The most commonly reported side effects of moxetumomab include capillary leak syndrome, haemolytic uraemic syndrome, and death, based on 71 FDA adverse event reports from 2009 to 2025. 4.2% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for moxetumomab.
These are voluntary reports and do not establish that moxetumomab caused these reactions.
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Other drugs that appear in adverse event reports alongside moxetumomab. 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.
15.5% of moxetumomab adverse event reports involve female patients and 63.4% involve male patients. The largest age group is elderly at 66%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking moxetumomab when the adverse event was reported.
Moxetumomab is sold under the brand name Lumoxiti.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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