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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ZANUBRUTINIB Cause Adverse event? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Adverse event have been filed in association with ZANUBRUTINIB (BRUKINSA). This represents 0.2% of all adverse event reports for ZANUBRUTINIB.

5
Reports of Adverse event with ZANUBRUTINIB
0.2%
of all ZANUBRUTINIB reports
4
Deaths
0
Hospitalizations

How Dangerous Is Adverse event From ZANUBRUTINIB?

Of the 5 reports, 4 (80.0%) resulted in death.

Is Adverse event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ZANUBRUTINIB. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does ZANUBRUTINIB Cause?

Off label use (376) Disease progression (224) Contusion (165) Myelosuppression (147) Fatigue (146) Rash (134) Death (120) White blood cell count decreased (119) Platelet count decreased (112) Anaemia (102)

What Other Drugs Cause Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which ZANUBRUTINIB Alternatives Have Lower Adverse event Risk?

ZANUBRUTINIB vs ZAVEGEPANT ZANUBRUTINIB vs ZEAXANTHIN ZANUBRUTINIB vs ZELBORAF ZANUBRUTINIB vs ZEMPLAR ZANUBRUTINIB vs ZENATANE

Related Pages

ZANUBRUTINIB Full Profile All Adverse event Reports All Drugs Causing Adverse event ZANUBRUTINIB Demographics