Does ZANUBRUTINIB Cause Product use issue? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Product use issue have been filed in association with ZANUBRUTINIB (BRUKINSA). This represents 0.6% of all adverse event reports for ZANUBRUTINIB.
18
Reports of Product use issue with ZANUBRUTINIB
0.6%
of all ZANUBRUTINIB reports
2
Deaths
7
Hospitalizations
How Dangerous Is Product use issue From ZANUBRUTINIB?
Of the 18 reports, 2 (11.1%) resulted in death, 7 (38.9%) required hospitalization, and 2 (11.1%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZANUBRUTINIB. However, 18 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which ZANUBRUTINIB Alternatives Have Lower Product use issue Risk?
ZANUBRUTINIB vs ZAVEGEPANT
ZANUBRUTINIB vs ZEAXANTHIN
ZANUBRUTINIB vs ZELBORAF
ZANUBRUTINIB vs ZEMPLAR
ZANUBRUTINIB vs ZENATANE