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Indication Statement:

Daily administration of Pulmozyme (dornase alfa) in conjunction with standard therapies is indicated in the management of cystic fibrosis (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 twelve months.

Important Safety Information

  • Pulmozyme should not be used in patients with known hypersensitivity to dornase alfa, or any ingredients of the product.
  • Pulmozyme should be used in conjunction with standard therapies for CF.
  • Most common reported adverse events associated with the use of Pulmozyme include: voice alteration, pharyngitis, laryngitis, rash, chest pain, and conjunctivitis.

Pulmozyme Access Solutions®

Proposed Mechanism of Action

How Pulmozyme targets DNA in CF mucus

Learn about the unique Pulmozyme MOA, and how CF often requires a multiple therapy approach for optimal disease management. (Ref. 1, 2)

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Please see Important Safety Information

A unique role in CF treatment

Pulmozyme has a unique MOA in that it specifically targets DNA in cystic fibrosis mucus. (Ref. 3, 4, 5) In in vitro studies, Pulmozyme has been shown to reduce the viscosity and viscoelasticity of mucus by cleaving extracellular DNA. (Ref. 3, 6, 7)

Mucus before and after Pulmozyme


However, managing cystic fibrosis often requires a multiple therapy approach for optimal disease management.
(Ref. 1,4,5)

What do other CF medicines do?

Other medicines before image

Antibiotics

Help to prevent and
treat infections (Ref. 8)

Bronchodilators

Help to relax
the air wall lining (Ref. 6)

Hydrators

Help to restore
airway surface liquid (Ref. 8)

CFTR Modulators

May help to impact sodium
chloride ion conduction (Ref. 8)

Other medicines after image

Next, learn about prescribing Pulmozyme as part of a treatment plan ›

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References
  1. Cystic Fibrosis Foundation. Therapies for Cystic Fibrosis. http://www.cff.org/treatments/Therapies/. Accessed August 17, 2010: 1.
  2. Flume PA, O'Sullivan BP, Robinson KA, et al. Cystic fibrosis pulmonary guidelines: chronic medications for maintenance of lung health. Am J Respir Crit Care Med. 2007;176:957.
  3. Pulmozyme Prescribing Information. South San Francisco, CA: Genentech, Inc.; 2005:1.
  4. Rubin BK. Taxonomy of mucoactive medications. In: Rubin BK, van der Schans CP, eds. Therapy for Mucus-Clearance Disorders. New York, NY: Marcel Dekker; 2004:137.
  5. Cystic Fibrosis Foundation. Drug Development Pipeline. http://www.cff.org/treatments/pipeline/. Accessed August 16, 2010:1.
  6. Puchelle E, de Bentzmann S, Zahm JM. Physical and functional properties of airway secretions in cystic fibrosis-therapeutic approaches. Respiration. 1995;62(suppl 1):6.
  7. King M. Mucolytics and mucus clearance. In: Rubin BK, van der Schans CP, eds. Therapy for Mucus-Clearance Disorders. New York, NY: Marcel Dekker Inc; 2004:211.
  8. Cystic Fibrosis Foundation. Frequently Asked Questions. http://www.cff.org/AboutCF/Faqs/. Accessed January 3, 2011:1.