The most commonly reported side effects of foscarbidopa include fall, infusion site reaction, and hallucination, based on 1,470 FDA adverse event reports from 2024 to 2025. 3.6% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for foscarbidopa.
These are voluntary reports and do not establish that foscarbidopa caused these reactions.
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Other drugs that appear in adverse event reports alongside foscarbidopa. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
37.6% of foscarbidopa adverse event reports involve female patients and 52.2% involve male patients. The largest age group is elderly at 59%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking foscarbidopa when the adverse event was reported.
Foscarbidopa is sold under the brand name Vyalev.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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