Customer Contact Center:
1-888-PLMZYME (756-9963)

Indication and Usage

Daily administration of Pulmozyme® (dornase alfa) Inhalation Solution along with standard therapies is indicated in the management of cystic fibrosis patients to improve lung function. In patients with a forced vital capacity (volume of air exhaled with maximum effort and speed) greater than or equal to 40% of predicted, daily administration of Pulmozyme has also been shown to reduce the risk of respiratory tract infections requiring the administration of injectable antibiotics.

In our pivotal study, safety and efficacy of daily administration has not been studied in patients beyond 12 months.

Important Safety Information

  • Pulmozyme should not be used in patients who are allergic to any of its ingredients. Pulmozyme should be used along with standard therapies for cystic fibrosis.
  • When starting Pulmozyme therapy, patients may experience change in or loss of their voice, discomfort in the throat, chest pain, red watery eyes, rash, dizziness, fever, or runny nose.
  • These side effects are usually mild and short-lived.

For further information, please see the Pulmozyme full Prescribing Information. If you have questions, please discuss them with your CF healthcare team.

Customer Contact Center

1-888-PLMZYME (756-9963)

Pulmozyme Access Solutions®

The CF Living community

Resource Center

CF Living is an online community for CF patients and caregivers to get information and learn about others living with this disease.

CF Living is a free program featuring helpful information for patients and caregivers. After you register, you’ll receive regular, personalized emails with relevant information about CF according to the age of the patient and you’ll also receive updates about exciting additions to

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The program includes topics surrounding:

  • Tips for managing treatment
  • Balancing CF with school or work
  • Recipes and nutritional information
  • Links to additional resources for support

When you join, you will also have the opportunity to receive one of the following:

  • A Pulmozyme Patient Kit with resources, information, and tips
  • A printed copy of an Illustrated Story about a student who faces challenges of CF and how he takes control
  • A USB Webkey that provides access to a webcast that discusses how CF can progress when symptoms are not visible

We look forward to you becoming part of the community!

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