decrease the dosage more slowly [see Warnings and Precautions (5.3) and Drug Abuse and Dependence (9.3)].

Clobazam Oral Suspension Oral Administration

Clobazam oral suspension can be taken with or without food [see Clinical Pharmacology (12.3)].

Shake clobazam oral suspension well before every administration.

Plasma concentrations at any given dose are generally higher in the elderly: proceed slowly with dose escalation. The starting dose should be 5 mg/day for all elderly patients. Then titrate elderly patients according to weight, but to half the dose presented in Table 1, as tolerated. If necessary and based upon clinical response, an additional titration to the maximum dose (20 mg/day or 40 mg/day, depending on weight) may be started on day 21 [see Use In Specific Populations (8.5)].

In CYP2C19 poor metabolizers, levels of N-desmethylclobazam, clobazam's active metabolite, will be increased. Therefore, in patients known to be CYP2C19 poor metabolizers, the starting dose should be 5 mg/day and dose titration should proceed slowly according to weight, but to half the dose presented in Table 1, as tolerated. If necessary and based upon clinical response, an additional titration to the maximum dose (20 mg/day or 40 mg/day, depending on the weight group) may be started on day 21 [see Use in Specific Populations (8.6), Clinical Pharmacology (12.5)].

No dose adjustment is required for patients with mild and moderate renal impairment. There is no experience with clobazam oral suspension in patients with severe renal impairment or end stage renal disease (ESRD). It is not known if clobazam or its active metabolite, N-desmethylclobazam, is dialyzable [see Use in Specific Populations (8.7), Clinical Pharmacology (12.3)].

Clobazam oral suspension is hepatically metabolized; however, there are limited data to characterize the effect of hepatic impairment on the pharmacokinetics of clobazam oral suspension. For this reason, proceed slowly with dosing escalations. For patients with mild to moderate hepatic impairment (Child-Pugh score 5 to 9), the starting dose should be 5 mg/day in both weight groups. Then titrate patients according to weight, but to half the dose presented in Table 1, as tolerated. If necessary and based upon clinical response, start an additional titration on day 21 to the maximum dose (20 mg/day or 40 mg/day, depending on the weight group). There is inadequate information about metabolism of clobazam oral suspension in patients with severe hepatic impairment. Therefore no dosing recommendation in those patients can be given [see Use in Specific Populations (8.8), Clinical Pharmacology (12.3)].

Oral Suspension: 2.5 mg/mL for oral administration. An off-white suspension.

{ "type": "p", "children": [], "text": "Oral Suspension: 2.5 mg/mL for oral administration. An off-white suspension." }

Clobazam oral suspension is contraindicated in patients with a history of hypersensitivity to the drug or its ingredients. Hypersensitivity reactions have included serious dermatological reactions [see Warnings and Precautions (5.6)].

{ "type": "p", "children": [], "text": "Clobazam oral suspension is contraindicated in patients with a history of hypersensitivity to the drug or its ingredients. Hypersensitivity reactions have included serious dermatological reactions [see Warnings and Precautions (5.6)].\n" }

Concomitant use of benzodiazepines, including clobazam, and opioids may result in profound sedation, respiratory depression, coma, and death. Because of these risks, reserve concomitant prescribing of benzodiazepines and opioids for patients for whom alternative treatment options are inadequate.

Observational studies have demonstrated that concomitant use of opioid analgesics and benzodiazepines increases the risk of drug-related mortality compared to use of opioids alone. If a decision is made to prescribe clobazam concomitantly with opioids, prescribe the lowest effective dosages and minimum durations of concomitant use, and follow patients closely for signs and symptoms of respiratory depression and sedation. Advise both patients and caregivers about the risks of respiratory depression and sedation when clobazam is used with opioids [see Drug Interactions (7.1)].

The use of benzodiazepines, including clobazam, exposes users to the risks of abuse, misuse, and addiction, which can lead to overdose or death. Abuse and misuse of benzodiazepines often (but not always) involve the use of doses greater than the maximum recommended dosage and commonly involve concomitant use of other medications, alcohol, and/or illicit substances, which is associated with an increased frequency of serious adverse outcomes, including respiratory depression, overdose, or death[see Drug Abuse and Dependence (9.2)].

Before prescribing clobazam and throughout treatment, assess each patient's risk for abuse, misuse, and addiction (e.g., using a standardized screening tool). Use of clobazam, particularly in patients at elevated risk, necessitates counseling about the risks and proper use of clobazam along with monitoring for signs and symptoms of abuse, misuse, and addiction. Prescribe the lowest effective dosage; avoid or minimize concomitant use of CNS depressants and other substances associated with abuse, misuse, and addiction (e.g., opioid analgesics, stimulants). If a substance use disorder Is suspected, evaluate the patient and institute (or refer them for) early treatment, as appropriate.

To reduce the risk of withdrawal reactions, use a gradual taper to discontinue clobazam or reduce the dosage [see Dosage and Administration (2.2)]. Patients at an increased risk of withdrawal adverse reactions after benzodiazepine discontinuation or rapid dosage reduction include those who take higher dosages, and those who have had longer durations of use.

Acute Withdrawal Reactions

The continued use of benzodiazepines, including clobazam, may lead to clinically significant physical dependence. Abrupt discontinuation or rapid dosage reduction of clobazam after continued use, or administration of flumazenil (a benzodiazepine antagonist) may precipitate acute withdrawal reactions, which can be life-threatening (e.g., seizures) [see Drug Abuse and Dependence (9.3)].

Protracted Withdrawal Syndrome

In some cases, benzodiazepine users have developed a protracted withdrawal syndrome with withdrawal symptoms lasting weeks to more than 12 months [see Drug Abuse and Dependence (9.3)].

Since clobazam has a central nervous system (CNS) depressant effect, patients or their caregivers should be cautioned against simultaneous use with other CNS depressant drugs or alcohol, and cautioned that the effects of other CNS depressant drugs or alcohol may be potentiated [see Drug Interactions (7.2)].

Clobazam causes somnolence and sedation. In clinical trials, somnolence or sedation was reported at all effective doses and was dose-related.

In general, somnolence and sedation begin within the first month of treatment and may diminish with continued treatment. Prescribers should monitor patients for somnolence and sedation, particularly with concomitant use of other central nervous system depressants. Prescribers should caution patients against engaging in hazardous activities requiring mental alertness, such as operating dangerous machinery or motor vehicles, until the effect of clobazam is known.

Serious skin reactions, including Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN), have been reported with clobazam in both children and adults during the postmarketing period. Patients should be closely monitored for signs or symptoms of SJS/TEN, especially during the first 8 weeks of treatment initiation or when re-introducing therapy. Clobazam should be discontinued at the first sign of rash, unless the rash Is clearly not drug-related. If signs or symptoms suggest SJS/TEN, use of this drug should not be resumed and alternative therapy should be considered [see contraindications (4)].

Antiepileptic drugs (AEDs), including clobazam, increase the risk of suicidal thoughts or behavior in patients taking these drugs for any indication. Patients treated with any AED for any indication should be monitored for the emergence or worsening of depression, suicidal thoughts or behavior, and/or any unusual changes in mood or behavior.

Pooled analyses of 199 placebo-controlled clinical trials (mono- and adjunctive therapy) of 11 different AEDs showed that patients randomized to one of the AEDs had approximately twice the risk (adjusted relative risk 1.8, 95% confidence interval [Cl]: 1.2, 2.7) of suicidal thinking or behavior compared to patients randomized to placebo. In these trials, which had a median treatment duration of 12 weeks, the estimated incidence rate of suicidal behavior or ideation among 27,863 AED-treated patients was 0.43%, compared to 0.24% among 16,029 placebo-treated patients, representing an increase of approximately one case of suicidal thinking or behavior for every 530 patients treated. There were four suicides in drug-treated patients in the trials and none in placebo-treated patients, but the number is too small to allow any conclusion about drug effect on suicide.

The Increased risk of suicidal thoughts or behavior with AEDs was observed as early as one week after starting drug treatment with AEDs and persisted for the duration of treatment assessed. Because most trials included in the analysis did not extend beyond 24 weeks, the risk of suicidal thoughts or behavior beyond 24 weeks could not be assessed.

The risk of suicidal thoughts or behavior was generally consistent among drugs in the data analyzed. The finding of increased risk with AEDs of varying mechanisms of action and across a range of indications suggests that the risk applies to all AEDs used for any indication. The risk did not vary substantially by age (5 to 100 years) in the clinical trials analyzed. Table 2 shows absolute and relative risk by indication for all evaluated AEDs.

<div class="scrollingtable"><table width="85%"> <caption> <span>Table 2: Risk by Indication for Antiepileptic Drugs in the Pooled Analysis</span> </caption> <col align="left" valign="middle" width="8%"/> <col align="center" valign="middle" width="23%"/> <col align="center" valign="middle" width="23%"/> <col align="center" valign="middle" width="23%"/> <col align="center" valign="middle" width="23%"/> <thead> <tr class="First Last"> <th align="left" class="Lrule Rrule">Indication</th><th align="center" class="Rrule">Placebo Patients with Events per 1,000 Patients</th><th align="center" class="Rrule">Drug Patients with Events per 1,000 Patients</th><th align="center" class="Rrule">Relative Risk:<br/>Incidence of Drug Events in Drug Patients/Incidence in Placebo Patients</th><th align="center" class="Rrule">Risk Difference:<br/>Additional Drug<br/>Patients with Events<br/>par 1,000 Patients</th> </tr> </thead> <tbody> <tr class="Botrule First"> <td align="left" class="Lrule Rrule">Epilepsy</td><td align="center" class="Rrule">1.0</td><td align="center" class="Rrule">3.4</td><td align="center" class="Rrule">3.5</td><td align="center" class="Rrule">2.4</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Psychiatric</td><td align="center" class="Rrule">5.7</td><td align="center" class="Rrule">8.5</td><td align="center" class="Rrule">1.5</td><td align="center" class="Rrule">2.9</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Other</td><td align="center" class="Rrule">1.0</td><td align="center" class="Rrule">1.8</td><td align="center" class="Rrule">1.9</td><td align="center" class="Rrule">0.9</td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule">Total</td><td align="center" class="Rrule">2.4</td><td align="center" class="Rrule">4.3</td><td align="center" class="Rrule">1.8</td><td align="center" class="Rrule">1.9</td> </tr> </tbody> </table></div>

The relative risk for suicidal thoughts or behavior was higher in clinical trials for epilepsy than in clinical trials for psychiatric or other conditions, but the absolute risk differences were similar for the epilepsy and psychiatric indications.

Anyone considering prescribing clobazam or any other AED must balance the risk of suicidal thoughts or behavior with the risk of untreated illness. Epilepsy and many other illnesses for which AEDs are prescribed are themselves associated with morbidity and mortality and an Increased risk of suicidal thoughts and behavior. Should suicidal thoughts and behavior emerge during treatment, the prescriber needs to consider whether the emergence of these symptoms in any given patient may be related to the illness being treated.

Patients, their caregivers, and families should be informed that AEDs increase the risk of suicidal thoughts and behavior and should be advised of the need to be alert for the emergence or worsening of the signs and symptoms of depression, any unusual changes in mood or behavior, or the emergence of suicidal thoughts, behavior, or thoughts about self-harm. Behaviors of concern should be reported immediately to healthcare providers.

Use of clobazam late in pregnancy can result in sedation (respiratory depression, lethargy, hypotonia) and/or withdrawal symptoms (hyperreflexia, irritability, restlessness, tremors, inconsolable crying and feeding difficulties) in the neonate [see Use in Specific Populations (8.1)]. Monitor neonates exposed to clobazam during pregnancy or labor for signs of sedation and monitor neonates exposed to clobazam during pregnancy for signs of withdrawal; manage these neonates accordingly.

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

During its development for the adjunctive treatment of seizures associated with LGS, clobazam was administered to 333 healthy volunteers and 300 patients with a current or prior diagnosis of LGS, including 197 patients treated for 12 months or more. The conditions and duration of exposure varied greatly and included single- and multiple-dose clinical pharmacology studies in healthy volunteers and two double-blind studies in patients with LGS (Study 1 and 2) [see Clinical Studies (14)]. Only Study 1 included a placebo group, allowing comparison of adverse reaction rates on clobazam at several doses to placebo.

Adverse Reactions Leading to Discontinuation in an LGS Placebo Controlled Clinical Trial (Study 1)

The adverse reactions associated with clobazam treatment discontinuation in ≥ 1% of patients in decreasing order of frequency included lethargy, somnolence, ataxia, aggression, fatigue, and insomnia.

Most common Adverse Reactions in an LGS Placebo Controlled Clinical Trial (Study 1)

Table 3 lists the adverse reactions that occurred in ≥ 5% of clobazam-treated patients (at any dose) and at a rate greater than placebo-treated patients, in the randomized, double-blind, placebo-controlled, parallel group clinical study of adjunctive AED therapy for 15 weeks (Study 1).

<div class="scrollingtable"><table width="85%"> <caption> <span>Table 3: Adverse Reactions Reported for ≥ 5% of Patients and More Frequently than Placebo in Any Treatment Group</span> </caption> <col align="left" valign="top" width="50%"/> <col align="center" valign="middle" width="10%"/> <col align="center" valign="middle" width="10%"/> <col align="center" valign="middle" width="10%"/> <col align="center" valign="middle" width="10%"/> <col align="center" valign="middle" width="10%"/> <thead> <tr class="First"> <th align="left" class="Lrule Rrule" rowspan="2"></th><th align="center" class="Rrule" rowspan="2">Placebo<br/>N=59<br/>%</th><th align="center" class="Botrule Rrule" colspan="3">Clobazam Dose Level</th><th align="center" class="Rrule" rowspan="2">All Clobazam<br/> N=179<br/> %</th> </tr> <tr class="Last"> <th align="center" class="Rrule">Low<a class="Sup" href="#footnote-1" name="footnote-reference-1">*</a> <br/>N=58<br/>%</th><th align="center" class="Rrule">Medium<a class="Sup" href="#footnote-2" name="footnote-reference-2">†</a> <br/>N=62<br/>%</th><th align="center" class="Rrule">High<a class="Sup" href="#footnote-3" name="footnote-reference-3">‡</a> <br/>N=59<br/>%</th> </tr> </thead> <tfoot> <tr> <td align="left" colspan="6"> <dl class="Footnote"> <dt> <a href="#footnote-reference-1" name="footnote-1">*</a> </dt> <dd>Maximum daily dose of 5 mg for ≤ 30 kg body weight; 10 mg for &gt; 30 kg body weight</dd> <dt> <a href="#footnote-reference-2" name="footnote-2">†</a> </dt> <dd>Maximum daily dose of 10 mg for ≤ 30 kg body weight; 20 mg for &gt; 30 kg body weight</dd> <dt> <a href="#footnote-reference-3" name="footnote-3">‡</a> </dt> <dd>Maximum daily dose of 20 mg for ≤ 30 kg body weight; 40 mg for &gt; 30 kg body weight</dd> </dl> </td> </tr> </tfoot> <tbody> <tr class="Botrule First"> <td align="left" class="Lrule Rrule" colspan="6"><span class="Bold">Gastrointestinal Disorders</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Vomiting</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">9</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">7</td><td align="center" class="Rrule">7</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Constipation</td><td align="center" class="Rrule">0</td><td align="center" class="Rrule">2</td><td align="center" class="Rrule">2</td><td align="center" class="Rrule">10</td><td align="center" class="Rrule">5</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Dysphagia</td><td align="center" class="Rrule">0</td><td align="center" class="Rrule">0</td><td align="center" class="Rrule">0</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">2</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="6"><span class="Bold">General Disorders and Administration Site Conditions</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Pyrexia</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">17</td><td align="center" class="Rrule">10</td><td align="center" class="Rrule">12</td><td align="center" class="Rrule">13</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Irritability</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">11</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">7</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Fatigue</td><td align="center" class="Rrule">2</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">5</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="6"><span class="Bold">Infections and Infestations</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Upper respiratory tract infection</td><td align="center" class="Rrule">10</td><td align="center" class="Rrule">10</td><td align="center" class="Rrule">13</td><td align="center" class="Rrule">14</td><td align="center" class="Rrule">12</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Pneumonia</td><td align="center" class="Rrule">2</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">7</td><td align="center" class="Rrule">4</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Urinary tract infection</td><td align="center" class="Rrule">0</td><td align="center" class="Rrule">2</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">4</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Bronchitis</td><td align="center" class="Rrule">0</td><td align="center" class="Rrule">2</td><td align="center" class="Rrule">0</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">2</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="6"><span class="Bold">Metabolism and Nutrition Disorders</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Decreased appetite</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">0</td><td align="center" class="Rrule">7</td><td align="center" class="Rrule">3</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Increased appetite</td><td align="center" class="Rrule">0</td><td align="center" class="Rrule">2</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">3</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="6"><span class="Bold">Nervous System Disorders</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Somnolence or Sedation</td><td align="center" class="Rrule">15</td><td align="center" class="Rrule">17</td><td align="center" class="Rrule">27</td><td align="center" class="Rrule">32</td><td align="center" class="Rrule">26</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">    Somnolence</td><td align="center" class="Rrule">12</td><td align="center" class="Rrule">16</td><td align="center" class="Rrule">24</td><td align="center" class="Rrule">25</td><td align="center" class="Rrule">22</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">    Sedation</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">2</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">9</td><td align="center" class="Rrule">5</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Lethargy</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">10</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">15</td><td align="center" class="Rrule">10</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Drooling</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">0</td><td align="center" class="Rrule">13</td><td align="center" class="Rrule">14</td><td align="center" class="Rrule">9</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Ataxia</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">2</td><td align="center" class="Rrule">10</td><td align="center" class="Rrule">5</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Psychomotor hyperactivity</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">4</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Dysarthria</td><td align="center" class="Rrule">0</td><td align="center" class="Rrule">2</td><td align="center" class="Rrule">2</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">3</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="6"><span class="Bold">Psychiatric Disorders</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Aggression</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">8</td><td align="center" class="Rrule">14</td><td align="center" class="Rrule">8</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Insomnia</td><td align="center" class="Rrule">2</td><td align="center" class="Rrule">2</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">7</td><td align="center" class="Rrule">5</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="6"><span class="Bold">Respiratory Disorders</span></td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule">  Cough</td><td align="center" class="Rrule">0</td><td align="center" class="Rrule">3</td><td align="center" class="Rrule">5</td><td align="center" class="Rrule">7</td><td align="center" class="Rrule">5</td> </tr> </tbody> </table></div>

These reactions are reported voluntarily from a population of uncertain size; therefore, it is not possible to estimate their frequency or establish a causal relationship to drug exposure. Adverse reactions are categorized by system organ class.

Blood Disorders: Anemia, eosinophilia, leukopenia, thrombocytopenia

Eye Disorders: Diplopia, vision blurred

Gastrointestinal Disorders: Abdominal distention

General Disorders and Administration Site Conditions: Hypothermia

Investigations: Hepatic enzyme increased

Musculoskeletal: Muscle spasms

Psychiatric Disorders: Agitation, anxiety, apathy, confusional state, depression, delirium, delusion, hallucination

Renal and Urinary Disorders: Urinary retention

Respiratory Disorders: Aspiration, respiratory depression

Skin and Subcutaneous Tissue Disorders: Rash, urticaria, angioedema, and facial and lip edema

The concomitant use of benzodiazepines and opioids increases the risk of respiratory depression because of actions at different receptor sites in the CNS that control respiration. Benzodiazepines interact at GABAA sites, and opioids interact primarily at mu receptors. When benzodiazepines and opioids are combined, the potential for benzodiazepines to significantly worsen opioid-related respiratory depression exists. Limit dosage and duration of concomitant use of benzodiazepines and opioids and follow patients closely for respiratory depression and sedation [see Warnings and Precautions (5.1)].

Concomitant use of clobazam with other CNS depressants may increase the risk of sedation and somnolence [see Warnings and Precautions (5.4)].

Alcohol, as a CNS depressant, will interact with clobazam in a similar way and also increases clobazam's maximum plasma exposure by approximately 50%. Therefore, caution patients or their caregivers against simultaneous use with other CNS depressant drugs or alcohol, and caution that the effects of other CNS depressant drugs or alcohol may be potentiated [see Warnings and Precautions (5.4)].

Hormonal Contraceptives

Clobazam is a weak CYP3A4 inducer. As some hormonal contraceptives are metabolized by CYP3A4, their effectiveness may be diminished when given with clobazam. Additional non-hormonal forms of contraception are recommended when using clobazam [see Clinical Pharmacology (12.3), Patient Counseling Information (17)].

Drugs Metabolized by CYP2D6

Clobazam inhibits CYP2D6. Dose adjustment of drugs metabolized by CYP2D6 may be necessary [see Clinical Pharmacology (12.3)].

Strong and moderate inhibitors of CYP2C19

Strong and moderate inhibitors of CYP2C19 may result in increased exposure to N-desmethylclobazam, the active metabolite of clobazam. This may increase the risk of dose-related adverse reactions. Dosage adjustment of clobazam may be necessary when co-administered with strong CYP2C19 inhibitors (e.g., fluconazole, fluvoxamine, ticlopidine) or moderate CYP2C19 inhibitors (e.g., omeprazole) [see Clinical Pharmacology (12.3)].

Pregnancy Registry

There is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to AEDs, such as clobazam, during pregnancy. Healthcare providers are encouraged to recommend that pregnant women taking clobazam enroll in the North American Antiepileptic Drug (NAAED) Pregnancy Registry by calling 1-888-233-2334 or online at http://www.aedpregnancyregistry.org/.

Risk summary

Neonates born to mothers using benzodiazepines late in pregnancy have been reported to experience symptoms of sedation and/or neonatal withdrawal [see Warnings and Precautions (5.8) and Clinical Considerations]. Available data from published observational studies of pregnant women exposed to benzodiazepines do not report a clear association with benzodiazepines and major birth defects (see Data).

Administration of clobazam to pregnant rats and rabbits during the period of organogenesis or to rats throughout pregnancy and lactation resulted in developmental toxicity, including increased incidences of fetal malformations and mortality, at plasma exposures for clobazam and its major active metabolite, N-desmethylclobazam, below those expected at therapeutic doses in patients [see Animal Data]. Data for other benzodiazepines suggest the possibility of long-term effects on neurobehavioral and immunological function in animals following prenatal exposure to benzodiazepines at clinically relevant doses. Clobazam should be used during pregnancy only if the potential benefit to the mother justifies the potential risk to the fetus. Advise a pregnant woman and women of childbearing age of the potential risk to a fetus.

The background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and of miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively.

Clinical Considerations

Fetal/Neonatal Adverse Reactions

Benzodiazepines cross the placenta and may produce respiratory depression, hypotonia, and sedation in neonates. Monitor neonates exposed to clobazam during pregnancy or labor for signs of sedation, respiratory depression, hypotonia, and feeding problems. Monitor neonates exposed to clobazam during pregnancy for signs of withdrawal. Manage these neonates accordingly [see Warnings and Precautions (5.8)].

Data

Human Data

Published data from observational studies on the use of benzodiazepines during pregnancy do not report a clear association with benzodiazepines and major birth defects. Although early studies reported an increased risk of congenital malformations with diazepam and chlordiazepoxide, there was no consistent pattern noted. In addition, the majority of more recent case-control and cohort studies of benzodiazepine use during pregnancy, which were adjusted for confounding exposures to alcohol, tobacco, and other medications, have not confirmed these findings.

Animal Data

In a study in which clobazam (0, 150, 450, or 750 mg/kg/day) was orally administered to pregnant rats throughout the period of organogenesis, embryofetal mortality and incidences of fetal skeletal variations were increased at all doses. The low-effect dose for embryofetal developmental toxicity in rats (150 mg/kg/day) was associated with plasma exposures (AUC) for clobazam and its major active metabolite, N-desmethylclobazam, lower than those in humans at the maximum recommended human dose (MRHD) of 40 mg/day.

Oral administration of clobazam (0, 10, 30, or 75 mg/kg/day) to pregnant rabbits throughout the period of organogenesis resulted in decreased fetal body weights, and increased incidences of fetal malformations (visceral and skeletal) at the mid and high doses, and an increase in embryofetal mortality at the high dose. Incidences of fetal variations were increased at all doses. The highest dose tested was associated with maternal toxicity (ataxia and decreased activity). The low-affect dose for embryofetal developmental toxicity in rabbits (10 mg/kg/day) was associated with plasma exposures for clobazam and N-desmethylclobazam lower than those in humans at the MRHD.

Oral administration of clobazam (0, 50, 350, or 750 mg/kg/day) to rats throughout pregnancy and lactation resulted in increased embryofetal mortality at the high dose, decreased pup survival at the mid and high doses and alterations in offspring behavior (locomotor activity) at all doses. The low-effect dose for adverse effects on pre- and postnatal development in rats (50 mg/kg/day) was associated with plasma exposures for clobazam and N-desmethylclobazam lower than those in humans at the MRHD.

Risk Summary

Clobazam is excreted in human milk (see Data). There are reports of sedation, poor feeding, and poor weight gain in infants exposed to benzodiazepines through breast milk. There are no data on the effects of clobazam on milk production. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for clobazam and any potential adverse effects on the breastfed infant from clobazam or from the underlying maternal condition.

Clinical Considerations

Adverse reactions such as somnolence and difficulty feeding have been reported in infants during breastfeeding in postmarketing experience with clobazam. Infants exposed to clobazam through breast milk should be monitored for sedation, poor feeding, and poor weight gain.

Data

Scientific literature on clobazam use during lactation is limited. After short-term administration, clobazam and N-desmethylclobazam are transferred into breast milk.

Administration of clobazam to rats prior to and during mating and early gestation resulted in adverse effects on fertility and early embryonic development at plasma exposures for clobazam and its major active metabolite, N-desmethylclobazam, below those in humans at the MRHD [see Nonclinical Toxicology (13.1)].

Safety and effectiveness in patients less than 2 years of age have not been established.

In a study in which clobazam (0, 4, 36, or 120 mg/kg/day) was orally administered to rats during the juvenile period of development (postnatal days 14 to 48), adverse effects on growth (decreased bone density and bone length) and behavior (altered motor activity and auditory startle response; learning deficit) were observed at the high dose. The effect on bone density, but not on behavior, was reversible when drug was discontinued. The no-effect level for juvenile toxicity (36 mg/kg/day) was associated with plasma exposures (AUG) to clobazam and its major active metabolite, N-desmethylclobazam, less than those expected at therapeutic doses in pediatric patients.

Clinical studies of clobazam did not include sufficient numbers of subjects aged 65 and over to detenmine whether they respond differently from younger subjects. However, elderly subjects appear to eliminate clobazam more slowly than younger subjects based on population pharmacokinetic analysis. For these reasons, the initial dose in elderly patients should be 5 mg/day. Patients should be titrated initially to 10 mg/day to 20 mg/day. Patients may be titrated further to a maximum daily dose of 40 mg if tolerated [see Dosage and Administration (2.4), Clinical Pharmacology (12.3)].

Concentrations of clobazam's active metabolite, N-desmethylclobazam, are higher in CYP2C19 poor metabolizers than in extensive metabolizers. For this reason, dosage modification is recommended [see Dosage and Administration (2.5), Clinical Pharmacology (12.3)].

The pharmacokinetics of clobazam were evaluated in patients with mild and moderate renal impairment. There were no significant differences in systemic exposure (AUC and Cmax) between patients with mild or moderate renal impairment and healthy subjects. No dose adjustment is required for patients with mild and moderate renal impairment. There is essentially no experience with clobazam in patients with severe renal impairment or ESRD. It is not known if clobazam or its active metabolite, N-desmethylclobazam, is dialyzable [see Dosage and Administration (2.6), Clinical Pharmacology (12.3)].

Clobazam is hepatically metabolized; however, there are limited data to characterize the effect of hepatic impairment on the pharmacokinetics of clobazam. For this reason, dosage adjustment is recommended in patients with mild to moderate hepatic impairment (Child-Pugh score 5 to 9). There is inadequate information about metabolism of clobazam in patients with severe hepatic impairment [see Dosage and Administration (2.7), Clinical Pharmacology (12.3)].

Clobazam oral suspension contains clobazam, a Schedule IV controlled substance.

Clobazam is a benzodiazepine and a CNS depressant with a potential for abuse and addiction. Abuse is the intentional, non-therapeutic use of a drug, even once, for its desirable psychological or physiological effects. Misuse is the intentional use, for therapeutic purposes, of a drug by an individual in a way other than prescribed by a health care provider or for whom it was not prescribed. Drug addiction is a cluster of behavioral, cognitive, and physiological phenomena that may include a strong desire to take the drug, difficulties in controlling drug use (e.g., continuing drug use despite harmful consequences, giving a higher priority to drug use than other activities and obligations), and possible tolerance or physical dependence. Even taking benzodiazepines as prescribed may put patients at risk for abuse and misuse of their medication. Abuse and misuse of benzodiazepines may lead to addiction.

Abuse and misuse of benzodiazepines often (but not always) involve the use of doses greater than the maximum recommended dosage and commonly involve concomitant use of other medications, alcohol, and/or illicit substances, which is associated with an increased frequency of serious adverse outcomes, including respiratory depression, overdose, or death. Benzodiazepines are often sought by individuals who abuse drugs and other substances, and by individuals with addictive disorders[see Warnings and Precautions (5.2)].

The following adverse reactions have occurred with benzodiazepine abuse and/or misuse: abdominal pain, amnesia, anorexia, anxiety, aggression, ataxia, blurred vision, confusion, depression, disinhibition, disorientation, dizziness, euphoria, impaired concentration and memory, indigestion, irritability, muscle pain, slurred speech, tremors, and vertigo.

The following severe adverse reactions have occurred with benzodiazepine abuse and/or misuse: delirium, paranoia, suicidal ideation and behavior, seizures, coma, breathing difficulty, and death. Death is more often associated with polysubstance use (especially benzodiazepines with other CNS depressants such as opioids and alcohol).

The World Health Organization epidemiology database contains reports of drug abuse, misuse, and overdoses associated with clobazam.

Physical Dependence

Clobazam may produce physical dependence from continued therapy. Physical dependence is a state that develops as a result of physiological adaptation in response to repeated drug use, manifested by withdrawal signs and symptoms after abrupt discontinuation or a significant dose reduction of a drug. Abrupt discontinuation or rapid dosage reduction of benzodiazepines or administration of flumazenil, a benzodiazepine antagonist, may precipitate acute withdrawal reactions, including seizures, which can be life-threatening. Patients at an increased risk of withdrawal adverse reactions after benzodiazepine discontinuation or rapid dosage reduction include those who take higher dosages i.e., higher and/or more frequent doses) and those who have had longer durations of use [see Warnings and Precautions (5.3)]. In clinical trials, cases of dependency were reported following abrupt discontinuation of clobazam.

To reduce the risk of withdrawal reactions, use a gradual taper to discontinue clobazam or reduce the dosage [see Dosage and Administration (2.2) and Warnings and Precautions (5.3)].

Acute Withdrawal Signs and Symptoms

Acute withdrawal signs and symptoms associated with benzodiazepines have included abnormal involuntary movements, anxiety, blurred vision, depersonalization, depression, derealization, dizziness, fatigue, gastrointestinal adverse reactions (e.g., nausea, vomiting, diarrhea, weight loss, decreased appetite), headache, hyperacusis, hypertension, irritability, insomnia, memory impairment, muscle pain and stiffness, panic attacks, photophobia, restlessness, tachycardia, and tremor. More severe acute withdrawal signs and symptoms, including life-threatening reactions, have included catatonia, convulsions, delirium tremens, depression, hallucinations, mania, psychosis, seizures, and suicidality.

Protracted Withdrawal Syndrome

Protracted withdrawal syndrome associated with benzodiazepines is characterized by anxiety, cognitive impairment, depression, insomnia, formication, motor symptoms (e.g., weakness, tremor, muscle twitches), paresthesia, and tinnitus that persists beyond 4 to 6 weeks after initial benzodiazepine withdrawal. Protracted withdrawal symptoms may last weeks to more than 12 months. As a result, there may be difficulty in differentiating withdrawal symptoms from potential re-emergence or continuation of symptoms for which the benzodiazepine was being used.

Tolerance

Tolerance to clobazam may develop from continued therapy. Tolerance is a physiological state characterized by a reduced response to a drug after repeated administration (i.e., a higher dose of a drug is required to produce the same effect that was once obtained at a lower dose). Tolerance to the therapeutic effect of clobazam may develop; however, little tolerance develops to the amnestic reactions and other cognitive impairments caused by benzodiazepines.

Overdosage of benzodiazepines is characterized by central nervous system depression ranging from drowsiness to coma. In mild to moderate cases, symptoms can include drowsiness, confusion, dysarthria, lethargy, hypnotic state, diminished reflexes, ataxia, and hypotonia. Rarely, paradoxical or disinhibitory reactions (including agitation, irritability, impulsivity, violent behavior, confusion, restlessness, excitement, and talkativeness) may occur. In severe overdosage cases, patients may develop respiratory depression and coma. Overdosage of benzodiazepines in combination with other CNS depressants (including alcohol and opioids) may be fatal [see Warnings and Precautions (5.2)]. Markedly abnormal (lowered or elevated) blood pressure, heart rate, or respiratory rate raise the concern that additional drugs and/or alcohol are involved in the overdosage.

{ "type": "p", "children": [], "text": "Overdosage of benzodiazepines is characterized by central nervous system depression ranging from drowsiness to coma. In mild to moderate cases, symptoms can include drowsiness, confusion, dysarthria, lethargy, hypnotic state, diminished reflexes, ataxia, and hypotonia. Rarely, paradoxical or disinhibitory reactions (including agitation, irritability, impulsivity, violent behavior, confusion, restlessness, excitement, and talkativeness) may occur. In severe overdosage cases, patients may develop respiratory depression and coma. Overdosage of benzodiazepines in combination with other CNS depressants (including alcohol and opioids) may be fatal [see Warnings and Precautions (5.2)]. Markedly abnormal (lowered or elevated) blood pressure, heart rate, or respiratory rate raise the concern that additional drugs and/or alcohol are involved in the overdosage." }

In managing benzodiazepine overdosage, employ general supportive measures, including intravenous fluids and airway maintenance. Flumazenil, a specific benzodiazepine receptor antagonist indicated for the complete or partial reversal of the sedative effects of benzodiazepines in the management of benzodiazepine overdosage, can lead to withdrawal and adverse reactions, including seizures, particularly in the context of mixed overdosage with drugs that increase seizure risk (e.g., tricyclic and tetracyclic antidepressants) and in patients with long-term benzodiazepine use and physical dependency. The risk of withdrawal seizures with flumazenil may be increased in patients with epilepsy. Flumazenil is contraindicated in patients who have received a benzodiazepine for control of a potentially life-threatening condition (e.g., status epilepticus). If the decision is made to use flumazenil, it should be used as an adjunct to, not as a substitute for, supportive management of benzodiazepine overdosage. See the flumazenil injection Prescribing Information.

{ "type": "p", "children": [], "text": "In managing benzodiazepine overdosage, employ general supportive measures, including intravenous fluids and airway maintenance. Flumazenil, a specific benzodiazepine receptor antagonist indicated for the complete or partial reversal of the sedative effects of benzodiazepines in the management of benzodiazepine overdosage, can lead to withdrawal and adverse reactions, including seizures, particularly in the context of mixed overdosage with drugs that increase seizure risk (e.g., tricyclic and tetracyclic antidepressants) and in patients with long-term benzodiazepine use and physical dependency. The risk of withdrawal seizures with flumazenil may be increased in patients with epilepsy. Flumazenil is contraindicated in patients who have received a benzodiazepine for control of a potentially life-threatening condition (e.g., status epilepticus). If the decision is made to use flumazenil, it should be used as an adjunct to, not as a substitute for, supportive management of benzodiazepine overdosage. See the flumazenil injection Prescribing Information." }

Consider contacting the Poison Help line (1-800-222-1222) or a medical toxicologist for additional overdosage management recommendations.

{ "type": "p", "children": [], "text": "Consider contacting the Poison Help line (1-800-222-1222) or a medical toxicologist for additional overdosage management recommendations." }

<div class="scrollingtable"><table width="85%"> <caption> <span>Table 4: Description</span> </caption> <col align="left" valign="top" width="50%"/> <col align="left" valign="top" width="50%"/> <tbody class="Headless"> <tr class="Botrule First"> <td align="left" class="Lrule Rrule">Established Name:</td><td align="left" class="Rrule">Clobazam Oral Suspension</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Dosage Forms:</td><td align="left" class="Rrule">Oral Suspension</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Route of Administration:</td><td align="left" class="Rrule">Oral</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Established Pharmacologic Class of Drug:</td><td align="left" class="Rrule">Benzodiazepine</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Chemical Name:</td><td align="left" class="Rrule">7-Chloro-1-methyl-5-phenyl-1 H-1,5 benzodiazepine- 2,4(<span class="Italics">3H,5H</span>)-dione</td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule">Structural Formula:</td><td align="left" class="Rrule"><img alt="Chemical Structure" src="/dailymed/image.cfm?name=clobazam-01.jpg&amp;setid=6332e71c-3b37-422c-838c-8a2489ac6009"/></td> </tr> </tbody> </table></div>

{ "type": "table", "children": [], "text": "<div class=\"scrollingtable\"><table width=\"85%\">\n<caption>\n<span>Table 4: Description</span>\n</caption>\n<col align=\"left\" valign=\"top\" width=\"50%\"/>\n<col align=\"left\" valign=\"top\" width=\"50%\"/>\n<tbody class=\"Headless\">\n<tr class=\"Botrule First\">\n<td align=\"left\" class=\"Lrule Rrule\">Established Name:</td><td align=\"left\" class=\"Rrule\">Clobazam Oral Suspension</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\">Dosage Forms:</td><td align=\"left\" class=\"Rrule\">Oral Suspension</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\">Route of Administration:</td><td align=\"left\" class=\"Rrule\">Oral</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\">Established Pharmacologic Class of Drug:</td><td align=\"left\" class=\"Rrule\">Benzodiazepine</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\">Chemical Name:</td><td align=\"left\" class=\"Rrule\">7-Chloro-1-methyl-5-phenyl-1 H-1,5 benzodiazepine- 2,4(<span class=\"Italics\">3H,5H</span>)-dione</td>\n</tr>\n<tr class=\"Last\">\n<td align=\"left\" class=\"Lrule Rrule\">Structural Formula:</td><td align=\"left\" class=\"Rrule\"><img alt=\"Chemical Structure\" src=\"/dailymed/image.cfm?name=clobazam-01.jpg&amp;setid=6332e71c-3b37-422c-838c-8a2489ac6009\"/></td>\n</tr>\n</tbody>\n</table></div>" }

Clobazam is a white or almost white, crystalline powder with a slightly bitter taste; is slightly soluble in water, sparingly soluble in ethanol, and freely soluble in methylene chloride. The melting range of clobazam is from 182°C to 185°C. The molecular formula is C16H13O2N2Cl and the molecular weight is 300.7.

{ "type": "p", "children": [], "text": "Clobazam is a white or almost white, crystalline powder with a slightly bitter taste; is slightly soluble in water, sparingly soluble in ethanol, and freely soluble in methylene chloride. The melting range of clobazam is from 182°C to 185°C. The molecular formula is C16H13O2N2Cl and the molecular weight is 300.7." }

Clobazam oral suspension is available for oral administration as an off-white suspension containing clobazam at a concentration of 2.5 mg/mL. Inactive ingredients include berry flavor, citric acid monohydrate, dibasic sodium phosphate dihydrate, magnesium aluminum silicate, maltitol solution, methylparaben, polysorbate 80, propylene glycol, propylparaben, purified water, simethicone emulsion, sucralose, xanthan gum.

{ "type": "p", "children": [], "text": "Clobazam oral suspension is available for oral administration as an off-white suspension containing clobazam at a concentration of 2.5 mg/mL. Inactive ingredients include berry flavor, citric acid monohydrate, dibasic sodium phosphate dihydrate, magnesium aluminum silicate, maltitol solution, methylparaben, polysorbate 80, propylene glycol, propylparaben, purified water, simethicone emulsion, sucralose, xanthan gum." }

The exact mechanism of action far clobazam, a 1,5-benzadiazepine, is not fully understood but is thought to involve potentiation of GABAergic neurotransmission resulting from binding at the benzodiazepine site of the GABAA receptor.

Effects on Electrocardiogram

The effect of clobazam 20 mg and 80 mg administered twice daily on OTc interval was evaluated in a randomized, evaluator-blinded, placebo-, and active-controlled (moxifloxacin 400 mg) parallel thorough QT study in 280 healthy subjects. In a study with demonstrated ability to detect small effects, the upper bound of the one-sided 95% confidence interval for the largest placebo-adjusted, baseline-corrected QTc based on the Fridericia correction method was below 10 ms, the threshold for regulatory concern. Thus, at a dose two times the maximum recommended dose, clobazam did not prolong the QTc interval to any clinically relevant extent.

The peak plasma levels (Cmax) and the area under the curve (AUG) of clobazam are dose-proportional over the dose range of 10 mg to 80 mg following single- or multiple-dose administration of clobazam. Based on a population pharmacokinetic analysis, the pharmacokinetics of clobazam are linear from 5 mg/day to 160 mg/day. Clobazam is converted to N-desmethylclobazam which has about 1/5 the activity of clobazam. The estimated mean elimination half-lives (t½) of clobazam and N-desmethylclobazam were 36 to 42 hours and 71 to 82 hours, respectively.

Absorption

Clobazam is rapidly and extensively absorbed following oral administration. The time to peak concentrations (Tmax) of clobazam tablets under fasted conditions ranged from 0.5 to 4 hours after single- or multiple-dose administrations. The relative bioavailability of clobazam tablets compared to an oral solution is approximately 100%. After single dose administration of the oral suspension under fasted conditions, the Tmax ranged from 0.5 to 2 hours. Based on exposure (Cmax and AUC) of clobazam, clobazam tablets and suspension were shown to have similar bioavailability under fasted conditions. The administration of clobazam tablets with food or when crushed in applesauce does not affect absorption. Although not studied, the oral bioavailability of the oral suspension is unlikely to be affected under fed conditions.

Distribution

Clobazam is lipophilic and distributes rapidly throughout the body. The apparent volume of distribution at steady-state was approximately 100 L. The in vitro plasma protein binding of clobazam and N-desmethylclobazam is approximately 80% to 90% and 70%, respectively.

Metabolism and Excretion

Clobazam is extensively metabolized in the liver, with approximately 2% of the dose recovered in urine and 1 % in feces as unchanged drug. The major metabolic pathway of clobazam involves N-demethylation, primarily by CYP3A4 and to a lesser extent by CYP2C19 and CYP2B6. N-desmethylclobazam, an active metabolite, is the major circulating metabolite in humans, and at therapeutic doses, plasma concentrations are 3 to 5 times higher than those of the parent compound. Based on animal and in vitro receptor binding data, estimates of the relative potency of N-desmethylclobazam compared to parent compound range from 1/5 to equal potency. N-desmethylclobazam is extensively metabolized, mainly by CYP2C19. N-desmethylclobazam and its metabolites comprise ~94% of the total drug-related components in urine. Following a single oral dose of radiolabeled drug, approximately 11% of the dose was excreted in the feces and approximately 82% was excreted in the urine.

The polymorphic CYP2C19 is the major contributor to the metabolism of the pharmacologically active N-desmethylclobazam [see Clinical Pharmacology (12.5)]. In CYP2C19 poor metabolizers, levels of N-desmethylclobazam were 5-fold higher in plasma and 2- to 3-told higher in the urine than in CYP2C19 extensive metabolizers.

Pharmacokinetics in Specific Populations

Age

Population pharmacokinetic analyses showed that the clearance of clobazam is lower in elderly subjects compared to other age groups (ages 2 to 64). Dosing should be adjusted in the elderly [see Dosage and Administration (2.4)].

Sex

Population pharmacokinetic analyses showed no difference in the clearance of clobazam between women and men.

Race

Population pharmacokinetic analyses including Caucasian (75%), African American (15%), and Asian (9%) subjects showed that there is no evidence of clinically significant effect of race on the clearance of clobazam.

Renal Impairment

The effect of renal impairment on the pharmacokinetics of clobazam was evaluated in patients with mild (creatinine clearance [CLCR] > 50 to 80 mL/min; N=6) and moderate (CLCR=30 to 50 mL/min; N=6) renal dysfunction, with matching healthy controls (N=6), following administration of multiple doses of clobazam 20 mg/day. There were insignificant changes in Cmax (3% to 24%) and AUC (≤ 13%) tor clobazam or N-desmethylclobazam in patients with mild or moderate renal impairment compared to patients with normal renal function. Patients with severe renal impairment or ESRD were not included in this study.

Hepatic Impairment

There are limited data to characterize the effect of hepatic impairment on the pharmacokinetics of clobazam. In a small study, the pharmacokinetics of a 20 mg single oral dose of clobazam in 9 patients with liver impairment were compared to healthy controls (N=6). The Cmax and the mean plasma clearance of clobazam, as well as the Cmax of N-desmethylclobazam, showed no significant change compared to the healthy controls. The AUC values of N-desmethylclobazam in these patients were not available. Adjust dosage in patients with hepatic impairment [see Dosage and Administration (2.7)].

Drug Interaction Studies

In vitro studies:

Clobazam did not inhibit CYP1A2, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP3A4, UGT1A1, UGTIA4, UGT1A6, or UGT2B4 in vitro. N-desmethylclobazam showed weak inhibition of CYP2C9, UGT1A4, UGT1A6 and UGT2B4.

Clobazam and N-desmethylclobazam did not significantly increase CYP1A2 or CYP2C19 activities, but did induce CYP3A4 activity in a concentration-dependent manner. Clobazam and N-desmethylclobazam also increased UGT1A1 mRNA but at concentrations much higher than therapeutic levels. The potential tor clobazam or N-desmethylclobazam to induce CYP2B6 and CYP2C8 has not been evaluated.

Clobazam and N-desmethylclobazam do not inhibit P-glycoprotein (P-gp), but are P-gp substrates.

In vivo studies:

Potential for Clobazam to Affect Other Drugs

The effect of repeated 40 mg once-daily doses of clobazam on the pharmacokinetic profiles of single-dose dextromethorphan (CYP2D6 substrate), midazolam (CYP3A4 substrate), caffeine (CYP1A2 substrate), and tolbutamide (CYP2C9 substrate), was studied when these probe substrates were given as a drug cocktail (N=l 8).

Clobazam increased AUC and Cmax of dextromethorphan by 90% and 59%, respectively, reflecting its inhibition of CYP2D6 in vivo. Drugs metabolized by CYP2D6 may require dose adjustment when used with clobazam.

Clobazam decreased the ALIC and Cmax of midazolam by 27% and 24%, respectively, and increased the AUC and Cmax of the metabolite 1-hydroxymidazolam by 4-fold and 2-fold, respectively. This level of induction does not call for dosage adjustment of drugs that are primarily metabolized by CYP3A4 when used concomitantly with clobazam. Some hormonal contraceptives are metabolized by CYP3A4 and their effectiveness may be diminished when given with clobazam [see Drug Interactions (7.3)]. Repeated clobazam doses had no effect on caffeine and tolbutamide.

A population pharmacokinetic analysis indicated clobazam did not affect the exposure of valproic acid (a CYP2C9/2C19 substrate) or lamotrigine (a UGT substrate).

Potential for Other Drugs to Affect Clobazam

Co-administration of ketoconazole (a strong CYP3A4 inhibitor) 400 mg once-daily for 5 days increased clobazam AUC by 54%, with an insignificant effect on clobazam Cmax. There was no significant change in AUG and Cmax of N-desmethylclobazam (N=18).

Strong (e.g., fluconazole, fluvoxamine, ticlopidine) and moderate (e.g., omeprazole) inhibitors of CYP2C19 may result in up to a 5-fold increase in exposure to N-desmethylclobazam, the active metabolite of clobazam, based on extrapolation from pharmacogenomic data [see Clinical Pharmacology (12.5)]. Dosage adjustment of clobazam may be necessary when co-administered with strong or moderate CYP2C19 inhibitors [see Drug Interactions (7.4)].

The effects of concomitant antiepileptic drugs that are CYP3A4 inducers (phenobarbital, phenytoin, and carbamazepine), CYP2C19 inducers (valproic acid, phenobarbital, phenytoin, and carbamazepine), and CYP2C19 inhibitors (felbamate and oxcarbazepine) were evaluated using data from clinical trials. Results of population pharmacokinetic analysis show that these concomitant antiepileptic drugs did not significantly alter the pharmacokinetics of clobazam or N-desmethylclobazam at steady-state.

Alcohol has been reported to increase the maximum plasma exposure of clobazam by approximately 50%. Alcohol may have additive CNS depressant effects when taken with clobazam [see Warnings and Precautions (5.4), Drug Interactions (7.2)].

The polymorphic CYP2C19 is the main enzyme that metabolizes the pharmacologically active N-desmethylclobazam. Compared to CYP2C19 extensive metabolizers, N-desmethylclobazam AUC and Cmax are approximately 3 to 5 times higher in poor metabolizern (e.g., subjects with *2/*2 genotype) and 2 times higher in intermediate metabolizers (e.g., subjects with *1/*2 genotype). The prevalence of CYP2C19 poor metabolism differs depending on racial/ethnic background. Dosage in patients who are known CYP2C19 poor metabolizers may need to be adjusted [see Dosage and Administration (2.5)].

The systemic exposure of clobazam is similar for both CYP2C19 poor and extensive metabolizers.

Carcinogenesis

In mice, oral administration of clobazam (O, 6, 12, or 24 mg/kg/day) for 2 years did not result in an increase in tumors. The highest dose tested was approximately 3 times the maximum recommended human dose (MRHD) of 40 mg/day, based on body surface area (mg/m2).

In rats, oral administration of clobazam for 2 years resulted in increases in tumors of the thyroid gland (follicular cell adenoma and carcinoma) and liver (hepatocellular adenoma) at the mid and high doses. The low dose, not associated with an increase in tumors, was associated with plasma exposures (AUC) for clobazam and its major active metabolite, N-desmethylclobazam, less than that in humans at the MRHD.

Mutagenesis

Clobazam and the major active metabolite, N-desmethylclobazam, were negative for genotoxicity, based on data from a battery of in vitro (bacteria reverse mutation, mammalian clastogenicity) and in vivo (mouse micronucleus) assays.

Impairment of Fertility

In a fertility study in which clobazam (50,350, or 750 mg/kg/day, corresponding to 12, 84 and 181 times the oral Maximum Recommended Human Dose, MRHD, of 40 mg/day based on mg/m2 body surface) was orally administered to male and female rats prior to and during mating and continuing in females to gestation day 6, increases in abnormal sperm and pre-implantation loss were observed at the highest dose tested. The no-effect level for fertility and ear1y embryonic development in rats was associated with plasma exposures (AUC) tor clobazam and its major active metabolite, N-desmethylclobazam, less than those in humans at the maximum recommended human dose of 40 mg/day.

Study 1

Study 1 (N=238) was a randomized, double-blind, placebo-controlled study consisting of a 4-week baseline period followed by a 3-week titration period and 12-week maintenance period. Patients age 2 to 54 years with a current or prior diagnosis of LGS were stratified into 2 weight groups (12.5 kg to ≤ 30 kg or > 30 kg) and then randomized to placebo or one of three target maintenance doses of clobazam according to Table 5.

<div class="scrollingtable"><table width="85%"> <caption> <span>Table 5: Study 1 Total Daily Dose</span> </caption> <col align="left" valign="top" width="34%"/> <col align="center" valign="top" width="33%"/> <col align="center" valign="top" width="33%"/> <thead> <tr class="First Last"> <th align="left" class="Lrule Rrule"></th><th align="center" class="Rrule">≤ 30 kg Body Weight</th><th align="center" class="Rrule">&gt; 30 kg Body Weight</th> </tr> </thead> <tbody> <tr class="Botrule First"> <td align="left" class="Lrule Rrule">Low Dose</td><td align="center" class="Rrule">5 mg daily</td><td align="center" class="Rrule">10 mg daily</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Medium Dose</td><td align="center" class="Rrule">10 mg daily</td><td align="center" class="Rrule">20 mg daily</td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule">High Dose</td><td align="center" class="Rrule">20 mg daily</td><td align="center" class="Rrule">40 mg daily</td> </tr> </tbody> </table></div>

Doses above 5 mg/day were administered in two divided doses.

The primary efficacy measure was the percent reduction in the weekly frequency of drop seizures (atonic, tonic, or myoclonic), also known as drop attacks, from the 4-week baseline period to 12-week maintenance period.

The pre-dosing baseline mean weekly drop seizure frequency was 98, 100, 61, and 105 for the placebo, low-, medium-, and high-dose groups, respectively. Figure 1 presents the mean percent reduction in weekly drop seizures from this baseline. All dose groups of clobazam were statistically superior (p ≤ 0.05) to the placebo group. This effect appeared to be dose dependent.

<div class="scrollingtable"><table class="Noautorules" width="100%"> <col align="center" valign="top" width="100%"/> <thead> <tr> <th align="center">Figure 1: Mean Percent Reduction from Baseline in Weekly Drop Seizure Frequency (Study 1)</th> </tr> </thead> <tbody> <tr> <td align="center"><img alt="Figure 1" src="/dailymed/image.cfm?name=clobazam-02.jpg&amp;setid=6332e71c-3b37-422c-838c-8a2489ac6009"/></td> </tr> </tbody> </table></div>

Figure 2 shows changes from baseline in weekly drop seizure frequency by category tor patients treated with clobazam and placebo in Study 1. Patients in whom the seizure frequency increased are shown at left as "worse." Patients in whom the seizure frequency decreased are shown in five categories.

<div class="scrollingtable"><table class="Noautorules" width="100%"> <col align="center" valign="top" width="100%"/> <thead> <tr> <th align="center">Figure 2: Drop Seizure Response by Category for Clobazam and Placebo (Study 1)</th> </tr> </thead> <tbody> <tr> <td align="center"><img alt="Figure 2" src="/dailymed/image.cfm?name=clobazam-03.jpg&amp;setid=6332e71c-3b37-422c-838c-8a2489ac6009"/></td> </tr> </tbody> </table></div>

There was no evidence that tolerance to the therapeutic effect of clobazam developed during the 3-month maintenance period.

Study 2

Study 2 (N=68) was a randomized, double-blind comparison study of high- and low-dose clobazam, consisting of a 4-week baseline period followed by a 3-week titration period and 4-week maintenance period. Patients age 2 to 25 years with a current or prior diagnosis of LGS were stratified by weight, then randomized to either a low or high dose of clobazam, and then entered a 3-week titration period.

The primary efficacy measure was the percent reduction in the weekly frequency of drop seizures (atonic, tonic, or myoclonic), also known as drop attacks, from the 4-week baseline period to the 4-week maintenance period.

A statistically significantly greater reduction in seizure frequency was observed in the high-dose group compared to the low-dose group (median percent reduction of 93% vs 29%; p < 0.05).

Store oral suspension at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].

Risks from Concomitant Use with Opioids

Inform patients and caregivers that potentially fatal additive effects may occur if clobazam is used with opioids and not to use such drugs concomitantly unless supervised by a healthcare provider [see Warnings and Precautions (5.1), Drug Interactions (7.1)].

Abuse Misuse and Addiction

Inform patients that the use of clobazam, even at recommended dosages, exposes users to risks of abuse, misuse, and addiction, which can lead to overdose and death, especially when used in combination with other medications (e.g., opioid analgesics), alcohol, and/or illicit substances. Inform patients about the signs and symptoms of benzodiazepine abuse, misuse, and addiction; to seek medical help if they develop these signs and/or symptoms; and on the proper disposal of unused drug [see Warnings and Precautions (5.2) and Drug Abuse and Dependence (9.2)].

Withdrawal Reactions

Advise patients or caregivers that abrupt withdrawal of AEDs may increase their risk of seizure. Inform patients that the continued use of clobazam may lead to clinically significant physical dependence and that abrupt discontinuation or rapid dosage reduction of clobazam may precipitate acute withdrawal reactions, which can be life-threatening. Inform patients that in some cases, patients taking benzodiazepines have developed a protracted withdrawal syndrome with withdrawal symptoms lasting weeks to more than 12 months. Instruct patients that discontinuation or dosage reduction of clobazam may require a slow taper [see Warnings and Precautions (5.3) and Drug Abuse and Dependence (9.3)].

Somnolence or Sedation

Advise patients or caregivers to check with their healthcare provider before clobazam is taken with other CNS depressants such as other benzodiazepines, opioids, tricyclic antidepressants, sedating antihistamines, or alcohol [see Warnings and Precautions (5.4, 5.5)].

If applicable, caution patients about operating hazardous machinery, including automobiles, until they are reasonably certain that clobazam does not affect them adversely (e.g., impair judgment, thinking or motor skills).

Hypersensitivity

Inform patients or caregivers that clobazam is contraindicated in patients with a history of hypersensitivity to the drug or its ingredients [see Warnings and Precautions (5.6)].

Interactions with Hormonal Contraceptives

Counsel women to also use non-hormonal methods of contraception when clobazam is used with hormonal contraceptives and to continue these alternative methods for 28 days after discontinuing clobazam to ensure contraceptive reliability [see Drug Interactions (7.3), Clinical Pharmacology (12.3)].

Serious Dermatological Reactions

Advise patients or caregivers that serious skin reactions have been reported in patients taking clobazam. Serious skin reactions, including SJS/TEN, may need to be treated in a hospital and may be life-threatening. If a skin reaction occurs while taking clobazam, patients or caregivers should consult with healthcare providers immediately [see Warnings and Precautions (5.6)].

Suicidal Thinking and Behavior

Counsel patients, their caregivers, and their families that AEDs, including clobazam, may increase the risk of suicidal thoughts and behavior and advise them of the need to be alert for the emergence or worsening of symptoms of depression, any unusual changes in mood or behavior, or the emergence of suicidal thoughts, behavior, or thoughts of self-harm. Patients should report behaviors of concern immediately to healthcare providers [see Warnings and Precautions (5.7)].

Pregnancy

Advise pregnant females that the use of clobazam late in pregnancy can result in sedation (respiratory depression, lethargy, hypotonia) and/or withdrawal symptoms (hyperreflexia, irritability, restlessness, tremors, inconsolable crying, and feeding difficulties) in newborns [see Warnings and Precautions (5.8) and Use in Specific Populations (8.1)]. Instruct patients to notify their healthcare provider if they are pregnant.

Encourage patients to enroll in the North American Antiepileptic Drug (NAAED) Pregnancy Registry if they become pregnant while taking clobazam. The registry is collecting information about the safety of antiepileptic drugs during pregnancy [see Use in Specific Populations (8.1)].

Lactation

Counsel patients that clobazam, the active ingredient in clobazam oral suspension, is excreted in breast milk. Instruct patients to notify their healthcare provider if they are breast feeding or intend to breast feed. Instruct breastfeeding patients who have been administered clobazam to observe their infants for sedation, poor feeding and poor weight gain, and to seek medical attention if they notice these signs [see Use in Specific Populations (8.2)].

Packaged by: Precision Dose, Inc. South Beloit, IL 61080

{ "type": "p", "children": [], "text": "Packaged by:\nPrecision Dose, Inc.\nSouth Beloit, IL 61080" }

For inquiries call Precision Dose, Inc. at 1-800-397-9228 or email druginfo@precisiondose.com

{ "type": "p", "children": [], "text": "For inquiries call Precision Dose, Inc. at 1-800-397-9228 or email druginfo@precisiondose.com" }

Ll1567 Rev. 04/24

{ "type": "p", "children": [], "text": "Ll1567 Rev. 04/24" }

<div class="scrollingtable"><table width="100%"> <col align="left" valign="top" width="2%"/> <col align="left" valign="top" width="28%"/> <col align="left" valign="top" width="70%"/> <thead> <tr class="First Last"> <th align="center" class="Lrule Rrule" colspan="3">MEDICATION GUIDE<br/>Clobazam (kloe' ba zam)<br/>Oral Suspension, CIV</th> </tr> </thead> <tbody> <tr class="First"> <td align="left" class="Lrule Rrule" colspan="3"> <p class="First"> <a name="important"></a><span class="Bold">What is the most important information I should know about clobazam oral suspension?</span> </p> <ul class="Disc"> <li> <span class="Bold">Clobazam oral suspension is benzodiazepine medicine. Taking benzodiazepines with opioid medicines, alcohol, or other central nervous system (CNS) depressants (including street drugs) can cause severe drowsiness, breathing problems (respiratory depression), coma, and death.</span> Get emergency help right away if any of the following happens:<ul class="Circle"> <li>shallow or slowed breathing</li> <li>breathing stops (which may lead to the heart stopping)</li> <li>excessive sleepiness (sedation)</li> </ul> </li> </ul> Do not drive or operate heavy machinery until you know how taking clobazam oral suspension with opioids affects you. <ul class="Disc"> <li> <span class="Bold">Risk of abuse, misuse, and addiction. There is a risk of abuse, misuse, and addiction with benzodiazepines, including clobazam oral suspension, which can lead to overdose and serious side effects including coma and death.</span> <ul class="Circle"> <li> <span class="Bold">Serious side effects including coma and death have happened in people who have abused or misused benzodiazepines, including clobazam oral suspension.</span> These serious side effects may also include delirium, paranoia, suicidal thoughts or actions, seizures, and difficulty breathing. <span class="Bold">Call your healthcare provider or go to the nearest hospital emergency room right away if you get any of these serious side effects.</span> </li> <li> <span class="Bold">You can develop an addiction even if you take clobazam oral suspension as prescribed by your healthcare provider.</span> </li> <li> <span class="Bold">Take clobazam oral suspension exactly as your healthcare provider prescribed.</span> </li> <li>Do not share your clobazam oral suspension with other people.</li> <li>Keep clobazam oral suspension in a safe place and away from children.</li> </ul> </li> <li> <span class="Bold">Physical dependence and withdrawal reactions.</span> Clobazam oral suspension can cause physical dependence and withdrawal reactions.</li> <li> <span class="Bold">Do not suddenly stop taking clobazam oral suspension.</span> Stopping clobazam oral suspension suddenly can cause serious and life-threatening side effects, including unusual movements, responses, or expressions, siezures, sudden and severe mental or nervous system changes, depression, seeing or hearing things that others do not see or hear, an extreme increase in activity or talking, losing touch with reality, and suicidal thoughts or actions. <span class="Bold">Call your healthcare provider or go to the nearest hospital emergency room right away if you get any of these symptoms.</span> <ul class="Circle"> <li> <span class="Bold">Some people who suddenly stop benzodiazepines have symptoms that can last for several weeks to more than 12 months,</span> including, anxiety, trouble remembering, learning, or concentrating, depression, problems sleeping, felling like insects are crawling under your skin, weakness, shaking, muscle twitching, burning or prickling feeling in your hands, arms, legs or feet, and ringing in your ears.</li> <li>Physical dependence is not the same as drug addiction. Your your healthcare provider can tell you more about the differences between physical dependence and drug addiction.</li> <li>Do not take more clobazam oral suspension than prescribed or take clobazam oral suspension for longer than prescribed.</li> </ul> </li> <li> <span class="Bold">Clobazam oral suspension can make you sleepy or dizzy and can slow your thinking and motor skills.</span> <ul class="Circle"> <li>Do not drive, operate heavy machinery, or do other dangerous activities until you know how clobazam oral suspension affects you.</li> <li>Do not drink alcohol or take other drugs that may make you sleepy or dizzy while taking clobazam oral suspension without first talking to your healthcare provider. When taken with alcohol or drugs that cause sleepiness or dizziness, clobazam oral suspension may make your sleepiness or dizziness much worse.</li> </ul> </li> <li> <span class="Bold">Serious skin reactions have been seen when clobazam oral suspension is taken with other medicines and may require stopping its use.</span> Do not stop taking clobazam oral suspension without first talking to your healthcare provider.<ul class="Circle"> <li>A serious skin reaction can happen at any time during your treatment with clobazam oral suspension, but is more likely to happen within the first 8 weeks of treatment. These skin reactions may need to be treated right away.</li> <li>Call your healthcare provider immediately if you have skin blisters, rash, sores in the mouth, hives or any other allergic reaction.</li> </ul> </li> <li> <span class="Bold">Like other antiepileptic medicines, clobazam oral suspension may cause suicidal thoughts or actions in a very small number of people, about 1 in 500.</span> </li> <li> <span class="Bold">Call your healthcare provider right away if you have any of these symptoms especially if they are new, worse, or worry you:</span> </li> </ul> </td> </tr> <tr> <td align="left" class="Lrule"></td><td align="left"> <ul class="Circle"> <li>thoughts about suicide or dying</li> <li>new or worse depression</li> <li>trouble sleeping (insomnia)</li> <li>acting on dangerous impulses</li> <li>attempts to commit suicide</li> <li>feeling agitated or restless</li> <li>new or worse anxiety or irritability</li> </ul> </td><td align="left" class="Rrule"> <ul class="Circle"> <li>an extreme increase in activity and talking (mania)</li> <li>new or worse panic attacks</li> <li>acting aggressive, being angry or violent</li> <li>other unusual changes in behavior or mood</li> </ul> </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="3"><span class="Bold">How can I watch for early symptoms of suicidal thoughts and actions?</span> <ul class="Circle"> <li>Pay attention to any changes, especially sudden changes, in mood, behaviors, thoughts, or feelings.</li> <li>Keep all follow-up visits with your healthcare provider as scheduled.</li> </ul> Call your healthcare provider between visits as needed, especially if you are worried about symptoms.<br/>Stopping a seizure medicine suddenly in a patient who has epilepsy can cause seizures that will not stop (status epilepticus).<br/>Suicidal thoughts or actions can be caused by things other than medicines. If you have suicidal thoughts or actions, your healthcare provider may check for other causes. </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="3"><span class="Bold">What is clobazam oral suspension?</span> <ul class="Disc"> <li>Clobazam oral suspension is a prescription medicine used along with other medicines to treat seizures associated with Lennox-Gastaut syndrone in people 2 years of age or older.</li> <li> <span class="Bold">Clobazam oral suspension is a federally controlled substance (C-IV) because it contains clobazam that can be abused or lead to dependence.</span> Keep clobazam oral suspension in a safe place to prevent misuse and abuse. Selling or giving away clobazam oral suspension may harm others, and is againts the law. Tell your healthcare provider if you have ever abused or been dependent on alcohol, prescription medicines, or street drugs.</li> </ul> It is not known if clobazam oral suspension is safe and effective in children less than 2 years old. </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="3"><span class="Bold">Do not take clobazam oral suspension if you:</span> <ul class="Disc"> <li>are allergic to clobazam or any of the ingredients in clobazam oral suspension. See the end of this Medication Guide for a complete list of ingredients in clobazam oral suspension.</li> </ul> <span class="Bold">Before you take clobazam oral suspension, tell your healthcare provider about all your medical conditions, including if you:</span> <ul class="Disc"> <li>have liver or kidney problems</li> <li>have lung problems (respiratory disease)</li> <li>have or have had depression, mood problems, or suicidal thoughts or behavior</li> <li>use birth control medicine. Clobazam oral suspension may cause your birth control medicine to be less effective. Talk to your healthcare provider about the best birth control method to use.</li> <li>are pregnant or plan to become pregnant. <ul class="Circle"> <li>Taking clobazam oral suspension late in pregnancy may cause your baby to have symptoms of sedation (breathing problems, sluggishness, low muscle tone) and/or withdrawal symptoms 0itteriness, irritability, restlessness, shaking, excessive crying, feeding problems).</li> <li>Tell your healthcare provider right away if you become pregnant or think you are pregnant while taking clobazam oral suspension.</li> <li>If you become pregnant while taking clobazam oral suspension, talk to your healthcare provider about registering with the North American Antiepileptic Drug Pregnancy Registry. You can registerby calling 1-888-233-2334. For more information about the registry go to http://www.aedpregnancyregistry.org. The purpose of this registry is to collect information about the safety of antiepileptic drugs during pregnancy.</li> </ul> </li> <li>are breastfeeding or plan to breastfeed. Clobazam can pass into breast milk. <ul class="Circle"> <li>Breastfeeding during treatment with clobazam oral suspension may cause your baby to have sleepiness, feeding problems and decreased weight gain.</li> <li>Talk to your healthcare provider about the best way to feed your baby if you take clobazam oral suspension.</li> </ul> </li> </ul> <span class="Bold">Tell healthcare provider about all the medicines you take,</span> including prescription and over-the-counter medicines, vitamins, and herbal supplements. Taking clobazam oral suspension with certain other medicines can cause side effects or affect how well clobazam oral suspension or the other medicines work. Do not start or stop other medicines without talking to your healthcare provider. </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="3"><span class="Bold">How should I take clobazam oral suspension?</span> <ul class="Disc"> <li>Take clobazam oral suspension exactly as your healthcare provider tells you to take.</li> <li>Your healthcare provider will tell you how much clobazam oral suspension to take and when to take it.</li> <li>Clobazam oral suspension can be taken with or without food.</li> <li> <span class="Bold">Shake clobazam oral suspension right before you take each dose.</span> </li> <li>Your healthcare provider may change your dose if needed.</li> <li>Do not stop taking clobazam oral suspension without first talking to your healthcare provider.</li> <li>Stopping clobazam oral suspension suddenly can cause serious problems.</li> <li>If you take too much clobazam oral suspension, call your healthcare provider or go to the nearest hospital emergency room right away.</li> </ul> </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="3"><span class="Bold">What should I avoid while taking clobazam oral suspension?</span> <br/>See <span class="Bold">"<a href="#important">What is the most important information I should know about clobazam oral suspension?</a>"</span></td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="3"><span class="Bold">What are the possible side effects of clobazam oral suspension?<br/>Clobazam oral suspension may cause serious side effects, including:<br/>See "<a href="#important">What is the most important information I should know about clobazam oral suspension?</a>"<br/>The most common side effects of clobazam oral suspension include:</span></td> </tr> <tr> <td align="left" class="Lrule"></td><td align="left"> <ul class="Disc"> <li>sleepiness</li> <li>cough</li> <li>acting aggressive, being angry or violent</li> <li>tiredness</li> <li>drooling</li> <li>pain with urination</li> </ul> </td><td align="left" class="Rrule"> <ul class="Disc"> <li>difficulty sleeping</li> <li>problems with breathing</li> <li>constipation</li> <li>fever</li> <li>slurred speech</li> </ul> </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="3">These are not all the possible side effects of clobazam oral suspension.<br/>Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="3"><span class="Bold">How should I store clobazam oral suspension?</span> <ul class="Disc"> <li>Store clobazam oral suspension at room temperature between 68°F to 77°F (20°C to 25°C)</li> <li> <span class="Bold">Keep clobazam oral suspension and all medicines out of the reach of children.</span> </li> </ul> </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="3"><span class="Bold">General information about the safe and effective use of clobazam oral suspension.</span> <br/>Medicines are sometimes prescribed for purposes other than those listed in the Medication Guide. Do not use clobazam oral suspension for a condition for which it was not prescribed. Do not give clobazam oral suspension to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about clobazam oral suspension that is written for health professionals.</td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule" colspan="3"><span class="Bold">What are the ingredients in clobazam oral suspension?</span> <br/> <span class="Underline">Oral Suspension</span> <br/> <span class="Bold">Active ingredient:</span> clobazam<br/> <span class="Bold">Inactive ingredients:</span> berry flavor, citric acid monohydrate, dibasic sodium phosphate dihydrate, magnesium aluminum silicate, maltitol solution, methylparaben, polysorbate 80, propylene glycol, propylparaben, purified water, simethicone emulsion, sucralose, xanthan gum.<br/>Package by:<br/> <span class="Bold">Precision Dose, Inc.</span> <br/>South Beloit, IL 61080<br/>For inquiries call Precision Dose, Inc. at 1-800-397-9228 or email druginfo@precisiondose.com</td> </tr> </tbody> </table></div>

{ "type": "table", "children": [], "text": "<div class=\"scrollingtable\"><table width=\"100%\">\n<col align=\"left\" valign=\"top\" width=\"2%\"/>\n<col align=\"left\" valign=\"top\" width=\"28%\"/>\n<col align=\"left\" valign=\"top\" width=\"70%\"/>\n<thead>\n<tr class=\"First Last\">\n<th align=\"center\" class=\"Lrule Rrule\" colspan=\"3\">MEDICATION GUIDE<br/>Clobazam (kloe' ba zam)<br/>Oral Suspension, CIV</th>\n</tr>\n</thead>\n<tbody>\n<tr class=\"First\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"3\">\n<p class=\"First\">\n<a name=\"important\"></a><span class=\"Bold\">What is the most important information I should know about clobazam oral suspension?</span>\n</p>\n<ul class=\"Disc\">\n<li>\n<span class=\"Bold\">Clobazam oral suspension is benzodiazepine medicine. Taking benzodiazepines with opioid medicines, alcohol, or other central nervous system (CNS) depressants (including street drugs) can cause severe drowsiness, breathing problems (respiratory depression), coma, and death.</span> Get emergency help right away if any of the following happens:<ul class=\"Circle\">\n<li>shallow or slowed breathing</li>\n<li>breathing stops (which may lead to the heart stopping)</li>\n<li>excessive sleepiness (sedation)</li>\n</ul>\n</li>\n</ul>\t\t\t\t\t\t\t\t\tDo not drive or operate heavy machinery until you know how taking clobazam oral suspension with opioids affects you. \t\t\t\t\t\t\t\t\t<ul class=\"Disc\">\n<li>\n<span class=\"Bold\">Risk of abuse, misuse, and addiction. There is a risk of abuse, misuse, and addiction with benzodiazepines, including clobazam oral suspension, which can lead to overdose and serious side effects including coma and death.</span>\n<ul class=\"Circle\">\n<li>\n<span class=\"Bold\">Serious side effects including coma and death have happened in people who have abused or misused benzodiazepines, including clobazam oral suspension.</span> These serious side effects may also include delirium, paranoia, suicidal thoughts or actions, seizures, and difficulty breathing. <span class=\"Bold\">Call your healthcare provider or go to the nearest hospital emergency room right away if you get any of these serious side effects.</span>\n</li>\n<li>\n<span class=\"Bold\">You can develop an addiction even if you take clobazam oral suspension as prescribed by your healthcare provider.</span>\n</li>\n<li>\n<span class=\"Bold\">Take clobazam oral suspension exactly as your healthcare provider prescribed.</span>\n</li>\n<li>Do not share your clobazam oral suspension with other people.</li>\n<li>Keep clobazam oral suspension in a safe place and away from children.</li>\n</ul>\n</li>\n<li>\n<span class=\"Bold\">Physical dependence and withdrawal reactions.</span> Clobazam oral suspension can cause physical dependence and withdrawal reactions.</li>\n<li>\n<span class=\"Bold\">Do not suddenly stop taking clobazam oral suspension.</span> Stopping clobazam oral suspension suddenly can cause serious and life-threatening side effects, including unusual movements, responses, or expressions, siezures, sudden and severe mental or nervous system changes, depression, seeing or hearing things that others do not see or hear, an extreme increase in activity or talking, losing touch with reality, and suicidal thoughts or actions. <span class=\"Bold\">Call your healthcare provider or go to the nearest hospital emergency room right away if you get any of these symptoms.</span>\n<ul class=\"Circle\">\n<li>\n<span class=\"Bold\">Some people who suddenly stop benzodiazepines have symptoms that can last for several weeks to more than 12 months,</span> including, anxiety, trouble remembering, learning, or concentrating, depression, problems sleeping, felling like insects are crawling under your skin, weakness, shaking, muscle twitching, burning or prickling feeling in your hands, arms, legs or feet, and ringing in your ears.</li>\n<li>Physical dependence is not the same as drug addiction. Your your healthcare provider can tell you more about the differences between physical dependence and drug addiction.</li>\n<li>Do not take more clobazam oral suspension than prescribed or take clobazam oral suspension for longer than prescribed.</li>\n</ul>\n</li>\n<li>\n<span class=\"Bold\">Clobazam oral suspension can make you sleepy or dizzy and can slow your thinking and motor skills.</span>\n<ul class=\"Circle\">\n<li>Do not drive, operate heavy machinery, or do other dangerous activities until you know how clobazam oral suspension affects you.</li>\n<li>Do not drink alcohol or take other drugs that may make you sleepy or dizzy while taking clobazam oral suspension without first talking to your healthcare provider. When taken with alcohol or drugs that cause sleepiness or dizziness, clobazam oral suspension may make your sleepiness or dizziness much worse.</li>\n</ul>\n</li>\n<li>\n<span class=\"Bold\">Serious skin reactions have been seen when clobazam oral suspension is taken with other medicines and may require stopping its use.</span> Do not stop taking clobazam oral suspension without first talking to your healthcare provider.<ul class=\"Circle\">\n<li>A serious skin reaction can happen at any time during your treatment with clobazam oral suspension, but is more likely to happen within the first 8 weeks of treatment. These skin reactions may need to be treated right away.</li>\n<li>Call your healthcare provider immediately if you have skin blisters, rash, sores in the mouth, hives or any other allergic reaction.</li>\n</ul>\n</li>\n<li>\n<span class=\"Bold\">Like other antiepileptic medicines, clobazam oral suspension may cause suicidal thoughts or actions in a very small number of people, about 1 in 500.</span>\n</li>\n<li>\n<span class=\"Bold\">Call your healthcare provider right away if you have any of these symptoms especially if they are new, worse, or worry you:</span>\n</li>\n</ul>\n</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule\"></td><td align=\"left\">\n<ul class=\"Circle\">\n<li>thoughts about suicide or dying</li>\n<li>new or worse depression</li>\n<li>trouble sleeping (insomnia)</li>\n<li>acting on dangerous impulses</li>\n<li>attempts to commit suicide</li>\n<li>feeling agitated or restless</li>\n<li>new or worse anxiety or irritability</li>\n</ul>\n</td><td align=\"left\" class=\"Rrule\">\n<ul class=\"Circle\">\n<li>an extreme increase in activity and talking (mania)</li>\n<li>new or worse panic attacks</li>\n<li>acting aggressive, being angry or violent</li>\n<li>other unusual changes in behavior or mood</li>\n</ul>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"3\"><span class=\"Bold\">How can I watch for early symptoms of suicidal thoughts and actions?</span>\n<ul class=\"Circle\">\n<li>Pay attention to any changes, especially sudden changes, in mood, behaviors, thoughts, or feelings.</li>\n<li>Keep all follow-up visits with your healthcare provider as scheduled.</li>\n</ul>\t\t\t\t\t\t\t\t\tCall your healthcare provider between visits as needed, especially if you are worried about symptoms.<br/>Stopping a seizure medicine suddenly in a patient who has epilepsy can cause seizures that will not stop (status epilepticus).<br/>Suicidal thoughts or actions can be caused by things other than medicines. If you have suicidal thoughts or actions, your healthcare provider may check for other causes. \t\t\t\t\t\t\t\t\t</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"3\"><span class=\"Bold\">What is clobazam oral suspension?</span>\n<ul class=\"Disc\">\n<li>Clobazam oral suspension is a prescription medicine used along with other medicines to treat seizures associated with Lennox-Gastaut syndrone in people 2 years of age or older.</li>\n<li>\n<span class=\"Bold\">Clobazam oral suspension is a federally controlled substance (C-IV) because it contains clobazam that can be abused or lead to dependence.</span> Keep clobazam oral suspension in a safe place to prevent misuse and abuse. Selling or giving away clobazam oral suspension may harm others, and is againts the law. Tell your healthcare provider if you have ever abused or been dependent on alcohol, prescription medicines, or street drugs.</li>\n</ul>\t\t\t\t\t\t\t\t\tIt is not known if clobazam oral suspension is safe and effective in children less than 2 years old. \t\t\t\t\t\t\t\t\t</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"3\"><span class=\"Bold\">Do not take clobazam oral suspension if you:</span>\n<ul class=\"Disc\">\n<li>are allergic to clobazam or any of the ingredients in clobazam oral suspension. See the end of this Medication Guide for a complete list of ingredients in clobazam oral suspension.</li>\n</ul>\n<span class=\"Bold\">Before you take clobazam oral suspension, tell your healthcare provider about all your medical conditions, including if you:</span>\n<ul class=\"Disc\">\n<li>have liver or kidney problems</li>\n<li>have lung problems (respiratory disease)</li>\n<li>have or have had depression, mood problems, or suicidal thoughts or behavior</li>\n<li>use birth control medicine. Clobazam oral suspension may cause your birth control medicine to be less effective. Talk to your healthcare provider about the best birth control method to use.</li>\n<li>are pregnant or plan to become pregnant. \t\t\t\t\t\t\t\t\t\t<ul class=\"Circle\">\n<li>Taking clobazam oral suspension late in pregnancy may cause your baby to have symptoms of sedation (breathing problems, sluggishness, low muscle tone) and/or withdrawal symptoms 0itteriness, irritability, restlessness, shaking, excessive crying, feeding problems).</li>\n<li>Tell your healthcare provider right away if you become pregnant or think you are pregnant while taking clobazam oral suspension.</li>\n<li>If you become pregnant while taking clobazam oral suspension, talk to your healthcare provider about registering with the North American Antiepileptic Drug Pregnancy Registry. You can registerby calling 1-888-233-2334. For more information about the registry go to http://www.aedpregnancyregistry.org. The purpose of this registry is to collect information about the safety of antiepileptic drugs during pregnancy.</li>\n</ul>\n</li>\n<li>are breastfeeding or plan to breastfeed. Clobazam can pass into breast milk. \t\t\t\t\t\t\t\t\t\t<ul class=\"Circle\">\n<li>Breastfeeding during treatment with clobazam oral suspension may cause your baby to have sleepiness, feeding problems and decreased weight gain.</li>\n<li>Talk to your healthcare provider about the best way to feed your baby if you take clobazam oral suspension.</li>\n</ul>\n</li>\n</ul>\n<span class=\"Bold\">Tell healthcare provider about all the medicines you take,</span> including prescription and over-the-counter medicines, vitamins, and herbal supplements. Taking clobazam oral suspension with certain other medicines can cause side effects or affect how well clobazam oral suspension or the other medicines work. Do not start or stop other medicines without talking to your healthcare provider. \t\t\t\t\t\t\t\t\t</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"3\"><span class=\"Bold\">How should I take clobazam oral suspension?</span>\n<ul class=\"Disc\">\n<li>Take clobazam oral suspension exactly as your healthcare provider tells you to take.</li>\n<li>Your healthcare provider will tell you how much clobazam oral suspension to take and when to take it.</li>\n<li>Clobazam oral suspension can be taken with or without food.</li>\n<li>\n<span class=\"Bold\">Shake clobazam oral suspension right before you take each dose.</span>\n</li>\n<li>Your healthcare provider may change your dose if needed.</li>\n<li>Do not stop taking clobazam oral suspension without first talking to your healthcare provider.</li>\n<li>Stopping clobazam oral suspension suddenly can cause serious problems.</li>\n<li>If you take too much clobazam oral suspension, call your healthcare provider or go to the nearest hospital emergency room right away.</li>\n</ul>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"3\"><span class=\"Bold\">What should I avoid while taking clobazam oral suspension?</span>\n<br/>See <span class=\"Bold\">\"<a href=\"#important\">What is the most important information I should know about clobazam oral suspension?</a>\"</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"3\"><span class=\"Bold\">What are the possible side effects of clobazam oral suspension?<br/>Clobazam oral suspension may cause serious side effects, including:<br/>See \"<a href=\"#important\">What is the most important information I should know about clobazam oral suspension?</a>\"<br/>The most common side effects of clobazam oral suspension include:</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule\"></td><td align=\"left\">\n<ul class=\"Disc\">\n<li>sleepiness</li>\n<li>cough</li>\n<li>acting aggressive, being angry or violent</li>\n<li>tiredness</li>\n<li>drooling</li>\n<li>pain with urination</li>\n</ul>\n</td><td align=\"left\" class=\"Rrule\">\n<ul class=\"Disc\">\n<li>difficulty sleeping</li>\n<li>problems with breathing</li>\n<li>constipation</li>\n<li>fever</li>\n<li>slurred speech</li>\n</ul>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"3\">These are not all the possible side effects of clobazam oral suspension.<br/>Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"3\"><span class=\"Bold\">How should I store clobazam oral suspension?</span>\n<ul class=\"Disc\">\n<li>Store clobazam oral suspension at room temperature between 68°F to 77°F (20°C to 25°C)</li>\n<li>\n<span class=\"Bold\">Keep clobazam oral suspension and all medicines out of the reach of children.</span>\n</li>\n</ul>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"3\"><span class=\"Bold\">General information about the safe and effective use of clobazam oral suspension.</span>\n<br/>Medicines are sometimes prescribed for purposes other than those listed in the Medication Guide. Do not use clobazam oral suspension for a condition for which it was not prescribed. Do not give clobazam oral suspension to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about clobazam oral suspension that is written for health professionals.</td>\n</tr>\n<tr class=\"Last\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"3\"><span class=\"Bold\">What are the ingredients in clobazam oral suspension?</span>\n<br/>\n<span class=\"Underline\">Oral Suspension</span>\n<br/>\n<span class=\"Bold\">Active ingredient:</span> clobazam<br/>\n<span class=\"Bold\">Inactive ingredients:</span> berry flavor, citric acid monohydrate, dibasic sodium phosphate dihydrate, magnesium aluminum silicate, maltitol solution, methylparaben, polysorbate 80, propylene glycol, propylparaben, purified water, simethicone emulsion, sucralose, xanthan gum.<br/>Package by:<br/>\n<span class=\"Bold\">Precision Dose, Inc.</span>\n<br/>South Beloit, IL 61080<br/>For inquiries call Precision Dose, Inc. at 1-800-397-9228 or email druginfo@precisiondose.com</td>\n</tr>\n</tbody>\n</table></div>" }

This Medication Guide has been approved by the U.S. Food and Drug Administration.

{ "type": "p", "children": [], "text": "This Medication Guide has been approved by the U.S. Food and Drug Administration." }

Ll1567 Rev. 04/24

{ "type": "p", "children": [], "text": "Ll1567 Rev. 04/24" }

cloBAZam Oral Suspension CIV

{ "type": "p", "children": [], "text": "cloBAZam Oral Suspension CIV" }

10 mg/4 mL Delivers 4 mL

{ "type": "p", "children": [], "text": "10 mg/4 mL Delivers 4 mL" }

Each mL Contains: clobazam 2.5 mg

{ "type": "p", "children": [], "text": "Each mL Contains: clobazam 2.5 mg" }

Shake syringe well before each use.

{ "type": "p", "children": [], "text": "Shake syringe well before each use." }

Store at 20-25° (68-77°F)

{ "type": "p", "children": [], "text": "Store at 20-25° (68-77°F)" }

FOR ORAL ADMINISTRATION ONLY.

{ "type": "p", "children": [], "text": "FOR ORAL ADMINISTRATION ONLY." }

Pkg: Precision Dose, Inc. S. Beloit, IL 61080

{ "type": "p", "children": [], "text": "Pkg: Precision Dose, Inc. S. Beloit, IL 61080" }

Clobazam tablet is indicated for the adjunctive treatment of seizures associated with Lennox-Gastaut syndrome (LGS) in patients 2 years of age or older.

{ "type": "p", "children": [], "text": "Clobazam tablet is indicated for the adjunctive treatment of seizures associated with Lennox-Gastaut syndrome (LGS) in patients 2 years of age or older." }

A daily dose of clobazam tablets greater than 5 mg should be administered in divided doses twice daily; a 5 mg daily dose can be administered as a single dose. Dose patients according to body weight. Individualize dosing within each body weight group, based on clinical efficacy and tolerability. Each dose in Table 1 (e.g., 5 to 20 mg in ≤30 kg weight group) has been shown to be effective, although effectiveness increases with increasing dose [see Clinical Studies (14)]. Do not proceed with dose escalation more rapidly than weekly, because serum concentrations of clobazam and its active metabolite require 5 and 9 days, respectively, to reach steady-state.

Table 1. Recommended Total Daily Dosing by Weight Group

<div class="scrollingtable"><table border="0" cellpadding="0" cellspacing="0" width="798"> <colgroup> <col width="33.3333333333333%"/> <col width="33.3333333333333%"/> <col width="33.3333333333333%"/> </colgroup> <tbody class="Headless"> <tr class="Botrule First"> <td align="justify" class="Lrule Rrule" valign="top"> <br/> </td><td align="justify" class="Rrule" valign="top"><span class="Bold">≤30 kg Body Weight </span> <br/> </td><td align="justify" class="Rrule" valign="top"><span class="Bold">Greater than 30 kg Body Weight </span> <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="top">Starting Dose <br/> </td><td align="justify" class="Rrule" valign="top">5 mg <br/> </td><td align="justify" class="Rrule" valign="top">10 mg <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="top">Starting Day 7 <br/> </td><td align="justify" class="Rrule" valign="top">10 mg <br/> </td><td align="justify" class="Rrule" valign="top">20 mg <br/> </td> </tr> <tr class="Last"> <td align="justify" class="Lrule Rrule" valign="top">Starting Day 14 <br/> </td><td align="justify" class="Rrule" valign="top">20 mg <br/> </td><td align="justify" class="Rrule" valign="top">40 mg <br/> </td> </tr> </tbody> </table></div>

To reduce the risk of withdrawal reactions, increased seizure frequency, and status epilepticus, use a gradual taper to discontinue clobazam tablets or reduce the dosage. Taper by decreasing the total daily dose by 5 to 10 mg/day on a weekly basis until discontinued. If a patient develops withdrawal reactions, consider pausing the taper or increasing the dosage to the previous tapered dosage level. Subsequently decrease the dosage more slowly [see Warnings and Precautions (5.3) and Drug Abuse and Dependence (9.3)].

Clobazam Tablets Oral Administration Clobazam tablets can be taken with or without food. Clobazam tablets can be administered whole, broken in half along the score, or crushed and mixed in applesauce.

Plasma concentrations at any given dose are generally higher in the elderly: proceed slowly with dose escalation. The starting dose should be 5 mg/day for all elderly patients. Then titrate elderly patients according to weight, but to half the dose presented in Table 1, as tolerated. If necessary and based upon clinical response, an additional titration to the maximum dose (20 mg/day or 40 mg/day, depending on weight) may be started on day 21 [see Use in Specific Populations (8.5)].

In CYP2C19 poor metabolizers, levels of N-desmethylclobazam, clobazam’s active metabolite, will be increased. Therefore, in patients known to be CYP2C19 poor metabolizers, the starting dose should be 5 mg/day and dose titration should proceed slowly according to weight, but to half the dose presented in Table 1, as tolerated. If necessary and based upon clinical response, an additional titration to the maximum dose (20 mg/day or 40 mg/day, depending on the weight group) may be started on day 21 [see Use in Specific Populations (8.6), Clinical Pharmacology (12.5)].

No dose adjustment is required for patients with mild and moderate renal impairment. There is no experience with clobazam in patients with severe renal impairment or end stage renal disease (ESRD). It is not known if clobazam or its active metabolite, N-desmethylclobazam, is dialyzable [see Use in Specific Populations (8.7), Clinical Pharmacology (12.3)].

Clobazam is hepatically metabolized; however, there are limited data to characterize the effect of hepatic impairment on the pharmacokinetics of clobazam. For this reason, proceed slowly with dosing escalations. For patients with mild to moderate hepatic impairment (Child-Pugh score 5 to 9), the starting dose should be 5 mg/day in both weight groups. Then titrate patients according to weight, but to half the dose presented in Table 1, as tolerated. If necessary and based upon clinical response, start an additional titration on day 21 to the maximum dose (20 mg/day or 40 mg/day, depending on the weight group). There is inadequate information about metabolism of clobazam in patients with severe hepatic impairment. Therefore no dosing recommendation in those patients can be given [see Use in Specific Populations (8.8), Clinical Pharmacology (12.3)].

5 mg: White to off white round shaped uncoated tablets debossed with "C" on one side and "5" on other side.

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10 mg:  Off white oval shaped uncoated tablets with a functional score on one side and ‘C’ and ‘10’ debossed on other side.

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20 mg: Off white oval shaped uncoated tablets with a functional score on one side and ‘C’ and ‘20’ debossed on other side.

{ "type": "p", "children": [], "text": "\n20 mg: Off white oval shaped uncoated tablets with a functional score on one side and ‘C’ and ‘20’ debossed on other side." }

Clobazam is contraindicated in patients with a history of hypersensitivity to the drug or its ingredients. Hypersensitivity reactions have included serious dermatological reactions [see Warnings and Precautions (5.6, 5.7)].

{ "type": "p", "children": [], "text": "Clobazam is contraindicated in patients with a history of hypersensitivity to the drug or its ingredients. Hypersensitivity reactions have included serious dermatological reactions [see Warnings and Precautions (5.6, 5.7)].\n" }

Concomitant use of benzodiazepines, including clobazam, and opioids may result in profound sedation, respiratory depression, coma, and death. Because of these risks, reserve concomitant prescribing of benzodiazepines and opioids for patients for whom alternative treatment options are inadequate. Observational studies have demonstrated that concomitant use of opioid analgesics and benzodiazepines increases the risk of drug-related mortality compared to use of opioids alone. If a decision is made to prescribe clobazam concomitantly with opioids, prescribe the lowest effective dosages and minimum durations of concomitant use, and follow patients closely for signs and symptoms of respiratory depression and sedation. Advise both patients and caregivers about the risks of respiratory depression and sedation when clobazam is used with opioids [see Drug Interactions (7.1)].

The use of benzodiazepines, including clobazam, exposes users to the risks of abuse, misuse, and addiction, which can lead to overdose or death. Abuse and misuse of benzodiazepines often (but not always) involve the use of doses greater than the maximum recommended dosage and commonly involve concomitant use of other medications, alcohol, and/or illicit substances, which is associated with an increased frequency of serious adverse outcomes, including respiratory depression, overdose, or death [see Drug Abuse and Dependence (9.2)].

Before prescribing clobazam and throughout treatment, assess each patient’s risk for abuse, misuse, and addiction (e.g., using a standardized screening tool). Use of clobazam, particularly in patients at elevated risk, necessitates counseling about the risks and proper use of clobazam along with monitoring for signs and symptoms of abuse, misuse, and addiction. Prescribe the lowest effective dosage; avoid or minimize concomitant use of CNS depressants and other substances associated with abuse, misuse, and addiction (e.g., opioid analgesics, stimulants); and advise patients on the proper disposal of unused drug. If a substance use disorder is suspected, evaluate the patient and institute (or refer them for) early treatment, as appropriate.

To reduce the risk of withdrawal reactions, use a gradual taper to discontinue clobazam or reduce the dosage [see Dosage and Administration (2.2)]. Patients at an increased risk of withdrawal adverse reactions after benzodiazepine discontinuation or rapid dosage reduction include those who take higher dosages, and those who have had longer durations of use.

Acute Withdrawal Reactions

The continued use of benzodiazepines, including clobazam, may lead to clinically significant physical dependence. Abrupt discontinuation or rapid dosage reduction of clobazam after continued use, or administration of flumazenil (a benzodiazepine antagonist) may precipitate acute withdrawal reactions, which can be life-threatening (e.g., seizures) [see Drug Abuse and Dependence (9.3)].

Protracted Withdrawal Syndrome

In some cases, benzodiazepine users have developed a protracted withdrawal syndrome with withdrawal symptoms lasting weeks to more than 12 months [see Drug Abuse and Dependence (9.3)].

Since clobazam has a central nervous system (CNS) depressant effect, patients or their caregivers should be cautioned against simultaneous use with other CNS depressant drugs or alcohol, and cautioned that the effects of other CNS depressant drugs or alcohol may be potentiated [see Drug Interactions (7.2)].

Clobazam causes somnolence and sedation. In clinical trials, somnolence or sedation was reported at all effective doses and was dose-related. In general, somnolence and sedation begin within the first month of treatment and may diminish with continued treatment. Prescribers should monitor patients for somnolence and sedation, particularly with concomitant use of other central nervous system depressants. Prescribers should caution patients against engaging in hazardous activities requiring mental alertness, such as operating dangerous machinery or motor vehicles, until the effect of clobazam is known.

Serious skin reactions, including Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN), have been reported with clobazam in both children and adults during the postmarketing period. Patients should be closely monitored for signs or symptoms of SJS/TEN, especially during the first 8 weeks of treatment initiation or when re-introducing therapy. Clobazam should be discontinued at the first sign of rash, unless the rash is clearly not drug-related. If signs or symptoms suggest SJS/TEN, use of this drug should not be resumed and alternative therapy should be considered [see Contraindications (4)].

Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS), also known as multiorgan hypersensitivity, has been reported in patients taking antiepileptic drugs, including clobazam. These events can be fatal or life-threatening, particularly if diagnosis and treatment do not occur as early as possible. DRESS typically, although not exclusively, presents with fever, rash, lymphadenopathy, and/or facial swelling, in association with other organ system involvement, such as hepatitis, nephritis, hematological abnormalities, myocarditis, or myositis, sometimes resembling an acute viral infection. Eosinophilia is often present. Because this disorder is variable in its expression, other organ systems not noted here may be involved. It is important to note that early manifestations of hypersensitivity, such as fever or lymphadenopathy, may be present even though rash is not evident. If such signs or symptoms are present, the patient should be evaluated immediately. Clobazam should be discontinued if an alternative etiology for the signs or symptoms cannot be established [see Contraindications (4)].

Antiepileptic drugs (AEDs), including clobazam, increase the risk of suicidal thoughts or behavior in patients taking these drugs for any indication. Patients treated with any AED for any indication should be monitored for the emergence or worsening of depression, suicidal thoughts or behavior, and/or any unusual changes in mood or behavior. Pooled analyses of 199 placebo-controlled clinical trials (mono-and adjunctive therapy) of 11 different AEDs showed that patients randomized to one of the AEDs had approximately twice the risk (adjusted relative risk 1.8, 95% confidence interval [CI]: 1.2, 2.7) of suicidal thinking or behavior compared to patients randomized to placebo. In these trials, which had a median treatment duration of 12 weeks, the estimated incidence rate of suicidal behavior or ideation among 27,863 AED-treated patients was 0.43%, compared to 0.24% among 16,029 placebo-treated patients, representing an increase of approximately one case of suicidal thinking or behavior for every 530 patients treated. There were four suicides in drug-treated patients in the trials and none in placebo-treated patients, but the number is too small to allow any conclusion about drug effect on suicide. The increased risk of suicidal thoughts or behavior with AEDs was observed as early as one week after starting drug treatment with AEDs and persisted for the duration of treatment assessed. Because most trials included in the analysis did not extend beyond 24 weeks, the risk of suicidal thoughts or behavior beyond 24 weeks could not be assessed. The risk of suicidal thoughts or behavior was generally consistent among drugs in the data analyzed. The finding of increased risk with AEDs of varying mechanisms of action and across a range of indications suggests that the risk applies to all AEDs used for any indication. The risk did not vary substantially by age (5 to 100 years) in the clinical trials analyzed. Table 2 shows absolute and relative risk by indication for all evaluated AEDs. Table 2. Risk by Indication for Antiepileptic Drugs in the Pooled Analysis

<div class="scrollingtable"><table border="0" cellpadding="0" cellspacing="0" width="604"> <colgroup> <col width="15.7284768211921%"/> <col width="22.0198675496689%"/> <col width="15.7284768211921%"/> <col width="25.1655629139073%"/> <col width="21.3576158940397%"/> </colgroup> <tbody class="Headless"> <tr class="Botrule First"> <td class="Lrule Rrule" valign="top"><span class="Bold"></span> <br/> <span class="Bold">Indication</span> <br/> <br/> </td><td class="Rrule" valign="top"><span class="Bold"> Placebo Patients with Events per 1,000 Patients</span> <br/> <br/> </td><td class="Rrule" valign="top"><span class="Bold">Drug Patients with Events per 1,000 Patients</span> <br/> </td><td class="Rrule" valign="top"><span class="Bold">Relative Risk: Incidence of Drug Events in Drug Patients/Incidence in Placebo Patients</span> <br/> </td><td class="Rrule" valign="top"><span class="Bold">Risk Difference: Additional Drug Patients with Events per 1,000 Patients</span> <br/> </td> </tr> <tr class="Botrule"> <td align="center" class="Lrule Rrule" valign="middle">Epilepsy<br/> </td><td align="center" class="Rrule" valign="middle">1.0<br/> </td><td align="center" class="Rrule" valign="middle">3.4<br/> </td><td align="center" class="Rrule" valign="middle">3.5<br/> </td><td align="center" class="Rrule" valign="middle">2.4<br/> </td> </tr> <tr class="Botrule"> <td align="center" class="Lrule Rrule" valign="middle">Psychiatric<br/> </td><td align="center" class="Rrule" valign="middle">5.7<br/> </td><td align="center" class="Rrule" valign="middle">8.5<br/> </td><td align="center" class="Rrule" valign="middle">1.5<br/> </td><td align="center" class="Rrule" valign="middle">2.9<br/> </td> </tr> <tr class="Botrule"> <td align="center" class="Lrule Rrule" valign="middle">Other<br/> </td><td align="center" class="Rrule" valign="middle">1.0<br/> </td><td align="center" class="Rrule" valign="middle">1.8<br/> </td><td align="center" class="Rrule" valign="middle">1.9<br/> </td><td align="center" class="Rrule" valign="middle">0.9<br/> </td> </tr> <tr class="Last"> <td align="center" class="Lrule Rrule" valign="middle">Total<br/> </td><td align="center" class="Rrule" valign="middle">2.4<br/> </td><td align="center" class="Rrule" valign="middle">4.3<br/> </td><td align="center" class="Rrule" valign="middle">1.8<br/> </td><td align="center" class="Rrule" valign="middle">1.9<br/> </td> </tr> </tbody> </table></div>

The relative risk for suicidal thoughts or behavior was higher in clinical trials for epilepsy than in clinical trials for psychiatric or other conditions, but the absolute risk differences were similar for the epilepsy and psychiatric indications.

Anyone considering prescribing clobazam or any other AED must balance the risk of suicidal thoughts or behavior with the risk of untreated illness. Epilepsy and many other illnesses for which AEDs are prescribed are themselves associated with morbidity and mortality and an increased risk of suicidal thoughts and behavior. Should suicidal thoughts and behavior emerge during treatment, the prescriber needs to consider whether the emergence of these symptoms in any given patient may be related to the illness being treated. Patients, their caregivers, and families should be informed that AEDs increase the risk of suicidal thoughts and behavior and should be advised of the need to be alert for the emergence or worsening of the signs and symptoms of depression, any unusual changes in mood or behavior, or the emergence of suicidal thoughts, behavior, or thoughts about self-harm. Behaviors of concern should be reported immediately to healthcare providers.

Use of clobazam late in pregnancy can result in sedation (respiratory depression, lethargy, hypotonia) and/or withdrawal symptoms (hyperreflexia, irritability, restlessness, tremors, inconsolable crying, and feeding difficulties) in the neonate [see Use in Specific Populations (8.1)]. Monitor neonates exposed to clobazam during pregnancy or labor for signs of sedation and monitor neonates exposed to clobazam during pregnancy for signs of withdrawal; manage these neonates accordingly.

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

During its development for the adjunctive treatment of seizures associated with LGS, clobazam was administered to 333 healthy volunteers and 300 patients with a current or prior diagnosis of LGS, including 197 patients treated for 12 months or more. The conditions and duration of exposure varied greatly and included single-and multiple-dose clinical pharmacology studies in healthy volunteers and two double-blind studies in patients with LGS (Study 1 and 2) [see Clinical Studies (14)]. Only Study 1 included a placebo group, allowing comparison of adverse reaction rates on clobazam at several doses to placebo.

Adverse Reactions Leading to Discontinuation in an LGS Placebo Controlled Clinical Trial (Study 1) The adverse reactions associated with clobazam treatment discontinuation in ≥1% of patients in decreasing order of frequency included lethargy, somnolence, ataxia, aggression, fatigue, and insomnia. 

Most Common Adverse Reactions in an LGS Placebo Controlled Clinical Trial (Study 1)

Table 3 lists the adverse reactions that occurred in ≥5% of clobazam-treated patients (at any dose), and at a rate greater than placebo-treated patients, in the randomized, double-blind, placebo-controlled, parallel group clinical study of adjunctive AED therapy for 15 weeks (Study 1). 

Table 3. Adverse Reactions Reported for ≥5% of Patients and More Frequently than Placebo in Any Treatment Group

<div class="scrollingtable"><table border="0" cellpadding="0" cellspacing="0" width="668"> <colgroup> <col width="23.8380809595202%"/> <col width="15.592203898051%"/> <col width="14.8425787106447%"/> <col width="15.7421289355322%"/> <col width="14.8425787106447%"/> <col width="15.1424287856072%"/> </colgroup> <tbody class="Headless"> <tr class="Botrule First"> <td align="justify" class="Lrule Rrule" rowspan="2" valign="top"> <br/> </td><td align="justify" class="Rrule" rowspan="2" valign="top"> <br/> <br/> <br/> <br/> <span class="Bold">Placebo N=59 % </span> <br/> </td><td align="center" class="Rrule" colspan="3" valign="top"><span class="Bold">Clobazam Dose Level</span> <br/> </td><td align="justify" class="Rrule" rowspan="2" valign="top"> <br/> <br/> <br/> <span class="Bold">All Clobazam</span> <br/> <span class="Bold">N=179 </span> <br/> <span class="Bold">% </span> <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom"><span class="Bold">Low<span class="Sup">a</span></span> <br/> <span class="Bold">N=58 % </span> <br/> </td><td align="justify" class="Rrule" valign="bottom"><span class="Bold">Medium<span class="Sup">b</span></span><span class="Bold"><span class="Sup"> </span></span><span class="Bold">N=62 % </span> <br/> </td><td align="justify" class="Rrule" valign="top"> <br/> <br/> <span class="Bold">High<span class="Sup">c</span></span><span class="Bold"> </span><span class="Bold">N=59</span> <br/> <span class="Bold">% </span> <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" colspan="6" valign="top"><span class="Bold">Gastrointestinal Disorders </span> <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Vomiting <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">9 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">7 <br/> </td><td align="justify" class="Rrule" valign="bottom">7 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Constipation <br/> </td><td align="justify" class="Rrule" valign="bottom">0 <br/> </td><td align="justify" class="Rrule" valign="bottom">2 <br/> </td><td align="justify" class="Rrule" valign="bottom">2 <br/> </td><td align="justify" class="Rrule" valign="bottom">10 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Dysphagia <br/> </td><td align="justify" class="Rrule" valign="bottom">0 <br/> </td><td align="justify" class="Rrule" valign="bottom">0 <br/> </td><td align="justify" class="Rrule" valign="bottom">0 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">2 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" colspan="6" valign="top"><span class="Bold">General Disorders and Administration Site Conditions </span> <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Pyrexia <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">17 <br/> </td><td align="justify" class="Rrule" valign="bottom">10 <br/> </td><td align="justify" class="Rrule" valign="bottom">12 <br/> </td><td align="justify" class="Rrule" valign="bottom">13 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Irritability <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">11 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">7 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Fatigue <br/> </td><td align="justify" class="Rrule" valign="bottom">2 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" colspan="6" valign="top"><span class="Bold">Infections and Infestations </span> <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Upper respiratory tract infection <br/> </td><td align="justify" class="Rrule" valign="top">10 <br/> </td><td align="justify" class="Rrule" valign="top">10 <br/> </td><td align="justify" class="Rrule" valign="top">13 <br/> </td><td align="justify" class="Rrule" valign="top">14 <br/> </td><td align="justify" class="Rrule" valign="top">12 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Pneumonia <br/> </td><td align="justify" class="Rrule" valign="bottom">2 <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">7 <br/> </td><td align="justify" class="Rrule" valign="bottom">4 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Urinary tract infection <br/> </td><td align="justify" class="Rrule" valign="bottom">0 <br/> </td><td align="justify" class="Rrule" valign="bottom">2 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">4 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Bronchitis <br/> </td><td align="justify" class="Rrule" valign="bottom">0 <br/> </td><td align="justify" class="Rrule" valign="bottom">2 <br/> </td><td align="justify" class="Rrule" valign="bottom">0 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">2 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" colspan="6" valign="top"><span class="Bold">Metabolism and Nutrition Disorders </span> <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Decreased appetite <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">0 <br/> </td><td align="justify" class="Rrule" valign="bottom">7 <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Increased appetite <br/> </td><td align="justify" class="Rrule" valign="bottom">0 <br/> </td><td align="justify" class="Rrule" valign="bottom">2 <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" colspan="6" valign="bottom"><span class="Bold">Nervous System Disorders </span> <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Somnolence or Sedation <br/> </td><td align="justify" class="Rrule" valign="bottom">15 <br/> </td><td align="justify" class="Rrule" valign="bottom">17 <br/> </td><td align="justify" class="Rrule" valign="bottom">27 <br/> </td><td align="justify" class="Rrule" valign="bottom">32 <br/> </td><td align="justify" class="Rrule" valign="bottom">26 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Somnolence <br/> </td><td align="justify" class="Rrule" valign="bottom">12 <br/> </td><td align="justify" class="Rrule" valign="bottom">16 <br/> </td><td align="justify" class="Rrule" valign="bottom">24 <br/> </td><td align="justify" class="Rrule" valign="bottom">25 <br/> </td><td align="justify" class="Rrule" valign="bottom">22 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Sedation <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">2 <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">9 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Lethargy <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">10 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">15 <br/> </td><td align="justify" class="Rrule" valign="bottom">10 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Drooling <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">0 <br/> </td><td align="justify" class="Rrule" valign="bottom">13 <br/> </td><td align="justify" class="Rrule" valign="bottom">14 <br/> </td><td align="justify" class="Rrule" valign="bottom">9 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Ataxia<br/> </td><td align="justify" class="Rrule" valign="bottom">3<br/> </td><td align="justify" class="Rrule" valign="bottom">3<br/> </td><td align="justify" class="Rrule" valign="bottom">2<br/> </td><td align="justify" class="Rrule" valign="bottom">10<br/> </td><td align="justify" class="Rrule" valign="bottom">5<br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Psychomotor hyperactivity <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">4 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Dysarthria <br/> </td><td align="justify" class="Rrule" valign="bottom">0 <br/> </td><td align="justify" class="Rrule" valign="bottom">2 <br/> </td><td align="justify" class="Rrule" valign="bottom">2 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" colspan="6" valign="bottom"><span class="Bold">Psychiatric Disorders </span> <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Aggression <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">8 <br/> </td><td align="justify" class="Rrule" valign="bottom">14 <br/> </td><td align="justify" class="Rrule" valign="bottom">8 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="bottom">Insomnia <br/> </td><td align="justify" class="Rrule" valign="bottom">2 <br/> </td><td align="justify" class="Rrule" valign="bottom">2 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">7 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" colspan="6" valign="bottom"><span class="Bold">Respiratory Disorders </span> <br/> </td> </tr> <tr class="Last"> <td align="justify" class="Lrule Rrule" valign="bottom">Cough <br/> </td><td align="justify" class="Rrule" valign="bottom">0 <br/> </td><td align="justify" class="Rrule" valign="bottom">3 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td><td align="justify" class="Rrule" valign="bottom">7 <br/> </td><td align="justify" class="Rrule" valign="bottom">5 <br/> </td> </tr> </tbody> </table></div>

   aMaximum daily dose of 5 mg for ≤30 kg body weight; 10 mg for greater than 30 kg body weight

 bMaximum daily dose of 10 mg for ≤30 kg body weight; 20 mg for greater than 30 kg body weight

  cMaximum daily dose of 20 mg for ≤30 kg body weight; 40 mg for greater than 30 kg body weight

These reactions are reported voluntarily from a population of uncertain size; therefore, it is not possible to estimate their frequency or establish a causal relationship to drug exposure. Adverse reactions are categorized by system organ class.  Blood Disorders: Anemia, eosinophilia, leukopenia, thrombocytopenia  Eye Disorders: Diplopia, vision blurred Gastrointestinal Disorders: Abdominal distention General Disorders and Administration Site Conditions: Hypothermia Investigations: Hepatic enzyme increased Musculoskeletal: Muscle spasms Psychiatric Disorders: Agitation, anxiety, apathy, confusional state, depression, delirium, delusion, hallucination Renal and Urinary Disorders: Urinary retention Respiratory Disorders: Aspiration, respiratory depression Skin and Subcutaneous Tissue Disorders: Rash, urticaria, angioedema, and facial and lip edema

The concomitant use of benzodiazepines and opioids increases the risk of respiratory depression because of actions at different receptor sites in the CNS that control respiration. Benzodiazepines interact at GABAA sites, and opioids interact primarily at mu receptors. When benzodiazepines and opioids are combined, the potential for benzodiazepines to significantly worsen opioid-related respiratory depression exists. Limit dosage and duration of concomitant use of benzodiazepines and opioids, and follow patients closely for respiratory depression and sedation [see Warnings and Precautions (5.1)].

Concomitant use of clobazam with other CNS depressants may increase the risk of sedation and somnolence [see Warnings and Precautions (5.4)].

Alcohol, as a CNS depressant, will interact with clobazam in a similar way and also increases clobazam’s maximum plasma exposure by approximately 50%. Therefore, caution patients or their caregivers against simultaneous use with other CNS depressant drugs or alcohol, and caution that the effects of other CNS depressant drugs or alcohol may be potentiated [see Warnings and Precautions (5.4)]. 

Hormonal Contraceptives

Clobazam is a weak CYP3A4 inducer. As some hormonal contraceptives are metabolized by CYP3A4, their effectiveness may be diminished when given with clobazam. Additional non-hormonal forms of contraception are recommended when using clobazam [see Clinical Pharmacology (12.3), Patient Counseling Information (17)].

Drugs Metabolized by CYP2D6

Clobazam inhibits CYP2D6. Dose adjustment of drugs metabolized by CYP2D6 may be necessary [see Clinical Pharmacology (12.3)].

Strong and moderate inhibitors of CYP2C19

Strong and moderate inhibitors of CYP2C19 may result in increased exposure to N-desmethylclobazam, the active metabolite of clobazam. This may increase the risk of dose-related adverse reactions. Dosage adjustment of clobazam may be necessary when co-administered with strong CYP2C19 inhibitors (e.g., fluconazole, fluvoxamine, ticlopidine) or moderate CYP2C19 inhibitors (e.g., omeprazole) [see Clinical Pharmacology (12.3)]. 

Pregnancy Registry

There is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to AEDs, such as clobazam, during pregnancy. Healthcare providers are encouraged to recommend that pregnant women taking clobazam enroll in the North American Antiepileptic Drug (NAAED) Pregnancy Registry by calling 1-888-233-2334 or online at http://www.aedpregnancyregistry.org/.

Risk Summary

Neonates born to mothers using benzodiazepines late in pregnancy have been reported to experience symptoms of sedation and/or neonatal withdrawal [see Warnings and Precautions (5.9) and Clinical Considerations]. Available data from published observational studies of pregnant women exposed to benzodiazepines do not report a clear association with benzodiazepines and major birth defects (see Data).

Administration of clobazam to pregnant rats and rabbits during the period of organogenesis or to rats throughout pregnancy and lactation resulted in developmental toxicity, including increased incidences of fetal malformations and mortality, at plasma exposures for clobazam and its major active metabolite, N-desmethylclobazam, below those expected at therapeutic doses in patients [see Animal Data]. Data for other benzodiazepines suggest the possibility of long-term effects on neurobehavioral and immunological function in animals following prenatal exposure to benzodiazepines at clinically relevant doses. Clobazam should be used during pregnancy only if the potential benefit to the mother justifies the potential risk to the fetus. Advise a pregnant woman and women of childbearing age of the potential risk to a fetus.

The background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and of miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively.

Clinical Considerations

Fetal/Neonatal Adverse Reactions

Benzodiazepines cross the placenta and may produce respiratory depression, hypotonia, and sedation in neonates. Monitor neonates exposed to clobazam during pregnancy or labor for signs of sedation, respiratory depression, hypotonia, and feeding problems. Monitor neonates exposed to clobazam during pregnancy for signs of withdrawal. Manage these neonates accordingly [see Warnings and Precautions (5.9)].

Data

Human Data

Published data from observational studies on the use of benzodiazepines during pregnancy do not report a clear association with benzodiazepines and major birth defects. Although early studies reported an increased risk of congenital malformations with diazepam and chlordiazepoxide, there was no consistent pattern noted. In addition, the majority of more recent case-control and cohort studies of benzodiazepine use during pregnancy, which were adjusted for confounding exposures to alcohol, tobacco and other medications, have not confirmed these findings.

Animal Data

In a study in which clobazam (0, 150, 450, or 750 mg/kg/day) was orally administered to pregnant rats throughout the period of organogenesis, embryofetal mortality and incidences of fetal skeletal variations were increased at all doses. The low-effect dose for embryofetal developmental toxicity in rats (150 mg/kg/day) was associated with  plasma exposures (AUC) for clobazam and its major active metabolite, N-desmethylclobazam, lower than those in humans at the maximum recommended human dose (MRHD) of 40 mg/day.

Oral administration of clobazam (0, 10, 30, or 75 mg/kg/day) to pregnant rabbits throughout the period of organogenesis resulted in decreased fetal body weights, and increased incidences of fetal malformations (visceral and skeletal) at the mid and high doses, and an increase in embryofetal mortality at the high dose. Incidences of fetal variations were increased at all doses. The highest dose tested was associated with maternal toxicity (ataxia and decreased activity). The low-effect dose for embryofetal developmental toxicity in rabbits (10 mg/kg/day) was associated with plasma exposures  for clobazam and N-desmethylclobazam lower than those in humans at the MRHD.

Oral administration of clobazam (0, 50, 350, or 750 mg/kg/day) to rats throughout pregnancy and lactation resulted in increased embryofetal mortality at the high dose, decreased pup survival at the mid and high doses and alterations in offspring behavior (locomotor activity) at all doses. The low-effect dose for adverse effects on pre-and  postnatal development in rats (50 mg/kg/day) was associated with plasma exposures for clobazam and N-desmethylclobazam lower than those in humans at the MRHD.

Risk Summary

Clobazam is excreted in human milk (see Data). There are reports of sedation, poor feeding and poor weight gain in infants exposed to benzodiazepines through breast milk. There are no data on the effects of clobazam on milk production. The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for clobazam and any potential adverse effects on the breastfed infant from clobazam or from the underlying maternal condition.

Clinical Considerations

Adverse reactions such as somnolence and difficulty feeding have been reported in infants during breastfeeding in postmarketing experience with clobazam. Infants exposed to clobazam through breast milk should be monitored for sedation, poor feeding and poor weight gain.

Data

Scientific literature on clobazam use during lactation is limited. After short-term administration, clobazam and N-desmethylclobazam are transferred into breast milk.

Administration of clobazam to rats prior to and during mating and early gestation resulted in adverse effects on fertility and early embryonic development at plasma exposures for clobazam and its major active metabolite, N-desmethylclobazam, below those in humans at the MRHD [see Nonclinical Toxicology (13.1)].

Safety and effectiveness in patients less than 2 years of age have not been established. In a study in which clobazam (0, 4, 36, or 120 mg/kg/day) was orally administered to rats during the juvenile period of development (postnatal days 14 to 48), adverse effects on growth (decreased bone density and bone length) and behavior (altered motor activity and auditory startle response; learning deficit) were observed at the high dose. The effect on bone density, but not on behavior, was reversible when drug was discontinued. The no-effect level for juvenile toxicity (36 mg/kg/day) was associated with plasma exposures (AUC) to clobazam and its major active metabolite, N-desmethylclobazam, less than those expected at therapeutic doses in pediatric patients.

Clinical studies of clobazam did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. However, elderly subjects appear to eliminate clobazam more slowly than younger subjects based on population pharmacokinetic analysis. For these reasons, the initial dose in elderly patients should be 5 mg/day. Patients should be titrated initially to 10 to 20 mg/day. Patients may be titrated further to a maximum daily dose of 40 mg if tolerated [see Dosage and Administration (2.4), Clinical Pharmacology (12.3)].

Concentrations of clobazam’s active metabolite, N-desmethylclobazam, are higher in CYP2C19 poor metabolizers than in extensive metabolizers. For this reason, dosage modification is recommended [see Dosage and Administration (2.5),Clinical Pharmacology (12.3)].

The pharmacokinetics of clobazam were evaluated in patients with mild and moderate renal impairment. There were no significant differences in systemic exposure (AUC and Cmax) between patients with mild or moderate renal impairment and healthy subjects. No dose adjustment is required for patients with mild and moderate renal impairment. There is essentially no experience with clobazam in patients with severe renal impairment or ESRD. It is not known if clobazam or its active metabolite, N-desmethylclobazam, is dialyzable [see Dosage and Administration (2.6),Clinical Pharmacology (12.3)].

Clobazam is hepatically metabolized; however, there are limited data to characterize the effect of hepatic impairment on the pharmacokinetics of clobazam. For this reason, dosage adjustment is recommended in patients with mild to moderate hepatic impairment (Child-Pugh score 5 to 9). There is inadequate information about metabolism of clobazam in patients with severe hepatic impairment [see Dosage and Administration (2.7),Clinical Pharmacology (12.3)].

Clobazam tablet contains clobazam, a Schedule IV controlled substance.

Clobazam is a benzodiazepine and a CNS depressant with a potential for abuse and addiction. Abuse is the intentional, non-therapeutic use of a drug, even once, for its desirable psychological or physiological effects. Misuse is the intentional use, for therapeutic purposes, of a drug by an individual in a way other than prescribed by a health care provider or for whom it was not prescribed. Drug addiction is a cluster of behavioral, cognitive, and physiological phenomena that may include a strong desire to take the drug, difficulties in controlling drug use (e.g., continuing drug use despite harmful consequences, giving a higher priority to drug use than other activities and obligations), and possible tolerance or physical dependence. Even taking benzodiazepines as prescribed may put patients at risk for abuse and misuse of their medication. Abuse and misuse of benzodiazepines may lead to addiction.

Abuse and misuse of benzodiazepines often (but not always) involve the use of doses greater than the maximum recommended dosage and commonly involve concomitant use of other medications, alcohol, and/or illicit substances, which is associated with an increased frequency of serious adverse outcomes, including respiratory depression, overdose, or death. Benzodiazepines are often sought by individuals who abuse drugs and other substances, and by individuals with addictive disorders [see Warnings and Precautions (5.2)].

The following adverse reactions have occurred with benzodiazepine abuse and/or misuse: abdominal pain, amnesia, anorexia, anxiety, aggression, ataxia, blurred vision, confusion, depression, disinhibition, disorientation, dizziness, euphoria, impaired concentration and memory, indigestion, irritability, muscle pain, slurred speech, tremors, and vertigo.

The following severe adverse reactions have occurred with benzodiazepine abuse and/or misuse: delirium, paranoia, suicidal ideation and behavior, seizures, coma, breathing difficulty, and death. Death is more often associated with polysubstance use (especially benzodiazepines with other CNS depressants such as opioids and alcohol).

The World Health Organization epidemiology database contains reports of drug abuse, misuse, and overdoses associated with clobazam.

Physical Dependence

Clobazam may produce physical dependence from continued therapy. Physical dependence is a state that develops as a result of physiological adaptation in response to repeated drug use, manifested by withdrawal signs and symptoms after abrupt discontinuation or a significant dose reduction of a drug. Abrupt discontinuation or rapid dosage reduction of benzodiazepines or administration of flumazenil, a benzodiazepine antagonist, may precipitate acute withdrawal reactions, including seizures, which can be life-threatening. Patients at an increased risk of withdrawal adverse reactions after benzodiazepine discontinuation or rapid dosage reduction include those who take higher dosages (i.e., higher and/or more frequent doses) and those who have had longer durations of use [see Warnings and Precautions (5.3)]. In clinical trials, cases of dependency were reported following abrupt discontinuation of clobazam.

To reduce the risk of withdrawal reactions, use a gradual taper to discontinue clobazam or reduce the dosage [see Dosage and Administration (2.2) and Warnings and Precautions (5.3)].

Acute Withdrawal Signs and Symptoms

Acute withdrawal signs and symptoms associated with benzodiazepines have included abnormal involuntary movements, anxiety, blurred vision, depersonalization, depression, derealization, dizziness, fatigue, gastrointestinal adverse reactions (e.g., nausea, vomiting, diarrhea, weight loss, decreased appetite), headache, hyperacusis, hypertension, irritability, insomnia, memory impairment, muscle pain and stiffness, panic attacks, photophobia, restlessness, tachycardia, and tremor. More severe acute withdrawal signs and symptoms, including life-threatening reactions, have included catatonia, convulsions, delirium tremens, depression, hallucinations, mania, psychosis, seizures, and suicidality.

Protracted Withdrawal Syndrome

Protracted withdrawal syndrome associated with benzodiazepines is characterized by anxiety, cognitive impairment, depression, insomnia, formication, motor symptoms (e.g., weakness, tremor, muscle twitches), paresthesia, and tinnitus that persists beyond 4 to 6 weeks after initial benzodiazepine withdrawal. Protracted withdrawal symptoms may last weeks to more than 12 months. As a result, there may be difficulty in differentiating withdrawal symptoms from potential re-emergence or continuation of symptoms for which the benzodiazepine was being used.

Tolerance

Tolerance to clobazam may develop from continued therapy. Tolerance is a physiological state characterized by a reduced response to a drug after repeated administration (i.e., a higher dose of a drug is required to produce the same effect that was once obtained at a lower dose). Tolerance to the therapeutic effect of clobazam may develop; however, little tolerance develops to the amnestic reactions and other cognitive impairments caused by benzodiazepines.

Overdosage of benzodiazepines is characterized by central nervous system depression ranging from drowsiness to coma. In mild to moderate cases, symptoms can include drowsiness, confusion, dysarthria, lethargy, hypnotic state, diminished reflexes, ataxia, and hypotonia. Rarely, paradoxical or disinhibitory reactions (including agitation, irritability, impulsivity, violent behavior, confusion, restlessness, excitement, and talkativeness) may occur. In severe overdosage cases, patients may develop respiratory depression and coma. Overdosage of benzodiazepines in combination with other CNS depressants (including alcohol and opioids) may be fatal [see Warnings and Precautions (5.2)]. Markedly abnormal (lowered or elevated) blood pressure, heart rate, or respiratory rate raise the concern that additional drugs and/or alcohol are involved in the overdosage.

{ "type": "p", "children": [], "text": "Overdosage of benzodiazepines is characterized by central nervous system depression ranging from drowsiness to coma. In mild to moderate cases, symptoms can include drowsiness, confusion, dysarthria, lethargy, hypnotic state, diminished reflexes, ataxia, and hypotonia. Rarely, paradoxical or disinhibitory reactions (including agitation, irritability, impulsivity, violent behavior, confusion, restlessness, excitement, and talkativeness) may occur. In severe overdosage cases, patients may develop respiratory depression and coma. Overdosage of benzodiazepines in combination with other CNS depressants (including alcohol and opioids) may be fatal [see Warnings and Precautions (5.2)]. Markedly abnormal (lowered or elevated) blood pressure, heart rate, or respiratory rate raise the concern that additional drugs and/or alcohol are involved in the overdosage. " }

In managing benzodiazepine overdosage, employ general supportive measures, including intravenous fluids and airway maintenance. Flumazenil, a specific benzodiazepine receptor antagonist indicated for the complete or partial reversal of the sedative effects of benzodiazepines in the management of benzodiazepine overdosage, can lead to withdrawal and adverse reactions, including seizures, particularly in the context of mixed overdosage with drugs that increase seizure risk (e.g., tricyclic and tetracyclic antidepressants) and in patients with long-term benzodiazepine use and physical dependency. The risk of withdrawal seizures with flumazenil may be increased in patients with epilepsy. Flumazenil is contraindicated in patients who have received a benzodiazepine for control of a potentially life-threatening condition (e.g., status epilepticus). If the decision is made to use flumazenil, it should be used as an adjunct to, not as a substitute for, supportive management of benzodiazepine overdosage. See the flumazenil injection Prescribing Information.

{ "type": "p", "children": [], "text": "In managing benzodiazepine overdosage, employ general supportive measures, including intravenous fluids and airway maintenance. Flumazenil, a specific benzodiazepine receptor antagonist indicated for the complete or partial reversal of the sedative effects of benzodiazepines in the management of benzodiazepine overdosage, can lead to withdrawal and adverse reactions, including seizures, particularly in the context of mixed overdosage with drugs that increase seizure risk (e.g., tricyclic and tetracyclic antidepressants) and in patients with long-term benzodiazepine use and physical dependency. The risk of withdrawal seizures with flumazenil may be increased in patients with epilepsy. Flumazenil is contraindicated in patients who have received a benzodiazepine for control of a potentially life-threatening condition (e.g., status epilepticus). If the decision is made to use flumazenil, it should be used as an adjunct to, not as a substitute for, supportive management of benzodiazepine overdosage. See the flumazenil injection Prescribing Information. " }

Consider contacting the Poison Help line (1-800-222-1222) or a medical toxicologist for additional overdosage management recommendations. 

{ "type": "p", "children": [], "text": "Consider contacting the Poison Help line (1-800-222-1222) or a medical toxicologist for additional overdosage management recommendations. " }

Table 4. Description

{ "type": "p", "children": [], "text": "\nTable 4. Description\n" }

<div class="scrollingtable"><table border="0" cellpadding="0" cellspacing="0"> <tbody class="Headless"> <tr class="Botrule First"> <td class="Lrule Rrule" valign="middle">Established Name:</td><td class="Rrule" valign="middle">Clobazam Tablets</td> </tr> <tr class="Botrule"> <td class="Lrule Rrule" valign="middle">Dosage Forms:</td><td class="Rrule" valign="middle">Tablet</td> </tr> <tr class="Botrule"> <td class="Lrule Rrule" valign="middle">Route of Administration:</td><td class="Rrule" valign="middle">Oral </td> </tr> <tr class="Botrule"> <td class="Lrule Rrule" valign="middle">Established Pharmacologic Class of Drug:</td><td class="Rrule" valign="middle">Benzodiazepine</td> </tr> <tr class="Botrule"> <td class="Lrule Rrule" valign="middle">Chemical Name:</td><td class="Rrule" valign="middle">7-Chloro-1-methyl-5-phenyl-1H-1,5 benzodiazepine-2,4(3H,5H)-dione</td> </tr> <tr class="Last"> <td class="Lrule Rrule" valign="middle">Structural Formula:</td><td class="Rrule" valign="middle"><img alt="clob01.jpg" src="/dailymed/image.cfm?name=clob01.jpg&amp;setid=a77ffbdd-4e3e-4ec4-b0fa-b51ee610df0f"/></td> </tr> </tbody> </table></div>

{ "type": "table", "children": [], "text": "<div class=\"scrollingtable\"><table border=\"0\" cellpadding=\"0\" cellspacing=\"0\">\n<tbody class=\"Headless\">\n<tr class=\"Botrule First\">\n<td class=\"Lrule Rrule\" valign=\"middle\">Established Name:</td><td class=\"Rrule\" valign=\"middle\">Clobazam Tablets</td>\n</tr>\n<tr class=\"Botrule\">\n<td class=\"Lrule Rrule\" valign=\"middle\">Dosage Forms:</td><td class=\"Rrule\" valign=\"middle\">Tablet</td>\n</tr>\n<tr class=\"Botrule\">\n<td class=\"Lrule Rrule\" valign=\"middle\">Route of Administration:</td><td class=\"Rrule\" valign=\"middle\">Oral </td>\n</tr>\n<tr class=\"Botrule\">\n<td class=\"Lrule Rrule\" valign=\"middle\">Established Pharmacologic Class of Drug:</td><td class=\"Rrule\" valign=\"middle\">Benzodiazepine</td>\n</tr>\n<tr class=\"Botrule\">\n<td class=\"Lrule Rrule\" valign=\"middle\">Chemical Name:</td><td class=\"Rrule\" valign=\"middle\">7-Chloro-1-methyl-5-phenyl-1H-1,5 benzodiazepine-2,4(3H,5H)-dione</td>\n</tr>\n<tr class=\"Last\">\n<td class=\"Lrule Rrule\" valign=\"middle\">Structural Formula:</td><td class=\"Rrule\" valign=\"middle\"><img alt=\"clob01.jpg\" src=\"/dailymed/image.cfm?name=clob01.jpg&amp;setid=a77ffbdd-4e3e-4ec4-b0fa-b51ee610df0f\"/></td>\n</tr>\n</tbody>\n</table></div>" }

Clobazam is a white or almost white crystalline powder, freely soluble in dichloromethane. The melting range of clobazam is from 178ºC to 185ºC. The molecular formula is C16H13O2N2Cl and the molecular weight is 300.74. Each clobazam tablet contains  5 mg, 10 mg or 20 mg of clobazam. Tablets also contain as inactive ingredients: Pregelatinized starch, lactose monohydrate, magnesium stearate, colloidal silicon dioxide, and talc.

{ "type": "p", "children": [], "text": " Clobazam is a white or almost white crystalline powder, freely soluble in dichloromethane. The melting range of clobazam is from 178ºC to 185ºC. The molecular formula is C16H13O2N2Cl and the molecular weight is 300.74. Each clobazam tablet contains  5 mg, 10 mg or 20 mg of clobazam. Tablets also contain as inactive ingredients: Pregelatinized starch, lactose monohydrate, magnesium stearate, colloidal silicon dioxide, and talc." }

The exact mechanism of action for clobazam, a 1, 5-benzodiazepine, is not fully understood but is thought to involve potentiation of GABAergic neurotransmission resulting from binding at the benzodiazepine site of the GABAA receptor.

Effects on Electrocardiogram The effect of clobazam tablets 20 mg and 80 mg administered twice daily on QTc interval was evaluated in a randomized, evaluator-blinded, placebo-, and active-controlled (moxifloxacin 400 mg) parallel thorough QT study in 280 healthy subjects. In a study with demonstrated ability to detect small effects, the upper bound of the one-sided 95% confidence interval for the largest placebo-adjusted, baseline-corrected QTc based on the Fridericia correction method was below 10 ms, the threshold for regulatory concern. Thus, at a dose two times the maximum recommended dose, clobazam did not prolong the QTc interval to any clinically relevant extent.

The peak plasma levels (Cmax) and the area under the curve (AUC) of clobazam are dose-proportional over the dose range of 10 to 80 mg following single-or multiple-dose administration of clobazam. Based on a population pharmacokinetic analysis, the pharmacokinetics of clobazam are linear from 5 to 160 mg/day. Clobazam is converted to N-desmethylclobazam which has about 1/5 the activity of clobazam. The estimated mean elimination half-lives (t½) of clobazam and N-desmethylclobazam were 36 to 42 hours and 71 to 82 hours, respectively. Absorption Clobazam is rapidly and extensively absorbed following oral administration. The time to peak concentrations (Tmax) of clobazam tablets under fasted conditions ranged from 0.5 to 4 hours after single- or multiple-dose administrations. The relative bioavailability of clobazam tablets compared to an oral solution is approximately 100%. After single dose administration of the oral suspension under fasted conditions, the Tmax ranged from 0.5 to 2 hours. Based on exposure (Cmax and AUC) of clobazam, clobazam tablets and suspension were shown to have similar bioavailability under fasted conditions. The administration of clobazam tablets with food or when crushed in applesauce does not affect absorption. Although not studied, the oral bioavailability of the oral suspension is unlikely to be affected under fed conditions.

Distribution  Clobazam is lipophilic and distributes rapidly throughout the body. The apparent volume of distribution at steady state was approximately 100 L. The in vitro plasma protein binding of clobazam and N-desmethylclobazam is approximately 80% to 90% and 70%, respectively. Metabolism and Excretion  Clobazam is extensively metabolized in the liver, with approximately 2% of the dose recovered in urine and 1% in feces as unchanged drug. The major metabolic pathway of clobazam involves N-demethylation, primarily by CYP3A4 and to a lesser extent by CYP2C19 and CYP2B6. N-desmethylclobazam, an active metabolite, is the major circulating metabolite in humans, and at therapeutic doses, plasma concentrations are 3 to 5 times higher than those of the parent compound. Based on animal and in vitro receptor binding data, estimates of the relative potency of N-desmethylclobazam compared to parent compound range from 1/5 to equal potency. N-desmethylclobazam is extensively metabolized, mainly by CYP2C19. N-desmethylclobazam and its metabolites comprise ~94% of the total drug-related components in urine. Following a single oral dose of radiolabeled drug, approximately 11% of the dose was excreted in the feces and approximately 82% was excreted in the urine.

The polymorphic CYP2C19 is the major contributor to the metabolism of the pharmacologically active N-desmethylclobazam [see Clinical Pharmacology (12.5)]. In CYP2C19 poor metabolizers, levels of N-desmethylclobazam were 5-fold higher in plasma and 2-to 3-fold higher in the urine than in CYP2C19 extensive metabolizers.

Pharmacokinetics in Specific Populations Age Population pharmacokinetic analyses showed that the clearance of clobazam is lower in elderly subjects compared to other age groups (ages 2 to 64). Dosing should be adjusted in the elderly [see Dosage and Administration (2.4)]. Sex Population pharmacokinetic analyses showed no difference in the clearance of clobazam between women and men. Race Population pharmacokinetic analyses including Caucasian (75%), African American (15%), and Asian (9%) subjects showed that there is no evidence of clinically significant effect of race on the clearance of clobazam. Renal Impairment The effect of renal impairment on the pharmacokinetics of clobazam was evaluated in patients with mild (creatinine clearance [CLCR] greater than 50 to 80 mL/min; N=6) and moderate (CLCR=30 to 50 mL/min; N=6) renal dysfunction, with matching healthy controls (N=6), following administration of multiple doses of clobazam 20 mg/day. There were insignificant changes in Cmax (3% to 24%) and AUC (≤13%) for clobazam or N-desmethylclobazam in patients with mild or moderate renal impairment compared to patients with normal renal function. Patients with severe renal impairment or ESRD were not included in this study.

Hepatic Impairment There are limited data to characterize the effect of hepatic impairment on the pharmacokinetics of clobazam. In a small study, the pharmacokinetics of a 20 mg single oral dose of clobazam in 9 patients with liver impairment were compared to healthy controls (N=6). The Cmax and the mean plasma clearance of clobazam, as well as the Cmax of N-desmethylclobazam, showed no significant change compared to the healthy controls. The AUC values of N-desmethylclobazam in these patients were not available. Adjust dosage in patients with hepatic impairment [see Dosage and Administration (2.7)]. Drug Interaction Studies In vitro studies: Clobazam did not inhibit CYP1A2, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP3A4, UGT1A1, UGT1A4, UGT1A6, or UGT2B4 in vitro. N-desmethylclobazam showed weak inhibition of CYP2C9, UGT1A4, UGT1A6 and UGT2B4.

Clobazam and N-desmethylclobazam did not significantly increase CYP1A2 or CYP2C19 activities, but did induce CYP3A4 activity in a concentration-dependent manner. Clobazam and N-desmethylclobazam also increased UGT1A1 mRNA but at concentrations much higher than therapeutic levels. The potential for clobazam or N-desmethylclobazam to induce CYP2B6 and CYP2C8 has not been evaluated. Clobazam and N-desmethylclobazam do not inhibit P-glycoprotein (P-gp), but are P-gp substrates. In vivo studies:  Potential for clobazam to Affect Other Drugs The effect of repeated 40 mg once-daily doses of clobazam on the pharmacokinetic profiles of single-dose dextromethorphan (CYP2D6 substrate), midazolam (CYP3A4 substrate), caffeine (CYP1A2 substrate), and tolbutamide (CYP2C9 substrate), was studied when these probe substrates were given as a drug cocktail (N=18). Clobazam increased AUC and Cmax of dextromethorphan by 90% and 59%, respectively, reflecting its inhibition of CYP2D6 in vivo. Drugs metabolized by CYP2D6 may require dose adjustment when used with clobazam. Clobazam decreased the AUC and Cmax of midazolam by 27% and 24%, respectively, and increased the AUC and Cmax of the metabolite 1-hydroxymidazolam by 4-fold and 2-fold, respectively. This level of induction does not call for dosage adjustment of drugs that are primarily metabolized by CYP3A4 when used concomitantly with clobazam. Some hormonal contraceptives are metabolized by CYP3A4 and their effectiveness may be diminished when given with clobazam [see Drug Interactions (7.3)]. Repeated clobazam doses had no effect on caffeine and tolbutamide.

A population pharmacokinetic analysis indicated clobazam did not affect the exposure of valproic acid (a CYP2C9/2C19 substrate) or lamotrigine (a UGT substrate). Potential for Other Drugs to Affect Clobazam

Co-administration of ketoconazole (a strong CYP3A4 inhibitor) 400 mg once-daily for 5 days increased clobazam AUC by 54%, with an insignificant effect on clobazam Cmax. There was no significant change in AUC and Cmax of N-desmethylclobazam (N=18).

Strong (e.g., fluconazole, fluvoxamine, ticlopidine) and moderate (e.g., omeprazole) inhibitors of CYP2C19 may result in up to a 5-fold increase in exposure to N-desmethylclobazam, the active metabolite of clobazam, based on extrapolation from pharmacogenomic data [see Clinical Pharmacology (12.5)]. Dosage adjustment of clobazam may be necessary when co-administered with strong or moderate CYP2C19 inhibitors [see Drug Interactions (7.4)]. The effects of concomitant antiepileptic drugs that are CYP3A4 inducers (phenobarbital, phenytoin, and carbamazepine), CYP2C19 inducers (valproic acid, phenobarbital, phenytoin, and carbamazepine), and CYP2C19 inhibitors (felbamate and oxcarbazepine) were evaluated using data from clinical trials. Results of population pharmacokinetic analysis show that these concomitant antiepileptic drugs did not significantly alter the pharmacokinetics of clobazam or N-desmethylclobazam at steady-state.

Alcohol has been reported to increase the maximum plasma exposure of clobazam by approximately 50%. Alcohol may have additive CNS depressant effects when taken with clobazam [see Warnings and Precautions (5.4), Drug Interactions (7.2)].

The polymorphic CYP2C19 is the main enzyme that metabolizes the pharmacologically active N-desmethylclobazam. Compared to CYP2C19 extensive metabolizers, N-desmethylclobazam AUC and Cmax are approximately 3 to 5 times higher in poor metabolizers (e.g., subjects with *2/*2 genotype) and 2 times higher in intermediate metabolizers (e.g., subjects with *1/*2 genotype). The prevalence of CYP2C19 poor metabolism differs depending on racial/ethnic background. Dosage in patients who are known CYP2C19 poor metabolizers may need to be adjusted [see Dosage and Administration (2.5)]. The systemic exposure of clobazam is similar for both CYP2C19 poor and extensive metabolizers.

Carcinogenesis In mice, oral administration of clobazam (0, 6, 12, or 24 mg/kg/day) for 2 years did not result in an increase in tumors. The highest dose tested was approximately 3 times the maximum recommended human dose (MRHD) of 40 mg/day, based on body surface area (mg/m2). In rats, oral administration of clobazam for 2 years resulted in increases in tumors of the thyroid gland (follicular cell adenoma and carcinoma) and liver (hepatocellular adenoma) at the mid and high doses. The low dose, not associated with an increase in tumors, was associated with plasma exposures (AUC) for clobazam and its major active metabolite, N-desmethylclobazam, less than that in humans at the MRHD. Mutagenesis Clobazam and the major active metabolite, N-desmethylclobazam, were negative for genotoxicity, based on data from a battery of in vitro (bacteria reverse mutation, mammalian clastogenicity) and in vivo (mouse micronucleus) assays. Impairment of Fertility In a fertility study in which clobazam (50, 350, or 750 mg/kg/day, corresponding to 12, 84 and 181 times the oral Maximum Recommended Human Dose, MRHD, of 40 mg/day based on mg/m2 body surface) was orally administered to male and female rats prior to and during mating and continuing in females to gestation day 6, increases in abnormal sperm and pre-implantation loss were observed at the highest dose tested. The no-effect level for fertility and early embryonic development in rats was associated with plasma exposures (AUC) for clobazam and its major active metabolite, N-desmethylclobazam, less than those in humans at the maximum recommended human dose of 40 mg/day.

The effectiveness of clobazam for the adjunctive treatment of seizures associated with Lennox-Gastaut syndrome was established in two multicenter controlled studies (Study 1 and Study 2). Both studies were similar in terms of disease characteristics and concomitant AED treatments. The most common concomitant AED treatments at baseline included: valproate, lamotrigine, levetiracetam, and topiramate. Study 1 Study 1 (N=238) was a randomized, double-blind, placebo-controlled study consisting of a 4-week baseline period followed by a 3-week titration period and 12-week maintenance period. Patients age 2 to 54 years with a current or prior diagnosis of LGS were stratified into 2 weight groups (12.5 kg to ≤30 kg or greater than 30 kg) and then randomized to placebo or one of three target maintenance doses of clobazam according to Table 5.

{ "type": "p", "children": [], "text": "The effectiveness of clobazam for the adjunctive treatment of seizures associated with Lennox-Gastaut syndrome was established in two multicenter controlled studies (Study 1 and Study 2). Both studies were similar in terms of disease characteristics and concomitant AED treatments. The most common concomitant AED treatments at baseline included: valproate, lamotrigine, levetiracetam, and topiramate. \nStudy 1\n Study 1 (N=238) was a randomized, double-blind, placebo-controlled study consisting of a 4-week baseline period followed by a 3-week titration period and 12-week maintenance period. Patients age 2 to 54 years with a current or prior diagnosis of LGS were stratified into 2 weight groups (12.5 kg to ≤30 kg or greater than 30 kg) and then randomized to placebo or one of three target maintenance doses of clobazam according to Table 5." }

Table 5. Study 1 Total Daily Dose

{ "type": "p", "children": [], "text": "\nTable 5. Study 1 Total Daily Dose\n" }

<div class="scrollingtable"><table border="0" cellpadding="0" cellspacing="0" width="798"> <colgroup> <col width="33.3333333333333%"/> <col width="33.3333333333333%"/> <col width="33.3333333333333%"/> </colgroup> <tbody class="Headless"> <tr class="Botrule First"> <td align="justify" class="Lrule Rrule" valign="top"> <br/> </td><td align="justify" class="Rrule" valign="top"><span class="Bold">≤30 kg Body Weight </span> <br/> </td><td align="justify" class="Rrule" valign="top"><span class="Bold">Greater than 30 kg Body Weight </span> <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="top">Low Dose <br/> </td><td align="justify" class="Rrule" valign="top">5 mg daily <br/> </td><td align="justify" class="Rrule" valign="top">10 mg daily <br/> </td> </tr> <tr class="Botrule"> <td align="justify" class="Lrule Rrule" valign="top">Medium Dose <br/> </td><td align="justify" class="Rrule" valign="top">10 mg daily <br/> </td><td align="justify" class="Rrule" valign="top">20 mg daily <br/> </td> </tr> <tr class="Last"> <td align="justify" class="Lrule Rrule" valign="top">High Dose <br/> </td><td align="justify" class="Rrule" valign="top">20 mg daily <br/> </td><td align="justify" class="Rrule" valign="top">40 mg daily <br/> </td> </tr> </tbody> </table></div>

{ "type": "table", "children": [], "text": "<div class=\"scrollingtable\"><table border=\"0\" cellpadding=\"0\" cellspacing=\"0\" width=\"798\">\n<colgroup>\n<col width=\"33.3333333333333%\"/>\n<col width=\"33.3333333333333%\"/>\n<col width=\"33.3333333333333%\"/>\n</colgroup>\n<tbody class=\"Headless\">\n<tr class=\"Botrule First\">\n<td align=\"justify\" class=\"Lrule Rrule\" valign=\"top\"> <br/>\n</td><td align=\"justify\" class=\"Rrule\" valign=\"top\"><span class=\"Bold\">≤30 kg Body Weight </span>\n<br/>\n</td><td align=\"justify\" class=\"Rrule\" valign=\"top\"><span class=\"Bold\">Greater than 30 kg Body Weight </span>\n<br/>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"justify\" class=\"Lrule Rrule\" valign=\"top\">Low Dose <br/>\n</td><td align=\"justify\" class=\"Rrule\" valign=\"top\">5 mg daily <br/>\n</td><td align=\"justify\" class=\"Rrule\" valign=\"top\">10 mg daily <br/>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"justify\" class=\"Lrule Rrule\" valign=\"top\">Medium Dose <br/>\n</td><td align=\"justify\" class=\"Rrule\" valign=\"top\">10 mg daily <br/>\n</td><td align=\"justify\" class=\"Rrule\" valign=\"top\">20 mg daily <br/>\n</td>\n</tr>\n<tr class=\"Last\">\n<td align=\"justify\" class=\"Lrule Rrule\" valign=\"top\">High Dose <br/>\n</td><td align=\"justify\" class=\"Rrule\" valign=\"top\">20 mg daily <br/>\n</td><td align=\"justify\" class=\"Rrule\" valign=\"top\">40 mg daily <br/>\n</td>\n</tr>\n</tbody>\n</table></div>" }

Doses above 5 mg/day were administered in two divided doses. The primary efficacy measure was the percent reduction in the weekly frequency of drop seizures (atonic, tonic, or myoclonic), also known as drop attacks, from the 4-week baseline period to 12-week maintenance period. The pre-dosing baseline mean weekly drop seizure frequency was 98, 100, 61, and 105 for the placebo, low-, medium-, and high-dose groups, respectively. Figure 1 presents the mean percent reduction in weekly drop seizures from this baseline. All dose groups of clobazam were statistically superior (p ≤ 0.05) to the placebo group. This effect appeared to be dose dependent. Figure 1. Mean Percent Reduction from Baseline in Weekly Drop Seizure Frequency (Study 1) 

{ "type": "p", "children": [], "text": " Doses above 5 mg/day were administered in two divided doses. The primary efficacy measure was the percent reduction in the weekly frequency of drop seizures (atonic, tonic, or myoclonic), also known as drop attacks, from the 4-week baseline period to 12-week maintenance period. The pre-dosing baseline mean weekly drop seizure frequency was 98, 100, 61, and 105 for the placebo, low-, medium-, and high-dose groups, respectively. Figure 1 presents the mean percent reduction in weekly drop seizures from this baseline. All dose groups of clobazam were statistically superior (p ≤ 0.05) to the placebo group. This effect appeared to be dose dependent. \n\nFigure 1. Mean Percent Reduction from Baseline in Weekly Drop Seizure Frequency (Study 1) " }

Figure 2 shows changes from baseline in weekly drop seizure frequency by category for patients treated with clobazam and placebo in Study 1. Patients in whom the seizure frequency increased are shown at left as “worse.” Patients in whom the seizure frequency decreased are shown in five categories.

{ "type": "p", "children": [], "text": "\n Figure 2 shows changes from baseline in weekly drop seizure frequency by category for patients treated with clobazam and placebo in Study 1. Patients in whom the seizure frequency increased are shown at left as “worse.” Patients in whom the seizure frequency decreased are shown in five categories." }

Figure 2. Drop Seizure Response by Category for Clobazam and Placebo (Study 1)

{ "type": "p", "children": [], "text": "\nFigure 2. Drop Seizure Response by Category for Clobazam and Placebo (Study 1)\n\n\n" }

  There was no evidence that tolerance to the therapeutic effect of clobazam developed during the 3-month maintenance period. Study 2 Study 2 (N=68) was a randomized, double-blind comparison study of high- and low-dose clobazam, consisting of a 4-week baseline period followed by a 3-week titration period and 4-week maintenance period. Patients age 2 to 25 years with a current or prior diagnosis of LGS were stratified by weight, then randomized to either a low or high dose of clobazam, and then entered a 3-week titration period. The primary efficacy measure was the percent reduction in the weekly frequency of drop seizures (atonic, tonic, or myoclonic), also known as drop attacks, from the 4-week baseline period to the 4-week maintenance period. A statistically significantly greater reduction in seizure frequency was observed in the high-dose group compared to the low-dose group (median percent reduction of 93% vs 29%; p less than 0.05).

{ "type": "p", "children": [], "text": "  There was no evidence that tolerance to the therapeutic effect of clobazam developed during the 3-month maintenance period. \n\nStudy 2\n Study 2 (N=68) was a randomized, double-blind comparison study of high- and low-dose clobazam, consisting of a 4-week baseline period followed by a 3-week titration period and 4-week maintenance period. Patients age 2 to 25 years with a current or prior diagnosis of LGS were stratified by weight, then randomized to either a low or high dose of clobazam, and then entered a 3-week titration period. \n The primary efficacy measure was the percent reduction in the weekly frequency of drop seizures (atonic, tonic, or myoclonic), also known as drop attacks, from the 4-week baseline period to the 4-week maintenance period. \n A statistically significantly greater reduction in seizure frequency was observed in the high-dose group compared to the low-dose group (median percent reduction of 93% vs 29%; p less than 0.05). " }

5 mg: White to off white round shaped uncoated tablets debossed with "C" on one side and "5" on other side. 

{ "type": "p", "children": [], "text": "\n5 mg: White to off white round shaped uncoated tablets debossed with \"C\" on one side and \"5\" on other side. " }

10 mg:Off white oval shaped uncoated tablets with a functional score on one side and ‘C’ and ‘10’ debossed on other side.

{ "type": "p", "children": [], "text": "\n10 mg:Off white oval shaped uncoated tablets with a functional score on one side and ‘C’ and ‘10’ debossed on other side." }

20 mg: Off white oval shaped uncoated tablets with a functional score on one side and ‘C’ and ‘20’ debossed on other side.

{ "type": "p", "children": [], "text": "\n20 mg: Off white oval shaped uncoated tablets with a functional score on one side and ‘C’ and ‘20’ debossed on other side." }

NDC:

{ "type": "p", "children": [], "text": "\nNDC:\n" }

5 mg:  100’s HDPE Pack: NDC 67877-664-01 500’s HDPE Pack: NDC 67877-664-05 Cartons of 10 Tablets (1 x 10 Unit-dose) NDC 67877-664-33

{ "type": "p", "children": [], "text": "\n 5 mg: \n100’s HDPE Pack: NDC 67877-664-01 500’s HDPE Pack: NDC 67877-664-05 Cartons of 10 Tablets (1 x 10 Unit-dose) NDC 67877-664-33" }

10 mg:

{ "type": "p", "children": [], "text": "\n10 mg:\n" }

100’s HDPE Pack: NDC 67877-665-01

{ "type": "p", "children": [], "text": "100’s HDPE Pack: NDC 67877-665-01" }

500’s HDPE Pack: NDC 67877-665-05

{ "type": "p", "children": [], "text": "500’s HDPE Pack: NDC 67877-665-05" }

Cartons of 10 Tablets (1 x 10 Unit-dose) NDC 67877-665-33

{ "type": "p", "children": [], "text": "Cartons of 10 Tablets (1 x 10 Unit-dose) NDC 67877-665-33" }

20 mg:

{ "type": "p", "children": [], "text": "\n20 mg:\n" }

100’s HDPE Pack: NDC 67877-666-01

{ "type": "p", "children": [], "text": "100’s HDPE Pack: NDC 67877-666-01" }

500’s HDPE Pack: NDC 67877-666-05

{ "type": "p", "children": [], "text": "500’s HDPE Pack: NDC 67877-666-05" }

Cartons of 10 Tablets (1 x 10 Unit-dose) NDC 67877-666-33 

{ "type": "p", "children": [], "text": "Cartons of 10 Tablets (1 x 10 Unit-dose) NDC 67877-666-33 " }

Store at 20°C to 25°C (68°F to 77°F). [See USP Controlled Room Temperature].

{ "type": "p", "children": [], "text": "Store at 20°C to 25°C (68°F to 77°F). [See USP Controlled Room Temperature]." }

Advise the patient to read the FDA-approved patient labeling (Medication Guide). Risks from Concomitant Use with Opioids Inform patients and caregivers that potentially fatal additive effects may occur if clobazam is used with opioids and not to use such drugs concomitantly unless supervised by a healthcare provider [see Warnings and Precautions (5.1),Drug Interactions (7.1)].

{ "type": "p", "children": [], "text": "Advise the patient to read the FDA-approved patient labeling (Medication Guide). \n\nRisks from Concomitant Use with Opioids\n Inform patients and caregivers that potentially fatal additive effects may occur if clobazam is used with opioids and not to use such drugs concomitantly unless supervised by a healthcare provider [see Warnings and Precautions (5.1),Drug Interactions (7.1)]." }

Abuse, Misuse, and Addiction

{ "type": "p", "children": [], "text": "\nAbuse, Misuse, and Addiction \n" }

Inform patients that the use of clobazam, even at recommended dosages, exposes users to risks of abuse, misuse, and addiction, which can lead to overdose and death, especially when used in combination with other medications (e.g., opioid analgesics), alcohol, and/or illicit substances. Inform patients about the signs and symptoms of benzodiazepine abuse, misuse, and addiction; to seek medical help if they develop these signs and/or symptoms; and on the proper disposal of unused drug [see Warnings and Precautions (5.2) and Drug Abuse and Dependence (9.2)].

{ "type": "p", "children": [], "text": "Inform patients that the use of clobazam, even at recommended dosages, exposes users to risks of abuse, misuse, and addiction, which can lead to overdose and death, especially when used in combination with other medications (e.g., opioid analgesics), alcohol, and/or illicit substances. Inform patients about the signs and symptoms of benzodiazepine abuse, misuse, and addiction; to seek medical help if they develop these signs and/or symptoms; and on the proper disposal of unused drug [see Warnings and Precautions (5.2) and Drug Abuse and Dependence (9.2)].\n" }

Withdrawal Reactions

{ "type": "p", "children": [], "text": "\nWithdrawal Reactions \n" }

Advise patients or caregivers that abrupt withdrawal of AEDs may increase their risk of seizure. Inform patients that the continued use of clobazam may lead to clinically significant physical dependence and that abrupt discontinuation or rapid dosage reduction of clobazam may precipitate acute withdrawal reactions, which can be life-threatening. Inform patients that in some cases, patients taking benzodiazepines have developed a protracted withdrawal syndrome with withdrawal symptoms lasting weeks to more than 12 months. Instruct patients that discontinuation or dosage reduction of clobazam may require a slow taper [see Warnings and Precautions (5.3) and Drug Abuse and Dependence (9.3)].

{ "type": "p", "children": [], "text": "Advise patients or caregivers that abrupt withdrawal of AEDs may increase their risk of seizure. Inform patients that the continued use of clobazam may lead to clinically significant physical dependence and that abrupt discontinuation or rapid dosage reduction of clobazam may precipitate acute withdrawal reactions, which can be life-threatening. Inform patients that in some cases, patients taking benzodiazepines have developed a protracted withdrawal syndrome with withdrawal symptoms lasting weeks to more than 12 months. Instruct patients that discontinuation or dosage reduction of clobazam may require a slow taper [see Warnings and Precautions (5.3) and Drug Abuse and Dependence (9.3)].\n" }

Somnolence or Sedation  Advise patients or caregivers to check with their healthcare provider before clobazam is taken with other CNS depressants such as other benzodiazepines, opioids, tricyclic antidepressants, sedating antihistamines, or alcohol [see Warnings and Precautions (5.4, 5.5)]. If applicable, caution patients about operating hazardous machinery, including automobiles, until they are reasonably certain that clobazam does not affect them adversely (e.g., impair judgment, thinking or motor skills).   Hypersensitivity Inform patients or caregivers that clobazam is contraindicated in patients with a history of hypersensitivity to the drug or its ingredients [see Warnings and Precautions (5.6)]. Interactions with Hormonal Contraceptives Counsel women to also use non-hormonal methods of contraception when clobazam is used with hormonal contraceptives and to continue these alternative methods for 28 days after discontinuing clobazam to ensure contraceptive reliability [see Drug Interactions (7.3),Clinical Pharmacology (12.3)]. Serious Dermatological Reactions Advise patients or caregivers that serious skin reactions have been reported in patients taking clobazam. Serious skin reactions, including SJS/TEN, may need to be treated in a hospital and may be life-threatening. If a skin reaction occurs while taking clobazam, patients or caregivers should consult with healthcare providers immediately [see Warnings and Precautions (5.6)].

{ "type": "p", "children": [], "text": "\nSomnolence or Sedation\n  Advise patients or caregivers to check with their healthcare provider before clobazam is taken with other CNS depressants such as other benzodiazepines, opioids, tricyclic antidepressants, sedating antihistamines, or alcohol [see Warnings and Precautions (5.4, 5.5)]. If applicable, caution patients about operating hazardous machinery, including automobiles, until they are reasonably certain that clobazam does not affect them adversely (e.g., impair judgment, thinking or motor skills).  \nHypersensitivity\n Inform patients or caregivers that clobazam is contraindicated in patients with a history of hypersensitivity to the drug or its ingredients [see Warnings and Precautions (5.6)]. \n\nInteractions with Hormonal Contraceptives \n Counsel women to also use non-hormonal methods of contraception when clobazam is used with hormonal contraceptives and to continue these alternative methods for 28 days after discontinuing clobazam to ensure contraceptive reliability [see Drug Interactions (7.3),Clinical Pharmacology (12.3)]. \n\nSerious Dermatological Reactions\n Advise patients or caregivers that serious skin reactions have been reported in patients taking clobazam. Serious skin reactions, including SJS/TEN, may need to be treated in a hospital and may be life-threatening. If a skin reaction occurs while taking clobazam, patients or caregivers should consult with healthcare providers immediately [see Warnings and Precautions (5.6)]." }

DRESS/Multiorgan Hypersensitivity Instruct patients and caregivers that a fever or rash associated with signs of other organ system involvement (e.g., lymphadenopathy, hepatic dysfunction) may be drug-related and should be reported to their healthcare provider immediately. Clobazam should be discontinued immediately if a serious hypersensitivity reaction is suspected [see Warnings and Precautions (5.7)].

{ "type": "p", "children": [], "text": "\nDRESS/Multiorgan Hypersensitivity Instruct patients and caregivers that a fever or rash associated with signs of other organ system involvement (e.g., lymphadenopathy, hepatic dysfunction) may be drug-related and should be reported to their healthcare provider immediately. Clobazam should be discontinued immediately if a serious hypersensitivity reaction is suspected [see Warnings and Precautions (5.7)]." }

Suicidal Thinking and Behavior Counsel patients, their caregivers, and their families that AEDs, including clobazam, may increase the risk of suicidal thoughts and behavior and advise them of the need to be alert for the emergence or worsening of symptoms of depression, any unusual changes in mood or behavior, or the emergence of suicidal thoughts, behavior, or thoughts of self-harm. Patients should report behaviors of concern immediately to healthcare providers [see Warnings and Precautions (5.8)].  

{ "type": "p", "children": [], "text": "\nSuicidal Thinking and Behavior\n Counsel patients, their caregivers, and their families that AEDs, including clobazam, may increase the risk of suicidal thoughts and behavior and advise them of the need to be alert for the emergence or worsening of symptoms of depression, any unusual changes in mood or behavior, or the emergence of suicidal thoughts, behavior, or thoughts of self-harm. Patients should report behaviors of concern immediately to healthcare providers [see Warnings and Precautions (5.8)].  " }

Pregnancy

{ "type": "p", "children": [], "text": "\nPregnancy \n" }

Advise pregnant females that the use of clobazam late in pregnancy can result in sedation (respiratory depression, lethargy, hypotonia) and/or withdrawal symptoms (hyperreflexia, irritability, restlessness, tremors, inconsolable crying, and feeding difficulties) in newborns [see Warnings and Precautions (5.9) and Use in Specific Populations (8.1)]. Instruct patients to notify their healthcare provider if they are pregnant.

{ "type": "p", "children": [], "text": "Advise pregnant females that the use of clobazam late in pregnancy can result in sedation (respiratory depression, lethargy, hypotonia) and/or withdrawal symptoms (hyperreflexia, irritability, restlessness, tremors, inconsolable crying, and feeding difficulties) in newborns [see Warnings and Precautions (5.9) and Use in Specific Populations (8.1)]. Instruct patients to notify their healthcare provider if they are pregnant. " }

Encourage patients to enroll in the North American Antiepileptic Drug (NAAED) Pregnancy Registry if they become pregnant while taking clobazam. The registry is collecting information about the safety of antiepileptic drugs during pregnancy [see Use in Specific Populations (8.1)].

{ "type": "p", "children": [], "text": "Encourage patients to enroll in the North American Antiepileptic Drug (NAAED) Pregnancy Registry if they become pregnant while taking clobazam. The registry is collecting information about the safety of antiepileptic drugs during pregnancy [see Use in Specific Populations (8.1)]." }

Lactation

{ "type": "p", "children": [], "text": "\nLactation \n" }

Counsel patients that clobazam, the active ingredient in clobazam, is excreted in breast milk. Instruct patients to notify their healthcare provider if they are breastfeeding or intend to breastfeed. Instruct breastfeeding patients who have been administered clobazam to observe their infants for sedation, poor feeding and poor weight gain, and to seek medical attention if they notice these signs [see Use in Specific Populations (8.2)].

{ "type": "p", "children": [], "text": "Counsel patients that clobazam, the active ingredient in clobazam, is excreted in breast milk. Instruct patients to notify their healthcare provider if they are breastfeeding or intend to breastfeed. Instruct breastfeeding patients who have been administered clobazam to observe their infants for sedation, poor feeding and poor weight gain, and to seek medical attention if they notice these signs [see Use in Specific Populations (8.2)]." }

Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013, INDIA. Distributed by: Ascend Laboratories, LLC Bedminster, NJ 07921 Revised: January, 2025

{ "type": "p", "children": [], "text": "\n\n Manufactured by:\nAlkem Laboratories Ltd., Mumbai - 400 013, INDIA.\n\n Distributed by:\nAscend Laboratories, LLC Bedminster, NJ 07921\n\n\nRevised: January, 2025" }

For Medication Guide, please visit: www.ascendlaboratories.com/mg/clobazamtabs.pdf

{ "type": "p", "children": [], "text": "For Medication Guide, please visit: www.ascendlaboratories.com/mg/clobazamtabs.pdf" }

Clobazam (KLOE ba zam) Tablets, C-IV

{ "type": "p", "children": [], "text": "\nClobazam (KLOE ba zam) Tablets, C-IV\n" }

What is the most important information I should know about clobazam tablets?

{ "type": "p", "children": [], "text": "\nWhat is the most important information I should know about clobazam tablets? \n" }

{ "type": "ul", "children": [ "\nClobazam tablets are a benzodiazepine medicine. Taking benzodiazepines with opioid medicines, alcohol, or other central nervous system (CNS) depressants (including street drugs) can cause severe drowsiness, breathing problems (respiratory depression), coma, and death. Get emergency help right away if any of the following happens:" ], "text": "" }

{ "type": "ul", "children": [ "shallow or slowed breathing", "breathing stops (which may lead to the heart stopping)", "excessive sleepiness (sedation)" ], "text": "" }

Do not drive or operate heavy machinery until you know how taking clobazam tablets with opioids affects you.

{ "type": "p", "children": [], "text": "Do not drive or operate heavy machinery until you know how taking clobazam tablets with opioids affects you." }

{ "type": "ul", "children": [ "\nRisk of abuse, misuse, and addiction. There is a risk of abuse, misuse, and addiction with benzodiazepines, including clobazam tablets, which can lead to overdose and serious side effects including coma and death.\n" ], "text": "" }

{ "type": "ul", "children": [ "\nSerious side effects including coma and death have happened in people who have abused or misused benzodiazepines, including clobazam tablets. These serious side effects may also include delirium, paranoia, suicidal thoughts or actions, seizures, and difficulty breathing. Call your healthcare provider or go to the nearest hospital emergency room right away if you get any of these serious side effects.\n", "\nYou can develop an addiction even if you take clobazam tablets as prescribed by your healthcare provider.\n", "\nTake clobazam tablets exactly as your healthcare provider prescribed.\n", "Do not share your clobazam tablets with other people.", "Keep clobazam tablets in a safe place and away from children." ], "text": "" }

{ "type": "ul", "children": [ "\nPhysical dependence and withdrawal reactions. Clobazam tablets can cause physical dependence and withdrawal reactions.\n" ], "text": "" }

{ "type": "ul", "children": [ "\nDo not suddenly stop taking clobazam tablets. Stopping clobazam tablets suddenly can cause serious and life-threatening side effects, including, unusual movements, responses, or expressions, seizures, sudden and severe mental or nervous system changes, depression, seeing or hearing things that others do not see or hear, an extreme increase in activity or talking, losing touch with reality, and suicidal thoughts or actions. Call your healthcare provider or go to the nearest hospital emergency room right away if you get any of these symptoms.\n", "\nSome people who suddenly stop benzodiazepines have symptoms that can last for several weeks to more than 12 months, including, anxiety, trouble remembering, learning, or concentrating, depression, problems sleeping, feeling like insects are crawling under your skin, weakness, shaking, muscle twitching, burning or prickling feeling in your hands, arms, legs or feet, and ringing in your ears.", "Physical dependence is not the same as drug addiction. Your healthcare provider can tell you more about the differences between physical dependence and drug addiction.", "Do not take more clobazam tablets than prescribed or take clobazam tablets for longer than prescribed." ], "text": "" }

{ "type": "ul", "children": [ "\nClobazam tablets can make you sleepy or dizzy and can slow your thinking and motor skills.\n" ], "text": "" }

{ "type": "ul", "children": [ "Do not drive, operate heavy machinery, or do other dangerous activities until you know how clobazam tablets affects you.", "Do not drink alcohol or take other drugs that may make you sleepy or dizzy while taking clobazam tablets without first talking to your healthcare provider. When taken with alcohol or drugs that cause sleepiness or dizziness, clobazam tablets may make your sleepiness or dizziness much worse. " ], "text": "" }

{ "type": "ul", "children": [ "\nSerious skin reactions have been seen when clobazam tablets is taken with other medicines and may require stopping its use. Do not stop taking clobazam tablets without first talking to your healthcare provider." ], "text": "" }

{ "type": "ul", "children": [ "A serious skin reaction can happen at any time during your treatment with clobazam tablets, but is more likely to happen within the first 8 weeks of treatment. These skin reactions may need to be treated right away.", "Call your healthcare provider immediately if you have skin blisters, rash, sores in the mouth, hives or any other allergic reaction. " ], "text": "" }

{ "type": "ul", "children": [ "\nA serious allergic reaction that may affect your skin or other parts of your body such as your liver, kidneys, heart, or blood cells. This allergic reaction can be life-threatening and can cause death, particularly if it is not treated as early as possible. Call your healthcare provider right away if you have:" ], "text": "" }

<div class="scrollingtable"><table border="0" cellpadding="0" cellspacing="0" width="100%"> <colgroup> <col width="47.3153575615475%"/> <col width="52.6846424384525%"/> </colgroup> <tbody class="Headless"> <tr class="Botrule First"> <td class="Lrule Rrule" valign="top"> <br/> <ul class="Circle"> <li>a skin rash</li> </ul> </td><td class="Rrule" valign="top"> <ul class="Circle"> <li>fever or swollen glands that do not go away</li> </ul> </td> </tr> <tr class="Botrule"> <td class="Lrule Rrule" valign="top"> <ul class="Circle"> <li>swelling of your face</li> </ul> </td><td class="Rrule" valign="top"> <ul class="Circle"> <li>shortness of breath</li> </ul> </td> </tr> <tr class="Last"> <td class="Lrule Rrule" valign="top"> <ul class="Circle"> <li>dark urine</li> </ul> </td><td class="Rrule" valign="top"> <ul class="Circle"> <li>yellowing of the skin or whites of the eyes</li> </ul> </td> </tr> </tbody> </table></div>

{ "type": "table", "children": [], "text": "<div class=\"scrollingtable\"><table border=\"0\" cellpadding=\"0\" cellspacing=\"0\" width=\"100%\">\n<colgroup>\n<col width=\"47.3153575615475%\"/>\n<col width=\"52.6846424384525%\"/>\n</colgroup>\n<tbody class=\"Headless\">\n<tr class=\"Botrule First\">\n<td class=\"Lrule Rrule\" valign=\"top\">\n<br/>\n<ul class=\"Circle\">\n<li>a skin rash</li>\n</ul>\n</td><td class=\"Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>fever or swollen glands that do not go away</li>\n</ul>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td class=\"Lrule Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>swelling of your face</li>\n</ul>\n</td><td class=\"Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>shortness of breath</li>\n</ul>\n</td>\n</tr>\n<tr class=\"Last\">\n<td class=\"Lrule Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>dark urine</li>\n</ul>\n</td><td class=\"Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>yellowing of the skin or whites of the eyes</li>\n</ul>\n</td>\n</tr>\n</tbody>\n</table></div>" }

{ "type": "ul", "children": [ "\nLike other antiepileptic medicines, clobazam tablets may cause suicidal thoughts or actions in a very small number of people, about 1 in 500.\n" ], "text": "" }

Call your healthcare provider right away if you have any of these symptoms, especially if they are new, worse, or worry you:

{ "type": "p", "children": [], "text": "\nCall your healthcare provider right away if you have any of these symptoms, especially if they are new, worse, or worry you:\n" }

<div class="scrollingtable"><table border="0" cellpadding="0" cellspacing="0" width="0"> <colgroup> <col width="30.030487804878%"/> <col width="34.7560975609756%"/> <col width="35.2134146341463%"/> </colgroup> <tbody class="Headless"> <tr class="Botrule First"> <td class="Lrule Rrule" valign="top"> <ul class="Circle"> <li>thoughts about suicide or dying </li> </ul> </td><td class="Rrule" valign="top"> <ul class="Circle"> <li>attempts to commit suicide </li> </ul> </td><td class="Rrule" valign="top"> <ul class="Circle"> <li>new or worse depression </li> </ul> </td> </tr> <tr class="Botrule"> <td class="Lrule Rrule" valign="top"> <ul class="Circle"> <li>new or worse anxiety or irritability</li> </ul> </td><td class="Rrule" valign="top"> <ul class="Circle"> <li>feeling agitated or restless </li> </ul> </td><td class="Rrule" valign="top"> <ul class="Circle"> <li>an extreme increase in activity and talking (mania)</li> </ul> </td> </tr> <tr class="Botrule"> <td class="Lrule Rrule" valign="top"> <ul class="Circle"> <li>trouble sleeping (insomnia) </li> </ul> </td><td class="Rrule" valign="top"> <ul class="Circle"> <li>new or worse panic attacks</li> </ul> </td><td class="Rrule" valign="top"> <ul class="Circle"> <li>acting aggressive, being angry or violent </li> </ul> </td> </tr> <tr class="Last"> <td class="Lrule Rrule" valign="top"> <ul class="Circle"> <li>acting on dangerous impulses</li> </ul> </td><td class="Rrule" valign="top"> <ul class="Circle"> <li>other unusual changes in behavior or mood</li> </ul> </td><td class="Rrule" valign="top"> <br/> </td> </tr> </tbody> </table></div>

{ "type": "table", "children": [], "text": "<div class=\"scrollingtable\"><table border=\"0\" cellpadding=\"0\" cellspacing=\"0\" width=\"0\">\n<colgroup>\n<col width=\"30.030487804878%\"/>\n<col width=\"34.7560975609756%\"/>\n<col width=\"35.2134146341463%\"/>\n</colgroup>\n<tbody class=\"Headless\">\n<tr class=\"Botrule First\">\n<td class=\"Lrule Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>thoughts about suicide or dying </li>\n</ul>\n</td><td class=\"Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>attempts to commit suicide </li>\n</ul>\n</td><td class=\"Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>new or worse depression </li>\n</ul>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td class=\"Lrule Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>new or worse anxiety or irritability</li>\n</ul>\n</td><td class=\"Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>feeling agitated or restless </li>\n</ul>\n</td><td class=\"Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>an extreme increase in activity and talking (mania)</li>\n</ul>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td class=\"Lrule Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>trouble sleeping (insomnia) </li>\n</ul>\n</td><td class=\"Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>new or worse panic attacks</li>\n</ul>\n</td><td class=\"Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>acting aggressive, being angry or violent </li>\n</ul>\n</td>\n</tr>\n<tr class=\"Last\">\n<td class=\"Lrule Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>acting on dangerous impulses</li>\n</ul>\n</td><td class=\"Rrule\" valign=\"top\">\n<ul class=\"Circle\">\n<li>other unusual changes in behavior or mood</li>\n</ul>\n</td><td class=\"Rrule\" valign=\"top\"> <br/>\n</td>\n</tr>\n</tbody>\n</table></div>" }

How can I watch for early symptoms of suicidal thoughts and actions?

{ "type": "p", "children": [], "text": "\nHow can I watch for early symptoms of suicidal thoughts and actions?\n" }

{ "type": "ul", "children": [ "Pay attention to any changes, especially sudden changes, in mood, behaviors, thoughts, or feelings. ", "Keep all follow-up visits with your healthcare provider as scheduled. " ], "text": "" }

Call your healthcare provider between visits as needed, especially if you are worried about symptoms.

{ "type": "p", "children": [], "text": "Call your healthcare provider between visits as needed, especially if you are worried about symptoms." }

Stopping a seizure medicine suddenly in a patient who has epilepsy can cause seizures that will not stop (status epilepticus).

{ "type": "p", "children": [], "text": "Stopping a seizure medicine suddenly in a patient who has epilepsy can cause seizures that will not stop (status epilepticus)." }

Suicidal thoughts or actions can be caused by things other than medicines. If you have suicidal thoughts or actions, your healthcare provider may check for other causes.

{ "type": "p", "children": [], "text": "Suicidal thoughts or actions can be caused by things other than medicines. If you have suicidal thoughts or actions, your healthcare provider may check for other causes.\n" }

What are clobazam tablets?

{ "type": "p", "children": [], "text": "\nWhat are clobazam tablets?\n" }

{ "type": "ul", "children": [ "Clobazam tablets are a prescription medicine used along with other medicines to treat seizures associated with Lennox-Gastaut syndrome in people 2 years of age or older.", "\nClobazam tablets are a federally controlled substance (C-IV) because it contains clobazam that can be abused or lead to dependence. Keep clobazam tablets in a safe place to prevent misuse and abuse. Selling or giving away clobazam tablets may harm others, and is against the law. Tell your healthcare provider if you have ever abused or been dependent on alcohol, prescription medicines, or street drugs." ], "text": "" }

It is not known if clobazam tablets are safe and effective in children less than 2 years old.

{ "type": "p", "children": [], "text": "It is not known if clobazam tablets are safe and effective in children less than 2 years old.\n" }

Do not take clobazam tablets if you:

{ "type": "p", "children": [], "text": "\nDo not take clobazam tablets if you: \n" }

{ "type": "ul", "children": [ " are allergic to clobazam or any of the ingredients in clobazam tablets. See the end of this Medication Guide for a complete list of ingredients in clobazam tablets." ], "text": "" }

Before you take clobazam tablets, tell your healthcare provider about all your medical conditions, including if you:

{ "type": "p", "children": [], "text": "\nBefore you take clobazam tablets, tell your healthcare provider about all your medical conditions, including if you: \n" }

{ "type": "ul", "children": [ "have liver or kidney problems", "have lung problems (respiratory disease) ", "have or have had depression, mood problems, or suicidal thoughts or behavior", "use birth control medicine.  Clobazam tablets may cause your birth control medicine to be less effective. Talk to your healthcare provider about the best birth control method to use. ", "are pregnant or plan to become pregnant.\nTaking clobazam tablets late in pregnancy may cause your baby to have symptoms of sedation (breathing problems, sluggishness, low muscle tone), and/or withdrawal symptoms (jitteriness, irritability, restlessness, shaking, excessive crying, feeding problems). \nTell your healthcare provider right away if you become pregnant or think you are pregnant while taking clobazam tablets. \nIf you become pregnant while taking clobazam tablets, talk to your healthcare provider about registering with the North American Antiepileptic Drug Pregnancy Registry. You can register by calling 1-888-233-2334. For more information about the registry go to http://www.aedpregnancyregistry.org. The purpose of this registry is to collect information about the safety of antiepileptic drugs during pregnancy. \n\n", "are breastfeeding or plan to breastfeed. Clobazam can pass into breast milk. " ], "text": "" }

{ "type": "ul", "children": [ "Breastfeeding during treatment with clobazam tablets may cause your baby to have sleepiness, feeding problems, and decreased weight gain. ", "Talk to your healthcare provider about the best way to feed your baby if you take clobazam tablets. " ], "text": "" }

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Taking clobazam tablets with certain other medicines can cause side effects or affect how well clobazam tablets or the other medicines work. Do not start or stop other medicines without talking to your healthcare provider.

{ "type": "p", "children": [], "text": "\nTell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Taking clobazam tablets with certain other medicines can cause side effects or affect how well clobazam tablets or the other medicines work. Do not start or stop other medicines without talking to your healthcare provider." }

How should I take clobazam tablets?

{ "type": "p", "children": [], "text": "\nHow should I take clobazam tablets?\n" }

{ "type": "ul", "children": [ "Take clobazam tablets exactly as your healthcare provider tells you to take it.", "Your healthcare provider will tell you how much clobazam tablets to take and when to take it.", "Clobazam tablets can be taken whole, broken in half along the score, or crushed and mixed in applesauce.", "Clobazam tablets can be taken with or without food.", "Your healthcare provider may change your dose if needed. Do not change your dose of clobazam tablets without talking to your healthcare provider. ", "Do not stop taking clobazam tablets without first talking to your healthcare provider.", "Stopping clobazam tablets suddenly can cause serious problems.", " If you take too much clobazam tablets, call your healthcare provider or go to the nearest hospital emergency room right away. " ], "text": "" }

What should I avoid while taking clobazam tablets?

{ "type": "p", "children": [], "text": "\nWhat should I avoid while taking clobazam tablets? \n" }

See “What is the most important information I should know about clobazam tablets?”

{ "type": "p", "children": [], "text": " See “What is the most important information I should know about clobazam tablets?”\n" }

What are the possible side effects of clobazam tablets?

{ "type": "p", "children": [], "text": "\nWhat are the possible side effects of clobazam tablets?\n" }

Clobazam tablets may cause serious side effects, including: See “What is the most important information I should know about clobazam tablets?”

{ "type": "p", "children": [], "text": "\nClobazam tablets may cause serious side effects, including: See “What is the most important information I should know about clobazam tablets?”\n" }

The most common side effects of clobazam tablets include:

{ "type": "p", "children": [], "text": "\nThe most common side effects of clobazam tablets include:\n" }

<div class="scrollingtable"><table border="0" cellpadding="0" cellspacing="0"> <tbody class="Headless"> <tr class="Botrule First"> <td class="Lrule Rrule" valign="middle"> <ul class="Disc"> <li>sleepiness </li> </ul> </td><td class="Rrule" valign="middle"> <ul class="Disc"> <li>drooling </li> </ul> </td><td class="Rrule" valign="middle"> <ul class="Disc"> <li>constipation </li> </ul> </td> </tr> <tr class="Botrule"> <td class="Lrule Rrule" valign="middle"> <ul class="Disc"> <li> cough</li> </ul> </td><td class="Rrule" valign="middle"> <ul class="Disc"> <li> pain with urination</li> </ul> </td><td class="Rrule" valign="middle"> <ul class="Disc"> <li>fever</li> </ul> </td> </tr> <tr class="Botrule"> <td class="Lrule Rrule" valign="middle"> <ul class="Disc"> <li> acting aggressive, being angry or violent</li> </ul> </td><td class="Rrule" valign="middle"> <ul class="Disc"> <li> difficulty sleeping</li> </ul> </td><td class="Rrule" valign="middle"> <ul class="Disc"> <li>slurred speech</li> </ul> </td> </tr> <tr class="Last"> <td class="Lrule Rrule" valign="middle"> <ul class="Disc"> <li> tiredness</li> </ul> </td><td class="Rrule" valign="middle"> <ul class="Disc"> <li> problems with breathing</li> </ul> </td><td class="Rrule" valign="middle"> </td> </tr> </tbody> </table></div>

{ "type": "table", "children": [], "text": "<div class=\"scrollingtable\"><table border=\"0\" cellpadding=\"0\" cellspacing=\"0\">\n<tbody class=\"Headless\">\n<tr class=\"Botrule First\">\n<td class=\"Lrule Rrule\" valign=\"middle\">\n<ul class=\"Disc\">\n<li>sleepiness </li>\n</ul>\n</td><td class=\"Rrule\" valign=\"middle\">\n<ul class=\"Disc\">\n<li>drooling </li>\n</ul>\n</td><td class=\"Rrule\" valign=\"middle\">\n<ul class=\"Disc\">\n<li>constipation </li>\n</ul>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td class=\"Lrule Rrule\" valign=\"middle\">\n<ul class=\"Disc\">\n<li> cough</li>\n</ul>\n</td><td class=\"Rrule\" valign=\"middle\">\n<ul class=\"Disc\">\n<li> pain with urination</li>\n</ul>\n</td><td class=\"Rrule\" valign=\"middle\">\n<ul class=\"Disc\">\n<li>fever</li>\n</ul>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td class=\"Lrule Rrule\" valign=\"middle\">\n<ul class=\"Disc\">\n<li> acting aggressive, being angry or violent</li>\n</ul>\n</td><td class=\"Rrule\" valign=\"middle\">\n<ul class=\"Disc\">\n<li> difficulty sleeping</li>\n</ul>\n</td><td class=\"Rrule\" valign=\"middle\">\n<ul class=\"Disc\">\n<li>slurred speech</li>\n</ul>\n</td>\n</tr>\n<tr class=\"Last\">\n<td class=\"Lrule Rrule\" valign=\"middle\">\n<ul class=\"Disc\">\n<li> tiredness</li>\n</ul>\n</td><td class=\"Rrule\" valign=\"middle\">\n<ul class=\"Disc\">\n<li> problems with breathing</li>\n</ul>\n</td><td class=\"Rrule\" valign=\"middle\"> </td>\n</tr>\n</tbody>\n</table></div>" }

These are not all the possible side effects of clobazam tablets. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

{ "type": "p", "children": [], "text": "These are not all the possible side effects of clobazam tablets. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088." }

How should I store clobazam tablets?

{ "type": "p", "children": [], "text": "\nHow should I store clobazam tablets? \n" }

{ "type": "ul", "children": [ "Store clobazam tablets at room temperature between 68°F to 77°F (20°C to 25°C).\nTablets\n\n", "Keep clobazam tablets in a dry place." ], "text": "" }

{ "type": "ul", "children": [ "\nKeep clobazam tablets and all medicines out of the reach of children. \n" ], "text": "" }

General information about the safe and effective use of clobazam tablets.

{ "type": "p", "children": [], "text": "\nGeneral information about the safe and effective use of clobazam tablets. \n" }

Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use clobazam tablets for a condition for which it was not prescribed. Do not give clobazam tablets to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about clobazam tablets that is written for health professionals. 

{ "type": "p", "children": [], "text": " Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use clobazam tablets for a condition for which it was not prescribed. Do not give clobazam tablets to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about clobazam tablets that is written for health professionals. " }

What are the ingredients in clobazam tablets?

{ "type": "p", "children": [], "text": "\nWhat are the ingredients in clobazam tablets? \n" }

Tablets

{ "type": "p", "children": [], "text": "\nTablets\n" }

Active ingredient: clobazam

{ "type": "p", "children": [], "text": "\nActive ingredient: clobazam " }

Inactive ingredients: Pregelatinized starch, lactose monohydrate, magnesium stearate, Colloidal silicon dioxide, and talc.

{ "type": "p", "children": [], "text": "\nInactive ingredients: Pregelatinized starch, lactose monohydrate, magnesium stearate, Colloidal silicon dioxide, and talc. " }

Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013, INDIA. Distributed by: Ascend Laboratories, LLC Bedminster, NJ 07921

{ "type": "p", "children": [], "text": "\nManufactured by:\nAlkem Laboratories Ltd., Mumbai - 400 013, INDIA.\n\n Distributed by:\nAscend Laboratories, LLC Bedminster, NJ 07921" }

For more information about clobazam tablets, call Ascend Laboratories, LLC at 1-877-272-7901. 

{ "type": "p", "children": [], "text": "For more information about clobazam tablets, call Ascend Laboratories, LLC at 1-877-272-7901. " }

This Medication Guide has been approved by the U.S. Food and Drug Administration   

{ "type": "p", "children": [], "text": "This Medication Guide has been approved by the U.S. Food and Drug Administration    " }

Revised: January, 2025

{ "type": "p", "children": [], "text": "\nRevised: January, 2025" }

PT3324-07

{ "type": "p", "children": [], "text": "PT3324-07" }

NDC 67877-664-01 Clobazam Tablets 5 mg 100 Tablets

{ "type": "p", "children": [], "text": "NDC 67877-664-01\nClobazam Tablets 5 mg\n 100 Tablets" }

NDC 67877-665-01

{ "type": "p", "children": [], "text": "NDC 67877-665-01" }

Clobazam Tablets 10 mg  100 Tablets 

{ "type": "p", "children": [], "text": "\nClobazam Tablets 10 mg \n100 Tablets " }

NDC 67877-666-01

{ "type": "p", "children": [], "text": "NDC 67877-666-01" }

Clobazam Tablets 20 mg  100 Tablets

{ "type": "p", "children": [], "text": "\nClobazam Tablets 20 mg \n100 Tablets" }