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Dulaglutides safety profile is consistent with other GLP-1 receptor agonists, with transient nausea being the most frequently reported adverse event (14.6% incidence). Dose escalation from 0.75 to 1.5 mg is recommended after at least four weeks, based on individual glycemic control needs [57]

This contrasts with most PD literature, which suggests that younger patients generally have better compensatory resiliency and slower disease progression [67,68,69]

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