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The majority of study participants (81.6%) were female

The FDA Adverse Event Reporting System (FAERS) contains reports of arthralgia and musculoskeletal pain in patients taking GLP-1 receptor agonists, though these spontaneous reports have significant limitations including underreporting and inability to establish causation

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Consult your healthcare provider before making medical decisions, especially if bruising is frequent, large, worsening, painful, or connected to blood thinners or other bleeding concerns