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FDA labeling notes postmarketing reports of acute kidney injury in patients treated with semaglutide, the majority in people who had gastrointestinal reactions leading to dehydration, and it instructs patients to promptly report persistent nausea, vomiting, or diarrhea to their healthcare provider

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Fifth, most trials were performed on or led by Italian, and funded by Sigma-Tau, the manufacturer of ALC agent

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