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Alaris Pump Module Recall

On 12/26/2007, Cardinal Health notified its customers of a voluntary recall for all Alaris Pump modules, model 8100 (formerly known as Medley Pump module), shipped prior to September 27, 2007.

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Vioxx Settlement Alert

Merck & Co., Inc. has announced a plan to pay $4.85 billion to resolve Vioxx claims related to a heart attack, stroke, or sudden cardiac death. Lawsuits filed or tolled before November 9, 2007 can be considered for settlement under the plan.

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Global Sales of Trasylol Are Stopped

Bayer AG, maker of the antibleeding drug Trasylol, has announced that worldwide sales of the drug will be brought to a halt due to a clinical study linking Trasylol with a higher risk of death.

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FDA Requires Black Box Warning for Avandia

Due to the risk of congestive heart failure, the FDA is requiring that the type 2 diabetes drug Avandia be labeled with a black box warning detailing the risks.

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FDA Approves Cefotetan and Dextrose for Duplex Drug Delivery System

Duplex is now the only ready-to-use IV drug delivery system available for Cefotetan therapy in the United States.

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