FDA MedWatch - Orlistat (marketed as Alli and Xenical): Labeling Change

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Title: FDA MedWatch - Orlistat (marketed as Alli and Xenical): Labeling Change
MedWatch logo MedWatch - The FDA Safety Information and Adverse Event Reporting Program

Orlistat (marketed as Alli and Xenical): Labeling Change

Audience: Family Practice healthcare professionals, patients/consumers

FDA notified healthcare professionals and patients that it has approved a revised label for Xenical to include new safety information about cases of severe liver injury that have been reported rarely with the use of this medication. The agency is also adding a new warning about rare reports of severe liver injury to the OTC Drug Facts label for Alli.

Xenical and Alli are medications used for weight-loss that contain different strengths of the same active ingredient, orlistat. Xenical (orlistat 120 mg) is available by prescription and Alli (orlistat 60 mg) is sold over-the-counter without a prescription. This new safety information, originally announced in August 2009, is based on FDA's completed review of orlistat.

Healthcare professionals should weigh the benefits of weight-loss with the potential risks associated with Xenical and Alli before prescribing or recommending these medications to their patients; patients should stop use of orlistat and contact their healthcare professional if they develop the signs and symptoms of liver injury, including itching, yellow eyes or skin, dark urine, light-colored stools, or loss of appetite.

Read the complete MedWatch safety summary, including links to the FDA Drug Safety Communication and Questions and Answers pages, at:

http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm213448.htm


You are encouraged to report all serious adverse events and product quality problems to FDA MedWatch at www.fda.gov/medwatch/report.htm

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