Advisory issued for Advair Diskus, other asthma medications
Advisory issued for Advair Diskus, other asthma medicationsA health advisory has been issued regarding Advair Diskus and other asthma medications. What happened: On Nov. 18, 2005, the Food and Drug Administration (FDA) issued a public health advisory for three asthma medications, stating the medications may increase the risk of severe asthma episodes and possibly death if a severe asthma episode occurs. The three asthma medications included in the advisory are: Advair Diskus, Foradil Aerolizer and Serevent Diskus. All three medications are in a class of asthma drugs known as "long-acting beta-2-adrenergic agonists" or LABAs. These medicines are bronchodilator medicines that help relax the airways. In its advisory, the FDA said that although LABAs decrease how often asthma attacks occur, they may make the attacks that do occur more severe. FDA is asking the manufacturers of the three medications to update their product labels with the new health warning. What does this mean to you?: If you experience asthma attacks and you're taking one of these medications, you'll need to talk with your doctor to determine the best course of action. Here are details of what you need to know about what the FDA is now recommending:
RelatedLast Updated: 11/22/2005 © 1998-2013 Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. A single copy of these materials may be reprinted for noncommercial personal use only. "Mayo," "Mayo Clinic," "MayoClinic.com," "Mayo Clinic Health Information," "Reliable information for a healthier life" and the triple-shield Mayo logo are trademarks of Mayo Foundation for Medical Education and Research.
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