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These uncommon, but very serious adverse reactions, are typical of drug toxicities which, because of their rarity, may not be detected in clinical trials of drugs before marketing.

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That presumably was not unrelated to the fact that the OCC examiner at Riggs soon thereafter went to work for Riggs.

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Something like Acomplia could be the extra help that they need, he said.

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The FDA knew about liver toxicity with trovafloxacin before approval from animal studies .

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Based on a review of FDA documents, we hereby petition the Food and Drug Administration (FDA) as authorized by 21 U.

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Since the obese are often already at great risk of heart disease , this has dampened enthusiasm for the drug.

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However, one cannot study the subject, and avoid learning and being tested on clinical subjects.

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Phone calls and emails to Secretary to the Union Environment Ministry Prodipto Ghosh and to public relations chief Maria Doss went unanswered.

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