FDA Warnings Outline Actos Dangers

July 15, 2012

Warnings from the U.S. Food and Drug Administration (FDA) make clear that patients who take Actos (pioglitazone) treatments for longer than one year substantially increase the risk that they may develop bladder cancer. After five years of a decade long study, medical researchers concluded – and the FDA cautioned – that as cumulative pioglitazone exposure rises, the health risks associated with this often prescribed Type 2 diabetes medication increase as well.

 

Has your doctor prescribed a pioglitazone-based drug like Actos or Duetact? If the answer is yes, you may be at risk of dangerous side effects and, as a result, your legal rights may have been affected. Want to find out what your options are? Talk to the trained and dedicated professionals at Fears Nachawati today. With years of experience, our attorneys are prepared to advise you of your rights. For your free consultation, call us at 1.866.545.8364 or email mn@fnlawfirm.com. We’re ready to fight for you!

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