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It was licensed by the US Food and Drug Administration in 2005 and subsequently by the European Medicines Agency
Overall GLP-1 RAs were associated with increased risk of gastrointestinal system disorders (ROR, 1.46
Clinical trials have shown that participants using tirzepatide experienced an average loss of 15 to 20 percent of their body weight over a 72-week period
SURMOUNT-REAL UK five-year real-world safety study of tirzepatide
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