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FDA Investigating Reports of Liver Injury in Patients Using Weight Loss Drug Orlistat

Aug. 24, 2009 -- The FDA today announced that it is reviewing adverse event reports of liver injury in patients taking the weight loss drug orlistat, marketed as the prescription drug Xenical and the over-the-counter medication Alli.

Xenical was approved by the FDA in 1999; Alli was approved in 2007 as an over-the-counter weight loss aid for adults.

Between 1999 and October 2008, the FDA received 32 reports of serious liver injury in patients taking orlistat. That includes 27 cases that involved hospitalization and six cases of liver failure.

Thirty of the 32 reports occurred outside the U.S., the FDA notes. Orlistat is approved in about 100 countries.

The most commonly reported adverse events included yellowing of the skin or whites of the eyes (jaundice), weakness, and stomach pain.

The FDA is reviewing additional data submitted by orlistat makers on suspected cases of liver injury. The issue was also discussed in April 2009 at the FDA's Center for Drug Evaluation and Research Drug Safety Oversight Board.

"The issues here are complex, but FDA has benefited from the input of the Board, including comments from representatives from three FDA Centers and several other agencies in the Department of Health and Human Services," Steven Osborne, MD, executive director of the FDA's Drug Safety Oversight Board, states in an FDA news release.

The FDA is still analyzing the data and states that "no definite association between liver injury and orlistat has been established at this time." That means that it's not clear that orlistat caused the reported cases of liver injury. The FDA will release its findings on orlistat as soon as its review is completed.

In the meantime, the FDA isn't recommending any prescribing changes for orlistat and no changes in use of Xenical or Alli.

"Consumers taking Xenical should continue to take it as prescribed, and those using over-the-counter Alli should continue to use the product as directed," states the FDA.

The FDA also recommends that people who have used orlistat consult a health care professional if they experience symptoms possibly associated with development of liver injury, particularly weakness or fatigue, fever, jaundice, or brown urine. Other symptoms may include abdominal pain, nausea, vomiting, light-colored stools, itching, or loss of appetite.

Health care professionals and consumers can report side effects from orlistat -- or any other drug -- to the FDA's MedWatch Adverse Event Reporting program online or by calling 800-FDA-1088.

 

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