The most commonly reported side effects of brolucizumab include visual impairment, vitreous floaters, and vision blurred, based on 3,565 FDA adverse event reports from 2019 to 2025. 6.1% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for brolucizumab.
These are voluntary reports and do not establish that brolucizumab caused these reactions.
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Other drugs that appear in adverse event reports alongside brolucizumab. 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.
50.1% of brolucizumab adverse event reports involve female patients and 35.7% involve male patients. The largest age group is elderly at 84%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking brolucizumab when the adverse event was reported.
Showing 15 of 69 indications
Brolucizumab is sold under the brand name Beovu.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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