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Essentially two compounds were studied

Ototoxicity risk factors include the cumulative dose, impaired renal function, route of administration, cranial irradiation, previous sensorineural hearing loss, age under five years, concomitant use of ototoxic drugs, genetic susceptibility, and tumor localization (16)

Preclinical evidence consistently demonstrates that GLP-1 RAs can attenuate key pathophysiological mechanisms of PD [40, 53]

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Head-to-Head Comparison Side Effects: Similar but Not Identical GI side effects are the main event for both: nausea, diarrhea, vomiting, constipation