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Close monitoring of patients is essential during dose titration to assess treatment efficacy and safety and to minimize the risk of adverse events

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J Clin Pathol

Nov 2019;25(11):854-865

Trial discontinuation occurred in 16.6% of the semagalutide group due to adverse events including gastrointestinal (10%), nervous system (1.4%), and metabolism and nutrition (1.2%) disorders compared to 8.2% in the placebo group