The most commonly reported side effects of mesoridazine include insomnia, diabetes mellitus, and psychomotor hyperactivity, based on 40 FDA adverse event reports from 2004 to 2023. 7.5% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for mesoridazine.
These are voluntary reports and do not establish that mesoridazine caused these reactions.
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Other drugs that appear in adverse event reports alongside mesoridazine. 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.
45.0% of mesoridazine adverse event reports involve female patients and 55.0% involve male patients. The largest age group is adult at 88%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking mesoridazine when the adverse event was reported.
Mesoridazine is sold under the brand name Serentil.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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