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Other links at Articles > Business of Medicine |
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Bivalirudin "Nonapprovable" for ACUITY Indication
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The US FDA has issued a "not-approvable" letter to the Medicines Company for an additional dosing regimen of the drug covering upstream treatment of ACS initiated in the emergency department, based on the ACUITY trial. Heartwire
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FDA Approvals: Prilosec and Treanda
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The FDA has approved an expanded indication for omeprazole delayed-release capsules and oral suspension (Prilosec), and bendamustine intravenous infusion (Treanda). Medscape Medical News
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