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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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(Reminder: Ozempic follows a titration schedule, in which you gradually increase your dosage of the drug over a period of weeks to months until you find a dose thats effective and tolerable for you, i.e