<body bgcolor="#ffffff" text="#000000"> <a href="http://hyulo.free-best-hosting.com/?fp=BZ%2FnEWUQz0TqU7WGbYBOEKqXLcZ%2FsYGmkda7VIJNS%2F2qBEioThKqTtkk%2FPwa2sXIw21nAWRDbx7AUaw6bQ9ErQ%3D%3D&prvtof=n4PoUZVdqkYz5GQwYcjEH6pNfWU4Ix0Me156TMjue%2FI%3D&poru=5pBvvSH%2ByPNmSArOzR2KTlclNo8Qlh6MqYRY8jCsN%2FIhhNzLdZQIeZVFpa7%2FsDXwZggHNYqHL8gTIW16JTp54m51LsyajowHoPJlXIsCeI8mjZhKGfWul%2Bur5cPtAuEBUDc9sOvaMyf6sUUeG1wJGccEowWms%2B8e85XC6NOJGIhtv43vIKK9MIywhD4SEJnMr1VtF5hjvG6e4Cd16hF%2BPp1%2Bxl%2FxIge0RRrmtpReC5%2FaUY%2FQX20NqQwabqRQ32GavZ3V8lMk31TcZbc1AJ7ufg%3D%3D&result=aT01NC4xOTYuMzEuMTE3JnU9Q0NCb3QlMkYyLjArJTI4aHR0cCUzQSUyRiUyRmNvbW1vbmNyYXdsLm9yZyUyRmZhcSUyRiUyOSZoPXd3dy4yNC03LW5ld3MuY29tJmhyPXd3dy4yNC03LW5ld3MuY29tJTJGYXJjaGl2ZXMlMkY1MTMwJnJmPQ%3D%3D">Click here to proceed</a>. </body> Coumadin Recall Announced by Bristol-Myers Squibb | 24-7-news.com cialis online

Coumadin Recall Announced by Bristol-Myers Squibb

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Coumadin has been recalled by Bristol-Myers Squibb. According to the Food & Drug Administration (FDA), the recall is a precautionary measure based on the company’s determination that some of the tablets, over time, may not meet specifications for isopropanol. This ingredient is used to maintain the active ingredient, Coumadin, in the crystalline state, and could affect the therapeutic levels of the active ingredient.

Coumadin is prescribed to treat or prevent blood clots. A decrease of the active ingredient may increase the risk of clots, which could lead to heart attack or stroke. If there is too much active ingredient, there is an increased risk of bleeding.

The voluntary involves recall of three lots of physician sample blister packs of Coumadin® 1 mg tablets and five lots, of Coumadin 1 mg tablet hospital unit dose (HUD) blister packs with the following lot numbers:

• Physician Sample Blister Packs: Lot# 9A48931A, 9A48931B, 9A48931C, expiration January 2012

• HUD Blister Pack: Lot# 8F34006B, 8K44272A, 8K46168A, 9F44437A, and 9K58012B with expiry dates between June 2011 and November 2012.

The recall only involves Coumadin 1 mg tablet blister packs distributed in the U.S. and does not involve Coumadin 1 mg supplied in bottles or any other strengths and dosage forms of the product. Patients who may have the recalled product from the subject lots should contact their physicians to ensure that their anticoagulation therapy is not interrupted. To date, the company has not received any reports of adverse events related to this issue.

Bristol-Myers Squibb has issued recall communications to all physicians and other customers involved.

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