Does ZANUBRUTINIB Cause Condition aggravated? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Condition aggravated have been filed in association with ZANUBRUTINIB (BRUKINSA). This represents 0.6% of all adverse event reports for ZANUBRUTINIB.
16
Reports of Condition aggravated with ZANUBRUTINIB
0.6%
of all ZANUBRUTINIB reports
1
Deaths
8
Hospitalizations
How Dangerous Is Condition aggravated From ZANUBRUTINIB?
Of the 16 reports, 1 (6.3%) resulted in death, 8 (50.0%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZANUBRUTINIB. However, 16 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ZANUBRUTINIB Alternatives Have Lower Condition aggravated Risk?
ZANUBRUTINIB vs ZAVEGEPANT
ZANUBRUTINIB vs ZEAXANTHIN
ZANUBRUTINIB vs ZELBORAF
ZANUBRUTINIB vs ZEMPLAR
ZANUBRUTINIB vs ZENATANE