The most commonly reported side effects of pozelimab include meningococcal infection, seizure, and drug effect less than expected, based on 4 FDA adverse event reports from 2023 to 2025.
Percentages show how often each reaction appears relative to total reports for pozelimab.
These are voluntary reports and do not establish that pozelimab caused these reactions.
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Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside pozelimab. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
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.
75.0% of pozelimab adverse event reports involve female patients and 25.0% involve male patients. The largest age group is child at 50%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking pozelimab when the adverse event was reported.
Pozelimab is sold under the brand name Veopoz.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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