Does IBRUTINIB Cause Adverse event? 452 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 452 reports of Adverse event have been filed in association with IBRUTINIB (Imbruvica). This represents 0.6% of all adverse event reports for IBRUTINIB.
452
Reports of Adverse event with IBRUTINIB
0.6%
of all IBRUTINIB reports
61
Deaths
179
Hospitalizations
How Dangerous Is Adverse event From IBRUTINIB?
Of the 452 reports, 61 (13.5%) resulted in death, 179 (39.6%) required hospitalization, and 7 (1.5%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IBRUTINIB. However, 452 reports have been filed with the FAERS database.
What Other Side Effects Does IBRUTINIB Cause?
Death (8,007)
Off label use (5,446)
Fatigue (4,479)
Diarrhoea (3,903)
Atrial fibrillation (3,671)
Pneumonia (3,015)
Incorrect dose administered (2,752)
Contusion (2,712)
Fall (2,375)
Asthenia (2,200)
What Other Drugs Cause Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which IBRUTINIB Alternatives Have Lower Adverse event Risk?
IBRUTINIB vs IBUPROFEN
IBRUTINIB vs IBUPROFEN LYSINE
IBRUTINIB vs IBUPROFEN UNKNOWN PRODUCT
IBRUTINIB vs IBUPROFEN\IBUPROFEN
IBRUTINIB vs IBUPROFEN\PHENYLEPHRINE