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BMS Recalling Coumadin Tablets

By Drug Discovery Trends Editor | May 2, 2011

NEW YORK (AP) – Bristol-Myers Squibb Co. said it is recalling one production lot of its blood thinner Coumadin after finding an oversize tablet.

The company said it tested a returned bottle of Coumadin and found that one tablet was more potent than expected.

An excessive dose of Coumadin, or warfarin, could create an increased risk of bleeding.

The recall affects 5-milligram Coumadin tablets with an expiration date of Sept. 30, 2012. The production lot is number 9H49374A.

The New York drugmaker said it has notified the Food and Drug Administration about the recall. It said patients taking 5-milligram tablets should not stop taking them, but should talk to their pharmacist to find out if their prescription was filled with tablets that have been recalled.

Date: May 2, 2011
Source: Associated Press


Filed Under: Drug Discovery

 

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