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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 Multiple organ dysfunction syndrome? 15 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Multiple organ dysfunction syndrome have been filed in association with ZANUBRUTINIB (BRUKINSA). This represents 0.5% of all adverse event reports for ZANUBRUTINIB.

15
Reports of Multiple organ dysfunction syndrome with ZANUBRUTINIB
0.5%
of all ZANUBRUTINIB reports
12
Deaths
7
Hospitalizations

How Dangerous Is Multiple organ dysfunction syndrome From ZANUBRUTINIB?

Of the 15 reports, 12 (80.0%) resulted in death, 7 (46.7%) required hospitalization, and 1 (6.7%) were considered life-threatening.

Is Multiple organ dysfunction syndrome Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ZANUBRUTINIB. However, 15 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 Multiple organ dysfunction syndrome?

TACROLIMUS (1,847) CYCLOPHOSPHAMIDE (1,597) MYCOPHENOLATE MOFETIL (1,566) PREDNISONE (1,525) DEXAMETHASONE (1,355) METHOTREXATE (1,317) METHYLPREDNISOLONE (1,278) RITUXIMAB (1,188) PREDNISOLONE (1,154) CYCLOSPORINE (933)

Which ZANUBRUTINIB Alternatives Have Lower Multiple organ dysfunction syndrome Risk?

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

Related Pages

ZANUBRUTINIB Full Profile All Multiple organ dysfunction syndrome Reports All Drugs Causing Multiple organ dysfunction syndrome ZANUBRUTINIB Demographics