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It must complete Phase 3 trials and undergo FDA review before becoming available for prescription in Florida

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Other primary outcomes included PD motor complications as measured by MDS-UPDRS Part IV in endpoints of included studies, motor experiences of daily living in PD patients as measured by MDS-UPDRS Part II in endpoints of included studies, gastrointestinal adverse events of GLP-1 receptor agonists, including dyspepsia, vomiting, diarrhea, and constipation, as well as general adverse events such as headache and fatigue