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The goal of the study was to ascertain whether GI adverse events (GI AEs), such as nausea/vomiting, diarrhea, constipation, and dyspepsia (indigestion), during the dose escalation phase (baseline to week 12) and from baseline to the end of treatment, are responsible for the greater weight loss seen with semaglutide compared to other GLP-1RAs
Legality and safety vary: a generic produced in India under that country's legal framework is not FDA-approved for import into the U.S., and purchasing it exposes patients to customs seizure risk and product quality uncertainty
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Even a couple of samples to research
This is not caused by the medication itself but by the metabolic stress of rapid weight change
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