Drug Detail:Inbrija (Levodopa inhalation capsules [ lee-voe-doe-pa ])
Drug Class: Dopaminergic antiparkinsonism agents
Highlights of Prescribing Information
INBRIJA ® (levodopa inhalation powder), for oral inhalation use
Initial U.S. Approval: 1970
Indications and Usage for Inbrija
INBRIJA is an aromatic amino acid indicated for the intermittent treatment of OFF episodes in patients with Parkinson's disease treated with carbidopa/levodopa ( 1)
Inbrija Dosage and Administration
- For oral inhalation only. DO NOT swallow INBRIJA capsules. Only use INBRIJA capsules with the INBRIJA inhaler ( 2.1)
- Inhale the contents of two INBRIJA capsules (84 mg) as needed for OFF symptoms, up to 5 times daily ( 2.2)
- The maximum dose per OFF period is 84 mg, and the maximum recommended daily dosage of INBRIJA is 420 mg ( 2.2)
Dosage Forms and Strengths
Inhalation powder: INBRIJA capsules contain 42 mg levodopa for use with the INBRIJA inhaler ( 3)
Contraindications
INBRIJA is contraindicated in patients currently taking a nonselective monoamine oxidase (MAO) inhibitor or who have recently (within 2 weeks) taken a nonselective MAO inhibitor ( 4, 7.1)
Warnings and Precautions
- May cause falling asleep during activities of daily living ( 5.1)
- Avoid sudden discontinuation or rapid dose reduction to reduce the risk of withdrawal-emergent hyperpyrexia and confusion ( 5.2)
- Hallucinations/exacerbation of psychosis may occur. Patients with a major psychotic disorder should not be treated with INBRIJA ( 5.3, 7.2)
- Impulse Control Disorders: consider dose reduction or stopping INBRIJA ( 5.4)
- May cause or exacerbate dyskinesia: adjustment of levodopa therapy may be considered, including stopping INBRIJA ( 5.5)
- Not recommended in patients with asthma, COPD, or other chronic underlying lung disease ( 5.6)
Adverse Reactions/Side Effects
The most common adverse reactions (incidence ≥ 5% and higher than placebo) were cough, nausea, upper respiratory tract infection, and sputum discolored ( 6.1)
To report SUSPECTED ADVERSE REACTIONS, contact Acorda Therapeutics, Inc. at 1-800-367-5109 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Drug Interactions
- Monitor patients on MAO-B inhibitors for orthostatic hypotension ( 7.1)
- Dopamine D2 antagonists, isoniazid, and iron salts: May reduce the effectiveness of INBRIJA ( 7.2, 7.3)
Use In Specific Populations
Pregnancy: Based on animal data, may cause fetal harm ( 8.1)
See 17 for PATIENT COUNSELING INFORMATION and FDA-approved patient labeling.
Revised: 8/2020
Full Prescribing Information
1. Indications and Usage for Inbrija
INBRIJA is indicated for the intermittent treatment of OFF episodes in patients with Parkinson's disease treated with carbidopa/levodopa.
2. Inbrija Dosage and Administration
INBRIJA capsules are for oral inhalation only and should be used only with the INBRIJA inhaler.
2.1 Important Administration Instructions
INBRIJA capsules are for oral inhalation only and should be used only with the INBRIJA inhaler. INBRIJA capsules must not be swallowed as the intended effect will not be obtained. INBRIJA capsules should be stored in their blister package and only removed immediately before use [see How Supplied/Storage and Handling (16.2)] .
2.2 Recommended Dosage
INBRIJA should be taken when symptoms of an OFF period start to return.
The recommended dosage of INBRIJA is oral inhalation of the contents of two 42 mg capsules (84 mg) as needed, up to 5 times a day. The maximum dose per OFF period is 84 mg, and the maximum daily dosage is 420 mg. INBRIJA has been shown to be effective only in combination with carbidopa/levodopa [see Indications and Usage (1)].
3. Dosage Forms and Strengths
INBRIJA (levodopa inhalation powder) consists of INBRIJA capsules and the INBRIJA inhaler. INBRIJA capsules contain 42 mg dry powder formulation of levodopa in a white capsule with two black color bands, and "A42" printed on one side.
4. Contraindications
INBRIJA is contraindicated in patients currently taking a nonselective monoamine oxidase (MAO) inhibitor (e.g., phenelzine and tranylcypromine) or who have recently (within 2 weeks) taken a nonselective MAO inhibitor. Hypertension can occur if these drugs are used concurrently [see Drug Interactions (7.1)].
5. Warnings and Precautions
5.1 Falling Asleep During Activities of Daily Living and Somnolence
Patients treated with levodopa, the active ingredient in INBRIJA, have reported falling asleep while engaged in activities of daily living, including the operation of motor vehicles, which sometimes resulted in accidents. Although many of these patients reported somnolence, some reported no warning signs (sleep attack) and believed that they were alert immediately prior to the event. Some of these events have been reported more than 1 year after the initiation of treatment.
Prescribers should reassess patients for drowsiness or sleepiness. Prescribers should also be aware that patients may not acknowledge drowsiness or sleepiness until directly questioned about drowsiness or sleepiness during specific activities.
Before initiating treatment with INBRIJA, advise patients about the potential to develop drowsiness and ask about factors that may increase the risk for somnolence with INBRIJA such as the concomitant use of sedating medications and the presence of sleep disorders. Consider discontinuing INBRIJA in patients who report significant daytime sleepiness or episodes of falling asleep during activities that require active participation (e.g., conversations, eating, etc.).
If treatment with INBRIJA continues, patients should be advised not to drive and to avoid other activities that might result in harm if the patients become somnolent. There is insufficient information to establish that dose reduction will eliminate episodes of falling asleep while engaged in activities of daily living.
5.2 Withdrawal-Emergent Hyperpyrexia and Confusion
A symptom complex that resembles neuroleptic malignant syndrome (characterized by elevated temperature, muscular rigidity, altered consciousness, and autonomic instability), with no other obvious etiology, has been reported in association with rapid dose reduction, withdrawal of, or changes in dopaminergic therapy.
5.3 Hallucinations/Psychosis
In placebo-controlled trials [see Clinical Studies (14)], hallucinations were reported in less than 2% of patients treated with INBRIJA. Hallucinations may be responsive to reducing levodopa therapy. Hallucinations may be accompanied by confusion, insomnia, and excessive dreaming. Abnormal thinking and behavior may present with one or more symptoms, including paranoid ideation, delusions, hallucinations, confusion, psychotic-like behavior, disorientation, aggressive behavior, agitation, and delirium.
Because of the risk of exacerbating psychosis, patients with a major psychotic disorder should ordinarily not be treated with INBRIJA. In addition, medications that antagonize the effects of dopamine used to treat psychosis may exacerbate the symptoms of Parkinson's disease and may decrease the effectiveness of INBRIJA [see Drug Interactions (7.2)].
5.4 Impulse Control/Compulsive Behaviors
Patients treated with INBRIJA can experience intense urges to gamble, increased sexual urges, intense urges to spend money, binge eating, and/or other intense urges, and the inability to control these urges while taking one or more of the medications that increase central dopaminergic tone. In some cases, although not all, these urges were reported to have stopped when the dose was reduced or the medication was discontinued.
Because patients may not recognize these behaviors as abnormal, it is important for prescribers to specifically ask patients or their caregivers about the development of new or increased gambling urges, sexual urges, uncontrolled spending or other urges while being treated with INBRIJA. Consider stopping the medication if a patient develops such urges while taking INBRIJA.
5.5 Dyskinesia
INBRIJA may cause or exacerbate dyskinesias. If troublesome dyskinesias occur, prescribers may need to consider stopping treatment with INBRIJA and/or adjusting the patient's daily medications for the treatment of Parkinson's disease. In Study 1, 4% of patients treated with INBRIJA 84 mg reported dyskinesia, compared with 1% for patients on placebo [see Adverse Reactions (6.1)] .
5.6 Bronchospasm in Patients with Lung Disease
Because of the risk of bronchospasm, use of INBRIJA in patients with asthma, COPD, or other chronic underlying lung disease is not recommended.
In a double-blind, placebo-controlled, crossover clinical study, 25 otherwise healthy subjects with mild or moderate asthma on a stable regimen of asthma medication received placebo or INBRIJA 84 mg every 4 hours for a total of three doses. Cough was the most frequent adverse reaction, reported by 60% of subjects following administration of INBRIJA and 0% following administration of placebo. Following administration of INBRIJA, 10 subjects (40%) had temporary reductions from baseline (between 15% and 59%) for FEV 1; 4 of these subjects also had a reduction in FEV 1 following administration of placebo. Subjects with a reduction in FEV 1 remained asymptomatic and did not require rescue treatment.
5.7 Glaucoma
INBRIJA may cause increased intraocular pressure in patients with glaucoma. Monitor patients for increased intraocular pressure during therapy with INBRIJA.
5.8 Laboratory Test Abnormalities
Abnormalities in laboratory tests may include elevations of liver function tests such as alkaline phosphatase, AST, ALT, lactic dehydrogenase (LDH), and bilirubin. Abnormalities in blood urea nitrogen (BUN), hemolytic anemia and positive direct antibody test have also been reported.
Patients taking levodopa or carbidopa-levodopa may have increased levels of catecholamines and their metabolites in plasma and urine giving false positive results suggesting the diagnosis of pheochromocytoma in patients on levodopa and carbidopa-levodopa.
6. Adverse Reactions/Side Effects
The following serious adverse reactions are discussed below and elsewhere in the labeling:
- Falling Asleep During Activities of Daily Living and Somnolence [see Warnings and Precautions (5.1)]
- Withdrawal-Emergent Hyperpyrexia and Confusion [see Warnings and Precautions (5.2)]
- Hallucinations/Psychosis [see Warnings and Precautions (5.3)]
- Impulse Control/Compulsive Behaviors [see Warnings and Precautions (5.4)]
- Dyskinesia [see Warnings and Precautions (5.5)]
- Bronchospasm in Patients with Lung Disease [see Warnings and Precautions (5.6)]
- Glaucoma [see Warnings and Precautions (5.7)]
6.1 Clinical Trials Experience
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 clinical practice.
Adverse Reactions in Study 1
Table 1 lists the adverse reactions that occurred in at least 2% of patients with Parkinson's disease who were treated with INBRIJA 84 mg and higher than placebo for OFF periods in Study 1 [see Clinical Studies (14)]. Study 1 was a double-blind, placebo-controlled study, in which 114 patients received INBRIJA 84 mg (two 42 mg capsules) for an average of 2 doses per day, to a maximum of 5 times a day, and 112 patients received placebo. INBRIJA-treated patients were 45-82 years of age (mean 63.5 years of age) and were predominantly male (72%) and white (94%). All patients were also treated with oral carbidopa/levodopa. The most common adverse reactions (≥ 5% and higher than placebo) in Study 1 were cough, nausea, upper respiratory tract infection, and sputum discolored.
| Adverse Reactions | INBRIJA 84 mg
N=114 % | Placebo
N=112 % |
|---|---|---|
| Respiratory, thoracic and mediastinal disorders | ||
| Cough | 15 | 2 |
| Sputum discolored | 5 | 0 |
| Nasal discharge discoloration | 2 | 0 |
| Oropharyngeal pain | 2 | 0 |
| Gastrointestinal disorders | ||
| Nausea | 5 | 3 |
| Vomiting | 3 | 0 |
| Infections and infestations | ||
| Upper respiratory tract infection | 6 | 3 |
| Nasopharyngitis | 3 | 2 |
| Bronchitis/pneumonia | 2 | 0 |
| Nervous system disorders | ||
| Dyskinesia | 4 | 1 |
| Headache | 2 | 0 |
| Injury, poisoning and procedural complications | ||
| Fall | 3 | 2 |
| Laceration | 2 | 0 |
| Skin abrasion | 2 | 0 |
| General disorders and administration site conditions | ||
| Chest discomfort | 2 | 0 |
| Investigations | ||
| Blood bilirubin increased | 2 | 0 |
| Red blood cell count decreased | 2 | 0 |
| Musculoskeletal and connective tissue disorders | ||
| Pain in extremity | 2 | 1 |
| Psychiatric disorders | ||
| Insomnia | 2 | 1 |
| Vascular disorders | ||
| Orthostatic hypotension/blood pressure decreased | 2 | 0 |
6.2 Postmarketing Experience
The following adverse reaction has been identified during post approval use of INBRIJA. Because adverse reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure: sensation of choking immediately following administration.
7. Drug Interactions
7.1 Monoamine Oxidase (MAO) Inhibitors
The use of nonselective MAO inhibitors with INBRIJA is contraindicated [see Contraindications (4)] . Discontinue use of any nonselective MAO inhibitors at least two weeks prior to initiating INBRIJA.
The use of selective MAO-B inhibitors with INBRIJA may be associated with orthostatic hypotension. Monitor patients who are taking these drugs concurrently.
8. Use In Specific Populations
8.5 Geriatric Use
Of the Parkinson's disease patients in Study 1 who took INBRIJA 84 mg, 49% (n=56) were 65 years of age and older and 51% (n=58) were under 65 years of age. Of these patients, the following age-related differences in adverse reactions were reported in patients 65 years of age and older vs. in patients under 65 years of age, respectively: cough 25% vs. 5%; upper respiratory tract infection 11% vs. 2%; nausea 7% vs. 3%; vomiting 4% vs. 2%; pain in the extremities 4% vs. 0%; and discolored nasal discharge 4% vs. 0%.
10. Overdosage
Based on the limited available information, the acute symptoms of carbidopa/levodopa overdosage can be expected to arise from dopaminergic overstimulation. Using more than one dose (84 mg) to treat the same OFF period may result in CNS disturbances, with an increasing risk for cardiovascular disturbance (e.g., hypotension, tachycardia) and increased risk for new or worsening psychiatric problems at higher doses.
Reports of rhabdomyolysis and transient renal insufficiency suggest that levodopa overdosage may give rise to systemic complications.
Monitor patients and provide supportive care. Patients should receive electrocardiographic monitoring for the development of arrhythmias; if needed, appropriate antiarrhythmic therapy should be given. The possibility that the patient may have taken other drugs, increasing the risk of drug interactions (especially catechol-structured drugs) should be taken into consideration.
11. Inbrija Description
INBRIJA consists of a dry powder formulation of levodopa for oral inhalation with the INBRIJA inhaler. The inhalation powder is packaged in white hypromellose capsules.
Each capsule contains a spray-dried powder of 42 mg levodopa active ingredient with 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and sodium chloride.
The active component of INBRIJA is levodopa, an aromatic amino acid. Its chemical name is (2S)-2-amino-3-(3,4-dihydroxyphenyl) propanoic acid and its structural formula is:
Levodopa has a molecular weight of 197.19 g/mol and molecular formula C 9H 11NO 4. Levodopa is a white to slightly off-white powder and is readily soluble in formic acid, slightly soluble in water, and practically insoluble in ethanol and diethyl ether; it dissolves in dilute hydrochloric acid.
The INBRIJA inhaler is a plastic device with a blue body, blue cap, and white mouthpiece used for inhaling INBRIJA powder.
The INBRIJA inhaler is breath-actuated by the patient. Under standardized in vitro testing conditions, the INBRIJA inhaler delivered 36.1 mg of levodopa (emitted dose) for the 42 mg capsule from the mouthpiece. No significant difference in emitted dose was observed when varying the flow rate and volume from 20 liters per minute/1L up to 90 liters per minute/2L. Peak inspiratory flow rates (PIFR) achievable through the INBRIJA inhaler were evaluated in 24 adult patients with mild to moderate Parkinson's disease. The mean PIFR was 64 L/min (range 39–98 L/min) for patients in the ON state and 57 L/min (range 29–98 L/min) in the OFF state.
12. Inbrija - Clinical Pharmacology
12.1 Mechanism of Action
Levodopa, the metabolic precursor of dopamine, crosses the blood-brain barrier and presumably is converted to dopamine in the brain. This is thought to be the mechanism whereby levodopa relieves symptoms of Parkinson's disease.
12.3 Pharmacokinetics
In the presence of carbidopa, the pharmacokinetics of levodopa are dose-proportional in healthy subjects taking up to 84 mg of INBRIJA. In the presence of carbidopa, the terminal elimination half-life (t 1/2) of levodopa following a single administration of INBRIJA 84 mg was 2.3 hours.
14. Clinical Studies
The efficacy and safety of INBRIJA for the treatment of OFF episodes in patients with Parkinson's disease treated with oral carbidopa/levodopa was evaluated in a 12-week, randomized, placebo-controlled, double-blind study (Study 1; NCT02240030).
Study 1:
In Study 1, a total of 114 patients were treated with INBRIJA 84 mg (two 42 mg capsules), and 112 patients received placebo. Study medication could be administered up to five times a day. At baseline, patients had at least 2 hours of OFF time per day, and carbidopa/levodopa medication did not exceed 1600 mg levodopa per day. The mean UPDRS Part III scores at screening in the ON state were 14.9 for patients randomized to INBRIJA 84 mg and 16.1 for patients randomized to placebo. The UPDRS part III is designed to assess the severity of the cardinal motor findings (e.g., tremor, rigidity, bradykinesia, postural instability) in patients with Parkinson's disease.
The primary endpoint was the change in Unified Parkinson's Disease Rating Scale (UPDRS) Part III motor score from pre-dose OFF state to 30 minutes post-dose, measured at Week 12. The average use of INBRIJA 84 mg or placebo was approximately 2 doses per day. At Week 12, the reduction in UPDRS Part III motor score for INBRIJA 84 mg, compared to placebo at 30 minutes post-dose, were -9.8 and -5.9, respectively (See Table 2 and Figure 1). The proportion of patients who returned to an ON state and sustained that ON through 60 minutes post-dose was 58% for INBRIJA 84 mg and 36% for placebo (p=0.003).
| Treatment | Pre-dose (OFF) UPDRS Part III Motor Score
(mean) | Post-dose UPDRS Part III Motor Score
(mean) | Mean Change 30 minutes post-dose †,‡ | Difference from Placebo
(95% confidence interval) | p-value |
|---|---|---|---|---|---|
|
|||||
| Placebo | 32.1 | 25.3 | -5.9 | — | — |
| INBRIJA 84 mg | 29.0 | 19.3 | -9.8 | -3.92
(-6.84, -1.00) | 0.009 |
16. How is Inbrija supplied
16.1 How Supplied
INBRIJA 42 mg contains foil blister strips of INBRIJA (levodopa inhalation powder) white capsules with two black bands on the body and "A42" in black on the cap, and one INBRIJA inhaler.
- Carton containing 4 INBRIJA capsules (1 blister card containing 4 capsules) and 1 INBRIJA inhaler: NDC 10144-342-04
- Carton containing 12 INBRIJA capsules (3 blister cards containing 4 capsules each) and 1 INBRIJA inhaler: NDC 10144-342-12
- Carton containing 60 INBRIJA capsules (15 blister cards containing 4 capsules each) and 1 INBRIJA inhaler: NDC 10144-342-60
- Carton containing 92 INBRIJA capsules (23 blister cards containing 4 capsules each) and 1 INBRIJA inhaler: NDC 10144-342-92
INBRIJA inhaler consists of a blue cap, blue handle with "INBRIJA" imprinted on it, and white mouthpiece covering the capsule chamber.
16.2 Storage and Handling
Store in a dry place between 20°C to 25°C (68°F to 77°F), excursions permitted to 15°C to 30°C (59°F to 86°F).
INBRIJA capsules should always be stored in the blister packaging and only removed immediately before use. INBRIJA capsules should not be stored inside the INBRIJA inhaler.
INBRIJA capsules should be used only with the INBRIJA inhaler.
The INBRIJA inhaler should not be used to administer any other medicines.
17. Patient Counseling Information
Advise the patient to read the FDA-approved patient labeling (Patient Information and Instructions for Use).
| This Patient Information has been approved by the U.S. Food and Drug Administration | Issued: 12/2022 | ||
| PATIENT INFORMATION
INBRIJA ® (in-BRIH-jah) (levodopa inhalation powder) for oral inhalation use |
|||
| What is INBRIJA?
INBRIJA is an inhaled prescription levodopa medicine used to treat the return of Parkinson's symptoms (known as OFF episodes) in people with Parkinson's disease who are treated with carbidopa-levodopa medicines. It does not replace the regular carbidopa-levodopa medicines. It is not known if INBRIJA is safe or effective in children. |
|||
Do not use INBRIJA if you:
|
|||
Before you use INBRIJA, tell your healthcare provider about all of your medical conditions, including if you:
Using INBRIJA and certain other medicines may affect each other and cause serious side effects. Especially tell your healthcare provider if you take:
Know the medicines you take. Keep a list of them to show your healthcare provider and pharmacist each time you get a new medicine. |
|||
How should I use INBRIJA?
|
|||
What should I avoid while using INBRIJA?
|
|||
| What are the possible side effects of INBRIJA?
INBRIJA can cause serious side effects including:
|
|||
|
|
||
|
|||
|
|
||
| Get up slowly after sitting or lying down, especially if you have been sitting or lying down for a long time. Tell your healthcare provider if you have any of these symptoms. | |||
|
|||
How should I store INBRIJA?
|
|||
| General information about the safe and effective use of INBRIJA
Medicines are sometimes prescribed for purposes other than those listed in the Patient Information leaflet. Do not use INBRIJA for a condition for which it was not prescribed. Do not give INBRIJA 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 INBRIJA that is written for health professionals. |
|||
| What are the ingredients in INBRIJA?
Active ingredient: levodopa Inactive ingredients: 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), sodium chloride. For more information, go to www.INBRIJA.com, or call 1-800-367-5109. |
|||
INSTRUCTIONS FOR USE
INBRIJA
® (in-BRIH-jah)
(levodopa inhalation powder)
For Oral Inhalation Only
Read and follow these instructions before you start using INBRIJA and each time you get a refill. There may be new information. This leaflet does not take the place of talking to your healthcare provider about your medical condition or treatment.
Important Information about using INBRIJA
|
Overview:
A complete dose is 2 capsules.
You will load 1 capsule into the inhaler and breathe in (inhale). Then, you will remove the used capsule and load a second capsule into the inhaler and breathe in. Do not swallow INBRIJA capsules.
- Each carton contains 1 INBRIJA inhaler and capsules in sealed foil packages. When you open a new carton, always use the new inhaler supplied.
- Do not use capsules after the expiration date printed on the package.
- Do not load 2 capsules at the same time.
- Throw out all used capsules immediately after use.
- Throw out the inhaler after all capsules in the carton have been used.
- Make sure your hands are clean and dry when using the inhaler and capsules.
If you have any questions, ask your healthcare provider or pharmacist. If you have problems using INBRIJA, or if your INBRIJA inhaler becomes lost or damaged and you need a replacement, contact INBRIJA support at 1-800-367-5109. Then, call your healthcare provider for treatment instructions until you receive your replacement inhaler.
| Parts of your INBRIJA Inhaler
(see Figure A)
|
||
| Capsules | ||
| (see
Figure B)
Each carton includes strips of 4 capsules. |
|
|
| (see
Figure C)
Prepare and take a total of 2 capsules. Take each capsule 1 at a time for a full dose. |
|
|
| (see
Figure D)
Full Dose = 2 Capsules |
|
|
| Prepare Your Dose
Step 1. Gather Supplies Find a clean and dry surface. Make sure your hands are clean and dry. Get inhaler and strip of capsules. Tear off package of 2 capsules (see Figure E). |
|
|
| Step 2. Check Expiration
Check the expiration date on the package (see Figure F). |
|
|
| Step 3. Remove Blue Cap
Pull the cap straight off (see Figure G). Place the cap to the side. You will need it later to store the inhaler. |
|
|
| Step 4. Twist Off White Mouthpiece
Twist and pull off the mouthpiece to separate it from the handle (see Figure H). Place the mouthpiece and inhaler on a clean and dry surface. |
|
|
| Step 5. Remove 1 Capsule From Package
Carefully peel back the foil and take out 1 capsule (see Figure I). Do not try to push the capsule through the back of the foil package. Only remove 1 capsule at a time, and just before use. Do not use any capsule that looks crushed, damaged or wet. Throw it away and get a new capsule. |
|
|
| Step 6. Load Capsule
Hold the inhaler upright using the handle. Drop 1 capsule into the opening of the capsule chamber (see Figure J). Do not try to load 2 capsules at the same time. |
|
|
| Step 7. Attach White Mouthpiece
Line up the white arrows on the handle and mouthpiece (see Figure K). |
|
|
| Firmly push the mouthpiece and handle together until you hear a click. This punctures the capsule (see Figure L). |
|
|
| Release the mouthpiece. The mouthpiece will spring back and stay attached (see
Figure M).
Your inhaler is now ready to use. Do not push the handle and mouthpiece together more than 1 time. This may damage the capsule, and you may not get your full dose. If this happens throw the capsule away in your household trash and start over at Step 5. Make sure the mouthpiece is securely attached and will not fall off before moving to step 8. |
|
|
| Take Your Dose | ||
| Step 8. Breathe Out (Exhale)
Stand or sit with your head and chest upright. Hold the inhaler level and away from your mouth (see Figure N). Breathe out completely (see Figure N). Do not breathe into mouthpiece. |
|
|
| Step 9. Breathe In Deeply (Inhale)
While keeping the inhaler level, close your lips firmly around the mouthpiece (see Figure O). Take in a deep, comfortable breath until your lungs feel full. This normally takes several seconds. As you breathe in, you will hear and feel the capsule "whirl" (spin). The whirl means the inhaler is working and you are getting your medicine. If you cough or stop your dose, start again from the beginning of Step 8 using the same capsule. |
|
|
| Important: If you did not hear or feel the capsule "whirl" while inhaling you may need to take a deeper, longer breath or may need to clean the mouthpiece. Refer to Step 14 – Clean Mouthpiece. Start again from the beginning of Step 8 using the same capsule. | ||
| Step 10. Hold Breath, Then Breathe Out
Take the inhaler out of your mouth and hold your breath for 5 seconds (see Figure P). Then breathe out. |
|
|
| Step 11. Remove Capsule From Inhaler
Twist and pull off the mouthpiece (see Figure Q) and take out the used capsule (see Figure R). |
|
|
| Step 12. Dose With 2
nd Capsule
Repeat Steps 5 to 11 with the second capsule to finish the full dose (see Figure S). |
|
|
| Dispose and Store | ||
| Step 13. Throw Out Used Capsules Throw out used capsules in the household trash (see Figure T). |
|
|
| Step 14. Clean Mouthpiece
It is normal for some powder to remain in or on the inhaler. To avoid powder buildup, clean the powder off of the mouthpiece holes using a circular motion with a new dry cotton swab as needed. First, clean the holes from the top end of the mouthpiece (see Figure U). Next, clean the holes from the bottom end of the mouthpiece (see Figure V). You can also use a dry tissue to wipe the outside of the mouthpiece, as needed. Do not clean any other parts of the inhaler. Do not rinse the mouthpiece or get the inhaler wet. |
|
|
| Step 15. Store Inhaler
Make sure there are no capsules in the inhaler before you store it. Attach the mouthpiece to the handle by pushing until you hear a click (see Figure W). |
|
|
| Attach the cap over the mouthpiece (see
Figure X).
Your inhaler is now ready to store (see Figure Y). | ||
INBRIJA Storage, Cleaning and Disposal
Storing the Inhaler and Capsules
- Store the inhaler and capsules in a dry place at room temperature from 68°F to 77°F (20 to 25°C).
- Keep capsules inside their foil (blister) packages until just before you are ready to use them.
- Do not store capsules in the inhaler for a future dose.
- Keep the inhaler and capsules dry.
- Throw out the inhaler after all capsules in the carton have been used. Use the new inhaler that comes with your prescription refill.
- Keep INBRIJA and all medicines out of reach of children.
Cleaning the Inhaler
- It is normal for some powder to remain in or on the inhaler.
- If needed, to avoid powder buildup, you may use a dry cotton swab or a dry tissue to wipe the inside or outside of the mouthpiece.
Disposing of the Inhaler and Capsules
- Throw out all used capsules in your household trash.
- After all capsules in the carton have been used, throw out the inhaler and use a new carton containing a new inhaler and capsules.
This Instructions for Use has been approved by the U.S. Food and Drug Administration Rev: 08/2020
Marketed by:
Acorda Therapeutics, Inc.
Pearl River, NY 10965 USA
Inbrija ® is a trademark of Acorda Therapeutics, Inc. ©2022 Acorda Therapeutics, Inc. All rights reserved.
U.S. Patent Nos. 7182961, 8404276, 8545878, 8586093, 8685442, 8945612, 9155699, 9393210 and RE43711
2212342MFPI-0
PRINCIPAL DISPLAY PANEL - 42 mg Capsule Blister Pack Carton
NDC 10144-342-60
Rx ONLY
Inbrija®
(levodopa inhalation powder)
For Oral Inhalation Only
42 mg
capsules
CONTENTS:
60 capsules (15 blister
strips of 4 capsules each)
1 inhaler
Prescribing Information
Patient Information
Instructions for Use
Do not swallow
Inbrija® capsules
Inbrija® capsules are
for use with Inbrija®
inhaler only.
| INBRIJA
levodopa capsule |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Labeler - Acorda Therapeutics, Inc. (963845136) |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| Avista Pharma Solutions, Inc. | 079509111 | analysis(10144-342) | |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| Boston Analytical, Inc. | 080408849 | analysis(10144-342) | |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| Catalent Massachusetts LLC | 117922533 | manufacture(10144-342) | |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| Sharp Corporation | 143696495 | label(10144-342) , pack(10144-342) | |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| Ajinomoto Company, Inc. | 695028225 | api manufacture(10144-342) | |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| PPD Development Ireland Ltd. | 985036175 | analysis(10144-342) | |
