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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
For components distribution analysis in the ileum, mice given GQD_H were sacrificed at 30, 60, 120, and 240 min, and the ileal contents were collected
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