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The pivotal SURMOUNT trials that led to FDA approval of Mounjaro recorded musculoskeletal complaints at rates similar to placebo in most patient groups
Male WT mice and male GLP-1R knockout mice, aged 713 weeks with weighing 2030 g were included in this study [29]
While more than 70% of participants in both groups experienced adverse events (AEs), only about 2% in each group experienced a serious adverse event (SAE)
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