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Description
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Common reactions include nausea, diarrhea, constipation, vomiting, abdominal discomfort, reflux, and reduced appetite
In patients who did not receive IVT, the primary outcome occurred in 22 (64.7%) patients in the semaglutide group ( n = 34) and 15 (44.1%) patients in the standard therapy group ( n = 34) (adjusted RR 1.18, 95% CI 1.021.36, Fig
Months 6-12+ (maintenance and continued loss)
Purity is confirmed by high-performance liquid chromatography (HPLC) and identity by mass spectrometry (MS)
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