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
Hurt by a Defective Drug or Medical Device?
You can take legal action if you or a loved one is suffering due to a poorly made prescription drug or medical device. Contact a lawyer today.
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