The most commonly reported side effects of thiamine include off label use, nausea, and dyspnoea, based on 18,234 FDA adverse event reports from 2004 to 2025. 4.3% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for thiamine.
These are voluntary reports and do not establish that thiamine caused these reactions.
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Other drugs that appear in adverse event reports alongside thiamine. 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.
42.9% of thiamine adverse event reports involve female patients and 49.7% involve male patients. The largest age group is adult at 61%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking thiamine when the adverse event was reported.
Showing 15 of 409 indications
Thiamine is sold under brand names including M.v.i.-12 Lyophilized, M.v.i.-12 Adult.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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