The most commonly reported side effects of auranofin include drug hypersensitivity, nausea, and anaemia, based on 220 FDA adverse event reports from 2004 to 2024. 5.9% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for auranofin.
These are voluntary reports and do not establish that auranofin caused these reactions.
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Other drugs that appear in adverse event reports alongside auranofin. 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.
77.3% of auranofin adverse event reports involve female patients and 17.7% involve male patients. The largest age group is adult at 53%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking auranofin when the adverse event was reported.
Auranofin is sold under the brand name Ridaura.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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