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Gastrointestinal adverse events (affecting 79.6% in the cagrilintide-semaglutide group and 39.9% in the placebo group), including nausea, vomiting, diarrhea, constipation, or abdominal pain, were mainly transient and mild-to-moderate in severity
upper respiratory
颜色:2-in-1
2c) but not significantly different than that of the patients with the mild phenotype ( p = 0.383)
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