Do you still have questions about Pulmozyme?
It is important to take Pulmozyme as your doctor has prescribed. Pulmozyme has a distinct role in the fight against cystic fibrosis. One of the causes of thickened mucus in the lungs is extracellular DNA. As seen in laboratory studies, Pulmozyme uniquely cuts apart extracellular DNA by acting like an enzyme naturally found in the lungs. Cutting up extracellular DNA can help make mucus thinner and looser, which can make it easier to clear your lungs. In a clinical study of patients 5 years of age or older with a forced vital capacity (FVC) greater than or equal to 40% of predicted, Pulmozyme, when taken once-daily or twice-daily, was shown to improve lung function. If you have questions about the importance of taking Pulmozyme, talk to your doctor.
Every prescribed therapy plays a role to help you fight cystic fibrosis.
Pulmozyme is a mucolytic. In laboratory studies, Pulmozyme was shown to act like a protein already in your body to cut apart the sticky mucus your lungs produce, making it thinner and looser.
Gene-specific treatments, also called cystic fibrosis transmembrane conductance regulator (CFTR) modulators, were studied for use in patients with specific genetic mutations. Even though studies for these gene-specific treatments were not designed to look at the efficacy and safety of CFTR modulators in combination with existing treatments, patients in these studies stayed on their prescribed cystic fibrosis therapies (eg, Pulmozyme, tobramycin).
Please contact your doctor and/or CF Care Team to discuss your specific treatment plan and the distinct role each of your prescribed therapies plays.
Pulmozyme was approved by the US Food and Drug Administration (FDA) in 1993, and was the first drug developed specifically for cystic fibrosis.
Patients may experience the following when using Pulmozyme: change in or loss of voice, throat discomfort, rash, chest pain, red watery eyes, runny nose, lowering of lung function, fever, indigestion, and shortness of breath. There have been no reports of severe allergic reactions caused by the administration of Pulmozyme. Mild to moderate hives and mild skin rash have been observed and have been short-lived.
Pulmozyme is to be used with other standard cystic fibrosis
treatments and has demonstrated safety in children 5 years of age or
older, adolescents, and adults. The efficacy of Pulmozyme has not been
studied in patients less than 5 years of age. The safety of Pulmozyme,
2.5 mg by inhalation, was studied with 2 weeks of daily administration
in 65 patients with cystic fibrosis aged 3 months to < 5 years.
Overall, the nature of adverse events was similar to that seen in the
placebo-controlled trials in older patients. The number of patients
reporting cough was higher in the younger age group as compared to the
older age group (45%; compared to 30%) as was the number reporting
moderate to severe cough (37%; compared to 18%). The number of
patients reporting rhinitis was higher in the younger age group as
compared to the older age group (35%; compared to 27%) as was the
number reporting rash (6% as compared to 0%).
Pulmozyme should not be used in patients who are allergic to any of
You should call your doctor if you experience any of these side effects or if any of these side effects are severe, get worse, or do not go away.
You may feel more prepared if you talk to your doctor about what to expect before you begin Pulmozyme. Based on studies, patients taking Pulmozyme may experience change in or loss of their voice, discomfort in the throat, rash, chest pain, red watery eyes, runny nose, lowering of lung function, fever, indigestion, and shortness of breath. Mild to moderate hives and mild skin rash have been observed and have been short-lived. You should call your doctor if you experience any of these side effects or if any of these side effects are severe, get worse, or do not go away.
These are not all the possible side effects of Pulmozyme. Please see the full Pulmozyme Prescribing Information for additional Important Safety Information.
Pulmozyme may be an essential partner in your fight against cystic fibrosis. In cystic fibrosis, your lungs produce extra-thick, sticky mucus. Laboratory studies have shown that Pulmozyme makes mucus thinner and looser. See the clinical data and learn more about whether Pulmozyme is right for you.
The recommended dose for most cystic fibrosis patients is Pulmozyme 2.5 mg once-daily.
Some patients over 21 may benefit from twice-daily treatment. You should ask your doctor whether prescribing Pulmozyme 2.5 mg twice-daily may be right for you.
Treating cystic fibrosis is complicated so it is important to take all your treatments as prescribed by your doctor. As seen in laboratory studies, Pulmozyme works to help make mucus thinner and looser. Your doctor will prescribe other medicines to take in addition to Pulmozyme. These other medicines may include:
- Bronchodilators help open airways
- Hydrators help increase moisture in thick mucus
- Airway clearance techniques help physically loosen and move mucus out of the way
- Antibiotics help prevent and treat infections
- Gene-specific treatments, also known as cystic fibrosis transmembrane conductance regulator (CFTR) modulators, help keep a balance of salt and water in the lungs
The FDA has approved specific nebulizers/compressors to be used with Pulmozyme.
One nebulizer system is FDA-approved:
- eRapid® (PARI) Nebulizer System
The following nebulizers and compressors have been approved for use with Pulmozyme:
Hudson T Up-draft II® with Pulmo-Aide®
Marquest Acorn II® with Pulmo-Aide®
PARI LC® PLUS with PARI PRONEB®
PARI BABY™ with PARI PRONEB®
Durable Sidestream® with MOBILAIRE™
- Durable Sidestream® with Porta-Neb®
Please contact your doctor and/or CF Care Team for more information about nebulizers and compressors, and for guidance in choosing products that are right for you.
Pulmozyme comes in sterile, single-use ampules that should be used completely. Because Pulmozyme has no preservatives, the entire contents must be used or discarded.
It is important to store ampules of Pulmozyme in their protective foil pouch under refrigeration and protected from light. Refrigerate Pulmozyme during transport, and do not expose it to room temperatures for more than 24 hours.
Each ampule should be squeezed prior to use in order to check for leaks. Discard ampules if the solution is cloudy or discolored. Once opened, the entire contents of the ampule must be used or discarded.
Finding the time and place to take your treatments, like Pulmozyme, isn’t always easy. No one is perfect. But having a routine that fits your lifestyle can help you stay in control and assist in your fight against cystic fibrosis.
There are expiration dates stamped on each ampule. It is important to follow the stamped date and discard any ampules that expire.
Each sterile, single-use ampule of Pulmozyme (2.5 mg) is packaged in a protective foil pouch. The ampules should be left in their foil package and stored in the refrigerator. They should also be kept away from strong light. Refrigerate Pulmozyme during transport, and do not expose it to room temperatures for more than 24 hours.
Understanding cystic fibrosis
Cystic fibrosis is a genetic condition, which means that it is something you are born with. Cystic fibrosis is known to cause your lungs to produce extra-thick, sticky mucus. This mucus builds up and clogs your airways.
The lungs naturally produce a thin layer of mucus that helps protect the airways from dangerous bacteria that can cause infections.
For people living with cystic fibrosis, the mucus in the lungs is thicker than normal, and becomes a source of inflammation and infection that can lead to decreased lung function and exacerbation of infections.
Genentech Access Solutions may be able to help you understand how to get the medicine you need.
If you are eligible, there may be options to help you pay for Pulmozyme*:
Genentech co-pay cards
Referrals to independent co-pay assistance foundations
- The Genentech® Access to Care Foundation, or GATCF
*Patients must meet certain criteria.
To learn more about how we can help, contact us. Call (800) 690-3023 or visit Genentech-Access.com/Pulmozyme/patients.
For more information about Pulmozyme, talk to your doctor or call
1-888-PLMZYME (1-888-756-9963) to speak live with one of our