(Circulation. 1999;100:e133.)
© 1999 American Heart Association, Inc.
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1 Circulation Newswriter
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The settlement has yet to be approved by a federal judge, who must certify the suit. A similar attempt to settle product liability litigation by Interneuron Pharmaceuticals, Inc, met a stumbling block last September when the US District Court for the Eastern District of Pennsylvania rejected a proposed agreement between the company and the plaintiffs management committee on the grounds that the proposed settlement did not meet the requirements for limited fund class actions. Interneuron, which is based in Lexington, Mass, licensed dexfenfluramine from the closely held French drugmaker Laboratoires Servier SA and manufactured it for American Home Products Corp.
The American Home Products settlement will fund the following:
Fenfluramine and dexfenfluramine were withdrawn from the
market in September 1997 after physicians identified valvular
abnormalities in people who had taken the diet drug combination.
Concerns began when investigators at the Mayo Clinic and MeritCare
Medical
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