The most commonly reported side effects of belantamab include keratopathy, visual acuity reduced, and death, based on 2,653 FDA adverse event reports from 2012 to 2025. 3.4% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for belantamab.
These are voluntary reports and do not establish that belantamab caused these reactions.
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Other drugs that appear in adverse event reports alongside belantamab. 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.
21.0% of belantamab adverse event reports involve female patients and 28.7% involve male patients. The largest age group is elderly at 64%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking belantamab when the adverse event was reported.
Showing 15 of 29 indications
Belantamab is sold under the brand name Blenrep.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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