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The safety profile was consistent with GLP-1 receptor agonists, primarily featuring transient, mild-to-moderate gastrointestinal adverse events (e.g., nausea, 55%), with low discontinuation rates (6-8.4%)

The specific action taken is determined by consideration of all the available evidence and relevant legal precedents. The MHRA also stressed that labelling peptides for research purposes only a ruse used by many social media vendors and websites was not enough to avoid scrutiny

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It is unknown whether this downregulation is the primary cause of the disorder, but it is likely to be a contributing factor

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