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U.S. FDA panel rejects Johnson & Johnson drug for acute coronary syndrome-Reuters


Thursday, 16 Jan 2014 05:32pm EST 

Johnson & Johnson:Says that its anticoagulant Xarelto should not be approved to prevent further heart problems in patients who have recently suffered a heart attack, an advisory panel to the U.S. Food and Drug Administration concluded on Jan 16-Reuters.Says panel voted 10 to 0, with one abstention, that data presented by the company from a single clinical trial was not strong enough to justify approval, especially since some data from was missing.Says. 

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