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: InjuryBoardAlli, Xenical To Carry Liver Damage Warning
By Jane Akre
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Alli, Xenical Warning
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IMAGE SOURCE: Alli Web site /image of Alli |
A popular weight loss drug will be carrying a little more baggage on its warning label.
After 13 cases of severe liver injury, the orlistat label will contain a new warning about the potential of liver injury.
Orlistat is available by prescription as Xenical, and Alli, which is available over-the-counter.
Twelve of the 13 cases of liver damage were overseas and one case, from the use of Alli, was in the U.S.
Among those reports, two individuals died, and three needed a liver transplant.
About 40 million people worldwide have taken or are taking the drug. Dr. Eugene Schiff, a liver specialist at the University of Miami Miller School of Medicine tells Business Week that these cases are rare.
Alli is marketed by GlaxoSmithKline PLC at a lower dose (60 mg), while Xenical, the prescription version is made by Roche Holding AG (120 mg), which plans to monitor Xenical's safety and says it will share that information with federal regulators.
Liver Damage
Signs of liver injury include yellow eyes or skin, dark urine, light colored stools, loss of appetite or itching. Patients should stop using orlistat if they develop any of those symptoms.
"We are telling consumers and health-care providers to be vigilant should [patients] develop symptoms suggestive of liver impairment," said FDA spokeswoman Elaine Gansz Bobo who added that routine liver enzyme testing will not help predict who may be at increased risk.
"At this time, a cause-and-effect relationship of severe liver injury with [Xenical or Alli] use has not been established," the agency said in a statement.
Some of the patients experiencing reaction may have been taking other drugs as well.
Background
Approved in 1999, orlistat became the first nonprescription drug to treat obesity in American adults. By 2009, 32 reports of serious liver injury had been reported to the agency includes six cases of liver failure, with two occurring in the U.S. 27 of those patients had to be hospitalized.
In 2006, Public Citizen petitioned the FDA to remove orlistat from the market because 'the obesity treatment has been known to cause a significant increase in aberrant crypt foci (ACF), which are widely believed to be a precursor to colon cancer.'
For some, the costs associated with obesity are worth the drug risk. Thirty percent of Americans are considered obese, and another 36 percent are overweight, according to the National Center for Health Statistics. #
Originally posted at The Injury Board by Jane Akre
Full post as published by InjuryBoard on May 28, 2010 (boomark / email).
May 2010: New Safety Information For Xenical And Alli Regarding Cases Of Severe Liver Injury
FDA Had Been Investigating Reports Of Hepatotoxicity Involving Their Active Ingredient, Orlistat, For Past Year (Posted by Tom Lamb at DrugInjuryWatch.com) Xenical and Alli are relatively popular medications used for weight-loss that contain different strengths of the same active ingredient, orlistat...
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The FDA is reviewing diet drugs Alli and Xenical after 32 adverse event reports associated the drugs with liver injury. Alli is manufactured and marketed by GlaxoSmithKline and is available as an over-the-counter weight loss supplement...
FDA UIpdates Rare Cases of Liver Injury Reported with Use of Xenical, Alli
he U.S. Food and Drug Administration today advised consumers and health care professionals about potential rare occurrences of severe liver injury in patients taking the weight-loss medication orlistat, marketed as Xenical and Alli...
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Alli, the over-the-counter weight loss drug manufactured by GlaxoSmithKline and its prescription counterpart Xenical, manufactured by Roche, are being investigated by the FDA after more than two dozen adverse event reports have associated the drugs with liver injury...
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The weight-loss drugs Xenical and Alli are receiving an FDA review of reported liver injuries. Xenical is a prescription drug, marketed by Roche and approved in 1999. Alli is an over-the-counter drug, marketed by GlaxoSmithKline and approved in 2007...
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