About Rezulin

Rezulin (generically called troglitazone) is a prescription medication created by Warner Lambert's Parke-Davis division and designed to treat Type-2 diabetes- that is, a condition typically found in adults where the body becomes resistant to its own insulin. Even before its public release in 1997, Rezulin was known to pose a serious health risk to its users, causing side effects ranging from mild liver damage to complete liver failure. Because of this, on March 22, 2000, the sale and distribution of Rezulin was voluntarily discontinued at the request of the federal Food and Drug Administration.

Rezulin had been designed to help diabetes patients respond better to insulin. While other sugar- (glucose) lowering pills stimulate the pancreas into producing more insulin, Rezulin instead helped the body use its existing insulin more efficiently. As a result, blood glucose control could be improved in people taking Rezulin, while episodes of low blood glucose (hypoglycemia) levels could be reduced.

While there were benefits to the use of Rezulin, the FDA directly attributes numerous liver failure deaths and many additional cases of liver damage to the product.

Rezulin News Timeline

1997
January - Rezulin is approved by the FDA to treat Type II diabetes.
November - The FDA issues a warning about Rezulin (troglitazone). Recommended prescribing information is changed by the drug's manufacturer; new warning label information is added.
December - Approximately 150 adverse events associated with Rezulin have been reported to the FDA.
1998
June - The FDA and Rezulin manufacturer Parke-Davis agree to again tighten restrictions on the use of Rezulin.
July - Parke-Davis sends a letter to heathcare professionals warning to test for liver abnormalities and updating them on the changes in recommended use.
2001
March - Resulin sales are discontinued.

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Last Updated: May 11, 2010. 11:08:32 am.