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LONHALA MAGNAIR consists of LONHALA vials and a MAGNAIR nebulization system. LONHALA (glycopyrrolate) Inhalation Solution is a sterile, clear, colorless, aqueous solution for oral inhalation.
Glycopyrrolate USP, the active component of LONHALA Inhalation Solution, is chemically described as (3RS)-3-[(2SR)-(2-cyclopentyl-2-hydroxy-2-penylacetyl)oxy]-1,1-dimethlypyrrolidinium bromide. Glycopyrrolate is a synthetic quaternary ammonium compound that acts as a competitive antagonist at muscarinic acetylcholine receptors, also referred to as an anticholinergic. Glycopyrrolate, C19H28BrNO3, is a white, odorless, crystalline powder that is soluble in water and in alcohol. It has a molecular mass of 398.33. The structural formula is:
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The inactive ingredients in LONHALA are: citric acid monohydrate, sodium chloride, sodium hydroxide and water for injection.
LONHALA Inhalation Solution is supplied in low-density polyethylene (LDPE) unit dose vials, each containing 1.0 mL of the solution. Each unit-dose vial contains 25 mcg of glycopyrrolate in a sterile, isotonic saline solution, pH-adjusted to 4.0 with citric acid and sodium hydroxide.
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 14.2 mcg of glycopyrrolate (equivalent to 11.4 mcg glycopyrronium and 56.8% label claim). The mass median aerodynamic diameter (MMAD) of the nebulized aerosol particles/droplets is 3.71 μm 95% CI (2.92 - 4.49 μm) as determined using the Next Generation Impactor (NGI) method. The mean nebulization time was approximately 2 to 3 minutes.
LONHALA MAGNAIR is indicated for the long-term maintenance treatment of airflow obstruction in patients with chronic obstructive pulmonary disease (COPD), including chronic bronchitis and/or emphysema.
LONHALA vials should only be used with MAGNAIR [see OVERDOSE].
The recommended dose of LONHALA is the inhalation of the contents of one LONHALA vial twice-daily using MAGNAIR. LONHALA vials should only be administered with MAGNAIR. Patients should be instructed on the correct use of this drug product and device.
LONHALA MAGNAIR should be administered at the same time of the day, (1 vial in the morning and 1 vial in the evening), every day. More frequent administration or a greater number of inhalations (more than 1 vial twice daily) of LONHALA MAGNAIR is not recommended.
Store LONHALA vials in the foil pouch, and only remove IMMEDIATELY BEFORE USE with MAGNAIR.
No dosage adjustment is required for geriatric patients, patients with hepatic impairment, or patients with mild to moderate renal impairment.
LONHALA Inhalation Solution is supplied as a sterile, clear, colorless, aqueous solution for inhalation in a unit-dose single-use low-density polyethylene (LDPE) vial. Each 1 mL vial contains 25 mcg of glycopyrrolate.
LONHALA MAGNAIR is supplied as a 1 mL sterile, clear, colorless, aqueous solution in low-density polyethylene (LDPE) unit-dose vials overwrapped in foil. LONHALA MAGNAIR is available in a Starter Kit containing 60 unit-dose vials packaged with one MAGNAIR, and FDA approved patient labeling. LONHALA MAGNAIR is also supplied in a Refill Kit containing 60 unit-dose vials packaged with a MAGNAIR Replacement Handset and FDA approved patient labeling.
| Package Configuration | Dosage Strength | NDC |
| Starter Kit with 30 day supply (30 foil pouches with 2 vials per pouch) and complete MAGNAIR Nebulizer System | 25 mcg | NDC: 63402-201-00 |
| Refill Kit with 30 day supply (30 foil pouches with 2 vials per pouch) and MAGNAIR Replacement Handset | 25 mcg | NDC: 63402-301-01 |
Store LONHALA Inhalation Solution in the protective foil pouch at 20°-25°C (68°-77°F) [see USP Controlled Room Temperature].
Always use the MAGNAIR Replacement Handset parts that come with each LONHALA MAGNAIR refill prescription.
Keep out of the reach of children.
Manufactured by: PARI Respiratory Equipment, Inc., 2412 PARI Way, Midlothian, VA 23112. Revised: June 2019
The following adverse reactions are described in greater detail in other sections:
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
The LONHALA MAGNAIR safety database included 2379 subjects with COPD in two 12-week efficacy studies and one 48-week long-term safety study. A total of 431 subjects received treatment with LONHALA MAGNAIR 25 mcg twice-daily (BID). The safety data described below are based on the two 12-week trials and the one 48-week trial.
LONHALA MAGNAIR was studied in two 12-week placebo-controlled trials in subjects with COPD. In these trials, 431 subjects were treated with LONHALA MAGNAIR at the recommended dose of 25 mcg twice daily. The population had a mean age of 63 years (ranging from 40 to 87 years), with 56% males, 90% Caucasian, and a mean post-bronchodilator forced expiratory volume in one second (FEV1) percent predicted of 52% of predicted normal value (20%-80%) at study entry. The study population also included subjects with pre-existing cardiovascular disease as well as subjects with continued use of stable long-acting bronchodilator (LABA) ± inhaled corticosteroid (ICS) and ipratropium bromide background therapy. Subjects with unstable cardiac disease, narrow-angle glaucoma, or symptomatic prostatic hypertrophy or bladder outlet obstruction were excluded from these studies.
Table 1 shows the most common adverse reactions incidence greater than or equal to 2.0% in the LONHALA MAGNAIR group and higher than placebo in the two 12-week placebo-controlled trials.
The proportion of subjects who discontinued treatment due to adverse reactions was 5% for the LONHALA MAGNAIR-treated subjects and 9% for placebo-treated subjects.
Table 1. Adverse Reactions with LONHALA MAGNAIR ≥2.0% Incidence and Higher than Placebo
| Placebo (N=430) N (%) |
LONHALA MAGNAIR 25 mcg BID (N=431) N (%) |
|
| Dyspnea | 13 (3.0) | 21 (4.9) |
| Urinary Tract Infection | 6 (1.4) | 9 (2.1) |
Other adverse reactions defined as events with an incidence of ≥1.0% but less than 2.0% with LONHALA MAGNAIR but more common than with placebo included the following: wheezing, upper respiratory tract infection, nasopharyngitis, oedema peripheral, and fatigue.
In a long-term open-label safety trial, 1086 subjects were treated for up to 48-weeks with LONHALA MAGNAIR 50 mcg twice-daily (N=620) or tiotropium (N=466). The demographic and baseline characteristics of the long-term safety trial were similar to those of the placebo-controlled efficacy studies described above. The adverse reactions reported in the long-term safety trial were consistent with those observed in the placebo-controlled studies of 12-weeks. Adverse reactions that occurred at a frequency greater than that seen in either active treatment dose in the pooled 12-week placebo controlled studies and ≥ 2.0% were: diarrhea, edema peripheral, bronchitis, nasopharyngitis, pneumonia, sinusitis, upper respiratory tract infection, urinary tract infection, back pain, headache, Chronic Obstructive Pulmonary Disease, cough, dyspnea, oropharyngeal pain, and hypertension.
In clinical studies, concurrent administration of glycopyrrolate and other drugs commonly used in the treatment of COPD including sympathomimetics (long and short-acting beta2 agonists), anticholinergics (short-acting anti-muscarinic antagonists) and oral and inhaled steroids showed no increases in adverse drug reactions.
There is a potential for an additive interaction with concomitantly used anticholinergic medications. Therefore, avoid unnecessary co-administration of LONHALA MAGNAIR with other anticholinergic-containing drugs as this may lead to an increase in anticholinergic effects [see WARNINGS AND PRECAUTIONS and ADVERSE REACTIONS].
Included as part of the "PRECAUTIONS" Section
LONHALA MAGNAIR should not be initiated in patients during acutely deteriorating or potentially life-threatening episodes of COPD. LONHALA MAGNAIR has not been studied in subjects with acutely deteriorating COPD. The initiation of LONHALA MAGNAIR in this setting is not appropriate.
LONHALA MAGNAIR should not be used as rescue therapy for the treatment of acute episodes of bronchospasm. LONHALA MAGNAIR has not been studied in the relief of acute symptoms and extra doses should not be used for that purpose. Acute symptoms should be treated with an inhaled, short-acting beta2agonist.
COPD may deteriorate acutely over a period of hours or chronically over several days or longer. If LONHALA MAGNAIR no longer controls symptoms of bronchoconstriction the patient’s inhaled, short-acting beta2agonist becomes less effective; or the patient needs more inhalations of a short-acting beta2-agonist than usual, these may be markers of deterioration of disease. In this setting, a re-evaluation of the patient and the COPD treatment regimen should be undertaken at once. Increasing the daily dose of LONHALA MAGNAIR beyond the recommended dose is not appropriate in this situation.
As with other inhaled medicines, LONHALA MAGNAIR can produce paradoxical bronchospasm that may be life-threatening. If paradoxical bronchospasm occurs following dosing with LONHALA MAGNAIR, it should be treated immediately with an inhaled, short-acting bronchodilator; LONHALA MAGNAIR should be discontinued immediately, and alternative therapy instituted.
Immediate hypersensitivity reactions may occur after administration of LONHALA MAGNAIR. If signs suggesting allergic reactions occur, in particular, angioedema (including difficulties in breathing or swallowing, swelling of the tongue, lips, and face), urticaria, or skin rash, LONHALA MAGNAIR should be discontinued immediately and alternative therapy instituted.
LONHALA MAGNAIR should be used with caution in patients with narrow-angle glaucoma. Prescribers and patients should be alert for signs and symptoms of acute narrow-angle glaucoma (e.g., eye pain or discomfort, blurred vision, visual halos or colored images in association with red eyes from conjunctival congestion and corneal edema). Instruct patients to consult a physician immediately should any of these signs or symptoms develop.
LONHALA MAGNAIR should be used with caution in patients with urinary retention. Prescribers and patients should be alert for signs and symptoms of urinary retention (e.g., difficulty passing urine, painful urination), especially in patients with prostatic hyperplasia or bladder-neck obstruction. Instruct patients to consult a physician immediately should any of these signs or symptoms develop.
Advise the patient to read the FDA-approved patient labeling (PATIENT INFORMATION and Instructions for Use).
Inform patients that LONHALA MAGNAIR is not meant to relieve acute symptoms of COPD and extra doses should not be used for that purpose. Advise them to treat acute symptoms with a rescue inhaler such as albuterol. Provide patients with such medicine and instruct them in how it should be used [see WARNINGS AND PRECAUTIONS].
Instruct patients to seek medical attention immediately if they experience any of the following:
Patients should not stop therapy with LONHALA MAGNAIR without physician/provider guidance since symptoms may recur after discontinuation.
Inform patients that LONHALA MAGNAIR can cause paradoxical bronchospasm. If paradoxical bronchospasm occurs, instruct patients to discontinue LONHALA MAGNAIR.
Angle Glaucoma
Instruct patients to be alert for signs and symptoms of acute narrow-angle glaucoma (e.g., eye pain or discomfort, blurred vision, visual halos or colored images in association with red eyes from conjunctival congestion and corneal edema). Instruct patients to consult a physician immediately if any of these signs or symptoms develop.
Instruct patients to be alert for signs and symptoms of urinary retention (e.g., difficulty passing urine, painful urination). Instruct patients to consult a physician immediately if any of these signs or symptoms develop.
It is important for patients to understand how to correctly administer LONHALA vials using MAGNAIR [see Instructions for Use]. Instruct patients that LONHALA vials should only be administered via MAGNAIR and MAGNAIR should not be used for administering other medications. Patients should be instructed not to inject or swallow the LONHALA solution.
Instruct patients to store LONHALA vials in the sealed foil pouch and to only open the foil pouch to remove a LONHALA vial immediately before use. Inform patients that unopened vials should be returned to the opened foil pouch for use at their next treatment and discarded if not used within 7 days or it may not be as effective.
Inform patients to use one inhalation of LONHALA MAGNAIR orally twice daily (1 vial in the morning and 1 vial in the evening) at the same time every day.
Inform patients that if they miss a dose of LONHALA MAGNAIR, they should use their next vial at the usual time. Instruct patients to not use 2 vials at one time and to not use more than 2 vials in a day. Patients should throw the plastic dispensing vials away immediately after use. Due to their small size, the vials pose a danger of choking to young children.
Inform patients treated with LONHALA MAGNAIR that a Refill Kit will be provided to them on a monthly basis. The Refill Kit will include foil pouches containing 60 vials of LONHALA (2 vials of LONHALA in each pouch;1 vial per dose), and 1 MAGNAIR Replacement Handset (containing only these replacement parts: Medication cap, Handset body, Mouthpiece, and Aerosol head; Manufacturer’s Instructions for Use booklet).
Important
Instruct patients to throw away the old Handset parts after using 60 vials of LONHALA and use the replacement Handset parts with the next 60 vials of LONHALA.
Carcinogenicity studies of glycopyrrolate did not result in an increase in the incidence of tumors in a 2-year inhalation study of glycopyrrolate in Wistar rats at doses up to 0.56 mg/kg/day, approximately 143 times the MRHDID of LONHALA MAGNAIR in adults on an AUC basis. Also, no evidence of tumorigenicity occurred in a 26-week oral (gavage) study in male and female TgrasH2 mice that received glycopyrrolate at doses up to 93.8 and 125.1 mg/kg/day, respectively, approximately 66 times the MRHDID of LONHALA MAGNAIR.
Glycopyrrolate was not mutagenic in the following genotoxicity assays: the in vitro Ames assay, in vitro human lymphocyte chromosomal aberration assay, and in vivo rat bone marrow micronucleus assay.
Impairment of fertility was observed in male and female Wistar rats at a subcutaneous glycopyrrolate dose of 1.88 mg/kg/day (approximately and 2035 and 1136 times, respectively, the MRHD of LONHALA MAGNAIR on an AUC basis) based upon findings of decreased implantation sites and corresponding reduction of live fetuses. No effects on fertility and reproductive performance occurred in male and female rats at a subcutaneous glycopyrrolate dose of 0.63 mg/kg/day, approximately 384 times the MRHD of LONHALA MAGNAIR on an AUC basis).
There are no adequate and well-controlled studies in pregnant women. LONHALA MAGNAIR should only be used during pregnancy if the expected benefit to the patient outweighs the potential risk to the fetus. Women should be advised to contact their physician if they become pregnant while taking LONHALA MAGNAIR. In animal reproduction studies, there were no teratogenic effects in Wistar rats and New Zealand White rabbits at inhaled doses approximating 1521 and 580 times, respectively, the maximum recommended human daily inhalation dose (MRHDID) based on an AUC comparison [see Data].
The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. 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.
The potential effect of LONHALA MAGNAIR on labor and delivery is unknown. LONHALA MAGNAIR should be used during labor and delivery only if the potential benefit to the patient justifies the potential risk to the fetus.
Animal Data
Developmental studies in Wistar rats and New Zealand White rabbits in which glycopyrrolate was administered by inhalation during the period of organogenesis did not result in evidence of teratogenicity at exposures approximately 1521 and 580 times, respectively, the MRHDID of LONHALA MAGNAIR based on a comparison of plasma AUC levels (maternal doses up to 3.8 mg/kg/day in rats and 4.4 mg/kg/day in rabbits).
Glycopyrrolate had no effects on peri-natal and post-natal development in rats following subcutaneous exposure of approximately 1137 times the MRHDID of LONHALA MAGNAIR based on an AUC comparison (at a maternal dose of up to 1.885 mg/kg/day).
There are no data on the presence of glycopyrrolate or its metabolites in human milk, the effects on the breastfed infant, or the effects on milk production. However, in a study of lactating rats, glycopyrrolate was present in the milk [see Data]. The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for LONHALA MAGNAIR and any potential adverse effects on the breastfed infant from LONHALA MAGNAIR or from the underlying maternal condition.
Glycopyrrolate (and its metabolites) was detected in the milk of lactating rats following a single intravenous injection of 4 mg/kg of radiolabeled glycopyrrolate.
LONHALA MAGNAIR is not indicated for use in children. The safety and efficacy of LONHALA MAGNAIR in pediatric patients have not been established.
Based on available data, no adjustment of the dosage of LONHALA MAGNAIR in geriatric patients is warranted. LONHALA MAGNAIR can be used at the recommended dose in elderly patients 75 years of age and older.
Of the total number of subjects in clinical studies of LONHALA MAGNAIR, 41% were aged 65 and older, while 8% were aged 75 and older. No overall differences in safety or effectiveness were observed between these subjects and younger subjects, and other reported clinical experience has not identified differences in responses between the elderly and younger patients, but greater sensitivity of some older individuals cannot be ruled out.
No dose adjustment is required for patients with mild and moderate renal impairment. The effects of renal impairment on the pharmacokinetics of glycopyrrolate have not been studied [see CLINICAL PHARMACOLOGY].
No dose adjustment is required for patients with hepatic impairment. The effects of hepatic impairment on the pharmacokinetics of glycopyrrolate have not been studied [see CLINICAL PHARMACOLOGY].
An overdose of glycopyrrolate may lead to anticholinergic signs and symptoms such as nausea, vomiting, dizziness, lightheadedness, blurred vision, increased intraocular pressure (causing pain, vision disturbances, or reddening of the eye), obstipation or difficulties in voiding.
In COPD patients, orally inhaled administration of LONHALA MAGNAIR at a total daily dose of 200 mcg for 28 consecutive days (maximum of 1 mg) was well tolerated. Pharmacokinetic results from several studies conducted in COPD patients showed that a single, well tolerated dose of 1000 mcg had a Cmax of 1534 pg/mL and AUC0-inf of 5271 pg*hr/mL. These values are approximately 44 fold and 21 fold higher, respectively, than the estimated daily Cmax of 34.5 pg/mL and AUC0-inf of 255 pg*hr/mL for a 25 mcg BID dose regimen at steady-state.
LONHALA MAGNAIR is contraindicated in patients with a hypersensitivity to glycopyrrolate or any of the ingredients [see WARNINGS AND PRECAUTIONS].
Glycopyrrolate is a long-acting muscarinic antagonist, which is often referred to as an anticholinergic. It has similar affinity to the subtypes of muscarinic receptors M1 to M5. In the airways, it exhibits pharmacological effects through inhibition of M3 receptor at the smooth muscle leading to bronchodilation. The competitive and reversible nature of antagonism was shown with human and animal origin receptors and isolated organ preparations. In preclinical in vitro as well as in vivo studies, prevention of methacholine and acetylcholine induced bronchoconstrictive effects was dose-dependent and lasted longer than 24 hours. The clinical relevance of these findings is unknown. The bronchodilation following inhalation of glycopyrrolate is predominantly a site-specific effect.
In the dose ranging and confirmatory clinical studies, the administration of LONHALA MAGNAIR did not demonstrate any clinically relevant changes in cardiac function including: vital signs (heart rate, blood pressure), electrocardiograms (including QTc) and Holter monitoring. In addition, no major adverse cardiovascular events (MACE) were reported following the administration of LONHALA MAGNAIR 25 mcg in any clinical study.
Following oral inhalation using MAGNAIR, glycopyrrolate was rapidly absorbed and reached peak plasma levels <20 minutes post dose.
In patients with COPD, pharmacokinetic steady-state plasma levels of glycopyrrolate were reached within one week of the start of treatment. A twice daily dose regimen leads to approximately 2-3 fold accumulation of systemic glycopyrrolate exposure at steady-state.
The in vitro human plasma protein binding of glycopyrrolate was 38% to 41% at concentrations of 1 to 10 ng/mL.
In vitro metabolism studies show glycopyrrolate hydroxylation resulting in a variety of mono- and bishydroxylated metabolites and direct hydrolysis resulting in the formation of a carboxylic acid derivative (M9). Further in vitro investigations showed that multiple CYP isoenzymes contribute to the oxidative biotransformation of glycopyrrolate and the hydrolysis to M9 is likely to be catalyzed by members from the cholinesterase family pre-systemically and/or via first pass metabolism from the swallowed dose fraction of orally inhaled glycopyrrolate.
After intravenous administration of [3H]-labelled glycopyrrolate to humans, the mean urinary excretion of radioactivity in 48 hours amounted to 85% of the dose. A further 5% of the dose was found in the bile.
Renal elimination of parent drug accounts for about 60 to 70% of total clearance of systemically available glycopyrrolate whereas non-renal clearance processes account for about 30 to 40%. Biliary clearance contributes to the non-renal clearance, but the majority of non-renal clearance is thought to be due to metabolism.
In vitro inhibition studies demonstrated that glycopyrrolate has no relevant capacity to inhibit CYP1A2, CYP2A6, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP2E1 or CYP3A4/5, the efflux transporters MDR1, MRP2 or MXR, and the uptake transporters OATP1B1, OATP1B3, OAT1, OAT3, OCT1 or OCT2. In vitro enzyme induction studies did not indicate a clinically relevant induction by glycopyrrolate for cytochrome P450 isoenzymes, or for UGT1A1 and the transporters MDR1 and MRP2.
There is potential for additive interaction with concomitantly used anticholinergic medications. Therefore, avoid coadministration of LONHALA MAGNAIR with other anticholinergic-containing drugs as this may lead to an increase in anticholinergic effects [see WARNINGS AND PRECAUTIONS and ADVERSE REACTIONS].
A population pharmacokinetic analysis of data in COPD patients indicated no clinically relevant effect of age (41 to 80 years) or body weight (40.1 to 154.8 kg) on systemic exposure to glycopyrrolate. In addition, there was no evidence of clinically significant ethnic/race effect.
The effects of renal impairment on the pharmacokinetics of glycopyrrolate have not been studied [see Use In Specific Populations].
The effects of hepatic impairment on the pharmacokinetics of glycopyrrolate have not been studied. Glycopyrrolate is cleared predominantly from systemic circulation by renal excretion [see Use In Specific Populations].
The safety and efficacy of LONHALA MAGNAIR were evaluated in 2 dose-ranging studies, 2 placebo-controlled confirmatory studies (12-week studies), and a 48-week long-term safety study. The efficacy of LONHALA MAGNAIR is based primarily on the dose-ranging studies in 378 subjects with COPD and the 2 placebo-controlled confirmatory studies in 1293 subjects with COPD.
Dose selection for the confirmatory COPD studies for LONHALA MAGNAIR was supported by two studies. Study A was a randomized, double-blind, placebo-controlled, parallel arm study with a 28-day treatment period. The study included LONHALA MAGNAIR doses of placebo, 12.5 mcg, 25 mcg, 50 mcg, and 100 mcg twice daily. The Study demonstrated a dose-response effect on peak and trough FEV1 over 24-hour dosing period in subjects treated with LONHALA MAGNAIR twice daily [Figure 1 (Day 1) and Figure 2 (Day 28)]. The LS mean differences in trough FEV1 from baseline after 28 days compared to placebo for the 12.5 mcg, 25 mcg, 50 mcg, and 100 mcg twice daily doses were 0.117 L (95% CI: 0.037, 0.197); 0.128 L (95% CI: 0.048, 0.209), 0.146 L (95% CI: 0.067, 0.226), and 0.177 L (95% CI: 0.099, 0.255), respectively. In Study A, all subjects in each treatment group (N=282) had FEV1 AUC0-12h serial spirometry assessments while a subset of subjects (N=125; shown in Figure 1 and Figure 2 below) had extended FEV1 AUC12-24h assessments on Days 1 and 28.
Study B was a randomized, six-way, crossover study with 7-day treatment periods separated by 5-7-day washout periods. Study B included LONHALA MAGNAIR doses of placebo, 3 mcg, 6.25 mcg, 12.5 mcg, and 50 mcg twice daily with aclidinium bromide 400 mcg BID as an active control.
The dose-ranging results from Study A and Study B supported the evaluation of LONHALA MAGNAIR 25 mcg and 50 mcg twice-daily in the confirmatory COPD trials. The results of Study A are reported in Figure 1 below.
Figure 1: LS Mean Change from Baseline in FEV1 (L) Over Time on Day 1 (Study A)
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Figure 2: LS Mean Change from Baseline in FEV1 (L) Over Time on Day 28 (Study A)
 |
There were 2 confirmatory studies (Study 1 and Study 2) for LONHALA MAGNAIR. Both studies were randomized, double-blind, placebo-controlled, parallel-group 12-week studies in subjects with COPD designed to evaluate the efficacy of LONHALA MAGNAIR on lung function. These studies treated subjects who had a clinical diagnosis of COPD, were 40 years of age or older, had a history of smoking greater than or equal to 10 pack-years, a post –bronchodilator FEV1 less than or equal to 80% of predicted, and an FEV1/FVC ratio less than 0.7. Subjects also had pre-existing or concurrent cardiovascular disease and stable, background LABA ± ICS and SAMA use were permitted. Subjects in Study 1 and Study 2 had a mean age of 63 years, were primarily male (56%), Caucasian (90%), and current smokers (53%) with an average smoking history of 52 pack-years. At screening, the mean post-bronchodilator percent predicted FEV1 was 52% (range: 20% to 80%), the mean post-bronchodilator percent FEV1/FVC was 54% (range: 20% to 71%), and the mean percent reversibility was 18% (range: -33% to 86%).
Study 1 and Study 2 evaluated LONHALA MAGNAIR (glycopyrrolate) 25 mcg and 50 mcg twice-daily and placebo twice-daily. The primary endpoint was the change from baseline in trough FEV1 at Day 84 compared with placebo. LONHALA MAGNAIR twice-daily demonstrated a larger increase in LS mean change from baseline in trough FEV1 compared to placebo. Compared to LONHALA MAGNAIR 25 mcg twice daily, LONHALA MAGNAIR 50 mcg twice daily did not provide sufficient additional benefit on a variety of endpoints, including FEV1, to support use of higher doses. Table 2 presents the results from Studies 1 and 2 for LONHALA MAGNAIR 25 mcg twice daily.
Table 2. LS Mean change from baseline in Trough FEV1 (L) on Day 84 (ITT Population*)
| Treatment | N | Change from baseline LS Mean (SE) | Comparison | Treatment Difference LS Mean (SE) | 95% CI |
| Study 1 | |||||
| LONHALA MAGNAIR 25 mcg BID | 217 | 0.089 (0.014) |
LONHALA MAGNAIR -Placebo | 0.096 (0.019) |
0.059, 0.133 |
| Placebo | 218 | -0.008 (0.014) |
|||
| Study 2 | |||||
| LONHALA MAGNAIR 25 mcg BID | 214 | 0.092 (0.014) |
LONHALA MAGNAIR -Placebo | 0.081 (0.020) |
0.042, 0.120 |
| Placebo | 212 | 0.011 (0.015) |
|||
| *Study results are from a treatment policy strategy which analyzes all collected data, including data for some patients who discontinued study treatment prior to Week 12 and may have received other COPD treatment but were followed. Analyses of efficacy data measured only while on randomized blinded study treatment showed similar results. | |||||
In Study 1, serial spirometric evaluations throughout the 12-hour dosing interval were performed in a subset of subjects on Day 1 and Day 84. The spirometric curves from Study 1 on Day 1 and Day 84 are displayed in Figure 3 and Figure 4.
Figure 3: Mean Change from Baseline in FEV1 (L) Over Time on Day 1 (Substudy Population)
 |
Figure 4: Mean Change from Baseline in FEV1 (L) Over Time on Day 84 (Substudy Population)
 |
The peak FEV1 was defined as the highest postdose FEV1 within the first 12 hours after morning dosing for each subject on Days 1 and 84, respectively, for the substudy population.
The mean peak FEV1 improvement from baseline for LONHALA MAGNAIR on Day 1 and on Day 84 in the subset of subjects was 0.228 L and 0.214 L (Study 1) respectively.
The St. George’s Respiratory Questionnaire (SGRQ) was assessed in Studies 1 and 2. In Study 1, the SGRQ responder rate (defined as an improvement in score of 4 or more as threshold) for the LONHALA MAGNAIR 25 mcg treatment arm was 51% compared to 40% for placebo [Odds Ratio:1.55; 95% CI: 1.03, 2.33]. In Study 2, the SGRQ responder rate for the LONHALA MAGNAIR 25 mcg treatment arm was 41% compared to 29% for placebo [Odds Ratio: 1.72; 95% CI: 1.11, 2.67].
LONHALA MAGNAIR
(lon-HAH-luh MAGG-nair)
(glycopyrrolate)
inhalation solution, for oral inhalation use
Important: For oral inhalation only. Do not inject or swallow the LONHALA medicine. LONHALA vials are used only with the MAGNAIR device. Do not use MAGNAIR with any other medicine.
Read this Patient Information that comes with LONHALA MAGNAIR before you start using it and each time you get a refill. There may be new information. This Patient Information does not take the place of talking to your healthcare provider about your medical condition or treatment.
What is LONHALA MAGNAIR?
LONHALA MAGNAIR is an anticholinergic medicine known as glycopyrrolate.
Do not use LONHALA MAGNAIR if you:
Before using LONHALA MAGNAIR, tell your healthcare provider about all of your medical conditions, including if you:
Tell your healthcare provider about all the medicines you take, including prescription medicines and overthe-counter medicines, vitamins, and herbal supplements. LONHALA MAGNAIR may affect the way other medicines work, and other medicines can affect how LONHALA MAGNAIR works. Using LONHALA MAGNAIR with other medicines may cause serious side effects.
Especially tell your healthcare provider if you take anticholinergics (including umeclidinium, tiotropium, ipratropium, aclidinium, glycopyrrolate).
Know the medicines you take. Keep a list of your medicines with you and show it to your healthcare provider and pharmacist when you get a new medicine.
How should I use LONHALA MAGNAIR?
Read the step-by-step instructions for using LONHALA MAGNAIR at the end of this Patient
Information leaflet and the Manufacturer’s Instructions for Use booklet. The Manufacturer’s Instructions for Use booklet provides complete information about how to put together (assemble), prepare, use, care for, and trouble-shoot your MAGNAIR nebulizer system.
What are the possible side effects of LONHALA MAGNAIR?
LONHALA MAGNAIR can cause serious side effects, including:
If you have any of these symptoms, stop taking LONHALA MAGNAIR and call your healthcare provider right away before using another dose.
If you have any of these symptoms, stop taking LONHALA MAGNAIR and call your healthcare provider right away before taking another dose.
Common side effects of LONHALA MAGNAIR include shortness of breath, and urinary tract infections.
These are not all of the possible side effects of LONHALA MAGNAIR.
Call your doctor or pharmacist for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
How should I store LONHALA MAGNAIR?
After opening the protective foil pouch, unused LONHALA vials should be returned to, and stored in, the opened foil pouch. Once a foil pouch is opened, discard the vials if not used within 7 days.
General information about the safe and effective use of LONHALA MAGNAIR.
Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use LONHALA MAGNAIR for a condition for which it was not prescribed. Do not give LONHALA MAGNAIR to other people, even if they have the same symptoms you have. It may harm them.
You can ask your healthcare provider or pharmacist for information about LONHALA MAGNAIR that is written for healthcare professionals.
What are the ingredients in LONHALA MAGNAIR?
Active ingredient: glycopyrrolate
Inactive ingredients: citric acid monohydrate, sodium chloride, sodium hydroxide and water for injection.
Instructions for Use
LONHALA MAGNAIR
(lon-HAH-luh MAGG-nair)
(glycopyrrolate)
inhalation solution, for oral inhalation use
Read this Instructions for Use leaflet and the Manufacturer’s Instructions for Use booklet before you start using LONHALA MAGNAIR and each time you get a refill. There may be new information. This information does not take the place of talking to your healthcare provider about your medical condition or treatment. If you have any questions, ask your healthcare provider or pharmacist. The Manufacturer’s Instructions for Use booklet provides complete information about how to put together (assemble), prepare, use, care for, and troubleshoot your MAGNAIR nebulizer system.
Your LONHALA MAGNAIR:
MAGNAIR is a nebulizer system to be used by the patient, caregiver, or healthcare provider to deliver the medicine LONHALA. LONHALA MAGNAIR consists of both the MAGNAIR nebulizer system and the medicine LONHALA.
The following supplies come with your LONHALA MAGNAIR:
Starter Kit: Foil pouches containing 60 vials of LONHALA (2 vials of LONHALA in each pouch; 1 vial per dose), Instructional video, and 1 MAGNAIR Nebulizer System with carrying bag (including Manufacturer’s Instructions for Use booklet and Quick Reference Guide) (see the figure below).
Refill Kit: Foil pouches containing 60 vials of LONHALA (2 vials of LONHALA in each pouch; 1 vial per dose), and 1 MAGNAIR refill Handset (containing only these replacement parts: Medication cap, Handset body, Mouthpiece, and Aerosol head; Manufacturer’s Instructions for Use booklet).
Important: Throw away the old Handset parts after using 60 vials of LONHALA and use the replacement Handset parts in the Refill Kit with the next 60 vials of LONHALA.
 |
Important: Check to make sure that your MAGNAIR nebulizer system is working properly before you use LONHALA MAGNAIR for the first time. See the Manufacturer’s Instructions for Use that come with your MAGNAIR nebulizer system.
Step 1: Open the battery door on the Controller. Place your thumb on the black tab of the battery door and firmly push the tab to open the door.
Steps for Using Batteries with MAGNAIR
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Step 2: Put 4 AA batteries in the Controller as shown.
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Step 3: Close the battery door. You may hear a “Click”.
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Important: Make sure to have an extra set of batteries with you at all times if you choose not to use the AC adapter.
Steps for Using the AC Adapter with MAGNAIR
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Step 1: Plug the AC adapter into the Inlet on the battery door of the Controller.
Step 2: Plug the AC adapter into the wall outlet.
Assembling Your MAGNAIR
Step 1: Wash your hands.
Step 2: Open the top of the Handset body by lifting the clasp.
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Step 3: Insert the Aerosol head into the Handset body as shown. Do not touch the center of the Aerosol head. Notice that the Aerosol head has a small tab on the side. Align the small tab with the matching notch in the Handset body.
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Step 4: Close the Handset body. You may hear a “Click”.
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Step 5: Attach the Mouthpiece to the Handset body. Make sure the Blue valve is pressed down.
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Step 6: Connect the Controller to the Handset body using the Connection cord. You may hear a “Click”.
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Step 7: Connect the Controller to the Handset body using the Connection cord as shown.
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Using LONHALA MAGNAIR
Step 1: Open the foil pouch, enough to remove the 2 LONHALA vials and separate them. Return 1 vial to the opened foil pouch and store in the carrying bag to be used at the next treatment. Discard the vial if not used within 7 days.
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Step 2: Insert one LONHALA vial into the bottom of the Medication cap until it ”Clicks”.
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Important: Do not touch the part of the Handset body that pierces the vial.
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Step 3: Make sure the Aerosol head is installed before attaching the Medication cap because your medicine could leak and you will not get your full treatment. Place the Medication cap with LONHALA vial on the top of the Handset body.
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Step 4: To attach the Medication cap to the Handset body, turn the Medication cap in a clockwise direction as shown, until you hear a “Click”. The notch in the Medication cap (at the base of the opening) should line up with the blue line on the Handset body.
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Step 5: Insert the Mouthpiece into your mouth.
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Important: Do not tilt the Handset, loosen or remove the Medication cap, or unclasp the Handset body until the treatment is complete because you will not get your full treatment.
Step 6: Press the On/Off button to turn on the Controller as shown, and start your treatment.
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Step 7: Breathe in (inhale) and breathe out (exhale) normally through the Mouthpiece.
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At the end of your treatment, you will hear a beeping sound and the Controller will automatically shut off. Your treatment should take about 2 to 3 minutes.
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Cleaning the Handset
Step 1: Disconnect the Handset from the Connection cord.
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Step 2: Turn the Medication cap in a counterclockwise direction as shown, to remove it from the Handset body.
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Step 3: Place the top of the Medication cap into the palm of your hand and push up as shown to remove the LONHALA vial. Throw away the LONHALA vial into the wastebasket.
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Step 4: Remove the Mouthpiece from the Handset body by giving it a gentle twist and pull to separate from the Handset body.
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Step 5: Carefully loosen the Blue valve from the slot in the Mouthpiece. Make sure the valve is still attached on one side to the Mouthpiece.
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Step 6: Remove the Aerosol head from the Handset body by lifting the clasp on the side of the Handset body as shown.
Do not touch the center of the Aerosol head.
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Step 7: Set aside the Aerosol head to be cleaned separately (see Step 10). Rinse all Handset parts well with warm running water for about 10 seconds.
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Step 8: Wash all Handset parts in warm soapy water (water and clear liquid dishwashing soap) for about 10 seconds.
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Step 9: Rinse the Handset parts well with warm running water for about 10 seconds to remove all of the soap.
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Step 10: Clean the Aerosol head using the instructions in Steps 7 through 10.
10A. Rinse each side of the Aerosol head well with warm running water for about 10 seconds.
10B. Hold the Aerosol head by the handle and swish it back and forth in the warm soapy water for about 10 seconds.
10C. Then, rinse both sides of the Aerosol head well with warm running water for about 10 seconds on each side.
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Rinsing the Aerosol head well helps prevent clogging and ensure proper operation.
Step 11: Inspect all Handset parts to make sure they are completely clean. If any Handset parts are still dirty, soak the parts in warm soapy water for 5 more minutes. Rinse well with warm running water until the Handset parts are clean.
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Shake Handset parts to remove excess water. Air-dry all Handset parts on a lint-free towel.
Do not put the Handset parts back together until ready to use again for your next treatment of LONHALA.
Step 12: Store the Handset parts in the carrying bag provided.
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Warnings and Precautions:
Failure to follow the Warnings and Precautions below could cause serious injury or may lead to death in some cases:
Instructions for Use
MAGNAIR™
NEBULIZER SYSTEM INSTRUCTIONS FOR USE
For use with LONHALA™ (glycopyrrolate) Inhalation Solution only
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Assembly required. LONHALA vials packaged separately.
Warning
Read and understand these Instructions for Use and all safety precautions it contains. Improper use can cause serious or fatal injury/illness.
Warning
Read and understand the full Patient Information (PI) for information and warnings related to LONHALA. The PI is contained in the LONHALA box.
A. SAFETY PRECAUTIONS
These Instructions for Use contain information and safety precautions for MAGNAIRTM (MAGG-nair) Nebulizer System for use with LONHALATM (lon-HAL-luh) (glycopyrrolate) Inhalation Solution.
Warning
MAGNAIR is designed specifically for use only with LONHALA. To reduce the risk of severe or fatal injury/illness, Never use other medications in MAGNAIR. Read and follow all warnings and instructions in the Instructions for Use prior to using this device.
Save these Instructions for Use for future reference.
If for any reason you do not understand any part of these Instructions for Use, please contact the Sunovion Customer Service line 1-888-394-7377 before proceeding with your treatment.
Take special note of all safety precautions marked Danger and Warning.
IMPORTANT INFORMATION FOR USE
Read all Dangers and Warnings before using.
Dangers
To reduce the risk of serious or fatal injury from electrocution:
Do Not place or drop into water or other liquid. Do Not use while bathing.
Retrieve MAGNAIR only after it has been unplugged.
Warnings
Warnings
Technical electromagnetic compatibility data is available in tabular format upon request from PARI Pharma GmbH or on the Internet at https://www.pari.com/fileadmin/Electromagnetic-compatibility-4.pdf.
B. GETTING STARTED
Check to make sure you have all of the following MAGNAIR parts and become familiar with how to identify each piece. If any parts are missing, call the Sunovion Customer Service line (1-888-394-7377).
See Fig. B1.
Fig. B1 MAGNAIR Nebulizer System
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LONHALA vials packaged separately.
C. STEPS FOR USING BATTERIES OR AC ADAPTER WITH MAGNAIR
MAGNAIR is designed to be used with AA batteries or with the AC adapter.
STEPS FOR USING BATTERIES WITH MAGNAIR
Four (4) high quality AA batteries will provide approximately 2 weeks of treatment.
C1. Open the battery door on the Controller by placing your thumb on the black tab of the battery door and firmly pushing the tab to open the door. Note that the battery door is designed to have a tight fit. See Fig. C1.
Fig. C1 Open the battery door of the Controller.
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C2. Load the batteries.
Each battery chamber has a small figure that shows the proper position of each battery. Using the battery tips as guides and starting left-to-right, insert the batteries: tip out, tip in, tip out, tip in, See Fig. C2.
Fig. C2 Load the batteries.
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C3. Close the battery door.
To close the battery door, push it closed until you hear it Click into place. See Fig. C3.
NOTE: Rechargeable and disposable batteries vary considerably in terms of storage life and output. If used exclusively, batteries have an operating life of ~2 weeks, based on high quality disposable AA batteries that meet the specifications listed in Section H and following the cleaning procedure described in Section F.
To reduce the risk of battery leakage, it is recommended to remove the batteries if you plan to store the Controller for more than 30 consecutive days.
If you choose not to use the AC adapter, it is strongly recommended to have an extra set of batteries with you at all times.
Fig. C3 Close the battery door
of the Controller.
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STEPS FOR USING THE AC ADAPTER WITH MAGNAIR
The AC adapter will automatically adjust to the incoming voltage. The AC adapter will power MAGNAIR with and without installed batteries.
C4. Plug the AC adapter into the Controller.
To connect the AC adapter to the Controller, place the Controller on a flat, stable surface.
The inlet is located on the underside of the black battery door. Push the round end of the AC adapter cord into the inlet. Do Not try to insert the AC adapter into the blue colored part of the Controller. See Fig. C4-C5.
C5. Plug the AC adapter into the wall outlet.
NOTE: the AC adapter will not charge the batteries in the Controller. See Fig. C4-C5.
Fig. C4-C5 Plug the AC adapter into the inlet
on the black battery door of
the Controller. Then plug the
AC adapter into the wall outlet.
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D. ASSEMBLING YOUR MAGNAIR
Your Handset parts (Medication cap, Aerosol head, Handset body, and Mouthpiece) will be replaced when you receive your next supply of LONHALA. Discard your old Handset parts and use the new Handset parts every time you get a LONHALA MAGNAIR Refill Kit.
Warning
Clean the Handset before the first use and after every use. (See Section F.) Inspect all Handset parts to ensure they are clean and not damaged. Do Not leave the Aerosol head in the Handset body after use, and Do Not use dirty or damaged parts because this can impair the function of the Handset.
D1. Wash your hands.
D2. Open the top of the Handset body.
Lift the clasp on top of the Handset body slightly and flip it up to open. See Fig. D2.
Fig. D2 Open the Handset body.
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D3. Insert the Aerosol head into the Handset body as shown, taking care Not to touch the center of the Aerosol head. Hold the Aerosol head like you would hold a small frying pan so that the silver text side is facing up and the brown ring is facing down. Notice that the Aerosol head has a small tab on the side. Align the small tab with the matching notch in the Handset body. See Fig. D3.
Fig. D3 Insert the Aerosol head into the Handset body. Do not touch the center of the Aerosol head.
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D4. Close the Handset body, making sure the Aerosol head is properly inserted and the tab is aligned with the notch and level with the Handset body. You may hear a Click. If you do not close your Handset body completely or align the Aerosol head correctly, your medication may leak and you will not get your full treatment. See Fig. D4.
Do not force the top of the Handset body closed. If the top of the Handset body cannot close (no Click is heard), make sure that the Aerosol head is seated correctly and level.
Fig. D4 Close the Handset body.
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D5. Attach the Mouthpiece to the Handset body. Make sure the Blue valve is pressed down into the slot on the Mouthpiece and is positioned on the top of the Mouthpiece before attaching the Mouthpiece onto the Handset body. See Fig. D5.
Fig. D5 Attach the Mouthpiece.
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D6a. Connect the Controller to the Handset body using the Connection cord.
Fig. D6a. Connect the Connection cord te the Controller.
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D6b. Connect the Controller to the Handset body using the Connection cord as shown.
Fig. D6b Connect the other end of the Connection cord to the Handset body.
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E. USING LONHALA MAGNAIR
E1. With clean hands, open the foil pouch enough to remove the 2 LONHALA vials.
Manually separate by twisting apart the 2 LONHALA vials and return 1 vial back to the opened foil pouch and store in the Carrying bag to be used at the next treatment. Discard the vial if not used within 7 days. See Fig. E1.
Warning
MAGNAIR will only operate with vials containing LONHALA. Do not try to use any other type of medication with your MAGNAIR or use the vials in any other type of device.
Fig. E1 Remove the LONHALA vials and separate them.
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E2. Insert 1 LONHALA vial into the Medication cap.
The Medication cap has a top and a bottom. Insert a LONHALA vial with the flat tab first through the bottom of the Medication cap and press it in as far as it will go. You should hear a Click if the LONHALA vial was inserted correctly. See Fig. E2.
You should be able to hear a Click when the LONHALA vial is inserted correctly.
Fig. E2 Insert the LONHALA vial into
the bottom of the Medication
cap until it Clicks.
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E3. Prepare to attach the Medication cap. Do Not touch the part of the Handset body that pierces the LONHALA vial. See Fig E3a.
Make sure the Aerosol head is installed before attaching the Medication cap because your medicine could leak and you will not get your full treatment.
Place the Medication cap with the LONHALA vial on top of the Handset body. See Fig. E3b.
Turn the Medication cap in a clockwise direction. As you turn the Medication cap, the LONHALA vial will open and you should hear a Click. The notch (at the base of the opening) in the Medication cap should line up with the blue line on the Handset body. See Fig. E3c.
Fig. E3a Do not touch the part
that pierces the vial.
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Fig. E3b Place the Medication cap
with LONHALA vial
on top of the
Handset body.
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Fig. E3c Turn the Medication cap onto the
Handset body until you hear a Click.
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Warning
Do Not Loosen or remove the Medication cap or unclasp the Handset until treatment is completed because your medicine could leak and you will not get your full treatment.
E4. Insert the Mouthpiece into your mouth.
Fig. E4 Insert the Mouthpiece into your mouth. Do not tilt the Handset.
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E5. Turn on the Controller.
Fig. E5 Turn on the Controller.
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E6. Breathe in (inhale) and breathe out (exhale) normally through the Mouthpiece.
The Mouthpiece should remain in your mouth throughout the treatment period.
Do Not breathe through your nose.
While you are exhaling, you may see the blue flap lift and some mist escape. See Fig. E6.
Fig. E6 Inhale and exhale normally.
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E7. At the end of treatment, the Controller will automatically shut off.
When all of the medication has been delivered, you will hear 2 Beeps, the green LED light will turn off, and the Controller will automatically shut off.
Your treatment should take 2 to 3 minutes. See Fig. E7.
Fig. E7 Your treatment should take about 2 to 3 minutes.
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Warning
If you do not clean the Handset parts after every use, your treatment time might take more than 3 minutes. If the treatment is taking longer than 3 minutes, continue with your treatment until the Controller shuts off to make sure that you get your full treatment.
F. CLEANING THE HANDSET
Warning
To ensure proper operation and to reduce the risk of severe or fatal injury/illness.
Important: Rinse and clean the MAGNAIR Handset parts after every use. Use clear liquid dishwashing soap. Do Not use white dishwashing soap (e.g., Ivory or Dove) or antibacterial liquid dish soaps, as these may contain additives harmful to the Aerosol head. Do Not leave the Aerosol head in your Handset. Do Not wash the Controller, Connection cord, or AC adapter.
Caution
CLEANING THE HANDSET
F1. Disconnect the Handset from the Connection cord. See Fig. F1.
Fig. F1 Disconnect the Handset.
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F2. Turn the Medication cap in a counterclockwise direction as shown, to remove from the Handset body. See Fig. F2.
Fig. F2 Remove the Medication cap.
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F3. Remove the LONHALA vial.
Place the top of the Medication cap into the palm of your hand and push up as shown to remove the LONHALA vial.
Throw away the LONHALA vial into wastebasket. See Fig. F3.
Fig. F3 Remove the LONHALA vial.
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F4. Remove the Mouthpiece from the Handset body by giving it a gentle twist and pull to separate from the Handset body. See Fig. F4.
Fig. F4 Remove the Mouthpiece.
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F5. Loosen the blue valve. Carefully loosen the blue valve from the slot in the Mouthpiece. Make sure the valve is still attached on one side to the Mouthpiece. See Fig. F5.
Fig. F5 Loosen the blue valve.
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F6. Remove the Aerosol head from the Handset body by lifting the clasp on the side of the Handset. Then remove the Aerosol head by lifting the handle.
Do Not touch the center of the Aerosol head. See Fig. F6.
Set aside the Aerosol head to be cleaned separately in Step F10.
Fig. F6 Remove the Aerosol head from the Handset body. Do not touch the center of the Aerosol head.
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F7. Rinse each of the disassembled Handset parts well under warm (above 105°F) running tap water. (approx. 10 seconds). See Fig. F7.
Fig. F7 Rinse all Handset parts
with warm running water for
about 10 seconds.
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F8. Wash all Handset parts in warm (above 105°F), soapy water made by adding a few drops (~¼ teaspoon) of clear liquid dishwashing soap into a bowl (~1 quart) of clean warm tap water. Swish the Handset parts around in the soapy water to clean. See Fig. F8.
Fig. F8 Wash all Handset parts in warm soapy water for about 10 seconds.
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F9. Rinse the Handset parts well under running warm tap water (approximately 10 seconds). See Fig. F9.
Fig. F9 Rinse Handset parts well with warm running water for about 10 seconds.
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F10. Clean the Aerosol head following the instructions in Steps 7 through 10.
10A. Rinse both sides of the Aerosol head well with warm running water for about 10 seconds on each side.
10B. Wash the Aerosol head by holding the handle and swishing it back and forth in the warm soapy water for about 10 seconds.
10C. Rinse both sides of the Aerosol head well with warm running water for about 10 seconds on each side.
Rinsing the Aerosol head well helps prevent clogging and ensures proper operation.
Fig. 10A Rinse Aerosol head with warm running water for about 10 seconds.
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Fig. 10B Wash Aerosol head in warm soapy water for about 10 seconds.
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Fig. 10C Rinse Aerosol head with warm running water for about 10 seconds.
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F11. Inspect all Handset parts to make sure they are completely clean. If any Handset parts are still dirty, soak the parts in warm soapy water for 5 more minutes. Rinse well with warm running water until clean.
Warning
Contamination and moisture may affect the Aerosol head and encourage the growth of bacteria.
Therefore, it is important to remove the Aerosol head from the Handset body and clean the Handset parts after every use. If Handset parts are still dirty after cleaning, then soak and rinse as described in step F11.
F12. Air-dry all Handset parts.
Remove excess water by shaking all parts. Place all Handset parts on a dry, clean, lint-free towel and allow them to air-dry. Do Not dry using a paper towel.
Do Not touch the center of the Aerosol head. See Fig. F12.
Fig. F12 Air-dry all Handset parts.
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F13. Store disassembled Handset parts.
After the Handset parts are completely dry, place them in the provided Carrying bag or a dry, dust-free environment for storage.
Do Not put the Handset parts back together until ready to use again for your next treatment of LONHALA.
Warning
A damp environment encourages the growth of bacteria. Make sure all Handset parts are dried properly.
CARING FOR THE CONTROLLER, CONNECTION CORD AND AC ADAPTER
Warning
G. TROUBLESHOOTING
CONTROLLER FEEDBACK INDICATORS
| Controller AUDIBLE SIGNAL | Controller VISUAL SIGNAL | Conditions | Action Required | |
| 1 | 1 Brief Beep at start of dose. | Solid green LED for duration of dose. | Normal: generating aerosol mist, no errors detected. | No action required. MAGNAIR is on and working properly. |
| 2 | 1 Brief Beep at start of dose. | Flashing orange-green LED. | Low battery power. | Replace batteries or use AC adapter. |
| 3 | 1 Brief Beep at start of dose followed by a 2-tone Beep. | Green LED followed by flashing orange-green and then shuts off. | No connection detected. | Check connection between the Controller and the Handset. |
| Two Beeps occurred immediately after starting. | Check to confirm a LONHALA vial has been inserted and the Handset clasp is closed properly. | |||
| No drug detected. Two-tone Beep occurred 10-30 seconds after starting. | Tilt the Handset from side to side then tap the Handset to dislodge LONHALA and restart the Controller. | |||
| 4 | 1 Brief Beep. | LED starts green, then turns orange and shuts off. | Treatment interrupted. The Controller On/Off button has been intentionally or unintentionally pressed. | Press the Controller On/Off button to resume treatment. |
| 5 | 2 Brief Beeps. | LED flashes green for 2 seconds, and then shuts off. | Normal: end of dose. | No action required. LONHALA vial contents are empty. |
| 6 | 2-tone Beep. | LED flashes orange-green. | Maximum nebulization time reached (15 minutes). Aerosol head clogged. | Press On/Off to resume treatment if medication is still present. Clean the Aerosol head. |
POTENTIAL FAULTS AND POSSIBLE CAUSES / RESOLUTIONS
| Fault | Fault Possible Causes / Resolutions | ||
| 1 | MAGNAIR cannot be turned on – no green LED and no Beep. | No power | |
| The batteries are discharged. Replace them or use the AC adapter. | |||
| The batteries are not inserted correctly. Remove batteries and reinsert following diagram on the battery compartment. | |||
| The AC adapter is not connected correctly. Check the wall connection and the Controller connection. | |||
| 2 | The LED flashes orange-green, there is a 2-tone Beep and the Controller turns off. | No connection between Handset and Controller Check the connection between the Controller and the Handset. |
|
| 3 | No aerosol mist appears when MAGNAIR is first turned on, or MAGNAIR turns off after a few seconds. | Low power | |
| Check for bad batteries. | |||
| Missing or improper insertion/assembly of LONHALA vial Confirm that a new LONHALA vial has been inserted. |
|||
| Tap MAGNAIR slightly to move the liquid to the bottom of the LONHALA vial. If aerosol mist is still not generated after MAGNAIR has been restarted, the LONHALA vial may not have been pierced or is empty. Replace the vial if empty. | |||
| If partial dose has been received, contact your health care provider for instructions. | |||
| 4 | The indicator light (LED) flashes orange-green during operation. | Low battery power | |
| Replace the batteries or use the AC power. | |||
| 5 | Mist appears but the Controller turns off prematurely. | Low battery power | |
| Replace the batteries or use the AC power. | |||
| The Handset was not being held upright Hold the Handset upright and press the On/Off button. |
|||
| Insufficient medication | |||
| If partial dose has been received and/or medication spills, call your health care provider. | |||
| If Handset clasp is broken and/or does not close properly, call Sunovion Customer Service (1-888-394-7377). | |||
| 6 | MAGNAIR will not switch off automatically. | Turn MAGNAIR off by pressing the On/Off button. | |
| 7 | Aerosol mist continuously escapes in large volumes from the opening slots in the Medication cap. | Improper Handset assembly. Check that the Handset has been assembled correctly and the Blue valve flap is pushed down. | |
| 8 | The Medication cap will not close. | LONHALA vial is not seated properly. Press the LONHALA vial base toward the cap until you hear it snap into place.
|
|
| 9 | The LONHALA vial has been inserted incorrectly. | If the LONHALA vial has been inserted incorrectly, the following steps must be carried out: | |
|
|||
| 10 | Increasing or long inhalation time.1 Treatment time may vary up to 15 minutes if the Aerosol head has become clogged. | The Aerosol head may be clogged. Clean the Aerosol head by soaking it in soapy water for 5 minutes and rinse both sides well (Section F). | |
| 11 | Top of Handset body has become detached from bottom of Handset body. | Line up the hinge part on the top of the Handset body with the hinge portion of the bottom of the Handset body. Press firmly until the parts snap together. You should hear a Click.
|
|
| 1 If the fault cannot be eliminated after following these steps, call the Sunovion Customer Service line (1-888-394-7377) immediately. | |||
H. SPECIFICATIONS
ELECTRICAL
AC adapter
Input 100 V-240 V, 50 Hz/60 Hz
Output 7.5 V
Batteries
Disposable 4 x 1.5 V (high quality alkaline or photography-grade)
Rechargeable 4 x 1.2 V (Ni-Cd)
OPERATIONAL
Temperature 41° to 104°F (5° to 40°C)
Relative humidity (non-condensing) 15% to 93%
Air pressure 10 to 15 PSI (700 to 1060 hPa)
Aerosol output 0.85-1.15 mL
Aerosol output rate 0.4 mL/min
MECHANICAL
MAGNAIR Handset weight, without medication approx. 2.6 oz (73 g)
MAGNAIR Controller weight (with batteries) approx. 7.6 oz (220 g)
Nebulizer dimensions (W x H x D) 2.4 in. x 4.7 in. x 7.19 in. (6 x 12 x 18 cm)
Controller dimensions H 1.6 in. (4 cm), Ø 4.6 in. (11.6 cm)
TRANSPORT / STORAGE
Temperature -13° to 158° F (-25 to +70°C)
Relative humidity (non-condensing) 0 to 93%
Air pressure 7 to 15 PSI (500 to 1060 hPa)
HANDSET MATERIALS
Polypropylene, polyoxymethylene, polyamide, silicone, stainless steel, thermoplastic elastomers.
Does not contain any natural rubber (latex).
DISPOSAL
The MAGNAIR parts and batteries must be thrown away in accordance with local (state, county, or municipal) regulations.
PERFORMANCE CHARACTERISTICS
| LONHALA (glycopyrrolate) Inhalation Solution, 25 mcg/mL | Mean1 | 95% Confidence Range2 |
| Delivered dose by breath simulation (mcg) | 14.20 | 11.11–17.29 |
| Delivered dose by breath simulation (% Label Claim) | 56.80 | 44.45–69.16 |
| MMAD3 (μm) by NGI4 | 3.71 | 2.92–4.49 |
| Coarse Particles (Dia. >5 μm) by NGI (mcg) | 5.83 | 2.32–9.33 |
| Coarse Particles (Dia. >5 μm) by NGI in % of Delivered Dose | 27.72 | 11.20–44.24 |
| Fine Particles (Dia. ≤5 μm) by NGI (mcg) | 15.20 | 11.46–18.93 |
| Fine Particles (Dia. ≤5 μm) by NGI in % of Delivered Dose | 72.28 | 55.77–88.79 |
| Extra-Fine Particles (Dia. <1 μm) by NGI (mcg) | 0.11 | 0.03–0.20 |
| Extra-Fine Particles (Dia. <1 μm) by NGI in % of Delivered Dose | 0.55 | 0.15–0.94 |
| GSD5 by NGI | 1.66 | 1.49–1.83 |
| 1 n=15 devices from 3 device lots; 5 devices tested per drug product batch x 3 batches drug product 2 95% Confidence Range: Two-sided tolerance interval, Proportion of total population=0.95, Confidence (1- Alpha)=0.95 3 MMAD: Mass Median Aerodynamic Diameter 4 NGI: Next Generation Impactor 5 GSD: Geometric Standard Deviation |
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This Instructions for Use has been approved by the U.S. Food and Drug Administration.
