The most commonly reported side effects of methdilazine include hepatotoxicity, condition aggravated, and intervertebral disc disorder, based on 7 FDA adverse event reports from 2005 to 2021. 42.9% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for methdilazine.
These are voluntary reports and do not establish that methdilazine caused these reactions.
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Other drugs that appear in adverse event reports alongside methdilazine. 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.
71.4% of methdilazine adverse event reports involve female patients and 14.3% involve male patients. The largest age group is elderly at 67%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking methdilazine when the adverse event was reported.
Methdilazine is sold under the brand name Tacaryl.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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