The most commonly reported side effects of ethopropazine include hallucination, somnolence, and oedema peripheral, based on 31 FDA adverse event reports from 2007 to 2023. 41.9% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for ethopropazine.
These are voluntary reports and do not establish that ethopropazine caused these reactions.
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Other drugs that appear in adverse event reports alongside ethopropazine. 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.
29.0% of ethopropazine adverse event reports involve female patients and 61.3% involve male patients. The largest age group is elderly at 91%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking ethopropazine when the adverse event was reported.
Ethopropazine is sold under the brand name Parsidol.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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