The most commonly reported side effects of margetuximab include disease progression, dry gangrene, and nausea, based on 65 FDA adverse event reports from 2021 to 2025. 10.8% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for margetuximab.
These are voluntary reports and do not establish that margetuximab caused these reactions.
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Other drugs that appear in adverse event reports alongside margetuximab. 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.
75.4% of margetuximab adverse event reports involve female patients and 13.8% involve male patients. The largest age group is adult at 71%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking margetuximab when the adverse event was reported.
Showing 15 of 24 indications
Margetuximab is sold under the brand name Margenza.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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