FDA Panel Mulls Safety of Asthma Meds
THURSDAY, Dec. 11 -- The safety of four asthma medications will be weighed by a U.S. Food and Drug Administration expert panel as two days of hearings end Thursday.
The controversy over these drugs has been going on for several years, with two FDA officials recently calling for banning the use of these drugs for anyone under 17.
One expert thinks the problem is not with the drugs, but with their misuse.
"This is an over-interpretation of the risk without adequate consideration of benefit," said Dr. Miles Weinberger, a professor of pediatrics at the University of Iowa. "However, there has been irresponsible marketing of the products, salmeterol and formoterol, and irresponsible prescribing by many physicians."
"Since most patients with chronic asthma can be controlled with inhaled steroids alone, using these more expensive combination formulations as first line is inappropriate but strongly encouraged by marketing practices" of drug makers, Weinberger said.
The products under review are Advair (salmeterol, fluticasone), Foradil (formoterol), Serevent (salmeterol), and Symbicort (formoterol, budesonide). Advair and Symbicort are combination products containing both a long-acting beta agonist and an inhaled corticosteroid. These drugs relax airway muscles, letting asthma patients breathe more easily.
In the panel's first day of hearings Wednesday, FDA officials themselves were split over the risks of the drugs.
One official told the panel members that more than 14,000 people may have died since 1994 after taking the drugs, while another suggested that an even greater number might have died without them, according to The New York Times.
Last week, two FDA officials, who work in the agency's safety division, posted an assessment on the agency Web site, saying asthma sufferers of all ages should not take the medicines. But a third FDA official concluded that Advair and Symbicort are safe for adults, but that all four drugs should no longer be used by children 17 and younger, the Times said.
The panel is reviewing an FDA study of 110 trials that included 60,954 people and found an increase in asthma-related hospitalization, asthma-related intubation, and asthma-related death in asthmatic patients with the use of these drugs. The risk varied, however, depending on the particular drug studied.
For example, there were 20 asthma-related deaths, 16 among people taking long-acting beta agonists compared with four patients not taking these drugs. All the deaths were in patients taking Serevent, the FDA notes.
The increased risk was seen in three of the four drugs, Foradil, Serevent and Symbicort, but was not seen with Advair. The increased risk wasn't seen when a long-acting beta agonist was used along with an inhaled corticosteroid, the agency found.
The greatest risk appears to be among children aged 4 to 11; women also appeared to be at greater risk than men.
Weinberger thinks that long-acting beta agonists should be used only in combination with inhaled steroids.
"All trials of the combination of long-acting beta agonists and an inhaled steroid demonstrate substantial additive effect for patients not fully controlled on the inhaled steroid alone," Weinberger said. "The sensible approach is to use the combination products only after inadequate control is observed with an inhaled steroid alone."
The drug manufacturers believe there is adequate evidence that their products are safe and effective when used properly.
"AstraZeneca believes that Symbicort exhibits a favorable benefit-risk profile in patients 6 years of age and older. Symbicort offers an important therapeutic option for asthma patients who cannot be adequately controlled on other asthma controller medications [low- to medium-dose inhaled corticosteroids] or whose disease severity clearly warrants initiation of treatment with two maintenance therapies," the company said in a statement filed with the FDA.
GlaxoSmithKline said in its statement: "The combination of salmeterol with an inhaled corticosteroid provides unsurpassed asthma control to patients by improving lung function, preventing daytime and night-time symptoms and decreasing the use of rescue medications. For Advair, there was no evidence of increased risk for asthma-related death, asthma-related hospitalization, asthma-related intubation and all-cause death in any database. Therefore, no regulatory action is necessary for this product."
A third company, Novartis, noted that "given the benefits associated with long-acting beta 2-agonist use in asthma, Novartis believes that the benefit-risk ratio is in favor of formoterol use as currently reflected in labeling and treatment guidelines. Long-acting beta 2-agonists, including formoterol, remain an important therapeutic option in the treatment of patients with asthma."
In 2007, an FDA advisory panel urged that stronger label warnings focused on children be added to the packaging for Serevent and Advair.
In 2006, after a 2005 panel investigation focused mainly on the drugs' use by adults, the FDA ordered a strong "black box" warning on both medications that they "may increase the risk of asthma-related death."
For more information on asthma, visit the U.S. National Institutes of Health.
Posted: December 2008
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