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2,3 In REDEFINE 1, adverse events were mainly gastrointestinal, (79.6% in the CagriSema group vs 39.9% with placebo) including nausea (55% vs 12.6%), constipation (30.7% vs 11.6%), and vomiting (26.1% vs 4.1%)

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[DOI] [PMC free article] [PubMed] [Google Scholar] 107.Dub JJ, Sitnick MT, Schoiswohl G, Wills RC, Basantani MK, Cai L, et al

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