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While both groups had similar rates of adverse events (89% in the liraglutide group and 88% in the placebo group), the liraglutide group reported a higher incidence of gastrointestinal side effects due to dose escalations, however, none resulted in hospitalization

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[DOI] [PMC free article] [PubMed] [Google Scholar] 44.Fernandez-Marcos P.J., Nobrega-Pereira S