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As part of a preventive treatment plan for patients with cystic fibrosis (CF)…

Treat Cystic Fibrosis patients with Pulmozyme® along with other standard therapies to provide early benefit to their lungs.

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CF impairs mucus production and hampers lung function

Lung damage can exist before any perceived lung problems

Consider Pulmozyme as part of a treatment plan

Indication

Daily administration of Pulmozyme Inhalation Solution in conjunction with standard therapies is indicated in the management of CF patients to improve pulmonary function. In patients with an FVC ≥40% of predicted, daily administration of Pulmozyme has also been shown to reduce the risk of respiratory tract infections requiring parenteral antibiotics. Safety and efficacy of daily administration have not been demonstrated in patients for longer than 12 months.

Spotlight

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Watch and listen to how Pulmozyme works.
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Contribute to the Cystic Fibrosis Community by sharing your experience of living with CF with other patients and caregivers.

Important Safety Information

Pulmozyme should be used in conjunction with standard therapies for CF. The most common adverse events reported include voice alteration, pharyngitis, laryngitis, rash, chest pain, and conjunctivitis. Pulmozyme is contraindicated in patients with known hypersensitivity to dornase alfa, Chinese hamster ovary cell products, or any component of the product.

Pediatric Use

Because of the limited experience with the administration of Pulmozyme to patients younger than 5 years, its use should be considered only for those patients in whom there is a potential for benefit in pulmonary function or in risk of respiratory tract infection.

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