FDA approves Zontivity to reduce the risk of heart attacks and stroke in high-risk patients

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Title: FDA approves Zontivity to reduce the risk of heart attacks and stroke in high-risk patients

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05/08/2014 03:57 PM EDT

The U.S. Food and Drug Administration today approved Zontivity (vorapaxar) tablets to reduce the risk of heart attack, stroke, cardiovascular death, and need for procedures to restore the blood flow to the heart in patients with a previous heart attack or blockages in the arteries to the legs.

 

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