The most commonly reported side effects of mephenytoin include headache, maternal exposure timing unspecified, and patent ductus arteriosus, based on 28 FDA adverse event reports from 2004 to 2021. 7.1% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for mephenytoin.
These are voluntary reports and do not establish that mephenytoin caused these reactions.
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Other drugs that appear in adverse event reports alongside mephenytoin. 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.
50.0% of mephenytoin adverse event reports involve female patients and 10.7% involve male patients. The largest age group is adult at 64%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking mephenytoin when the adverse event was reported.
Mephenytoin is sold under the brand name Mesantoin.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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