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Widely Used Cardiac Surgery Drug Doubles Risk of Kidney Failure;Aprotinin Proven Unsafe 13 Years After Approval in Today's New England Journal of Medicine.

The America's Intelligence Wire

| January 25, 2006 | COPYRIGHT 2003 Financial Times Ltd. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

(From US Newswire)

To: Metro Desk, Health Reporter

Contact: Tyler Prell of The Hauser Group for IREF, 202-518-8047 (8 a.m. to 6 p.m. EST) or 202-210-1203 (all other times)

SAN BRUNO, Calif., Jan. 25 /U.S. Newswire/ -- Aprotinin -a a drug approved by the FDA, marketed internationally for the last 13 years, and given to an estimated one million surgery patients to limit bleeding -a has now been proven to double a patient's risk of kidney failure, and increase the risk of heart attack, heart failure, and stroke. These results -a published in this week's New England Journal of Medicine -a are based on an independent (non-commercial), observational study conducted by The Ischemia Research and Education Foundation (IREF), in association with the McSPI Research Group -- nonprofit biomedical research organizations dedicated to saving and extending lives.

"Our study provides compelling evidence of aprotinin's serious risks, and strongly suggests discontinuation of use and replacement with either of the two alternative generic and far less costly medications proven safe in this study," said IREF and McSPI founder and principal scientist, Dennis T. Mangano, Ph.D., M.D. "Certainly, our findings -a coming on the heels of the Vioxx experience -a indicate that the problem of drug safety is not only ubiquitous,…

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