Plavix FDA Warning

Reported by: KPSP Local 2 News Services
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Updated: 3/12/2010 4:40 pm
Experts don't expect to see genetic testing become standard procedure for patients taking the blood-thinner Plavix.

The Food and Drug Administration is adding its strongest black-box warning to the label, saying that some patients don't respond to the drug.

The agency said patients with a genetic variation can't metabolize it. And it says that puts them at increased risk for heart attack and stroke.

Patients can determine if they are "poor metabolizers" by taking a genetic test. The FDA recommends that these patients use other blood thinners, like aspirin.

But genetic tests cost around $500. And a New Jersey cardiologist, Dr. Louis Teichholz, says it's "premature to say that everyone who gets Plavix needs to be tested."

He said the black-box warning could push more doctors to prescribe Effient, a competing blood thinner launched last summer by Eli Lilly.
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