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"Patients taking GLP-1s often experience symptoms of dry mouth, which include increased cavities and periodontal disease," Walton told HuffPost via email

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The firms own SOP states that OOS results must be immediately reported to Quality and the pharmacist-in-charge, and that investigation, root cause analysis, recall, and customer notification procedures shall be followed when applicable. The FDA pointedly notes that the when applicable language effectively makes investigation and notification optional rather than mandatory

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