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FDA Health Alert: heart-surgery med Trasylol may increase the risk of death and stroke


September 30, 2006

On Friday, the Food and Drug Administration (FDA) announced that German pharmaceutical giant Bayer A.G., had failed to alert federal drug officials that their popular heart-surgery drug Trasylol, might increase the health risks of death and stroke. The drug company had known of those risks after learning the results of a large-scale study it conducted.

According to an article in the New York Times, Bayer scientists even attended a public meeting with the FDA in late September to discuss the drug's risks but did not mention the large-scale study conducted by the company with its very troubling results.

Another study, published in January in the New England Journal of Medicine, found that the Trasylol, which is given to patients before heart surgery, may increase the risks of kidney failure, heart attack and stroke.

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see also:

Learn More Side Effects of Trasylol Include Kidney Failure--Lawyers Investigate
Trasylol has been found to cause kidney problems--free legal review

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Voluntary recall of Dextroamphetamine Sulfate drug used to treat ADHD

Drugs What You Need to Know about the Link Between Gleevec and Heart Failure
Link Between Gleevec and Heart Failure--New Precautions added to Label

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