The most commonly reported side effects of naxitamab include hypotension, pain, and hypertension, based on 236 FDA adverse event reports from 2011 to 2025.
Percentages show how often each reaction appears relative to total reports for naxitamab.
These are voluntary reports and do not establish that naxitamab caused these reactions.
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Other drugs that appear in adverse event reports alongside naxitamab. 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.
28.8% of naxitamab adverse event reports involve female patients and 28.4% involve male patients. The largest age group is child at 59%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking naxitamab when the adverse event was reported.
Naxitamab is sold under the brand name Danyelza.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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