The most commonly reported side effects of metharbital include complex regional pain syndrome, musculoskeletal pain, and oedema peripheral, based on 2 FDA adverse event reports from 2009 to 2015. 50.0% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for metharbital.
These are voluntary reports and do not establish that metharbital caused these reactions.
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Other drugs that appear in adverse event reports alongside metharbital. 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
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.
0.0% of metharbital adverse event reports involve female patients and 100.0% involve male patients. The largest age group is neonate at 50%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking metharbital when the adverse event was reported.
Metharbital is sold under the brand name Gemonil.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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