Why was there an FDA recall of Actos?

In 2007, the FDA determined that Actos should require a stronger warning to alert patients to the chance that the drug could cause, or worsen, heart failure.  Actos received one of the highest warnings, a “black box” warning label change signifying potential serious side effects from Actos

The information on this page is meant to provide a general overview of the law. The laws in your state and/or city may deviate significantly from those described here. If you have specific questions related to your situation you should speak with a local attorney.

Additional Actos Articles

Search LawInfo's Actos Resources