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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 Sepsis? 44 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 44 reports of Sepsis have been filed in association with ZANUBRUTINIB (BRUKINSA). This represents 1.6% of all adverse event reports for ZANUBRUTINIB.

44
Reports of Sepsis with ZANUBRUTINIB
1.6%
of all ZANUBRUTINIB reports
16
Deaths
24
Hospitalizations

How Dangerous Is Sepsis From ZANUBRUTINIB?

Of the 44 reports, 16 (36.4%) resulted in death, 24 (54.5%) required hospitalization, and 2 (4.5%) were considered life-threatening.

Is Sepsis Listed in the Official Label?

Yes, Sepsis is listed as a known adverse reaction in the official FDA drug label for ZANUBRUTINIB.

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 Sepsis?

RITUXIMAB (4,043) CYCLOPHOSPHAMIDE (4,041) METHOTREXATE (3,933) ADALIMUMAB (3,169) DEXAMETHASONE (3,150) LENALIDOMIDE (2,956) VINCRISTINE (2,791) DOXORUBICIN (2,740) PREDNISONE (2,634) PREDNISOLONE (2,281)

Which ZANUBRUTINIB Alternatives Have Lower Sepsis Risk?

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

Related Pages

ZANUBRUTINIB Full Profile All Sepsis Reports All Drugs Causing Sepsis ZANUBRUTINIB Demographics