Does ZANUBRUTINIB Cause Hepatic function abnormal? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Hepatic function abnormal have been filed in association with ZANUBRUTINIB (BRUKINSA). This represents 0.5% of all adverse event reports for ZANUBRUTINIB.
15
Reports of Hepatic function abnormal with ZANUBRUTINIB
0.5%
of all ZANUBRUTINIB reports
0
Deaths
10
Hospitalizations
How Dangerous Is Hepatic function abnormal From ZANUBRUTINIB?
Of the 15 reports, 10 (66.7%) required hospitalization, and 1 (6.7%) were considered life-threatening.
Is Hepatic function abnormal 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 Hepatic function abnormal?
NIVOLUMAB (1,131)
PEMBROLIZUMAB (1,079)
METHOTREXATE (1,054)
CABOZANTINIB S-MALATE (912)
CYCLOPHOSPHAMIDE (824)
BEVACIZUMAB (769)
PACLITAXEL (603)
LENVATINIB (528)
ATORVASTATIN (520)
CYCLOSPORINE (508)
Which ZANUBRUTINIB Alternatives Have Lower Hepatic function abnormal Risk?
ZANUBRUTINIB vs ZAVEGEPANT
ZANUBRUTINIB vs ZEAXANTHIN
ZANUBRUTINIB vs ZELBORAF
ZANUBRUTINIB vs ZEMPLAR
ZANUBRUTINIB vs ZENATANE