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It is not evaluated or approved by the FDA, EMA, or any other regulatory authority for human or animal consumption, diagnostics, or therapeutic purposes
3 In the REIMAGINE 1 trial, the most commonly reported adverse events (AEs) were gastrointestinal (GI)-related, occurring in 33/62 (53%) participants in the CagriSema 2.4 mg/2.4 mg group, 28/63 (44%) participants in the CagriSema 1 mg/1 mg group, and 13/64 (20%) participants in the placebo group
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Every extra week you spend at each titration step reduces your probability of experiencing intolerable GI effects at the target dose
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