Limitation of Use:

ARIKAYCE has only been studied in patients with refractory MAC lung disease defined as patients who did not achieve negative sputum cultures after a minimum of 6 consecutive months of a multidrug background regimen therapy. The use of ARIKAYCE is not recommended for patients with non-refractory MAC lung disease.

ARIKAYCE is for oral inhalation use only. Administer by nebulization only with the Lamira® Nebulizer System. Refer to the Instructions for Use for full administration information on use of ARIKAYCE with the Lamira Nebulizer System.

Instruct patients using a bronchodilator ('reliever') to first use the bronchodilator following the bronchodilator leaflet for use information before using ARIKAYCE.

Pre-treatment with short-acting selective beta-2 agonists should be considered for patients with known hyperreactive airway disease, chronic obstructive pulmonary disease, asthma, or bronchospasm [see Warnings and Precautions (5.3)].

The recommended dosage of ARIKAYCE in adults is once daily inhalation of the contents of one 590 mg/8.4 mL ARIKAYCE vial (590 mg of amikacin) using the Lamira Nebulizer System [see Clinical Studies (14)].

Administer ARIKAYCE with the Lamira Nebulizer System only. ARIKAYCE should be at room temperature before use. Prior to opening, shake the ARIKAYCE vial well for at least 10 to 15 seconds until the contents appear uniform and well mixed. The ARIKAYCE vial is opened by flipping up the plastic top of the vial then pulling downward to loosen the metal ring. The metal ring and the rubber stopper should be removed carefully. The contents of the ARIKAYCE vial can then be poured into the medication reservoir of the nebulizer handset.

If a daily dose of ARIKAYCE is missed, administer the next dose the next day. Do NOT double the dose to make up for the missed dose.

ARIKAYCE is supplied as a sterile, white, milky, aqueous, liposome suspension for oral inhalation in a unit-dose glass vial containing amikacin 590 mg/8.4 mL (equivalent to amikacin sulfate 788 mg/8.4 mL).

{ "type": "p", "children": [], "text": "ARIKAYCE is supplied as a sterile, white, milky, aqueous, liposome suspension for oral inhalation in a unit-dose glass vial containing amikacin 590 mg/8.4 mL (equivalent to amikacin sulfate 788 mg/8.4 mL)." }

ARIKAYCE is contraindicated in patients with a known hypersensitivity to any aminoglycoside.

{ "type": "p", "children": [], "text": "ARIKAYCE is contraindicated in patients with a known hypersensitivity to any aminoglycoside." }

Hypersensitivity pneumonitis has been reported with the use of ARIKAYCE in the clinical trials. Hypersensitivity pneumonitis (reported as allergic alveolitis, pneumonitis, interstitial lung disease, allergic reaction to ARIKAYCE) was reported at a higher frequency in patients treated with ARIKAYCE plus a background regimen (3.1%) compared to patients treated with a background regimen alone (0%). Most patients with hypersensitivity pneumonitis discontinued treatment with ARIKAYCE and received treatment with corticosteroids [see Adverse Reactions (6.1)].

If hypersensitivity pneumonitis occurs, discontinue ARIKAYCE and manage the patient as medically appropriate.

Hemoptysis has been reported with the use of ARIKAYCE in the clinical trials. Hemoptysis was reported at a higher frequency in patients treated with ARIKAYCE plus a background regimen (18.4%) compared to patients treated with a background regimen alone (13.4%) [see Adverse Reactions (6.1)]. If hemoptysis occurs, manage the patients as medically appropriate.

Bronchospasm has been reported with the use of ARIKAYCE in the clinical trials. Bronchospasm (reported as asthma, bronchial hyperreactivity, bronchospasm, dyspnea, dyspnea exertional, prolonged expiration, throat tightness, wheezing) was reported at a higher frequency in patients treated with ARIKAYCE plus a background regimen (28.7%) compared to patients treated with a background regimen alone (10.7%) [see Adverse Reactions (6.1)]. If bronchospasm occurs during the use of ARIKAYCE, treat the patients as medically appropriate.

Exacerbations of underlying pulmonary disease have been reported with the use of ARIKAYCE in the clinical trials. Exacerbations of underlying pulmonary disease (reported as chronic obstructive pulmonary disease, infective exacerbation of chronic obstructive pulmonary disease, infective exacerbation of bronchiectasis) have been reported at a higher frequency in patients treated with ARIKAYCE plus a background regimen (15.2%) compared to patients treated with background regimen alone (9.8%) [see Adverse Reactions (6.1)]. If exacerbations of underlying pulmonary disease occur during the use of ARIKAYCE, treat the patients as medically appropriate.

Serious and potentially life-threatening hypersensitivity reactions, including anaphylaxis, have been reported in patients taking ARIKAYCE. Signs and symptoms include acute onset of skin and mucosal tissue hypersensitivity reactions (hives, itching, flushing, swollen lips/tongue/uvula), respiratory difficulty (shortness of breath, wheezing, stridor, cough), gastrointestinal symptoms (nausea, vomiting, diarrhea, crampy abdominal pain), and cardiovascular signs and symptoms of anaphylaxis (tachycardia, low blood pressure, syncope, incontinence, dizziness). Before therapy with ARIKAYCE is instituted, evaluate for previous hypersensitivity reactions to aminoglycosides. If anaphylaxis or a hypersensitivity reaction occurs, discontinue ARIKAYCE and institute appropriate supportive measures.

Ototoxicity with use of ARIKAYCE

Ototoxicity has been reported with the use of ARIKAYCE in the clinical trials. Ototoxicity (including deafness, dizziness, presyncope, tinnitus, and vertigo) were reported with a higher frequency in patients treated with ARIKAYCE plus a background regimen (17%) compared to patients treated with background regimen alone (9.8%). This was primarily driven by tinnitus (8.1% in ARIKAYCE plus background regimen vs. 0.9% in the background regimen alone arm) and dizziness (6.3% in ARIKAYCE plus background regimen vs. 2.7% in the background regimen alone arm) [see Adverse Reactions (6.1)].

Closely monitor patients with known or suspected auditory or vestibular dysfunction during treatment with ARIKAYCE. If ototoxicity occurs, manage the patient as medically appropriate, including potentially discontinuing ARIKAYCE.

Risk of Ototoxicity Due to Mitochondrial DNA Variants

Cases of ototoxicity with aminoglycosides have been observed in patients with certain variants in the mitochondrially encoded 12S rRNA gene (MT-RNR1), particularly the m.1555A>G variant. Ototoxicity occurred in some patients even when their aminoglycoside serum levels were within the recommended range. Mitochondrial DNA variants are present in less than 1% of the general US population, and the proportion of the variant carriers who may develop ototoxicity as well as the severity of ototoxicity is unknown. In case of known maternal history of ototoxicity due to aminoglycoside use or a known mitochondrial DNA variant in the patient, consider alternative treatments other than aminoglycosides unless the increased risk of permanent hearing loss is outweighed by the severity of infection and lack of safe and effective alternative therapies.

Nephrotoxicity was observed during the clinical trials of ARIKAYCE in patients with MAC lung disease but not at a higher frequency than the background regimen alone [see Adverse Reactions (6.1)]. Nephrotoxicity has been associated with the aminoglycosides. Close monitoring of patients with known or suspected renal dysfunction may be needed when prescribing ARIKAYCE.

Patients with neuromuscular disorders were not enrolled in ARIKAYCE clinical trials. Aminoglycosides may aggravate muscle weakness by blocking the release of acetylcholine at neuromuscular junctions. Closely monitor patients with known or suspected neuromuscular disorders, such as myasthenia gravis. If neuromuscular blockade occurs, it may be reversed by the administration of calcium salts but mechanical respiratory assistance may be necessary.

Aminoglycosides can cause fetal harm when administered to a pregnant woman. Aminoglycosides, including ARIKAYCE, may be associated with total, irreversible, bilateral congenital deafness in pediatric patients exposed in utero. Patients who use ARIKAYCE during pregnancy, or become pregnant while taking ARIKAYCE should be apprised of the potential hazard to the fetus [see Use in Specific Populations (8.1)].

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.

Overview of Clinical Trials for Safety Evaluation

Within the refractory NTM clinical program, 404 patients that participated in three clinical trials were treated with ARIKAYCE at the dose of 590 mg/day (median duration of exposure to ARIKAYCE was 236.5 days).

Trial 1 (NCT#02344004) was an open-label, randomized (2:1), multi-center Phase 3 trial in patients with refractory Mycobacterium avium complex (MAC) lung disease. Patients were randomized to either 8 months of ARIKAYCE plus a background regimen (n=223) or background regimen alone (n=112).

Trial 2 (NCT#02628600) was a single-arm extension of Trial 1 for refractory MAC lung disease patients that failed to achieve negative sputum cultures after 6 months of treatment or had a relapse or recurrence by Month 6 from either study arm of Trial 1. A total of 163 patients (n=90 from the prior background regimen alone arm of Trial 1, and n=73 from the prior ARIKAYCE plus background regimen arm in Trial 1) participated in the trial.

Trial 3 (NCT#01315236) was a double-blind, randomized, placebo-controlled Phase 2 study in patients with refractory nontuberculous mycobacterial (NTM) lung disease caused by MAC and Mycobacterium abscessus. Patients were randomized to either ARIKAYCE plus background regimen (N=44) or an inhaled diluted empty liposome placebo plus background regimen (N=45) for 84 days.

Across all clinical trials of patients with and without refractory NTM lung infection, 818 patients were exposed to multiple doses of ARIKAYCE.

Adverse Reactions Leading to Treatment Discontinuation

In the three NTM studies, there was a higher incidence of premature discontinuation of ARIKAYCE. In Trial 1, 34.5% discontinued ARIKAYCE prematurely; most were due to adverse reactions (18.8%) and withdrawal by subject (9.9%). In the comparator arm, 10.7% of subjects discontinued their background regimen, with 0.9% due to adverse reactions and 5.4% due to withdrawal by subject. In Trial 2 (the single-arm extension of Trial 1), 37.8% of patients starting on ARIKAYCE discontinued prematurely with 24.4% discontinuing due to adverse reactions. In Trial 3, all 9 (20.5%) premature discontinuations occurred in the ARIKAYCE plus background regimen-treated patients and there were no premature discontinuations in the placebo plus background regimen arm.

Serious Adverse Reactions in Trials 1 and 3

In Trial 1, 19.7% of patients treated with ARIKAYCE plus background regimen reported SAR as compared to 16.1% of patients treated with background regimen alone. In addition, in Trial 1 [2 to 1 randomization, ARIKAYCE plus background regimen versus background regimen alone], there were 80 hospitalizations in 41 patients (18.4%) treated with ARIKAYCE plus background regimen compared to 29 hospitalizations in 15 patients (13.4%) treated with background regimen alone. The most common SARs and reasons for hospitalization in the ARIKAYCE plus background regimen arm were related to exacerbation of underlying pulmonary disease and lower respiratory tract infections, such as pneumonia.

In Trial 3, 18.2% of patients treated with ARIKAYCE plus background regimen reported SARs compared to 8.9% of patients treated with background regimen plus inhaled placebo.

Common Adverse Reactions

The incidence of adverse reactions in Trial 1 are displayed in Table 1. Only those adverse reactions with a rate of at least 5% in the ARIKAYCE plus background regimen group and greater than the background regimen alone group, are shown.

<div class="scrollingtable"><table width="80%"> <caption> <span>Table 1: Adverse Reactions in ≥ 5% of ARIKAYCE-treated MAC Patients and More Frequent than Background Regimen Alone in Trial 1</span> </caption> <col align="left" valign="top" width="60%"/> <col align="center" valign="top" width="20%"/> <col align="center" valign="top" width="20%"/> <thead> <tr class="First"> <th align="center" class="Lrule Rrule">Adverse Reaction</th><th align="center" class="Rrule">ARIKAYCE plus Background Regimen</th><th align="center" class="Rrule">Background Regimen Alone</th> </tr> <tr class="Last"> <th align="left" class="Lrule Rrule"></th><th align="center" class="Rrule">(N=223)<br/>n (%)</th><th align="center" class="Rrule">(N=112)<br/>n (%)</th> </tr> </thead> <tfoot> <tr> <td align="left" colspan="3"> <dl class="Footnote"> <dt> <a href="#footnote-reference-1" name="footnote-1">*</a> </dt> <dd>Includes aphonia and dysphonia</dd> <dt> <a href="#footnote-reference-2" name="footnote-2">†</a> </dt> <dd>Includes cough, productive cough, and upper airway cough syndrome</dd> <dt> <a href="#footnote-reference-3" name="footnote-3">‡</a> </dt> <dd>Includes asthma, bronchial hyperreactivity, bronchospasm, dyspnea, dyspnea exertional, prolonged expiration, throat tightness, and wheezing</dd> <dt> <a href="#footnote-reference-4" name="footnote-4">§</a> </dt> <dd>Includes back pain, arthralgia, myalgia, pain/body aches, muscle spasm and musculoskeletal pain</dd> <dt> <a href="#footnote-reference-5" name="footnote-5">¶</a> </dt> <dd>Includes oropharyngeal pain, oropharyngeal discomfort, throat irritation, pharyngeal erythema, upper airway inflammation, pharyngeal edema<span class="Bold">,</span> vocal cord inflammation, laryngeal pain, laryngeal erythema, laryngitis</dd> <dt> <a href="#footnote-reference-6" name="footnote-6">#</a> </dt> <dd>Includes deafness, deafness neurosensory, deafness unilateral, dizziness, hypoacusis, presyncope, tinnitus, vertigo, balance disorders</dd> <dt> <a href="#footnote-reference-7" name="footnote-7">Þ</a> </dt> <dd>Includes COPD, infective exacerbation of COPD, infective exacerbation of bronchiectasis</dd> <dt> <a href="#footnote-reference-8" name="footnote-8">ß</a> </dt> <dd>Includes atypical pneumonia, empyema, infection pleural effusion, lower respiratory tract infection, lung infection, lung infection pseudomonas, pneumonia, pneumonia aspiration, pneumonia pseudomonas, pseudomonas infection, and respiratory tract infection</dd> <dt> <a href="#footnote-reference-9" name="footnote-9">à</a> </dt> <dd>Includes vomiting and post-tussive vomiting</dd> <dt> <a href="#footnote-reference-10" name="footnote-10">è</a> </dt> <dd>Includes rash, rash maculo-papular, drug eruption, and urticaria</dd> <dt> <a href="#footnote-reference-11" name="footnote-11">ð</a> </dt> <dd>Includes increased sputum, sputum purulent, and sputum discolored</dd> </dl> </td> </tr> </tfoot> <tbody> <tr class="Botrule First"> <td align="left" class="Lrule Rrule">Dysphonia<a class="Sup" href="#footnote-1" name="footnote-reference-1">*</a></td><td align="center" class="Rrule">106 (48)</td><td align="center" class="Rrule">2 (2)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Cough<a class="Sup" href="#footnote-2" name="footnote-reference-2">†</a></td><td align="center" class="Rrule">88 (40)</td><td align="center" class="Rrule">19 (17)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Bronchospasm<a class="Sup" href="#footnote-3" name="footnote-reference-3">‡</a></td><td align="center" class="Rrule">64 (29)</td><td align="center" class="Rrule">12 (11)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Hemoptysis</td><td align="center" class="Rrule">41 (18)</td><td align="center" class="Rrule">15 (13)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Musculoskeletal pain<a class="Sup" href="#footnote-4" name="footnote-reference-4">§</a></td><td align="center" class="Rrule">40 (18)</td><td align="center" class="Rrule">10 (9)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Upper airway irritation<a class="Sup" href="#footnote-5" name="footnote-reference-5">¶</a></td><td align="center" class="Rrule">39 (18)</td><td align="center" class="Rrule">2 (2)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Ototoxicity<a class="Sup" href="#footnote-6" name="footnote-reference-6">#</a></td><td align="center" class="Rrule">38 (17)</td><td align="center" class="Rrule">11 (10)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Fatigue and asthenia</td><td align="center" class="Rrule">36 (16)</td><td align="center" class="Rrule">11 (10)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Exacerbation of underlying pulmonary disease<a class="Sup" href="#footnote-7" name="footnote-reference-7">Þ</a></td><td align="center" class="Rrule">34 (15)</td><td align="center" class="Rrule">11 (10)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Diarrhea</td><td align="center" class="Rrule">28 (13)</td><td align="center" class="Rrule">5 (5)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Nausea</td><td align="center" class="Rrule">26 (12)</td><td align="center" class="Rrule">4 (4)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Headache</td><td align="center" class="Rrule">22 (10)</td><td align="center" class="Rrule">5 (5)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Pneumonia<a class="Sup" href="#footnote-8" name="footnote-reference-8">ß</a></td><td align="center" class="Rrule">20 (9)</td><td align="center" class="Rrule">10 (9)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Pyrexia</td><td align="center" class="Rrule">17 (8)</td><td align="center" class="Rrule">5 (5)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Weight decreased</td><td align="center" class="Rrule">16 (7)</td><td align="center" class="Rrule">1 (1)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Vomiting<a class="Sup" href="#footnote-9" name="footnote-reference-9">à</a></td><td align="center" class="Rrule">15 (7)</td><td align="center" class="Rrule">4 (4)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Rash<a class="Sup" href="#footnote-10" name="footnote-reference-10">è</a></td><td align="center" class="Rrule">14 (6)</td><td align="center" class="Rrule">1 (1)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Change in sputum<a class="Sup" href="#footnote-11" name="footnote-reference-11">ð</a></td><td align="center" class="Rrule">13 (6)</td><td align="center" class="Rrule">1 (1)</td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule">Chest discomfort</td><td align="center" class="Rrule">12 (5)</td><td align="center" class="Rrule">3 (3)</td> </tr> </tbody> </table></div>

Selected adverse drug reactions that occurred in <5% of patients and at higher frequency in ARIKAYCE-treated patients in Trial 1 are presented in Table 2.

<div class="scrollingtable"><table width="80%"> <caption> <span>Table 2: Selected Adverse Reactions in &lt; 5% of ARIKAYCE-treated MAC Patients and More Frequent than Background Regimen Alone in Trial 1</span> </caption> <col align="left" valign="top" width="60%"/> <col align="center" valign="top" width="20%"/> <col align="center" valign="top" width="20%"/> <thead> <tr class="First Last"> <th align="center" class="Lrule Rrule" valign="top">Adverse Reaction</th><th align="center" class="Rrule">ARIKAYCE plus Background Regimen<br/>N=223<br/>n (%)</th><th align="center" class="Rrule">Background Regimen Alone<br/>N=112<br/>n (%)</th> </tr> </thead> <tfoot> <tr> <td align="left" colspan="3"> <dl class="Footnote"> <dt> <a href="#footnote-reference-12" name="footnote-12">*</a> </dt> <dd>Includes anxiety and anxiety disorder</dd> <dt> <a href="#footnote-reference-13" name="footnote-13">†</a> </dt> <dd>Includes oral candidiasis and oral fungal infection</dd> <dt> <a href="#footnote-reference-14" name="footnote-14">‡</a> </dt> <dd>Includes allergic alveolitis, interstitial lung disease, and pneumonitis</dd> <dt> <a href="#footnote-reference-15" name="footnote-15">§</a> </dt> <dd>Includes acute respiratory failure and respiratory failure</dd> <dt> <a href="#footnote-reference-16" name="footnote-16">¶</a> </dt> <dd>Includes pneumothorax, pneumothorax spontaneous and pneumomediastinum</dd> <dt> <a href="#footnote-reference-17" name="footnote-17">#</a> </dt> <dd>Includes muscle weakness and neuropathy peripheral</dd> </dl> </td> </tr> </tfoot> <tbody> <tr class="Botrule First"> <td align="left" class="Lrule Rrule">Anxiety<a class="Sup" href="#footnote-12" name="footnote-reference-12">*</a></td><td align="center" class="Rrule">10 (5)</td><td align="center" class="Rrule">0 (0)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Oral fungal infection<a class="Sup" href="#footnote-13" name="footnote-reference-13">†</a></td><td align="center" class="Rrule">9 (4)</td><td align="center" class="Rrule">2 (2)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Bronchitis</td><td align="center" class="Rrule">8 (4)</td><td align="center" class="Rrule">3 (3)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Dysgeusia</td><td align="center" class="Rrule">7 (3)</td><td align="center" class="Rrule">0 (0)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Hypersensitivity pneumonitis<a class="Sup" href="#footnote-14" name="footnote-reference-14">‡</a></td><td align="center" class="Rrule">7 (3)</td><td align="center" class="Rrule">0 (0)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Dry mouth</td><td align="center" class="Rrule">6 (3)</td><td align="center" class="Rrule">0 (0)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Epistaxis</td><td align="center" class="Rrule">6 (3)</td><td align="center" class="Rrule">1 (1)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Respiratory failure<a class="Sup" href="#footnote-15" name="footnote-reference-15">§</a></td><td align="center" class="Rrule">6 (3)</td><td align="center" class="Rrule">2 (2)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Pneumothorax<a class="Sup" href="#footnote-16" name="footnote-reference-16">¶</a></td><td align="center" class="Rrule">5 (2)</td><td align="center" class="Rrule">1 (1)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Exercise tolerance decreased</td><td align="center" class="Rrule">3 (1)</td><td align="center" class="Rrule">0 (0)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Balance disorder</td><td align="center" class="Rrule">3 (1)</td><td align="center" class="Rrule">0 (0)</td> </tr> <tr class="Botrule Last"> <td align="left" class="Lrule Rrule">Neuromuscular disorder<a class="Sup" href="#footnote-17" name="footnote-reference-17">#</a></td><td align="center" class="Rrule">2 (1)</td><td align="center" class="Rrule">0 (0)</td> </tr> </tbody> </table></div>

Refer to Table 1 and Table 2 for the incidence rate of hypersensitivity pneumonitis, bronchospasm, cough, dysphonia, exacerbation of underlying disease, hemoptysis, ototoxicity, upper airway irritation, and neuromuscular disorders [see Warnings and Precautions (5.1, 5.2, 5.3, 5.4, 5.6, 5.7)].

The following adverse reactions have been identified from postmarketing surveillance. Because these adverse reactions are reported voluntarily from a population of unknown size, precise estimates of frequency cannot be made and a causal relationship to drug exposure cannot be established.

Immune System Disorders: hypersensitivity, anaphylaxis [see Warnings and Precautions (5.5)]

Avoid concomitant use of ARIKAYCE with medications associated with neurotoxicity, nephrotoxicity, and ototoxicity.

Some diuretics can enhance aminoglycoside toxicity by altering aminoglycoside concentrations in serum and tissue. Avoid concomitant use of ARIKAYCE with ethacrynic acid, furosemide, urea, or intravenous mannitol.

Risk Summary

There are no data on ARIKAYCE use in pregnant women to evaluate for any drug-associated risk of major birth defects, miscarriage or adverse maternal or fetal outcomes. Although systemic absorption of amikacin following oral inhalation is expected to be low [see Clinical Pharmacology (12.3)], systemic exposure to aminoglycoside antibacterial drugs, including ARIKAYCE, may be associated with total, irreversible, bilateral congenital deafness when administered to pregnant women [see Warnings and Precautions (5.9)]. Advise pregnant women of the potential risk to a fetus.

Animal reproductive toxicology studies have not been conducted with inhaled amikacin. Subcutaneous administration of amikacin to pregnant rats (up to 100 mg/kg/day) and mice (up to 400 mg/kg/day) during organogenesis was not associated with fetal malformations. Ototoxicity was not adequately evaluated in offspring in animal studies.

The estimated background risk of major birth defects and miscarriage for the indicated populations 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.

Data

Animal Data

No animal reproductive toxicology studies have been conducted with ARIKAYCE or non-liposomal amikacin administered by inhalation.

Amikacin was subcutaneously administered to pregnant rats (Gestation Days 8-14) and mice (Gestation Days 7-13) at doses of 25, 100, or 400 mg/kg to assess developmental toxicity. These doses did not cause fetal visceral or skeletal malformations in mice. The high dose was excessively maternally toxic in rats (nephrotoxicity and mortality were observed), precluding the evaluation of offspring at this dose. Fetal malformations were not observed at the low or mid dose in rats. Postnatal development of the rats and mice exposed to these doses of amikacin in utero did not differ significantly from control.

Ototoxicity was not adequately evaluated in offspring in animal developmental toxicology studies.

Risk Summary

There is no information regarding the presence of ARIKAYCE in human milk, the effects on the breastfed infant, or the effects on milk production after administration of ARIKAYCE by inhalation. Although limited published data on other routes of administration of amikacin indicate that amikacin is present in human milk, systemic absorption of ARIKAYCE following inhaled administration is expected to be low [see Clinical Pharmacology (12.3)]. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for ARIKAYCE and any potential adverse effects on the breastfed child from ARIKAYCE or from the underlying maternal condition.

Safety and effectiveness of ARIKAYCE in pediatric patients below 18 years of age have not been established.

In the NTM clinical trials, of the total number of patients receiving ARIKAYCE, 208 (51.5%) were ≥ 65 years and 59 (14.6%) were ≥ 75 years. No overall differences in safety and effectiveness were observed between elderly subjects and younger subjects. Because elderly patients are more likely to have decreased renal function, it may be useful to monitor renal function [see Warnings and Precautions (5.7)].

ARIKAYCE has not been studied in patients with hepatic impairment. No dose adjustments based on hepatic impairment are required since amikacin is not hepatically metabolized [see Clinical Pharmacology (12.3)].

ARIKAYCE has not been studied in patients with renal impairment. Given the low systemic exposure to amikacin following administration of ARIKAYCE, clinically relevant accumulation of amikacin is unlikely to occur in patients with renal impairment. However, renal function should be monitored in patients with known or suspected renal impairment, including elderly patients with potential age-related decreases in renal function [see Warnings and Precautions (5.7), Use in Specific Populations (8.5)].

Adverse reactions specifically associated with overdose of ARIKAYCE have not been identified. Acute toxicity should be treated with immediate withdrawal of ARIKAYCE, and baseline tests of renal function should be undertaken.

{ "type": "p", "children": [], "text": "Adverse reactions specifically associated with overdose of ARIKAYCE have not been identified. Acute toxicity should be treated with immediate withdrawal of ARIKAYCE, and baseline tests of renal function should be undertaken. " }

Hemodialysis may be helpful in removing amikacin from the body.

{ "type": "p", "children": [], "text": "Hemodialysis may be helpful in removing amikacin from the body. " }

In all cases of suspected overdosage, physicians should contact the Regional Poison Control Center for information about effective treatment. In the case of any overdosage, the possibility of drug interactions with alterations in drug disposition should be considered.

{ "type": "p", "children": [], "text": "In all cases of suspected overdosage, physicians should contact the Regional Poison Control Center for information about effective treatment. In the case of any overdosage, the possibility of drug interactions with alterations in drug disposition should be considered." }

The active ingredient in ARIKAYCE (amikacin liposome inhalation suspension) is amikacin sulfate USP, an aminoglycoside antibacterial. Its chemical name is D-Streptamine, O-3-amino-3-deoxy-α-D-glucopyranosyl-(1→6)-O-[6-amino-6-deoxy-α-D-glucopyranosyl-(1→4)]-N1-(4-amino-2-hydroxy-1-oxobutyl)-2-deoxy-, (S)-, sulfate (1:2) salt with a chemical formula of C22H43N5O13∙2H2SO4 with a molecular weight of 781.76. Its structural formula is:

{ "type": "p", "children": [], "text": "The active ingredient in ARIKAYCE (amikacin liposome inhalation suspension) is amikacin sulfate USP, an aminoglycoside antibacterial. Its chemical name is D-Streptamine, O-3-amino-3-deoxy-α-D-glucopyranosyl-(1→6)-O-[6-amino-6-deoxy-α-D-glucopyranosyl-(1→4)]-N1-(4-amino-2-hydroxy-1-oxobutyl)-2-deoxy-, (S)-, sulfate (1:2) salt with a chemical formula of C22H43N5O13∙2H2SO4 with a molecular weight of 781.76. Its structural formula is:" }

ARIKAYCE is a white milky suspension consisting of amikacin sulfate encapsulated in liposomes and is supplied in a unit-dose 10 mL clear glass vial containing amikacin 590 mg/8.4 mL (equivalent to amikacin sulfate 788 mg/8.4 mL) as a sterile aqueous liposomal suspension for oral inhalation. ARIKAYCE consists of amikacin sulfate encapsulated in liposomes at a targeted concentration of 70 mg amikacin/mL with the pH range of 6.1 to 7.1 and lipid to amikacin weight ratio in the range of 0.60 to 0.79. The inactive ingredients are cholesterol, dipalmitoylphosphatidylcholine (DPPC), sodium chloride, sodium hydroxide (for pH adjustment), and water for injection.

{ "type": "p", "children": [], "text": "ARIKAYCE is a white milky suspension consisting of amikacin sulfate encapsulated in liposomes and is supplied in a unit-dose 10 mL clear glass vial containing amikacin 590 mg/8.4 mL (equivalent to amikacin sulfate 788 mg/8.4 mL) as a sterile aqueous liposomal suspension for oral inhalation. ARIKAYCE consists of amikacin sulfate encapsulated in liposomes at a targeted concentration of 70 mg amikacin/mL with the pH range of 6.1 to 7.1 and lipid to amikacin weight ratio in the range of 0.60 to 0.79. The inactive ingredients are cholesterol, dipalmitoylphosphatidylcholine (DPPC), sodium chloride, sodium hydroxide (for pH adjustment), and water for injection. " }

ARIKAYCE is administered only using a Lamira Nebulizer System [see Dosage and Administration (2.1)]. Like all other nebulized treatments, the amount delivered to the lungs will depend upon patient factors. Under standardized in vitro testing per USP<1601> adult breathing pattern (500 mL tidal volume, 15 breaths per minute, and inhalation: exhalation ratio of 1:1), the mean delivered dose from the mouthpiece was approximately 312 mg of amikacin sulfate (53% of label claim). The mass median aerodynamic diameter (MMAD) of the nebulized aerosol droplets is about 4.7 µm (4.1 – 5.3 µm) as determined using the Next Generation Impactor (NGI) method. A percentage of the amikacin in the liposome is released by the nebulization process, thus nebulized ARIKAYCE delivers a combination of free and liposomal amikacin.

{ "type": "p", "children": [], "text": "ARIKAYCE is administered only using a Lamira Nebulizer System [see Dosage and Administration (2.1)]. Like all other nebulized treatments, the amount delivered to the lungs will depend upon patient factors. Under standardized in vitro testing per USP<1601> adult breathing pattern (500 mL tidal volume, 15 breaths per minute, and inhalation: exhalation ratio of 1:1), the mean delivered dose from the mouthpiece was approximately 312 mg of amikacin sulfate (53% of label claim). The mass median aerodynamic diameter (MMAD) of the nebulized aerosol droplets is about 4.7 µm (4.1 – 5.3 µm) as determined using the Next Generation Impactor (NGI) method. A percentage of the amikacin in the liposome is released by the nebulization process, thus nebulized ARIKAYCE delivers a combination of free and liposomal amikacin." }

ARIKAYCE is an antibacterial drug [see Microbiology (12.4)].

ARIKAYCE exposure-response relationships and the time course of pharmacodynamic response are unknown.

Sputum Concentrations

Following once daily inhalation of 590 mg ARIKAYCE in Mycobacterium avium complex (MAC) patients, sputum concentrations at 1 to 4 hours post-inhalation were 1720, 884, and 1300 mcg/g at 1, 3, and 6 months, respectively. High variability in amikacin concentrations were observed (CV% >100%). After 48 to 72 hours post-inhalation, amikacin sputum concentrations decreased to approximately 5% of those at 1 to 4 hours post-inhalation.

Serum Concentrations

Following 3 months of once daily inhalation of 590 mg ARIKAYCE in MAC patients, the mean serum AUC0-24 was 23.5 mcg*hr/mL (range: 8.0 to 46.5 mcg*hr/mL; n=12) and the mean serum Cmax was 2.8 mcg/mL (range: 1.0 to 4.4 µg/mL; n=12). The maximum Cmax and AUC0-24 were below the mean Cmax of approximately 76 mcg/mL and AUC0-24 of 154 mcg*hr/mL observed for intravenous administration of amikacin sulfate for injection at the approved dosage of 15 mg/kg once daily in healthy adults.

Absorption

The bioavailability of ARIKAYCE is expected to vary primarily from individual differences in nebulizer efficiency and airway pathology.

Distribution

The protein binding of amikacin in serum is ≤ 10%.

Elimination

Following inhalation of ARIKAYCE in MAC patients, the apparent serum half-life of amikacin ranged from approximately 5.9 to 19.5 hrs.

Metabolism

Amikacin does not undergo appreciable metabolism.

Excretion

Systemically absorbed amikacin following ARIKAYCE administration is eliminated principally via glomerular filtration. On average, 7.42% (ranging from 0.72 to 22.60%; n=14) of the total ARIKAYCE dose was excreted in urine as unchanged drug compared to 94% following intravenous administration of amikacin sulfate for injection. Unabsorbed amikacin, following ARIKAYCE inhalation, is probably eliminated primarily by cellular turnover and expectoration.

Drug Interaction Studies

No clinical drug interaction studies have been conducted with ARIKAYCE [see Drug Interactions (7)].

Mechanism of Action

Amikacin is a polycationic, semisynthetic, bactericidal aminoglycoside. Amikacin enters the bacterial cell by binding to negatively charged components of the bacterial cell wall disrupting the overall architecture of the cell wall. The primary mechanism of action is the disruption and inhibition of protein synthesis in the target bacteria by binding to the 30S ribosomal subunit.

Resistance

The mechanism of resistance to amikacin in mycobacteria has been linked to mutations in the rrs gene of the 16S rRNA. In clinical trials, MAC isolates developing an amikacin MIC of > 64 mcg/mL after baseline were observed in a higher proportion of subjects treated with ARIKAYCE [see Clinical Studies (14)].

Interaction with Other Antimicrobials

There has been no in vitro signal for antagonism between amikacin and other antimicrobials against MAC based on fractional inhibitory concentration (FIC) and macrophage survival assays. In select instances, some degree of synergy between amikacin and other agents has been observed, as for example, synergy between aminoglycosides, including amikacin, and the beta-lactam class has been documented.

In a 2-year inhalation carcinogenicity study, rats were exposed to ARIKAYCE for 15-25, 50-70, or 155-170 minutes per day for 96-104 weeks. These provided approximate inhaled doses of 5, 15, and 45 mg/kg/day. Squamous cell carcinoma was observed in the lungs of 2 of 120 rats administered the highest dose tested. Maximum serum AUC levels of amikacin in the rats at steady state were approximately 1.3, 2.8, and 7.6 mcg∙hr/mL at the low, mid, and high doses, respectively, compared with 23.5 mcg∙hr/mL (8.0 to 46.5 mcg∙hr/mL) measured in humans. The squamous cell carcinomas may be the result of a high lung burden of particulates from ARIKAYCE in the rat lung. The relevance of the lung tumor findings with regards to humans receiving ARIKAYCE is unknown.

No evidence of mutagenicity or genotoxicity was observed in a battery of in vitro and in vivo genotoxicity studies with a liposome-encapsulated amikacin formulation similar to ARIKAYCE (in vitro microbial mutagenesis test, in vitro mouse lymphoma mutation assay, in vitro chromosomal aberration study, and an in vivo micronucleus study in rats).

No fertility studies were conducted with ARIKAYCE. Intraperitoneal administration of amikacin to male and female rats at doses up to 200 mg/kg/day prior to mating through Day 7 of gestation were not associated with impairment of fertility or adverse effects on early embryonic development.

To provide information about chronic dosing of ARIKAYCE to another animal species, a 9-month inhalation toxicology study was conducted in dogs. Foamy alveolar macrophages associated with clearance of the inhaled product were present at dose-related incidence and severity, but they were not associated with inflammation, tissue hyperplasia, or the presence of preneoplastic or neoplastic changes. Dogs were exposed to ARIKAYCE for up to 90 minutes per day, providing inhaled amikacin doses of approximately 5, 10, and 30 mg/kg/day.

Trial 1 (NCT#02344004) was an open-label, randomized (2:1), multi-center trial in patients with refractory Mycobacterium avium complex (MAC) lung disease as confirmed by at least 2 sputum culture results. Patients were considered to have refractory MAC lung disease if they did not achieve negative sputum cultures after a minimum duration of 6 consecutive months of background regimen therapy that was either ongoing or stopped no more than 12 months before the screening visit. Patients were randomized to either ARIKAYCE plus a background regimen or background regimen alone. The surrogate endpoint for assessing efficacy was based on achieving culture conversion (3 consecutive monthly negative sputum cultures) by Month 6. The date of conversion was defined as the date of the first of the 3 negative monthly cultures, which had to be achieved by Month 4 in order to meet the endpoint by Month 6. Patients who achieved culture conversion by Month 6 were continued on study drug (ARIKAYCE plus background regimen or background regimen alone based on their randomization) for a total of 12 months after the first negative sputum culture.

{ "type": "p", "children": [], "text": "Trial 1 (NCT#02344004) was an open-label, randomized (2:1), multi-center trial in patients with refractory Mycobacterium avium complex (MAC) lung disease as confirmed by at least 2 sputum culture results. Patients were considered to have refractory MAC lung disease if they did not achieve negative sputum cultures after a minimum duration of 6 consecutive months of background regimen therapy that was either ongoing or stopped no more than 12 months before the screening visit. Patients were randomized to either ARIKAYCE plus a background regimen or background regimen alone. The surrogate endpoint for assessing efficacy was based on achieving culture conversion (3 consecutive monthly negative sputum cultures) by Month 6. The date of conversion was defined as the date of the first of the 3 negative monthly cultures, which had to be achieved by Month 4 in order to meet the endpoint by Month 6. Patients who achieved culture conversion by Month 6 were continued on study drug (ARIKAYCE plus background regimen or background regimen alone based on their randomization) for a total of 12 months after the first negative sputum culture." }

A total of 336 patients were randomized (ARIKAYCE plus background regimen, n=224; background regimen alone, n=112) (ITT population), with a mean age of 64.7 years and there was a higher percentage of females (69.3%) than males (30.7%) in the study. At the time of enrollment, of the 336 subjects in the ITT population, 302 (89.9%) were either on a guideline-based regimen for MAC or off guideline-based therapy for MAC for less than 3 months while 34 (10.1%) were off treatment for 3 to 12 months prior to enrollment. At screening, patients were stratified by smoking status (current smoker or not) and by whether patients were on treatment or off treatment for at least 3 months. Most patients at screening were not current smokers (89.3%) and had underlying bronchiectasis (62.5%). At baseline, 329 patients were on a multidrug background regimen that included a macrolide (93.3%), a rifamycin (86.3%), or ethambutol (81.4%). Overall, 55.6% of subjects were receiving a triple-drug background regimen consisting of a macrolide, a rifamycin and ethambutol.

{ "type": "p", "children": [], "text": "A total of 336 patients were randomized (ARIKAYCE plus background regimen, n=224; background regimen alone, n=112) (ITT population), with a mean age of 64.7 years and there was a higher percentage of females (69.3%) than males (30.7%) in the study. At the time of enrollment, of the 336 subjects in the ITT population, 302 (89.9%) were either on a guideline-based regimen for MAC or off guideline-based therapy for MAC for less than 3 months while 34 (10.1%) were off treatment for 3 to 12 months prior to enrollment. At screening, patients were stratified by smoking status (current smoker or not) and by whether patients were on treatment or off treatment for at least 3 months. Most patients at screening were not current smokers (89.3%) and had underlying bronchiectasis (62.5%). At baseline, 329 patients were on a multidrug background regimen that included a macrolide (93.3%), a rifamycin (86.3%), or ethambutol (81.4%). Overall, 55.6% of subjects were receiving a triple-drug background regimen consisting of a macrolide, a rifamycin and ethambutol." }

The proportion of patients achieving culture conversion (3 consecutive monthly negative sputum cultures) by Month 6 was significantly (p<0.0001) greater for ARIKAYCE plus background regimen (65/224, 29.0%) compared to background regimen alone (10/112, 8.9%). Of those receiving ARIKAYCE plus background regimen, 18.3% (41/224) achieved culture conversion by Month 6 and sustained sputum culture conversion (defined as consecutive negative sputum cultures with no positive culture on solid media or no more than 2 consecutive positive cultures on liquid media following culture conversion) for up to 12 months of treatment after the first culture that defined culture conversion, compared to 2.7% (3/112) of patients receiving background regimen alone (p<0.0001). At 3 months after the completion of treatment, 16.1% (36/224) of patients who had received ARIKAYCE plus background regimen maintained durable culture conversion, compared to 0% of patients who had received background regimen alone (p<0.0001).

{ "type": "p", "children": [], "text": "The proportion of patients achieving culture conversion (3 consecutive monthly negative sputum cultures) by Month 6 was significantly (p<0.0001) greater for ARIKAYCE plus background regimen (65/224, 29.0%) compared to background regimen alone (10/112, 8.9%). Of those receiving ARIKAYCE plus background regimen, 18.3% (41/224) achieved culture conversion by Month 6 and sustained sputum culture conversion (defined as consecutive negative sputum cultures with no positive culture on solid media or no more than 2 consecutive positive cultures on liquid media following culture conversion) for up to 12 months of treatment after the first culture that defined culture conversion, compared to 2.7% (3/112) of patients receiving background regimen alone (p<0.0001). At 3 months after the completion of treatment, 16.1% (36/224) of patients who had received ARIKAYCE plus background regimen maintained durable culture conversion, compared to 0% of patients who had received background regimen alone (p<0.0001). " }

In Trial 1, 23/224 (10.3%) of patients had MAC isolates that developed MIC of > 64 mcg/mL while receiving treatment with ARIKAYCE. In the background regimen alone arm, 4/112 (3.6%) of patients had MAC isolates that developed amikacin MIC of > 64 mcg/mL.

{ "type": "p", "children": [], "text": "In Trial 1, 23/224 (10.3%) of patients had MAC isolates that developed MIC of > 64 mcg/mL while receiving treatment with ARIKAYCE. In the background regimen alone arm, 4/112 (3.6%) of patients had MAC isolates that developed amikacin MIC of > 64 mcg/mL. " }

Additional endpoints to assess the clinical benefit of ARIKAYCE, for example, change from baseline in six-minute walk test distance and the Saint George's Respiratory Questionnaire, did not demonstrate clinical benefit by Month 6.

{ "type": "p", "children": [], "text": "Additional endpoints to assess the clinical benefit of ARIKAYCE, for example, change from baseline in six-minute walk test distance and the Saint George's Respiratory Questionnaire, did not demonstrate clinical benefit by Month 6. " }

ARIKAYCE (amikacin liposome inhalation suspension), 590 mg/8.4 mL, is supplied in a sterile, unit-dose 10-mL glass vial. The product is dispensed as a 28-vial kit.

Each carton contains a 28-day supply of medication (28 vials). In addition to the ARIKAYCE vials in the carton, one Lamira Nebulizer Handset and four Lamira Aerosol Heads are provided.

NDC 71558-590-28

The Lamira Nebulizer System contains a controller, a spare Aerosol Head, a spare Handset, Power Cord and accessories.

Store ARIKAYCE vials refrigerated at 2°C to 8°C (36°F to 46°F) until expiration date on vial. Do not freeze. Once expired, discard any unused drug.

ARIKAYCE can be stored at room temperature up to 25°C (77°F) for up to 4 weeks. Once at room temperature, any unused drug must be discarded at the end of 4 weeks.

Important Instructions for Administration of ARIKAYCE

Instruct patients to read the Instructions for Use before starting ARIKAYCE. Instruct patients to only use the Lamira® Nebulizer System to administer ARIKAYCE. Advise the patient or caregiver not to use the Lamira Nebulizer System with any other medicine.

Hypersensitivity Pneumonitis and Bronchospasm (Difficulty Breathing)

Advise patients to inform their healthcare provider if they experience shortness of breath or wheezing after administration of ARIKAYCE. Advise patients with a history of reactive airway disease, asthma, or bronchospasm, to administer ARIKAYCE after using a short-acting bronchodilator [see Warnings and Precautions (5.1, 5.3)].

Hemoptysis or Cough

Advise patients to inform their healthcare provider if they cough up blood or experience episodic cough either during or after ARIKAYCE administration particularly in the first month after starting ARIKAYCE [see Warnings and Precautions (5.2) and Adverse Reactions (6.1)].

Exacerbations of Underlying Pulmonary Disease

Advise patients to inform their healthcare provider if they experience worsening of their lung disease after starting ARIKAYCE [see Warnings and Precautions (5.4)].

Dysphonia or Difficulty Speaking

Advise patients to inform their healthcare provider if they have difficulty speaking. Difficulty speaking or loss of ability to speak has been reported with ARIKAYCE [see Adverse Reactions (6.1)].

Anaphylaxis and Hypersensitivity Reactions

Advise patients and caregivers that serious and potentially life-threatening hypersensitivity reactions, that require immediate treatment could occur. Advise the patient to discontinue ARIKAYCE and seek immediate medical attention if any signs or symptoms of a hypersensitivity reaction occur [see Warnings and Precautions (5.5)].

Ototoxicity (Ringing in the Ears)

Advise patients to inform their healthcare provider if they experience ringing in the ears, dizziness, or any changes in hearing because ARIKAYCE has been associated with hearing loss [see Warnings and Precautions (5.6)].

Advise the patient not to operate heavy machinery or do dangerous activities while inhaling ARIKAYCE through the Lamira Nebulizer System because ARIKAYCE can cause symptoms such as dizziness or respiratory symptoms.

Nephrotoxicity or Kidney Damage

Advise patients to inform their health care provider if they have kidney problems because kidney damage has been reported with aminoglycosides [see Warnings and Precautions (5.7)].

Neuromuscular Blockade

Advise patients to inform their healthcare provider of known neuromuscular disease (e.g., myasthenia gravis) [see Warnings and Precautions (5.8)].

Embryo-Fetal Toxicity

Advise pregnant women that aminoglycosides, including ARIKAYCE, may cause irreversible congenital deafness when administered during pregnancy [see Warnings and Precautions (5.9) and Use in Special Populations (8.1)].

Manufactured for:

{ "type": "p", "children": [], "text": "Manufactured for:" }

Insmed Incorporated Bridgewater, NJ 08807

{ "type": "p", "children": [], "text": "Insmed Incorporated Bridgewater, NJ 08807" }

Insmed® and ARIKAYCE® are trademarks of Insmed Incorporated. Lamira® is a trademark of PARI Pharma GmbH.

{ "type": "p", "children": [], "text": "Insmed® and ARIKAYCE® are trademarks of Insmed Incorporated. Lamira® is a trademark of PARI Pharma GmbH." }

© 2018 Insmed Incorporated. All rights reserved.

{ "type": "p", "children": [], "text": "© 2018 Insmed Incorporated. All rights reserved." }

For patent information: www.insmed.com/program-patents

{ "type": "p", "children": [], "text": "For patent information: www.insmed.com/program-patents" }

<div class="scrollingtable"><table width="100%"> <col align="left" valign="top" width="2%"/> <col align="left" valign="top" width="25%"/> <col align="left" valign="top" width="25%"/> <col align="left" valign="top" width="33%"/> <col align="right" valign="top" width="15%"/> <tfoot> <tr class="First Last"> <td align="left" colspan="4">This Medication Guide has been approved by the U.S. Food and Drug Administration</td><td align="right">Issued 01/2025</td> </tr> </tfoot> <tbody class="Headless"> <tr class="Botrule First"> <td align="center" class="Lrule Rrule" colspan="5"><span class="Bold">MEDICATION GUIDE<br/>ARIKAYCE (ar' i kase) LIMITED POPULATION</span> <br/>(amikacin liposome inhalation suspension)<br/> for oral inhalation use</td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">Important: For oral inhalation only.</span></td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold"><a name="important"></a>What is the most important information I should know about ARIKAYCE?</span></td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">ARIKAYCE can cause serious side effects, including:</span> <ul class="Disc"> <li> <span class="Bold">allergic inflammation of the lungs:</span> These respiratory problems may be symptoms of allergic inflammation of the lungs and often come with:</li> </ul> </td> </tr> <tr> <td align="left" class="Lrule"></td><td align="left"> <ul class="Circle"> <li>fever</li> <li>coughing</li> <li>fast breathing </li> </ul> </td><td align="left"> <ul class="Circle"> <li>wheezing</li> <li>shortness of breath</li> </ul> </td><td align="left"></td><td align="right" class="Rrule"></td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"> <ul class="Disc"> <li> <span class="Bold">coughing up of blood (hemoptysis):</span> Coughing up blood is a serious and common side effect of ARIKAYCE.</li> <li> <span class="Bold">severe breathing problems</span>: Severe breathing problems can be symptoms of bronchospasm. Bronchospasm is a serious and common side effect of ARIKAYCE. Bronchospasm symptoms include:</li> </ul> </td> </tr> <tr> <td align="left" class="Lrule"></td><td align="left"> <ul class="Circle"> <li>shortness of breath</li> <li>wheezing</li> </ul> </td><td align="left"> <ul class="Circle"> <li>difficult or labored breathing</li> <li>coughing or chest tightness</li> </ul> </td><td align="left"></td><td align="right" class="Rrule"></td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"> <ul> <li> <span class="Bold">worsening of chronic obstructive pulmonary disease (COPD):</span> This is a serious and common side effect of ARIKAYCE.</li> </ul> </td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"> <ul class="Disc"> <li> <span class="Bold">serious allergic reactions: </span> Serious allergic reactions that may lead to death have happened to people who take ARIKAYCE. Stop taking ARIKAYCE right away and get emergency medical help if you have any of the following symptoms of a serious allergic reaction:</li> </ul> </td> </tr> <tr> <td align="left" class="Lrule"></td><td align="left"> <ul class="Circle"> <li>hives</li> <li>itching</li> <li>redness or blushing of the skin (flushing)</li> <li>swollen lips, tongue or throat</li> <li>trouble breathing or wheezing</li> <li>shortness of breath</li> </ul> </td><td align="left"> <ul class="Circle"> <li>noisy high-pitched breathing (stridor)</li> <li>cough</li> <li>nausea</li> <li>vomiting</li> <li>diarrhea</li> <li>feel cramps in your stomach area</li> </ul> </td><td align="left"> <ul class="Circle"> <li>fast heart rate</li> <li>feeling light headed</li> <li>feeling faint</li> <li>loss of control of the bowels or bladder (incontinence)</li> <li>dizziness</li> </ul> </td><td align="right" class="Rrule"></td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">While using ARIKAYCE these side effects may become serious enough that treatment in a hospital is needed. </span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">Call your healthcare provider or get medical help right away if</span> you have any of these serious side effects while taking ARIKAYCE. Your healthcare provider may ask you to stop using ARIKAYCE for a short period of time or completely stop using ARIKAYCE. </td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">What is ARIKAYCE?</span></td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5">ARIKAYCE is a prescription medicine used to treat adults with refractory (difficult to treat) <span class="Italics">Mycobacterium avium</span> complex (MAC) lung disease as part of a combination antibacterial drug treatment plan (regimen).</td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5">It is not known if ARIKAYCE is safe and effective in children younger than 18 years of age.</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="5">This product was approved by FDA using the Limited Population pathway. This means FDA has approved this drug for a limited and specific patient population, and studies on the drug may have only answered focused questions about its safety and effectiveness.</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">Do not use ARIKAYCE if you:</span> <ul class="Disc"> <li>are allergic to any aminoglycoside, or any of the ingredients in ARIKAYCE. See "<span class="Bold"><a href="#ingredients">What are the ingredients in ARIKAYCE?</a></span>" at the end of this leaflet for a complete list of ingredients in ARIKAYCE.</li> </ul> </td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">Before using ARIKAYCE, tell your healthcare provider about all of your medical conditions, including if you:</span> <ul class="Disc"> <li>have asthma, chronic obstructive pulmonary disease (COPD), shortness of breath or wheezing (bronchospasm).</li> <li>have been told you have poor lung function.</li> <li>have or have had hearing problems (including noises in your ears such as ringing or hissing), hearing loss, or your mother has had hearing problems after taking an aminoglycoside.</li> <li>have been told you have certain gene variants (a change in the gene) related to hearing abnormalities inherited from your mother.</li> <li>have dizziness or sense of the room spinning.</li> <li>have kidney problems.</li> <li>have neuromuscular disease such as myasthenia gravis.</li> <li>are pregnant or plan to become pregnant. It is not known if ARIKAYCE can harm your unborn baby. ARIKAYCE is in a class of medicines that may be connected with complete deafness in babies at birth. The deafness affects both ears and cannot be changed.</li> <li>are breastfeeding or plan to breastfeed. It is not known if the medicine in ARIKAYCE passes into your breast milk and if it can harm your baby. Talk to your healthcare provider about the best way to feed your baby during treatment with ARIKAYCE.</li> </ul> </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">Tell your healthcare provider about all the medicines you take, including</span> prescription medicines and over-the-counter medicines, vitamins, and herbal supplements. </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">How should I use ARIKAYCE?</span> <ul class="Disc"> <li> <span class="Bold">Read the step-by-step instructions for using ARIKAYCE at the end of the Medication Guide and the full Instructions for Use provided in your kit</span>. The manufacturer's Instructions for Use provides complete information about how to put together (assemble), prepare, use, clean, and disinfect your Lamira<span class="Sup">®</span> Nebulizer System.</li> <li> <span class="Bold">Do not</span> use ARIKAYCE unless you understand the directions provided. If you have questions talk to your health care provider or call Insmed inLighten™ Patient Support at 1-833-LIGHT-00 (1-833-544-4800).</li> <li>Use ARIKAYCE exactly as your healthcare provider tells you to use it. Do not use ARIKAYCE more often than prescribed for you.</li> <li>Only use ARIKAYCE with the Lamira Nebulizer System.</li> <li>Inhale each daily dose of ARIKAYCE 1 time each day through the Lamira Nebulizer Handset. <span class="Bold">Do not</span> use more than 1 vial of ARIKAYCE in a day.</li> <li>Do not use ARIKAYCE after the expiration date on the vial. If you forget to take your daily dose of ARIKAYCE, take your next dose at your usual time the next day.</li> <li> <span class="Bold">Do not</span> double the dose to make up for the missed dose.</li> <li> <span class="Bold">Do not</span> stop using ARIKAYCE or other medicines to treat your MAC lung disease unless told to do so by your healthcare provider. </li> <li>If you use too much ARIKAYCE, call your healthcare provider or go to the nearest emergency room right away.</li> </ul> </td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">What are the possible side effects of ARIKAYCE?</span></td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">ARIKAYCE may cause serious side effects, including:</span> <ul class="Disc"> <li> <span class="Bold">See "<a href="#important">What is the most important information I should know about ARIKAYCE?</a>"</span> </li> <li> <span class="Bold">hearing loss or ringing in the ears (ototoxicity).</span> Ototoxicity is a serious and common side effect of ARIKAYCE. Tell your healthcare provider right away if you have hearing loss or you hear noises in your ears such as ringing or hissing. Tell your healthcare provider if you start having problems with balance or dizziness (vertigo).</li> <li> <span class="Bold">worsening kidney problems (nephrotoxicity).</span> ARIKAYCE is in a class of medicines which may cause worsening kidney problems. Your healthcare provider may do a blood test to check how well your kidneys are working during your treatment with ARIKAYCE.</li> <li> <span class="Bold">worsening muscle weakness (neuromuscular blockade). </span>ARIKAYCE is in a class of medicines which can cause muscle weakness to get worse in people who already have problems with muscle weakness (myasthenia gravis).</li> </ul> </td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">The most common side effects of ARIKAYCE include:</span></td> </tr> <tr> <td align="left" class="Lrule" colspan="2"> <ul class="Disc"> <li>changes in your voice and hoarseness (dysphonia)</li> <li>tiredness (fatigue)</li> <li>headache</li> <li>rash</li> <li>cough during or after a dose of ARIKAYCE, especially in the first month after starting treatment.</li> </ul> </td><td align="left"> <ul class="Disc"> <li>sore throat</li> <li>diarrhea</li> <li>fever</li> <li>decreased weight</li> <li>chest discomfort</li> </ul> </td><td align="left"> <ul class="Disc"> <li>muscle pain</li> <li>nausea</li> <li>vomiting</li> <li>increased sputum</li> </ul> </td><td align="right" class="Rrule"></td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5">These are not all of the possible side effects of ARIKAYCE. </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="5">Call your doctor or pharmacist for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.</td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">How should I store ARIKAYCE?</span> <ul class="Disc"> <li>Store ARIKAYCE vials refrigerated between 36°F to 46°F (2°C to 8°C) until the expiration date on the vial. Do not freeze. </li> <li>After ARIKAYCE has been stored in the refrigerator, any unused medicine must be thrown away (disposed of) after the expiration date on the vial. </li> <li>Store ARIKAYCE vials at room temperature between 68°F to 77°F (20°C to 25°C) for up to 4 weeks.</li> <li>After ARIKAYCE has been stored at room temperature any unused medicine must be thrown away (disposed of) at the end of 4 weeks.</li> <li>Use an opened ARIKAYCE vial right away.</li> <li>Throw away the ARIKAYCE vial right away after use.</li> </ul> </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">Keep ARIKAYCE and all medicines out of the reach of children.</span></td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">General information about safe and effective use of ARIKAYCE</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="5">Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use ARIKAYCE for a condition for which it was not prescribed. Do not give ARIKAYCE 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 ARIKAYCE that is written for health professionals.</td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold"><a name="ingredients"></a>What are the ingredients in ARIKAYCE?</span></td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">Active ingredient:</span> amikacin sulfate</td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">Inactive ingredients</span>: Dipalmitoylphosphatidylcholine (DPPC), cholesterol, sodium chloride, sodium hydroxide (for pH adjustment), and water for injection</td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5">Manufactured for: Insmed Incorporated, 700 US Highway 202/206, Bridgewater, NJ 08807-1704</td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="5">© 2018 Insmed Incorporated. All rights reserved. Insmed<span class="Sup">®</span>, ARIKAYCE<span class="Sup">®</span>, and inLighten™ are trademarks of Insmed Incorporated. Lamira® is a trademark of PARI Pharma GmbH.</td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule" colspan="5">For more information, call Insmed inLighten Patient Support at: 1- 833-LIGHT-00 (1-833-544-4800)</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=\"25%\"/>\n<col align=\"left\" valign=\"top\" width=\"25%\"/>\n<col align=\"left\" valign=\"top\" width=\"33%\"/>\n<col align=\"right\" valign=\"top\" width=\"15%\"/>\n<tfoot>\n<tr class=\"First Last\">\n<td align=\"left\" colspan=\"4\">This Medication Guide has been approved by the U.S. Food and Drug Administration</td><td align=\"right\">Issued 01/2025</td>\n</tr>\n</tfoot>\n<tbody class=\"Headless\">\n<tr class=\"Botrule First\">\n<td align=\"center\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">MEDICATION GUIDE<br/>ARIKAYCE (ar' i kase) LIMITED POPULATION</span>\n<br/>(amikacin liposome inhalation suspension)<br/> for oral inhalation use</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">Important: For oral inhalation only.</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\"><a name=\"important\"></a>What is the most important information I should know about ARIKAYCE?</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">ARIKAYCE can cause serious side effects, including:</span>\n<ul class=\"Disc\">\n<li>\n<span class=\"Bold\">allergic inflammation of the lungs:</span> These respiratory problems may be symptoms of allergic inflammation of the lungs and often come with:</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>fever</li>\n<li>coughing</li>\n<li>fast breathing </li>\n</ul>\n</td><td align=\"left\">\n<ul class=\"Circle\">\n<li>wheezing</li>\n<li>shortness of breath</li>\n</ul>\n</td><td align=\"left\"></td><td align=\"right\" class=\"Rrule\"></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\">\n<ul class=\"Disc\">\n<li>\n<span class=\"Bold\">coughing up of blood (hemoptysis):</span> Coughing up blood is a serious and common side effect of ARIKAYCE.</li>\n<li>\n<span class=\"Bold\">severe breathing problems</span>: Severe breathing problems can be symptoms of bronchospasm. Bronchospasm is a serious and common side effect of ARIKAYCE. Bronchospasm symptoms include:</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>shortness of breath</li>\n<li>wheezing</li>\n</ul>\n</td><td align=\"left\">\n<ul class=\"Circle\">\n<li>difficult or labored breathing</li>\n<li>coughing or chest tightness</li>\n</ul>\n</td><td align=\"left\"></td><td align=\"right\" class=\"Rrule\"></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\">\n<ul>\n<li>\n<span class=\"Bold\">worsening of chronic obstructive pulmonary disease (COPD):</span> This is a serious and common side effect of ARIKAYCE.</li>\n</ul>\n</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\">\n<ul class=\"Disc\">\n<li>\n<span class=\"Bold\">serious allergic reactions: </span> Serious allergic reactions that may lead to death have happened to people who take ARIKAYCE. Stop taking ARIKAYCE right away and get emergency medical help if you have any of the following symptoms of a serious allergic reaction:</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>hives</li>\n<li>itching</li>\n<li>redness or blushing of the skin (flushing)</li>\n<li>swollen lips, tongue or throat</li>\n<li>trouble breathing or wheezing</li>\n<li>shortness of breath</li>\n</ul>\n</td><td align=\"left\">\n<ul class=\"Circle\">\n<li>noisy high-pitched breathing (stridor)</li>\n<li>cough</li>\n<li>nausea</li>\n<li>vomiting</li>\n<li>diarrhea</li>\n<li>feel cramps in your stomach area</li>\n</ul>\n</td><td align=\"left\">\n<ul class=\"Circle\">\n<li>fast heart rate</li>\n<li>feeling light headed</li>\n<li>feeling faint</li>\n<li>loss of control of the bowels or bladder (incontinence)</li>\n<li>dizziness</li>\n</ul>\n</td><td align=\"right\" class=\"Rrule\"></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">While using ARIKAYCE these side effects may become serious enough that treatment in a hospital is needed. </span></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">Call your healthcare provider or get medical help right away if</span> you have any of these serious side effects while taking ARIKAYCE. Your healthcare provider may ask you to stop using ARIKAYCE for a short period of time or completely stop using ARIKAYCE. \t\t\t\t\t\t\t\t \t\t\t\t\t\t\t\t\t</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">What is ARIKAYCE?</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\">ARIKAYCE is a prescription medicine used to treat adults with refractory (difficult to treat) <span class=\"Italics\">Mycobacterium avium</span> complex (MAC) lung disease as part of a combination antibacterial drug treatment plan (regimen).</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\">It is not known if ARIKAYCE is safe and effective in children younger than 18 years of age.</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\">This product was approved by FDA using the Limited Population pathway. This means FDA has approved this drug for a limited and specific patient population, and studies on the drug may have only answered focused questions about its safety and effectiveness.</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">Do not use ARIKAYCE if you:</span>\n<ul class=\"Disc\">\n<li>are allergic to any aminoglycoside, or any of the ingredients in ARIKAYCE. See \"<span class=\"Bold\"><a href=\"#ingredients\">What are the ingredients in ARIKAYCE?</a></span>\" at the end of this leaflet for a complete list of ingredients in ARIKAYCE.</li>\n</ul>\n</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">Before using ARIKAYCE, tell your healthcare provider about all of your medical conditions, including if you:</span>\n<ul class=\"Disc\">\n<li>have asthma, chronic obstructive pulmonary disease (COPD), shortness of breath or wheezing (bronchospasm).</li>\n<li>have been told you have poor lung function.</li>\n<li>have or have had hearing problems (including noises in your ears such as ringing or hissing), hearing loss, or your mother has had hearing problems after taking an aminoglycoside.</li>\n<li>have been told you have certain gene variants (a change in the gene) related to hearing abnormalities inherited from your mother.</li>\n<li>have dizziness or sense of the room spinning.</li>\n<li>have kidney problems.</li>\n<li>have neuromuscular disease such as myasthenia gravis.</li>\n<li>are pregnant or plan to become pregnant. It is not known if ARIKAYCE can harm your unborn baby. ARIKAYCE is in a class of medicines that may be connected with complete deafness in babies at birth. The deafness affects both ears and cannot be changed.</li>\n<li>are breastfeeding or plan to breastfeed. It is not known if the medicine in ARIKAYCE passes into your breast milk and if it can harm your baby. Talk to your healthcare provider about the best way to feed your baby during treatment with ARIKAYCE.</li>\n</ul>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">Tell your healthcare provider about all the medicines you take, including</span> prescription medicines and over-the-counter medicines, vitamins, and herbal supplements. </td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">How should I use ARIKAYCE?</span>\n<ul class=\"Disc\">\n<li>\n<span class=\"Bold\">Read the step-by-step instructions for using ARIKAYCE at the end of the Medication Guide and the full Instructions for Use provided in your kit</span>. The manufacturer's Instructions for Use provides complete information about how to put together (assemble), prepare, use, clean, and disinfect your Lamira<span class=\"Sup\">®</span> Nebulizer System.</li>\n<li>\n<span class=\"Bold\">Do not</span> use ARIKAYCE unless you understand the directions provided. If you have questions talk to your health care provider or call Insmed inLighten™ Patient Support at 1-833-LIGHT-00 (1-833-544-4800).</li>\n<li>Use ARIKAYCE exactly as your healthcare provider tells you to use it. Do not use ARIKAYCE more often than prescribed for you.</li>\n<li>Only use ARIKAYCE with the Lamira Nebulizer System.</li>\n<li>Inhale each daily dose of ARIKAYCE 1 time each day through the Lamira Nebulizer Handset. <span class=\"Bold\">Do not</span> use more than 1 vial of ARIKAYCE in a day.</li>\n<li>Do not use ARIKAYCE after the expiration date on the vial. If you forget to take your daily dose of ARIKAYCE, take your next dose at your usual time the next day.</li>\n<li>\n<span class=\"Bold\">Do not</span> double the dose to make up for the missed dose.</li>\n<li>\n<span class=\"Bold\">Do not</span> stop using ARIKAYCE or other medicines to treat your MAC lung disease unless told to do so by your healthcare provider. </li>\n<li>If you use too much ARIKAYCE, call your healthcare provider or go to the nearest emergency room right away.</li>\n</ul>\n</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">What are the possible side effects of ARIKAYCE?</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">ARIKAYCE may cause serious side effects, including:</span>\n<ul class=\"Disc\">\n<li>\n<span class=\"Bold\">See \"<a href=\"#important\">What is the most important information I should know about ARIKAYCE?</a>\"</span>\n</li>\n<li>\n<span class=\"Bold\">hearing loss or ringing in the ears (ototoxicity).</span> Ototoxicity is a serious and common side effect of ARIKAYCE. Tell your healthcare provider right away if you have hearing loss or you hear noises in your ears such as ringing or hissing. Tell your healthcare provider if you start having problems with balance or dizziness (vertigo).</li>\n<li>\n<span class=\"Bold\">worsening kidney problems (nephrotoxicity).</span> ARIKAYCE is in a class of medicines which may cause worsening kidney problems. Your healthcare provider may do a blood test to check how well your kidneys are working during your treatment with ARIKAYCE.</li>\n<li>\n<span class=\"Bold\">worsening muscle weakness (neuromuscular blockade). </span>ARIKAYCE is in a class of medicines which can cause muscle weakness to get worse in people who already have problems with muscle weakness (myasthenia gravis).</li>\n</ul>\n</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">The most common side effects of ARIKAYCE include:</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule\" colspan=\"2\">\n<ul class=\"Disc\">\n<li>changes in your voice and hoarseness (dysphonia)</li>\n<li>tiredness (fatigue)</li>\n<li>headache</li>\n<li>rash</li>\n<li>cough during or after a dose of ARIKAYCE, especially in the first month after starting treatment.</li>\n</ul>\n</td><td align=\"left\">\n<ul class=\"Disc\">\n<li>sore throat</li>\n<li>diarrhea</li>\n<li>fever</li>\n<li>decreased weight</li>\n<li>chest discomfort</li>\n</ul>\n</td><td align=\"left\">\n<ul class=\"Disc\">\n<li>muscle pain</li>\n<li>nausea</li>\n<li>vomiting</li>\n<li>increased sputum</li>\n</ul>\n</td><td align=\"right\" class=\"Rrule\"></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\">These are not all of the possible side effects of ARIKAYCE. </td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\">Call your doctor or pharmacist 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 align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">How should I store ARIKAYCE?</span>\n<ul class=\"Disc\">\n<li>Store ARIKAYCE vials refrigerated between 36°F to 46°F (2°C to 8°C) until the expiration date on the vial. Do not freeze. </li>\n<li>After ARIKAYCE has been stored in the refrigerator, any unused medicine must be thrown away (disposed of) after the expiration date on the vial. </li>\n<li>Store ARIKAYCE vials at room temperature between 68°F to 77°F (20°C to 25°C) for up to 4 weeks.</li>\n<li>After ARIKAYCE has been stored at room temperature any unused medicine must be thrown away (disposed of) at the end of 4 weeks.</li>\n<li>Use an opened ARIKAYCE vial right away.</li>\n<li>Throw away the ARIKAYCE vial right away after use.</li>\n</ul>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">Keep ARIKAYCE and all medicines out of the reach of children.</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">General information about safe and effective use of ARIKAYCE</span></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\">Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use ARIKAYCE for a condition for which it was not prescribed. Do not give ARIKAYCE 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 ARIKAYCE that is written for health professionals.</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\"><a name=\"ingredients\"></a>What are the ingredients in ARIKAYCE?</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">Active ingredient:</span> amikacin sulfate</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\"><span class=\"Bold\">Inactive ingredients</span>: Dipalmitoylphosphatidylcholine (DPPC), cholesterol, sodium chloride, sodium hydroxide (for pH adjustment), and water for injection</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\">Manufactured for: Insmed Incorporated, 700 US Highway 202/206, Bridgewater, NJ 08807-1704</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\">© 2018 Insmed Incorporated. All rights reserved. Insmed<span class=\"Sup\">®</span>, ARIKAYCE<span class=\"Sup\">®</span>, and inLighten™ are trademarks of Insmed Incorporated. Lamira® is a trademark of PARI Pharma GmbH.</td>\n</tr>\n<tr class=\"Last\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"5\">For more information, call Insmed inLighten Patient Support at: 1- 833-LIGHT-00 (1-833-544-4800)</td>\n</tr>\n</tbody>\n</table></div>" }

ARIKAYCE® LIMITED POPULATION(amikacin liposome inhalation suspension)

{ "type": "p", "children": [], "text": "\nARIKAYCE® LIMITED POPULATION(amikacin liposome inhalation suspension)\n" }

For oral inhalation useLamira® Nebulizer System

{ "type": "p", "children": [], "text": "\nFor oral inhalation useLamira® Nebulizer System\n" }

Before using your Lamira Nebulizer System, be sure you read and understand the detailed information in the full Instructions for Use that comes with the Lamira Nebulizer System. This will provide more complete information about how to put together (assemble), prepare, use, clean, and disinfect your Lamira Nebulizer System. If you do not understand any part of the instructions, contact Insmed inLighten™ Patient Support at 1-833-LIGHT-00 (1-833-544-4800) before using the Lamira Nebulizer System.

{ "type": "p", "children": [], "text": "Before using your Lamira Nebulizer System, be sure you read and understand the detailed information in the full Instructions for Use that comes with the Lamira Nebulizer System. This will provide more complete information about how to put together (assemble), prepare, use, clean, and disinfect your Lamira Nebulizer System. If you do not understand any part of the instructions, contact Insmed inLighten™ Patient Support at 1-833-LIGHT-00 (1-833-544-4800) before using the Lamira Nebulizer System." }

<div class="scrollingtable"><table width="100%"> <col align="left" valign="top" width="45%"/> <col align="left" valign="top" width="55%"/> <tbody class="Headless"> <tr class="Botrule First"> <td align="left" class="Lrule Rrule" colspan="2"><span class="Bold">Gather your ARIKAYCE medicine. The ARIKAYCE 28-day kit contains:</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="2"> <ul class="Disc"> <li>1 ARIKAYCE Quick Start Guide</li> <li>1 Instructions for Use insert</li> <li>1 Full Prescribing Information insert</li> <li>1 Lamira Nebulizer Handset </li> <li>4 Lamira Aerosol Heads (1 in each weekly box)</li> <li>28 vials (1 vial each day) of ARIKAYCE (7 in each weekly box)</li> </ul> </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="2"><span class="Bold">Check to make sure you have all the necessary parts for your Lamira Nebulizer System:</span></td> </tr> <tr> <td align="left" class="Lrule"> <dl> <dt>a.</dt> <dd>Carrying Case</dd> <dt>b.</dt> <dd>Connection Cord</dd> <dt>c.</dt> <dd>Controller</dd> <dt>d.</dt> <dd>A/C Power Supply</dd> <dt>e.</dt> <dd>"AA" Batteries</dd> </dl> </td><td align="left" class="Rrule"> <p class="First"> <img alt="Figure" src="/dailymed/image.cfm?name=arikayce-03.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></p> </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule">Spare Lamira Nebulizer Handset:<dl> <dt>f.</dt> <dd>Medication Cap and Seal </dd> <dt>g.</dt> <dd>Medication Reservoir </dd> <dt>h.</dt> <dd>Blue Valve</dd> <dt>i.</dt> <dd>Aerosol Chamber</dd> <dt>j.</dt> <dd> Mouthpiece</dd> <dt>k.</dt> <dd>Spare Aerosol Head</dd> </dl> </td><td align="center" class="Rrule"><img alt="Figure" src="/dailymed/image.cfm?name=arikayce-04.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="2"><span class="Bold">You will also need the following supplies that do not come in your ARIKAYCE 28-day kit that will help you care for your Lamira Nebulizer System: </span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="2"> <ul class="Disc"> <li>Clear liquid soap for cleaning the Handset and Aerosol Head</li> <li>Distilled water for disinfecting the Handset and Aerosol Head</li> </ul> </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="2"><span class="Bold">Choose your power supply and get it ready. </span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"> <dl> <dt class="Bold">a.</dt> <dd> <span class="Bold">4 "AA" batteries</span> </dd> </dl> </td><td align="center" class="Rrule"><img alt="Figure" src="/dailymed/image.cfm?name=arikayce-05.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></td> </tr> <tr class="Botrule"> <td align="center" class="Lrule Rrule" colspan="2"><span class="Bold">or</span></td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule"> <dl> <dt class="Bold">b.</dt> <dd> <span class="Bold">A/C Power Supply</span> <ul class="Disc"> <li>Plug the A/C Power Supply into the Controller.</li> <li>Plug the A/C Power Supply into the wall outlet.</li> </ul> </dd> </dl> <br/> <span class="Bold">Do not insert the A/C Power into the front of the Controller. </span></td><td align="center" class="Rrule"><img alt="Figure" src="/dailymed/image.cfm?name=arikayce-06.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></td> </tr> </tbody> </table></div>

{ "type": "table", "children": [], "text": "<div class=\"scrollingtable\"><table width=\"100%\">\n<col align=\"left\" valign=\"top\" width=\"45%\"/>\n<col align=\"left\" valign=\"top\" width=\"55%\"/>\n<tbody class=\"Headless\">\n<tr class=\"Botrule First\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"2\"><span class=\"Bold\">Gather your ARIKAYCE medicine. The ARIKAYCE 28-day kit contains:</span></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"2\">\n<ul class=\"Disc\">\n<li>1 ARIKAYCE Quick Start Guide</li>\n<li>1 Instructions for Use insert</li>\n<li>1 Full Prescribing Information insert</li>\n<li>1 Lamira Nebulizer Handset </li>\n<li>4 Lamira Aerosol Heads (1 in each weekly box)</li>\n<li>28 vials (1 vial each day) of ARIKAYCE (7 in each weekly box)</li>\n</ul>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"2\"><span class=\"Bold\">Check to make sure you have all the necessary parts for your Lamira Nebulizer System:</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule\">\n<dl>\n<dt>a.</dt>\n<dd>Carrying Case</dd>\n<dt>b.</dt>\n<dd>Connection Cord</dd>\n<dt>c.</dt>\n<dd>Controller</dd>\n<dt>d.</dt>\n<dd>A/C Power Supply</dd>\n<dt>e.</dt>\n<dd>\"AA\" Batteries</dd>\n</dl>\n</td><td align=\"left\" class=\"Rrule\">\n<p class=\"First\">\n<img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-03.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></p>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule\">Spare Lamira Nebulizer Handset:<dl>\n<dt>f.</dt>\n<dd>Medication Cap and Seal </dd>\n<dt>g.</dt>\n<dd>Medication Reservoir </dd>\n<dt>h.</dt>\n<dd>Blue Valve</dd>\n<dt>i.</dt>\n<dd>Aerosol Chamber</dd>\n<dt>j.</dt>\n<dd>\tMouthpiece</dd>\n<dt>k.</dt>\n<dd>Spare Aerosol Head</dd>\n</dl>\n</td><td align=\"center\" class=\"Rrule\"><img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-04.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"2\"><span class=\"Bold\">You will also need the following supplies that do not come in your ARIKAYCE 28-day kit that will help you care for your Lamira Nebulizer System: </span></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"2\">\n<ul class=\"Disc\">\n<li>Clear liquid soap for cleaning the Handset and Aerosol Head</li>\n<li>Distilled water for disinfecting the Handset and Aerosol Head</li>\n</ul>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"2\"><span class=\"Bold\">Choose your power supply and get it ready. </span></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\">\n<dl>\n<dt class=\"Bold\">a.</dt>\n<dd>\n<span class=\"Bold\">4 \"AA\" batteries</span>\n</dd>\n</dl>\n</td><td align=\"center\" class=\"Rrule\"><img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-05.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"center\" class=\"Lrule Rrule\" colspan=\"2\"><span class=\"Bold\">or</span></td>\n</tr>\n<tr class=\"Last\">\n<td align=\"left\" class=\"Lrule Rrule\">\n<dl>\n<dt class=\"Bold\">b.</dt>\n<dd>\n<span class=\"Bold\">A/C Power Supply</span>\n<ul class=\"Disc\">\n<li>Plug the A/C Power Supply into the Controller.</li>\n<li>Plug the A/C Power Supply into the wall outlet.</li>\n</ul>\n</dd>\n</dl>\n<br/>\n<span class=\"Bold\">Do not insert the A/C Power into the front of the Controller. </span></td><td align=\"center\" class=\"Rrule\"><img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-06.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></td>\n</tr>\n</tbody>\n</table></div>" }

Cleaning and Disinfecting

{ "type": "p", "children": [], "text": "\nCleaning and Disinfecting \n" }

Before first use, rinse, clean, and disinfect your Handset and Aerosol Head. Moving forward, rinse, clean, and disinfect the Handset including the Aerosol Head after every use.

{ "type": "p", "children": [], "text": "\nBefore first use, rinse, clean, and disinfect your Handset and Aerosol Head. Moving forward, rinse, clean, and disinfect the Handset including the Aerosol Head after every use.\n" }

When you receive your Handset and Aerosol Head, they will not be sterile. Cleaning and disinfecting your Handset and Aerosol Head is important to reduce the risk of infection, illness, and contamination.

{ "type": "p", "children": [], "text": "When you receive your Handset and Aerosol Head, they will not be sterile. Cleaning and disinfecting your Handset and Aerosol Head is important to reduce the risk of infection, illness, and contamination." }

<div class="scrollingtable"><table width="100%"> <col align="left" valign="top" width="45%"/> <col align="left" valign="top" width="55%"/> <tbody class="Headless"> <tr class="Botrule First"> <td align="left" class="Lrule Rrule" colspan="2"> <dl> <dt class="Bold">1.</dt> <dd> <span class="Bold">Cleaning the Handset and Aerosol Head Reminder:</span> Before first use, rinse and clean the Handset and Aerosol Head. Moving forward, rinse and clean the Handset including the Aerosol Head right after each use.</dd> </dl> </td> </tr> <tr> <td align="left" class="Lrule Rrule"> <dl> <dt class="Bold">•</dt> <dd>Take apart (disassemble) the Handset for cleaning </dd> <dt class="Bold">•</dt> <dd> <span class="Bold">Gently wipe away any drops of medicine</span> from the Medication Reservoir (a), Aerosol Chamber (b), and Mouthpiece (c) before rinsing, to reduce antibiotics added to water systems.<br/> <span class="Bold">Use only plain, dry paper towels or wipes.</span> Do not use towels or wipes that have any chemicals added to them such as alcohol, lotion, or baby wipes.</dd> </dl> </td><td align="left" class="Rrule"> <p class="First"> <img alt="Figure" src="/dailymed/image.cfm?name=arikayce-07.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></p> </td> </tr> <tr> <td align="left" class="Lrule Rrule"> <dl> <dt> </dt> <dd> <span class="Bold">Be careful not to harm the parts. Do not wipe Aerosol Head. </span> </dd> <dt> </dt> <dd> <span class="Bold">Throw away paper towels by disposing in trash with solid waste.</span> </dd> </dl> </td><td align="right" class="Rrule"> <p class="First"> <img alt="Figure" src="/dailymed/image.cfm?name=arikayce-08.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></p> </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"> <dl> <dt class="Bold">•</dt> <dd>Rinse each of the parts under warm running tap water for <span class="Bold">10 seconds</span>. Rinse the Aerosol Head for <span class="Bold">10 seconds on each side.</span> </dd> </dl> </td><td align="left" class="Rrule"><img alt="Figure" src="/dailymed/image.cfm?name=arikayce-09.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"> <ul class="Disc"> <li>Clean all Handset parts by adding a few drops of clear liquid dish soap and warm tap water to a clean tub or bowl. Cover the Handset parts in the warm soapy water and soak for <span class="Bold">5 minutes</span>, shaking them periodically. Then rinse them thoroughly under warm running tap water. </li> </ul> </td><td align="left" class="Rrule"><img alt="Figure" src="/dailymed/image.cfm?name=arikayce-10.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="2"> <dl> <dt class="Bold">2.</dt> <dd> <span class="Bold">Disinfecting the Handset and Aerosol Head Before First Use Reminder: </span>Disinfect the Handset and Aerosol Head before first use.</dd> </dl> </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"> <ul class="Disc"> <li>Be sure your Handset and Aerosol Head are clean before you disinfect.</li> <li>Make sure the pot has enough distilled water to completely cover all the Handset parts, including the Aerosol Head. </li> <li>Heat the water to a boil in a clean pot.</li> <li>Place the Handset parts, including the Aerosol Head, into the boiling water.</li> <li>Boil for a full <span class="Bold">5 minutes</span>. Note: It may be helpful to use a timer.</li> </ul> </td><td align="left" class="Rrule"><img alt="Figure" src="/dailymed/image.cfm?name=arikayce-11.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></td> </tr> <tr class="Botrule Last"> <td align="left" class="Lrule Rrule"> <ul class="Disc"> <li>Air dry on a <span class="Bold">lint-free</span> towel. When fully dry, wrap up the parts in a lint-free towel for storage. You can put them together again just before taking your next treatment.</li> </ul> </td><td align="center" class="Rrule"> <p class="First"> <img alt="Figure" src="/dailymed/image.cfm?name=arikayce-12.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></p> </td> </tr> </tbody> </table></div>

{ "type": "table", "children": [], "text": "<div class=\"scrollingtable\"><table width=\"100%\">\n<col align=\"left\" valign=\"top\" width=\"45%\"/>\n<col align=\"left\" valign=\"top\" width=\"55%\"/>\n<tbody class=\"Headless\">\n<tr class=\"Botrule First\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"2\">\n<dl>\n<dt class=\"Bold\">1.</dt>\n<dd>\n<span class=\"Bold\">Cleaning the Handset and Aerosol Head Reminder:</span> Before first use, rinse and clean the Handset and Aerosol Head. Moving forward, rinse and clean the Handset including the Aerosol Head right after each use.</dd>\n</dl>\n</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\">\n<dl>\n<dt class=\"Bold\">•</dt>\n<dd>Take apart (disassemble) the Handset for cleaning </dd>\n<dt class=\"Bold\">•</dt>\n<dd>\n<span class=\"Bold\">Gently wipe away any drops of medicine</span> from the Medication Reservoir (a), Aerosol Chamber (b), and Mouthpiece (c) before rinsing, to reduce antibiotics added to water systems.<br/>\n<span class=\"Bold\">Use only plain, dry paper towels or wipes.</span> Do not use towels or wipes that have any chemicals added to them such as alcohol, lotion, or baby wipes.</dd>\n</dl>\n</td><td align=\"left\" class=\"Rrule\">\n<p class=\"First\">\n<img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-07.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></p>\n</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\">\n<dl>\n<dt> </dt>\n<dd>\n<span class=\"Bold\">Be careful not to harm the parts. Do not wipe Aerosol Head. </span>\n</dd>\n<dt> </dt>\n<dd>\n<span class=\"Bold\">Throw away paper towels by disposing in trash with solid waste.</span>\n</dd>\n</dl>\n</td><td align=\"right\" class=\"Rrule\">\n<p class=\"First\">\n<img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-08.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></p>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\">\n<dl>\n<dt class=\"Bold\">•</dt>\n<dd>Rinse each of the parts under warm running tap water for <span class=\"Bold\">10 seconds</span>. Rinse the Aerosol Head for <span class=\"Bold\">10 seconds on each side.</span>\n</dd>\n</dl>\n</td><td align=\"left\" class=\"Rrule\"><img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-09.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\">\n<ul class=\"Disc\">\n<li>Clean all Handset parts by adding a few drops of clear liquid dish soap and warm tap water to a clean tub or bowl. Cover the Handset parts in the warm soapy water and soak for <span class=\"Bold\">5 minutes</span>, shaking them periodically. Then rinse them thoroughly under warm running tap water. </li>\n</ul>\n</td><td align=\"left\" class=\"Rrule\"><img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-10.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"2\">\n<dl>\n<dt class=\"Bold\">2.</dt>\n<dd>\n<span class=\"Bold\">Disinfecting the Handset and Aerosol Head Before First Use Reminder: </span>Disinfect the Handset and Aerosol Head before first use.</dd>\n</dl>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\">\n<ul class=\"Disc\">\n<li>Be sure your Handset and Aerosol Head are clean before you disinfect.</li>\n<li>Make sure the pot has enough distilled water to completely cover all the Handset parts, including the Aerosol Head. </li>\n<li>Heat the water to a boil in a clean pot.</li>\n<li>Place the Handset parts, including the Aerosol Head, into the boiling water.</li>\n<li>Boil for a full <span class=\"Bold\">5 minutes</span>. Note: It may be helpful to use a timer.</li>\n</ul>\n</td><td align=\"left\" class=\"Rrule\"><img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-11.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></td>\n</tr>\n<tr class=\"Botrule Last\">\n<td align=\"left\" class=\"Lrule Rrule\">\n<ul class=\"Disc\">\n<li>Air dry on a <span class=\"Bold\">lint-free</span> towel. When fully dry, wrap up the parts in a lint-free towel for storage. You can put them together again just before taking your next treatment.</li>\n</ul>\n</td><td align=\"center\" class=\"Rrule\">\n<p class=\"First\">\n<img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-12.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></p>\n</td>\n</tr>\n</tbody>\n</table></div>" }

Assembling Your Handset

{ "type": "p", "children": [], "text": "\nAssembling Your Handset\n" }

<div class="scrollingtable"><table width="100%"> <col align="left" valign="top" width="45%"/> <col align="left" valign="top" width="55%"/> <tbody class="Headless"> <tr class="Botrule First"> <td align="left" class="Lrule Rrule"> <p class="First"> <span class="Bold">Step 1: Wash your hands with </span><span class="Bold Underline">soap and water</span><span class="Bold">, and dry them well.</span> </p> </td><td align="center" class="Rrule"><img alt="Figure" src="/dailymed/image.cfm?name=arikayce-13.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"><span class="Bold">Step 2: Insert the Blue Valve.</span> <br/>Open the Handset by gently pulling up on the tab of the Medication Reservoir.<br/>Insert the Blue Valve so that it rests on top of the Aerosol Chamber with the 2 valve flaps facing down (valve flaps not bent).</td><td align="center" class="Rrule"><img alt="Figure" src="/dailymed/image.cfm?name=arikayce-14.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></td> </tr> <tr> <td align="left" class="Lrule Rrule"><span class="Bold">Step 3: Insert the Aerosol Head.</span></td><td align="left" class="Rrule"></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Grasp the Aerosol Head by the 2 flexible plastic tabs on each side. Be sure the text "Lamira<span class="Sup">®</span>" is facing toward you and is at the top of the Aerosol Head.<br/>Squeeze the 2 flexible plastic tabs together while inserting the Aerosol Head into the Medication Reservoir.<br/>Close the Handset when you are done (no gaps along blue valve edge).<br/> <span class="Bold">Do not touch the silver part of the Aerosol Head at any time.</span> <br/> <span class="Bold">After the Aerosol Head has been used 7 times, throw away (dispose of) and replace with a new one during the cleaning process. Lamira Handset is to be used for 28 days.</span></td><td align="center" class="Rrule"><img alt="Figure" src="/dailymed/image.cfm?name=arikayce-15.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/><br/> <img alt="Figure" src="/dailymed/image.cfm?name=arikayce-15a.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"><span class="Bold">Step 4: Attach the Mouthpiece to your Handset with the Blue Flap facing up</span>.</td><td align="center" class="Rrule"><img alt="Figure" src="/dailymed/image.cfm?name=arikayce-16.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></td> </tr> <tr> <td align="left" class="Lrule Rrule"><span class="Bold">Step 5: Finally, attach the Handset to the Controller. </span></td><td align="left" class="Rrule"></td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule"> <dl> <dt class="Bold">a.</dt> <dd> <span class="Bold">Attach the Connection Cord to the Handset</span>. <dl> <dt>a1.</dt> <dd>Line up the bottom of the Connector with the bottom of the Handset.</dd> <dt>a2.</dt> <dd>Push upward against the Handset until you hear the pieces snap together.</dd> </dl> </dd> </dl> <dl> <dt class="Bold">b.</dt> <dd> <span class="Bold">Connect the Connection Cord to the Controller.</span> </dd> </dl> </td><td align="center" class="Rrule"><img alt="Figure" src="/dailymed/image.cfm?name=arikayce-17.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></td> </tr> </tbody> </table></div>

{ "type": "table", "children": [], "text": "<div class=\"scrollingtable\"><table width=\"100%\">\n<col align=\"left\" valign=\"top\" width=\"45%\"/>\n<col align=\"left\" valign=\"top\" width=\"55%\"/>\n<tbody class=\"Headless\">\n<tr class=\"Botrule First\">\n<td align=\"left\" class=\"Lrule Rrule\">\n<p class=\"First\">\n<span class=\"Bold\">Step 1: Wash your hands with </span><span class=\"Bold Underline\">soap and water</span><span class=\"Bold\">, and dry them well.</span>\n</p>\n</td><td align=\"center\" class=\"Rrule\"><img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-13.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\"><span class=\"Bold\">Step 2: Insert the Blue Valve.</span>\n<br/>Open the Handset by gently pulling up on the tab of the Medication Reservoir.<br/>Insert the Blue Valve so that it rests on top of the Aerosol Chamber with the 2 valve flaps facing down (valve flaps not bent).</td><td align=\"center\" class=\"Rrule\"><img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-14.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\"><span class=\"Bold\">Step 3: Insert the Aerosol Head.</span></td><td align=\"left\" class=\"Rrule\"></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\">Grasp the Aerosol Head by the 2 flexible plastic tabs on each side. Be sure the text \"Lamira<span class=\"Sup\">®</span>\" is facing toward you and is at the top of the Aerosol Head.<br/>Squeeze the 2 flexible plastic tabs together while inserting the Aerosol Head into the Medication Reservoir.<br/>Close the Handset when you are done (no gaps along blue valve edge).<br/>\n<span class=\"Bold\">Do not touch the silver part of the Aerosol Head at any time.</span>\n<br/>\n<span class=\"Bold\">After the Aerosol Head has been used 7 times, throw away (dispose of) and replace with a new one during the cleaning process. Lamira Handset is to be used for 28 days.</span></td><td align=\"center\" class=\"Rrule\"><img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-15.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/><br/>\n<img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-15a.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\"><span class=\"Bold\">Step 4: Attach the Mouthpiece to your Handset with the Blue Flap facing up</span>.</td><td align=\"center\" class=\"Rrule\"><img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-16.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\"><span class=\"Bold\">Step 5: Finally, attach the Handset to the Controller. </span></td><td align=\"left\" class=\"Rrule\"></td>\n</tr>\n<tr class=\"Last\">\n<td align=\"left\" class=\"Lrule Rrule\">\n<dl>\n<dt class=\"Bold\">a.</dt>\n<dd>\n<span class=\"Bold\">Attach the Connection Cord to the Handset</span>. \t\t\t\t\t\t\t\t\t\t\t\t<dl>\n<dt>a1.</dt>\n<dd>Line up the bottom of the Connector with the bottom of the Handset.</dd>\n<dt>a2.</dt>\n<dd>Push upward against the Handset until you hear the pieces snap together.</dd>\n</dl>\n</dd>\n</dl>\n<dl>\n<dt class=\"Bold\">b.</dt>\n<dd>\n<span class=\"Bold\">Connect the Connection Cord to the Controller.</span>\n</dd>\n</dl>\n</td><td align=\"center\" class=\"Rrule\"><img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-17.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></td>\n</tr>\n</tbody>\n</table></div>" }

Taking ARIKAYCE

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

Your ARIKAYCE should be at room temperature before use to make sure that your Lamira Nebulizer System operates properly. Do not use other medicines in your Handset.

{ "type": "p", "children": [], "text": "Your ARIKAYCE should be at room temperature before use to make sure that your Lamira Nebulizer System operates properly. Do not use other medicines in your Handset.\n" }

Bring ARIKAYCE to room temperature by removing it from the refrigerator at least 45 minutes before use. Do not use if your ARIKAYCE has been frozen.

{ "type": "p", "children": [], "text": "Bring ARIKAYCE to room temperature by removing it from the refrigerator at least 45 minutes before use. Do not use if your ARIKAYCE has been frozen.\n" }

<div class="scrollingtable"><table width="100%"> <col align="left" valign="top" width="45%"/> <col align="left" valign="top" width="55%"/> <tbody class="Headless"> <tr class="Botrule First"> <td align="left" class="Lrule Rrule"><span class="Bold">Step 1: Get your ARIKAYCE ready.</span> <ul class="Disc"> <li>Place the Handset on a clean, flat, stable surface.</li> <li>Shake the ARIKAYCE vial for a <span class="Bold">minimum of</span> 10 to 15 seconds, <span class="Bold">AND UNTIL THE MEDICINE LOOKS THE SAME THROUGHOUT AND WELL MIXED.</span> </li> </ul> </td><td align="center" class="Rrule"><img alt="Figure" src="/dailymed/image.cfm?name=arikayce-18.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="2"><span class="Bold">How to open the ARIKAYCE vial</span></td> </tr> <tr> <td align="left" class="Lrule Rrule"> <ul class="Disc"> <li> <span class="Bold">Lift the orange cap</span> from the vial.</li> </ul> </td><td align="left" class="Rrule"> <p class="First"> <img alt="Figure" src="/dailymed/image.cfm?name=arikayce-19.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></p> </td> </tr> <tr> <td align="left" class="Lrule Rrule"> <ul class="Disc"> <li> <span class="Bold">Grip the metal ring</span> on top of the vial and pull it down gently until 1 side breaks away from the vial but do not pull the tab completely off.</li> </ul> </td><td align="left" class="Rrule"> <p class="First"> <img alt="Figure" src="/dailymed/image.cfm?name=arikayce-20.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></p> </td> </tr> <tr> <td align="left" class="Lrule Rrule"> <ul class="Disc"> <li> <span class="Bold">Pull the metal band</span> from around the vial top in a circular motion until it comes off completely.</li> </ul> </td><td align="left" class="Rrule"> <p class="First"> <img alt="Figure" src="/dailymed/image.cfm?name=arikayce-21.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></p> </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"> <ul class="Disc"> <li> <span class="Bold">Carefully remove</span> the rubber stopper.</li> </ul> </td><td align="left" class="Rrule"> <p class="First"> <img alt="Figure" src="/dailymed/image.cfm?name=arikayce-22.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></p> </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"> <ol class="LittleAlpha"> <li>Open the vial and pour the ARIKAYCE into the Medication Reservoir. </li> <li>Attach the Medication Cap.</li> </ol> </td><td align="center" class="Rrule"><img alt="Figure" src="/dailymed/image.cfm?name=arikayce-23.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></td> </tr> <tr> <td align="left" class="Lrule Rrule"><span class="Bold">Step 2: Sit in a relaxed, upright position.</span></td><td align="left" class="Rrule"></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"> <ul class="Disc"> <li>Press and hold down on the On/Off button for a few seconds to turn the Lamira on. </li> <li>Mist will begin to flow. </li> </ul> </td><td align="right" class="Rrule"><img alt="Figure" src="/dailymed/image.cfm?name=arikayce-24.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"><span class="Bold">Step 3: Insert the Mouthpiece (but do not cover the blue flap) and take slow, deep breaths</span>. <ul class="Disc"> <li>Then, breathe normally in and out through the Mouthpiece until your treatment is complete.</li> <li>Treatment should take about 14 minutes but could take up to 20 minutes.</li> </ul> <p class="First"> <span class="Bold">Be sure to hold the Handset level throughout the treatment.</span> </p> </td><td align="left" class="Rrule"> <p class="First"> <img alt="Figure" src="/dailymed/image.cfm?name=arikayce-25.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></p> </td> </tr> <tr> <td align="left" class="Lrule Rrule"><span class="Bold">Step 4: Check that your treatment has ended.</span></td><td align="left" class="Rrule"></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"> <ul class="Disc"> <li>The Lamira will beep 2 times.</li> <li>A Checkmark will briefly appear on the screen.</li> <li>The Controller will automatically shut off.</li> <li>Remove the Medication Cap and <span class="Bold">check the Medication Reservoir to make sure that no more than a few drops of ARIKAYCE remains. If ARIKAYCE remains, replace the Medication Cap, press the On/Off button, and complete your dose.</span> </li> </ul> </td><td align="left" class="Rrule"> <p class="First"> <img alt="Figure" src="/dailymed/image.cfm?name=arikayce-26.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40"/></p> </td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule" colspan="2"><span class="Bold">For any issues you may have with your Lamira Nebulizer System, see Section J – Frequently Asked Questions and Section K – Troubleshooting of the full Instructions for Use that comes with your medicine. </span></td> </tr> </tbody> </table></div>

{ "type": "table", "children": [], "text": "<div class=\"scrollingtable\"><table width=\"100%\">\n<col align=\"left\" valign=\"top\" width=\"45%\"/>\n<col align=\"left\" valign=\"top\" width=\"55%\"/>\n<tbody class=\"Headless\">\n<tr class=\"Botrule First\">\n<td align=\"left\" class=\"Lrule Rrule\"><span class=\"Bold\">Step 1: Get your ARIKAYCE ready.</span>\n<ul class=\"Disc\">\n<li>Place the Handset on a clean, flat, stable surface.</li>\n<li>Shake the ARIKAYCE vial for a <span class=\"Bold\">minimum of</span> 10 to 15 seconds, <span class=\"Bold\">AND UNTIL THE MEDICINE LOOKS THE SAME THROUGHOUT AND WELL MIXED.</span>\n</li>\n</ul>\n</td><td align=\"center\" class=\"Rrule\"><img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-18.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"2\"><span class=\"Bold\">How to open the ARIKAYCE vial</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\">\n<ul class=\"Disc\">\n<li>\n<span class=\"Bold\">Lift the orange cap</span> from the vial.</li>\n</ul>\n</td><td align=\"left\" class=\"Rrule\">\n<p class=\"First\">\n<img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-19.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></p>\n</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\">\n<ul class=\"Disc\">\n<li>\n<span class=\"Bold\">Grip the metal ring</span> on top of the vial and pull it down gently until 1 side breaks away from the vial but do not pull the tab completely off.</li>\n</ul>\n</td><td align=\"left\" class=\"Rrule\">\n<p class=\"First\">\n<img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-20.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></p>\n</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\">\n<ul class=\"Disc\">\n<li>\n<span class=\"Bold\">Pull the metal band</span> from around the vial top in a circular motion until it comes off completely.</li>\n</ul>\n</td><td align=\"left\" class=\"Rrule\">\n<p class=\"First\">\n<img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-21.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></p>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\">\n<ul class=\"Disc\">\n<li>\n<span class=\"Bold\">Carefully remove</span> the rubber stopper.</li>\n</ul>\n</td><td align=\"left\" class=\"Rrule\">\n<p class=\"First\">\n<img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-22.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></p>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\">\n<ol class=\"LittleAlpha\">\n<li>Open the vial and pour the ARIKAYCE into the Medication Reservoir. </li>\n<li>Attach the Medication Cap.</li>\n</ol>\n</td><td align=\"center\" class=\"Rrule\"><img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-23.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\"><span class=\"Bold\">Step 2: Sit in a relaxed, upright position.</span></td><td align=\"left\" class=\"Rrule\"></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\">\n<ul class=\"Disc\">\n<li>Press and hold down on the On/Off button for a few seconds to turn the Lamira on. </li>\n<li>Mist will begin to flow. </li>\n</ul>\n</td><td align=\"right\" class=\"Rrule\"><img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-24.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\"><span class=\"Bold\">Step 3: Insert the Mouthpiece (but do not cover the blue flap) and take slow, deep breaths</span>. \t\t\t\t\t\t\t\t\t<ul class=\"Disc\">\n<li>Then, breathe normally in and out through the Mouthpiece until your treatment is complete.</li>\n<li>Treatment should take about 14 minutes but could take up to 20 minutes.</li>\n</ul>\n<p class=\"First\">\n<span class=\"Bold\">Be sure to hold the Handset level throughout the treatment.</span>\n</p>\n</td><td align=\"left\" class=\"Rrule\">\n<p class=\"First\">\n<img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-25.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></p>\n</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\"><span class=\"Bold\">Step 4: Check that your treatment has ended.</span></td><td align=\"left\" class=\"Rrule\"></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\">\n<ul class=\"Disc\">\n<li>The Lamira will beep 2 times.</li>\n<li>A Checkmark will briefly appear on the screen.</li>\n<li>The Controller will automatically shut off.</li>\n<li>Remove the Medication Cap and <span class=\"Bold\">check the Medication Reservoir to make sure that no more than a few drops of ARIKAYCE remains. If ARIKAYCE remains, replace the Medication Cap, press the On/Off button, and complete your dose.</span>\n</li>\n</ul>\n</td><td align=\"left\" class=\"Rrule\">\n<p class=\"First\">\n<img alt=\"Figure\" src=\"/dailymed/image.cfm?name=arikayce-26.jpg&amp;setid=499ab990-2b21-474f-aaba-d86388965f40\"/></p>\n</td>\n</tr>\n<tr class=\"Last\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"2\"><span class=\"Bold\">For any issues you may have with your Lamira Nebulizer System, see Section J – Frequently Asked Questions and Section K – Troubleshooting of the full Instructions for Use that comes with your medicine. </span></td>\n</tr>\n</tbody>\n</table></div>" }

Cleaning your Lamira Handset and Aerosol Head After Use

{ "type": "p", "children": [], "text": "\nCleaning your Lamira Handset and Aerosol Head After Use\n" }

{ "type": "ul", "children": [ "\nRinse, clean, and disinfect handset right away after each use to reduce infection, illness, and contamination.\n", "\nDisinfect the Handset and Aerosol Head after every use.\n", "\nSee \"Cleaning and Disinfecting\" at the beginning of the Instructions for Use on how to properly clean and disinfect your handset and aerosol head.\n" ], "text": "" }

© 2018 Insmed Incorporated. All rights reserved. Insmed®, ARIKAYCE®, and inLighten™ are trademarks of Insmed Incorporated. Lamira® is a trademark of PARI Pharma GmbH.

{ "type": "p", "children": [], "text": "© 2018 Insmed Incorporated. All rights reserved. Insmed®, ARIKAYCE®, and inLighten™ are trademarks of Insmed Incorporated. Lamira® is a trademark of PARI Pharma GmbH." }

This Instructions for Use has been approved by the U.S. Food and Drug Administration.Issued: 01/2025

{ "type": "p", "children": [], "text": "This Instructions for Use has been approved by the U.S. Food and Drug Administration.Issued: 01/2025" }

1-833-LIGHT-00 (1-833-544-4800)

{ "type": "p", "children": [], "text": "1-833-LIGHT-00 (1-833-544-4800)" }

Contains 28 sterile unit-dose vials Each vial contains amikacin 590 mg/8.4 mL (equivalent to amikacin sulfate 788 mg/8.4 mL)

{ "type": "p", "children": [], "text": "Contains 28 sterile unit-dose vials Each vial contains amikacin 590 mg/8.4 mL (equivalent to amikacin sulfate 788 mg/8.4 mL)" }

For oral inhalation only

{ "type": "p", "children": [], "text": "For oral inhalation only" }

ARIKAYCE® (amikacin liposome inhalation suspension)590 mg/8.4 mL vials

{ "type": "p", "children": [], "text": "ARIKAYCE®\n(amikacin liposome inhalation suspension)590 mg/8.4 mL vials" }

Limited Population*

{ "type": "p", "children": [], "text": "Limited Population*" }

insmed®

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

Attention Patients: Store refrigerated until expiration date on vial. Do not freeze. Once expired, discard any unused medicine. ARIKAYCE can be stored at room temperature up to 25°C (77°F) for up to 4 weeks. Once at room temperature, any unused medicine must be discarded at the end of 4 weeks.

{ "type": "p", "children": [], "text": "Attention Patients: Store refrigerated until expiration date on vial. Do not freeze. Once expired, discard any unused medicine. ARIKAYCE can be stored at room temperature up to 25°C (77°F) for up to 4 weeks. Once at room temperature, any unused medicine must be discarded at the end of 4 weeks." }

*See the full prescribing information for ARIKAYCE for information about the limited population

{ "type": "p", "children": [], "text": "*See the full prescribing information for ARIKAYCE for information about the limited population" }

ARIKAYCE.COM

{ "type": "p", "children": [], "text": "ARIKAYCE.COM" }