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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. community AHP and their allies lobbied for a second hearing and, despite fresh evidence that the community drug was dangerous and not particularly effective, the FDA approved it in 1996. A year and 18 million prescriptions later, it transpired that as many as 30 per cent of the people who community 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, which has been approved for use in the NHS under the brand name Reductil, has been the subject of a $50 million marketing campaign in the US, aimed at doctors and their weight-conscious middle-aged female patients.
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