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FDA requires disclosure of suicide risk for anti-baldness drug

U.S. health regulators rejected a request to remove popular anti-baldness pill Propecia and its generic versions from the market, but for the first time required patient notification about reports of suicidal behavior in men taking the drug.

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FDA requires disclosure of suicide risk for anti-baldness drug

By Dan Levine (Reuters) - U.S. health regulators rejected a request to remove popular anti-baldness pill Propecia and its generic versions from the ma.

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Lawsuit Brings Renewed Attention to Finasteride Adverse Events

Lawsuit Brings Renewed Attention to Finasteride Adverse Events
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