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Su2057: a genetic risk score associated with nausea resulting from GLP-1 receptor agonist treatment: a post-hoc analysis of a randomized controlled trial of liraglutide
Discontinuation of treatment due to gastrointestinal adverse events was more frequent with any dose of tirzepatide (risk ratios ranging from 6.39 to 10.65) or semaglutide (risk ratios ranging from 4.99 to 8.91) compared with placebo (Fig
The safety of each medication can depend on individual health factors and proper administration
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