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Values presented as percentage of total Adverse events are presented for all participants who were randomised and took at least one dose of treatment, regardless of whether they discontinued * For the T2D trial, this was limited to ‘supraventricular arrhythmias and cardiac conduction disorders’ ** For the obesity trial these are presented as hepatic disorder / biliary disorder separately NA : Not applicable In the obesity trial, serious adverse events (SAEs) occurred in 4% of participants with retatrutide use overall (0–6% across groups) vs
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Warnings: This product is not meant for human consumption or ingestion, it is meant to reconstitute chemicals for research purpose only
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