Rezulin
   

Rezulin®, the brand name for the generic drug troglitazone, was manufactured by Parke-Davis, a division of Warner-Lambert Company. Rezulin® first came on the market in the United States in March, 1997, after receiving "fast track" approval from the United States Food and Drug Administration (FDA) as a treatment for patients suffering from Type II diabetes, which is also known as non-insulin dependent diabetes (NIDD) or adult onset diabetes mellitus (AODM).

In March, 2000, by which time approximately one-million diabetics in the United States had been treated with Rezulin®, the drug was removed from the market by the FDA after determining that severe liver toxicity was associated with its use. In fact, many cases of liver failure, including as many as 90 deaths, had been reported to the FDA as of the time Rezulin® was taken off the market.

Symptoms in the early stages of liver damage may be difficult to detect. Symptoms that may manifest in advanced stages include yellow eyes, abdominal pain, nausea, clay-colored stools, and dark urine. Severe liver damage caused by Rezulin® may result in death or necessitate a liver transplant.

Currently there are many individual and class-action lawsuits pending against Parke-Davis and Warner-Lambert nationwide. The individual suits seek compensatory and punitive damages against the defendant manufacturers for negligence, strict liability, breach of warranty and/or fraud based on the allegation that the claimants (or claimants' decedents) who used Rezulin® suffered severe liver damage or death as a result of taking the drug. The pending class action suits seek an agreement from the manufacturers to pay the costs of the medical monitoring necessary to detect latent liver and/or cardiac damage in those individuals who took Rezulin®.

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