The most commonly reported side effects of ansuvimab include postpartum haemorrhage, premature delivery, and maternal exposure during pregnancy, based on 3 FDA adverse event reports from 2024 to 2025.
Percentages show how often each reaction appears relative to total reports for ansuvimab.
These are voluntary reports and do not establish that ansuvimab 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 ansuvimab. 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.
66.7% of ansuvimab adverse event reports involve female patients and 33.3% involve male patients. The largest age group is neonate at 33%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking ansuvimab when the adverse event was reported.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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