Does ZANUBRUTINIB Cause Product use complaint? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Product use complaint have been filed in association with ZANUBRUTINIB (BRUKINSA). This represents 0.6% of all adverse event reports for ZANUBRUTINIB.
17
Reports of Product use complaint with ZANUBRUTINIB
0.6%
of all ZANUBRUTINIB reports
1
Deaths
2
Hospitalizations
How Dangerous Is Product use complaint From ZANUBRUTINIB?
Of the 17 reports, 1 (5.9%) resulted in death, 2 (11.8%) required hospitalization.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZANUBRUTINIB. However, 17 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 complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
Which ZANUBRUTINIB Alternatives Have Lower Product use complaint Risk?
ZANUBRUTINIB vs ZAVEGEPANT
ZANUBRUTINIB vs ZEAXANTHIN
ZANUBRUTINIB vs ZELBORAF
ZANUBRUTINIB vs ZEMPLAR
ZANUBRUTINIB vs ZENATANE