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In 1995, the FDA turned down an application by a subsidiary of American Home Products to market a more powerful form of fenfluramine, Redux. They were concerned by reports that a hundred people in Europe - where Redux was produced - had developed a rare, incurable and fatal respiratory disease after taking it. AHP and their allies lobbied for a second hearing and, despite fresh evidence that the drug organizations was dangerous and not particularly effective, the FDA organizations approved it in 1996. A year and 18 million prescriptions later, it transpired organizations that as many as 30 per cent of the people who took Redux had suffered some damaging side effect. The FDA withdrew it from the market, but not before hundreds of people had become seriously, and in some cases terminally, ill. In 2001, AHP set aside $12 billion to settle lawsuits brought on account of the drug.Meridia,
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