The most commonly reported side effects of ublituximab include infusion related reaction, fatigue, and headache, based on 3,086 FDA adverse event reports from 2015 to 2025. 2.2% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for ublituximab.
These are voluntary reports and do not establish that ublituximab caused these reactions.
Report severity
Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside ublituximab. 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.
22.9% of ublituximab adverse event reports involve female patients and 8.1% involve male patients. The largest age group is adult at 87%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking ublituximab when the adverse event was reported.
Showing 15 of 24 indications
Ublituximab is sold under the brand name Briumvi.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
Ask OpenClaim about your specific drug combination. Get a sourced report using FDA data, drug labels, and medical literature.