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Press Release 20100302
On March 19, 2010 @ 9:45 am In
Leading patient education organization to asthma patients: Talk to your healthcare provider about FDA 12-hour bronchodilator warnings
New Orleans, March 2, 2010—Allergy & Asthma Network Mothers of Asthmatics (AANMA) encourages patients to make informed decisions about recent U.S. Food and Drug Administration (FDA) recommendations affecting patients using asthma medications known as long-acting beta agonists (LABAs) or 12-hour bronchodilators: Advair, Foradil, Serevent and Symbicort.
This was also the message presented by allergists speaking this week at the American Academy of Allergy, Asthma and Immunology (AAAAI) annual meeting in New Orleans. Allergists are concerned that FDA’s recommendations are not consistent with Expert Panel Report 3: Guidelines for the Diagnosis and Management of Asthma (EPR3) or with significant clinical practice in real-world settings. Furthermore, experts stated that FDA may have given more credence to some research that EPR3 authors considered unsupported by evidence.
“FDA’s recommendations and public statements have serious implications for patients, particularly if patients using these medications suddenly decide to stop taking them because they don’t know whose advice to follow,” said Nancy Sander, AANMA president and founder. “Patients and families are advised to continue taking medication as prescribed and to avoid known allergens and irritants. Never use these medications more frequently than every 12 hours. Anyone using these medications on a daily basis should be in the care of an asthma specialist.”
“The key for asthma care is gaining and maintaining control of the asthma,” said Stuart Stoloff, MD, a member of the EPR3 panel and Chairman of AANMA’s Board of Directors. “This requires open and ongoing communication between patients and healthcare providers, including regularly scheduled well visits to monitor levels of control and follow-up visits when medications are changed.”
Allergists at the AAAAI meeting said that safety data concerning 12-hour bronchodilators had been carefully reviewed when the EPR3 Guidelines update was developed in 2007 and that no new data published since warrants any change to the Guidelines recommendations.
The recommendations issued by FDA on February 18 covered two basic issues:
The physicians speaking at the AAAAI meeting said they agree that it’s best to combine a LABA and an ICS, rather than using a LABA alone, and they said that these medications offer an important treatment option. “As a practicing physician, my experience is that combination medications [containing a 12-hour bronchodilator along with an inhaled corticosteroid in one dose] have changed how effective I’ve been able to be as a physician,” said William Busse, MD, chairman of the NIH Expert Panel 3. “We don’t see asthma patients being admitted into the hospital like before.”
But this is where agreement with FDA’s recommendation ends. Stanley Szefler, MD, also a member of Expert Panel 3, emphasized the importance of continuing to use a 12-hour bronchodilator if it’s helping a patient manage symptoms. “It doesn’t make sense to bring a patient to [a level of] good control and then stop what got them there,” he said. “It’s a lot like achieving good blood pressure, then stopping the medication. We are concerned that patients will achieve control and then stop the medication,” which he said could lead to dangerous consequences which could include death.
The FDA announcement:
“AANMA Provides Straight Answers to FDA’s Announcement about Asthma Medications”
Read AANMA’s article about 12-hour bronchodilators:
Find an Allergist. Find Relief.
Founded in 1985, Allergy & Asthma Network Mothers of Asthmatics is the leading national nonprofit family organization dedicated to eliminating suffering and death due to asthma, allergies and related conditions. AANMA’s core areas of expertise are education, advocacy and outreach. The organization’s www.aanma.org website and award-winning publications, Allergy & Asthma Today  magazine and The MA Report  online newsletter, are consumer lifelines to medical news and healthy living.
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URL to article: http://www.aanma.org/press-room/press-releases/press-release-20100302/
URLs in this post:
 Guidelines for the Diagnosis and Management of Asthma : http://www.nhlbi.nih.gov/guidelines/asthma/
 www.fda.gov/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/ucm200776.htm: http://www.fda.gov/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/ucm200776.htm
 www.aanma.org/2010/02/aanma-provides-straight-answers-to-fdas-announcement-about-asthma-medications: http://www.aanma.org/2010/02/aanma-provides-straight-answers-to-fdas-announcement-about-asthma-medications
 www.aanma.org/2009/03/fda-considers-safety-of-12-hour-bronchodilators: http://www.aanma.org/2009/03/fda-considers-safety-of-12-hour-bronchodilators
 http://allergyandasthmarelief.org: http://allergyandasthmarelief.org
 Allergy & Asthma Today: http://www.aanma.org/publication/aat-subscription/
 The MA Report: http://www.aanma.org/publication/ma-report/
 www.aanma.org: http://www.aanma.org
 Take A Weekly Breather: http://aanmablog.blogspot.com
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