Cystic Fibrosis
Medications
Medicines for cystic fibrosis help keep the lungs as healthy as possible, reduce and control mucus in the lungs, and replace digestive enzymes.
Medication Choices
Medicines for cystic fibrosis include:
Medicine to treat infections
- Antibiotics (such as azithromycin, Keflex or Cipro, and TOBI [tobramycin])
Medicines to open breathing tubes in the lungs or keep them open
- Bronchodilators (such as albuterol or salmeterol)
- Anticholinergics (such as Atrovent)
Medicines to control the amount and thickness of mucus
- DNase (such as Pulmozyme)
- Mucolytics (such as Mucomyst)
Medicines to reduce inflammation
- Nonsteroidal anti-inflammatory drugs (NSAIDs) (such as Motrin)
- Membrane stabilizers (such as Intal or Tilade)
- Corticosteroids (such as prednisone, Medrol, or Flovent Diskus)
Medicines to replace the effect of digestive enzymes
- Enzyme replacement therapy (such as Creon or Pancrease)
What To Think About
Some medicines work better for some people than for others. A medicine that works well for one person may not work for someone else. It can take time to find the medicines that work best for you or your child.
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| Author: | Debby Golonka, MPH | Last Updated: June 26, 2007 |
| Medical Review: | Michael J. Sexton, MD - Pediatrics Susanna McColley, MD - Pediatric Pulmonology | |
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