Does ZANUBRUTINIB Cause Dyspnoea? 61 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 61 reports of Dyspnoea have been filed in association with ZANUBRUTINIB (BRUKINSA). This represents 2.2% of all adverse event reports for ZANUBRUTINIB.
61
Reports of Dyspnoea with ZANUBRUTINIB
2.2%
of all ZANUBRUTINIB reports
3
Deaths
28
Hospitalizations
How Dangerous Is Dyspnoea From ZANUBRUTINIB?
Of the 61 reports, 3 (4.9%) resulted in death, 28 (45.9%) required hospitalization, and 1 (1.6%) were considered life-threatening.
Is Dyspnoea Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZANUBRUTINIB. However, 61 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 Dyspnoea?
ALBUTEROL (21,856)
TREPROSTINIL (16,348)
AMBRISENTAN (13,367)
PREDNISONE (12,830)
BUDESONIDE\FORMOTEROL (11,158)
TIOTROPIUM (10,863)
ADALIMUMAB (10,547)
DUPILUMAB (10,310)
FLUTICASONE\SALMETEROL (9,783)
MEPOLIZUMAB (9,192)
Which ZANUBRUTINIB Alternatives Have Lower Dyspnoea Risk?
ZANUBRUTINIB vs ZAVEGEPANT
ZANUBRUTINIB vs ZEAXANTHIN
ZANUBRUTINIB vs ZELBORAF
ZANUBRUTINIB vs ZEMPLAR
ZANUBRUTINIB vs ZENATANE