FDA Panel Asks: Are Asthma Drugs Safe?
Serevent, Symbicort, Foradil Safety Focus of Triple FDA Panel Meeting
WebMD News Archive
Dec. 9, 2008 - Are the commonly prescribed asthma drugs Serevent, Symbicort, and Foradil
That's the question facing a three-way meeting of the FDA's advisory panels
on asthma, drug safety, and pediatrics.
Analysis of data pulled from clinical trials shows that patients taking
Serevent, Symbicort, or Foradil have a small increased risk of asthma-related
hospitalization. This is especially true for kids 4 to 11.
The same analysis shows that patients taking Serevent have a small but
significantly increased risk of asthma-related death.
A fourth related drug, Advair, was not linked to these risks in the FDA
analysis. Advair is a combination of an inhaled corticosteroid and the
long-acting beta-agonist (LABA) Serevent. Symbicort is a combination of a
different inhaled corticosteroid and a different LABA, Foradil.
Nobody is suggesting the drugs don't help a lot of children and adults with
asthma. But do the drugs benefits outweigh their risks? The drugs already carry
the FDA's top-level "black box" warning -- but are more warnings or
restrictions needed? That's what the panel must decide in their two-day joint
meeting, scheduled for Dec. 10-11.
Inhaled asthma drugs
- Inhaled short-acting beta-agonists, often called rescue inhalers, which
open the airways to fight the bronchial spasms that make it hard to breathe.
These drugs are taken only as needed.
Inhaled corticosteroids, which fight lung
inflammation. These drugs are taken every day for long-term asthma control.
- Inhaled long-acting beta-agonists, LABAs, which open the airways to prevent
bronchial spasms for long-term asthma
control. These drugs are taken every day to prevent asthma attacks.
- Intal and Tilade, which are another class of inhaled anti-inflammatory
drugs. They are not steroids. Intal and Tilade are not under safety
When Serevent was first introduced, doctors didn't fully appreciate how
important it was to fight inflammation as well as bronchial spasms. In early
trials of the drug, fewer than half of patients took a corticosteroid along
In the early 1990s, a U.K. trial suggested there might be too many deaths
among patients taking Serevent. This didn't stop the FDA from approving the
drug -- but after a series of nagging adverse-event reports, Serevent maker GSK
agreed to conduct a large safety study.