The most commonly reported side effects of cefoxitin include off label use, drug resistance, and drug reaction with eosinophilia and systemic symptoms, based on 1,453 FDA adverse event reports from 2004 to 2025. 4.2% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for cefoxitin.
These are voluntary reports and do not establish that cefoxitin caused these reactions.
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Other drugs that appear in adverse event reports alongside cefoxitin. 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.
52.2% of cefoxitin adverse event reports involve female patients and 41.3% involve male patients. The largest age group is adult at 58%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking cefoxitin when the adverse event was reported.
Showing 15 of 195 indications
Cefoxitin is sold under the brand name Mefoxin In Sodium Chloride 0.9% In Plastic Container.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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