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Internal emails discussing adverse event patterns, safety committee meeting minutes, communications with FDA about label changes, and analyses of adverse event database reports all provide key evidence that the company knew about gastroparesis risks before adequately warning patients and doctors

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To answer this question, they tested the participants hemoglobin A1C (HbA1C) a measure of average glucose over two to three months at the start of the trial and after the participants had taken semaglutide or the placebo for 20 weeks

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