Dornase Alfa (Oral Inhalation) (Monograph)
Brand name: Pulmozyme
Drug class: Mucolytic Agents
Introduction
Mucolytic agent; biosynthetic (recombinant DNA origin) form of human deoxyribonuclease I (DNase I).
Uses for Dornase Alfa (Oral Inhalation)
Cystic Fibrosis
Adjunctive therapy in pediatric and adult patients with cystic fibrosis to improve pulmonary function.
Reduces the frequency of respiratory infections requiring parenteral anti-infective therapy in patients with forced vital capacity (FVC) ≥40%.
Designated an orphan drug by FDA for this use.
Guidelines recommend the use of dornase alfa for patients with asymptomatic, mild, moderate, or severe cystic fibrosis to improve lung function and reduce exacerbations.
Parapneumonic Effusions and Empyema
Although safety and efficacy not established, limited data suggest dornase alfa may be used intrapleurally in conjunction with alteplase for complicated parapneumonic effusions and empyema† [off-label].
Chronic Rhinosinusitis Secondary to Cystic Fibrosis
Although safety and efficacy not established, limited data suggest dornase alfa may be used for the treatment of chronic rhinosinusitis secondary to cystic fibrosis in pediatric patients† [off-label] .
Dornase Alfa (Oral Inhalation) Dosage and Administration
General
Other General Considerations
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Only administer dornase alfa with specific jet nebulizers and vibrating mesh nebulizers listed in the manufacturer’s product labeling. Data are not available to support the administration of dornase alfa with other nebulizer systems.
Administration
Oral Inhalation
Administer by oral inhalation via a jet nebulizer or vibrating mesh nebulizer.
The Table lists recommended jet nebulizers and compressor systems for use with dornase alfa. Manufacturer states recommended vibrating mesh nebulizers for use with dornase alfa include the eRapid™ Nebulizer System, consisting of the eRapid™ Nebulizer Handset with eBase™ Controller, Innospire Go, Pulmogine Vibrating Mesh Nebulizer, AireHealth Nebulizer, and Intelligent Mesh Nebulizer.
Jet Nebulizer |
Compressor |
---|---|
Hudson T Up-draft II |
Pulmo-Aide or legally marketed compressor of identical pressure and flow rate |
Marquest Acorn II |
Pulmo-Aide or legally marketed compressor of identical pressure and flow rate |
PARI LC Plus |
PARI PRONEBor legally marketed compressor of identical pressure and flow rate |
PARI BABY |
PARI PRONEB or legally marketed compressor of identical pressure and flow rate |
Durable Sidestream |
Porta-Neb ,MOBILAIRE, or legally marketed compressor of identical pressure and flow rate |
Do not dilute or mix the oral inhalation solution with any other drugs in the nebulizer.
Consult Instructions for Use provided by the manufacturer for detailed information on proper administration and maintenance techniques via various nebulization systems.
Oral inhalation solution contains no preservatives; once the single-use ampule is opened, use the entire contents or discard the remainder.
Dosage
Each single-use ampule delivers 2.5 mg of dornase alfa (2.5 mL of undiluted solution).
Pediatric Patients
Cystic Fibrosis
Oral Inhalation
2.5 mg once daily. Some patients may benefit from twice daily administration.
Adults
Cystic Fibrosis
Oral Inhalation
2.5 mg once daily. Some patients may benefit from twice daily administration.
Special Populations
Hepatic Impairment
No specific dosage recommendations at this time.
Renal Impairment
No specific dosage recommendations at this time.
Geriatric Use
No specific dosage recommendations at this time.
Cautions for Dornase Alfa (Oral Inhalation)
Contraindications
-
Known hypersensitivity to dornase alfa, Chinese hamster ovary cell products, or any ingredient in the formulation.
Warnings/Precautions
Specific Populations
Pregnancy
No adequate and well-controlled studies in pregnant women. Animal reproductive data have shown no evidence of fetal harm at doses up to 600 times the maximum recommended human dose.
Lactation
Not known whether dornase alfa distributed into human milk. Consider developmental and health benefits of breastfeeding along with mother’s clinical need for the drug and the potential for adverse effects to the breast-fed child.
Pediatric Use
Safety and efficacy established in pediatric patients. Use of dornase alfa in pediatric patients 5–17 years of age supported by evidence from a clinical trial. Use of dornase alfa in pediatric patients <5 years of age supported by extrapolated efficacy data from pediatric patients ≥5 years of age and additional safety data.
Geriatric Use
Clinical studies did not include sufficient numbers of patients ≥65 years of age.
Hepatic Impairment
Not evaluated in hepatic impairment.
Renal Impairment
Not evaluated in renal impairment.
Common Adverse Effects
Adverse effects (≥3%): voice alteration, pharyngitis, rash, laryngitis, chest pain, conjunctivitis, rhinitis, decrease in FVC ≥10%, fever, dyspnea.
Drug Interactions
Manufacturer states no clinically significant drug-drug interactions.
Dornase Alfa (Oral Inhalation) Pharmacokinetics
Absorption
Bioavailability
Following oral inhalation, serum DNase concentrations were not increased above normal endogenous levels.
Onset
After oral inhalation, sputum concentrations measurable within 15 minutes.
Distribution
Extent
Not known whether distributed into human milk.
Elimination
Metabolism
Expected to undergo metabolism via proteases in biological fluids.
Half-life
3-4 hours after IV administration.
Stability
Storage
Oral Inhalation
Solution for nebulization
Store in protective foil at 2-8ºC; keep refrigerated during transport, and do not expose to room temperature for ≥60 hours total.
Actions
-
Selectively cleaves extracellular DNA (e.g., in purulent pulmonary secretions); does not appear to affect sputum in the absence of an inflammatory response to infection (i.e., in those with nonpurulent sputum) nor does it affect pulmonary function in healthy individuals.
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Reduces sputum viscosity and viscoelasticity.
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Mechanism of action not fully elucidated; appears to improve the transportability of purulent mucus via ciliary activity and cough.
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Reduces airflow obstruction, improves pulmonary function (increased FVC and forced expiratory volume at 1 second [FEV1]), and improves mucociliary clearance in patients with cystic fibrosis.
Advice to Patients
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Advise patients and caregivers on the proper storage of dornase alfa; must be stored in the refrigerator and protected from heat and light. Refrigerate dornase alfa during transport, and do not allow it to be exposed to room temperature for more than 60 hours total.
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Instruct patients and caregivers to squeeze ampules prior to each use to check for leaks, and to discard the ampule if the solution appears cloudy or discolored. Once the ampule is opened, the contents must be used immediately or discarded.
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Inform patients and caregivers that dornase alfa must not be diluted or mixed with other drugs in the nebulizer.
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Advise patients and caregivers to read and follow the manufacturer's instruction manual for the proper use and maintenance of the jet nebulizer/compressor system, or the vibrating mesh nebulizer used in dornase alfa delivery.
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Advise women to inform their clinician if they are or plan to become pregnant or plan to breast-feed.
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Advise patients to inform their clinician of existing or contemplated concomitant therapy, including prescription and OTC drugs and dietary and herbal supplements, as well as any concomitant illnesses.
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Advise patients of other important precautionary information.
Additional Information
The American Society of Health-System Pharmacists, Inc. represents that the information provided in the accompanying monograph was formulated with a reasonable standard of care, and in conformity with professional standards in the field. Readers are advised that decisions regarding use of drugs are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and that the information contained in the monograph is provided for informational purposes only. The manufacturer’s labeling should be consulted for more detailed information. The American Society of Health-System Pharmacists, Inc. does not endorse or recommend the use of any drug. The information contained in the monograph is not a substitute for medical care.
Preparations
Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.
Please refer to the ASHP Drug Shortages Resource Center for information on shortages of one or more of these preparations.
Routes |
Dosage Forms |
Strengths |
Brand Names |
Manufacturer |
---|---|---|---|---|
Oral Inhalation |
Solution, for nebulization |
1 mg/mL (2.5 mg) |
Pulmozyme |
Genentech |
AHFS DI Essentials™. © Copyright 2025, Selected Revisions September 10, 2024. American Society of Health-System Pharmacists, Inc., 4500 East-West Highway, Suite 900, Bethesda, Maryland 20814.
† Off-label: Use is not currently included in the labeling approved by the US Food and Drug Administration.
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