The most commonly reported side effects of polatuzumab include disease progression, off label use, and death, based on 8,732 FDA adverse event reports from 2013 to 2025. 5.3% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for polatuzumab.
These are voluntary reports and do not establish that polatuzumab caused these reactions.
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Other drugs that appear in adverse event reports alongside polatuzumab. 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.
33.0% of polatuzumab adverse event reports involve female patients and 46.6% involve male patients. The largest age group is elderly at 58%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking polatuzumab when the adverse event was reported.
Showing 15 of 121 indications
Polatuzumab is sold under the brand name Polivy.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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