Cystic Fibrosis Articles A-Z
Prenatal Testing for Cystic Fibrosis
Prenatal testing for cystic fibrosis is performed by amniocentesis or chorionic villus biopsy. This eMedTV article discusses these options in detail and includes information on a test that can determine if you are a carrier of cystic fibrosis.
Pulmozyme is a drug that can help improve lung function in people with cystic fibrosis. This eMedTV segment takes an in-depth look at the drug, explaining how it works, possible side effects, tips and precautions for those taking it, and more.
This eMedTV resource explores Pulmozyme and breastfeeding. It explains the results of animal studies, discusses why the drug is unlikely to pass through breast milk in humans, and describes what to do if you are taking Pulmozyme while breastfeeding.
This eMedTV page takes a look at Pulmozyme and pregnancy. It describes the results of animal studies, explains how the FDA rates the safety of drugs during pregnancy, and discusses what a doctor will consider if you become pregnant while taking it.
Various factors can affect a person's Pulmozyme dosage, which this eMedTV segment describes. General dosing guidelines for the medication are also provided, as are helpful tips and suggestions for those taking Pulmozyme to treat cystic fibrosis.
No known Pulmozyme drug interactions exist at this time. However, as this eMedTV Web page explains, while the drug has been studied with other cystic fibrosis medications, interactions with other drugs have not been specifically studied.
This eMedTV article explains why it is unknown what effects, if any, could result from a Pulmozyme overdose. The results of studies on the subject are described, as are factors that can play a role and treatment options, should symptoms appear.
Although most people have no problems when taking Pulmozyme, side effects are possible. Therefore, this eMedTV resource lists common side effects of the drug, as well as rare side effects and side effects that may need prompt medical attention.
Pulmozyme uses, as this eMedTV article explains, pertain to the improvement of lung function in people with cystic fibrosis. This article describes how the drug works, discusses its use in children, and explores possible off-label Pulmozyme uses.
Pulmozyme Warnings and Precautions
Understanding Pulmozyme warnings and precautions can help ensure a safe treatment process. This page of the eMedTV archives contains some of the most common, including a list of people who should avoid the drug and things to discuss with your doctor.
This eMedTV segment focuses on cystic fibrosis (CF), a disease of the mucus and sweat glands. This article covers specific organs affected by CF and describes some symptoms of the condition. Sistic fibrosis is a common misspelling of cystic fibrosis.
Treatment for cystic fibrosis involves antibiotics, chest physical therapy, and exercise. This eMedTV resource describes these options in detail and explains why the main goal of cystic fibrosis treatment is to control infections in the lungs.