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Parkinsons disease drug therapies in the clinical trial pipeline: 2022 update

43,44 Given these neutral-to-concerning results, there is currently no evidence to support initiating GLP-1RAs for the primary treatment of HFrEF

Nausea was the primary adverse event, occurring in 67% of participants at the highest dose but predominantly mild-to-moderate in severity

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Deficiency causes megaloblastic anemia and subacute combined degeneration of the spinal cord

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