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Tuesday 25 October 2005

Pemoline to Exit U.S. Market

By: Kate Traynor

The Food and Drug Administration (FDA) announced yesterday that pemoline will no longer be available in the United States because the risks of liver toxicity associated with the drug's use outweigh the benefits of the therapy.

Pemoline, an older remedy for attention-deficit/hyperactivity disorder (ADHD), was sold by Abbott Laboratories under the brand name Cylert until May 2005, when the company discontinued the product. According to FDA's announcement, manufacturers of generic versions of the drug have now agreed to stop marketing their formulations of the drug in this country.

FDA, through its MedWatch drug safety reporting system, stated that pemoline products will remain available until existing stocks held by wholesalers and pharmacies are exhausted. Clinicians who prescribed pemoline for patients with ADHD must select another drug, the agency stated.

Pemoline was considered second-line therapy for ADHD. FDA noted that many other medications are currently available to treat the condition, including products with once-daily dosing and one drug that is not classified as a controlled substance.

FDA stated that it had received 13 reports of liver failure that resulted in liver transplant or death among patients receiving pemoline despite the existence of strong warnings in the product's labeling. Although the use of pemoline declined drastically after the addition to the labeling, in 1999, of a boxed warning about the risk of liver failure, one case of liver failure occurred after the label was revised, according to the agency.

Overall, FDA stated, the reporting rate for liver failure among pemoline users is 10 to 25 times higher than would be expected in the general population.

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