Does IBRUTINIB Cause Product use issue? 753 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 753 reports of Product use issue have been filed in association with IBRUTINIB (Imbruvica). This represents 1.0% of all adverse event reports for IBRUTINIB.
753
Reports of Product use issue with IBRUTINIB
1.0%
of all IBRUTINIB reports
160
Deaths
268
Hospitalizations
How Dangerous Is Product use issue From IBRUTINIB?
Of the 753 reports, 160 (21.2%) resulted in death, 268 (35.6%) required hospitalization, and 9 (1.2%) 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 IBRUTINIB. However, 753 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 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 IBRUTINIB Alternatives Have Lower Product use issue Risk?
IBRUTINIB vs IBUPROFEN
IBRUTINIB vs IBUPROFEN LYSINE
IBRUTINIB vs IBUPROFEN UNKNOWN PRODUCT
IBRUTINIB vs IBUPROFEN\IBUPROFEN
IBRUTINIB vs IBUPROFEN\PHENYLEPHRINE