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24 May 2012
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The US Food and Drug Administration’s (FDA) Cardiovascular and Renal Drugs Advisory Committee voted against Johnson & Johnson and Bayer’s co-developed oral anticoagulant drug Xarelto (rivaroxaban),
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22 May 2012
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An advisory committee to the US Food and Drug Administration (FDA) gave US-based manufacturer Johnson & Johnson’s (J&J) blood thinner Xarelto (rixaroxaban), experimentally used to treat acute coronary
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