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

Speak to an Experienced Actos Attorney Today

This article is intended to be helpful and informative. But even common legal matters can become complex and stressful. A qualified actos lawyer can address your particular legal needs, explain the law, and represent you in court. Take the first step now and contact a local actos attorney to discuss your specific legal situation.

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