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To clarify how integrated safety data operates in practice, the following areas are addressed: Clinical safety monitoring during development Pharmacovigilance Adverse Event Assessment Post-approval safety oversight and signal detection Regulatory documentation and data traceability Clinical Safety Monitoring During Drug Development Clinical teams monitor safety data continuously during trials to detect emerging risks early

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The full therapeutic effect may take 16-20 weeks to manifest, particularly with the Wegovy titration schedule

Shorter telomeres are associated with accelerated biological aging, increased disease risk, and reduced tissue repair capacity