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Whether this represents true peptide-related adverse events or confounding lifestyle factors remains unclear without controlled trials
Alexander, T
If you are taking retatrutide as part of a clinical trial , any adverse events including changes in mood or mental health must be reported to your trial team and trial sponsor in accordance with the UK Clinical Trials Regulations and MHRA guidance on adverse event and Suspected Unexpected Serious Adverse Reaction (SUSAR) reporting
Changing the frequency of your injections, though, should only be done at the direction of your clinician
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