The most commonly reported side effects of zanubrutinib include off label use, disease progression, and white blood cell count decreased, based on 3,541 FDA adverse event reports from 2019 to 2025. 3.5% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for zanubrutinib.
These are voluntary reports and do not establish that zanubrutinib caused these reactions.
Report severity
Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside zanubrutinib. 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.
11.9% of zanubrutinib adverse event reports involve female patients and 17.9% involve male patients. The largest age group is elderly at 71%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking zanubrutinib when the adverse event was reported.
Showing 15 of 136 indications
Zanubrutinib is sold under the brand name Brukinsa.
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.