The most commonly reported side effects of floxuridine include hepatic steatosis, steatohepatitis, and diarrhoea, based on 156 FDA adverse event reports from 2004 to 2025. 10.3% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for floxuridine.
These are voluntary reports and do not establish that floxuridine caused these reactions.
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Other drugs that appear in adverse event reports alongside floxuridine. 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.
33.3% of floxuridine adverse event reports involve female patients and 37.2% involve male patients. The largest age group is adult at 72%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking floxuridine when the adverse event was reported.
Showing 15 of 48 indications
Floxuridine is sold under the brand name Fudr.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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