Please Note: Schmidt & Clark, LLP, is no longer accepting Symbicort Lawsuits. If you feel that you may have a potential case, we urge you to contact another law firm adequately suited to handle your case.
The U.S. Food & Drug Administration (FDA) recently required AstraZeneca, the maker of the popular asthma inhaler Symbicort (budesonide and formoterol) to add new warnings on the product labeling warning of an increased risk of hospitalization and death.
The Problem With LABAs
Symbicort belongs to a class of inhalers called Long-Acting Beta-Agonists (LABAs).
Symbicort inhalers relax the muscles in bronchial passages, allowing more air to flow. The medication generally provides immediate relief to asthma sufferers but unfortunately, does not treat the underlying inflammation. This creates the risk of a life-threatening condition.