Does IBRUTINIB Cause Intentional product use issue? 161 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 161 reports of Intentional product use issue have been filed in association with IBRUTINIB (Imbruvica). This represents 0.2% of all adverse event reports for IBRUTINIB.
161
Reports of Intentional product use issue with IBRUTINIB
0.2%
of all IBRUTINIB reports
31
Deaths
25
Hospitalizations
How Dangerous Is Intentional product use issue From IBRUTINIB?
Of the 161 reports, 31 (19.3%) resulted in death, 25 (15.5%) required hospitalization, and 3 (1.9%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IBRUTINIB. However, 161 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which IBRUTINIB Alternatives Have Lower Intentional product use issue Risk?
IBRUTINIB vs IBUPROFEN
IBRUTINIB vs IBUPROFEN LYSINE
IBRUTINIB vs IBUPROFEN UNKNOWN PRODUCT
IBRUTINIB vs IBUPROFEN\IBUPROFEN
IBRUTINIB vs IBUPROFEN\PHENYLEPHRINE