Does IBRUTINIB Cause Condition aggravated? 201 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 201 reports of Condition aggravated have been filed in association with IBRUTINIB (Imbruvica). This represents 0.3% of all adverse event reports for IBRUTINIB.
201
Reports of Condition aggravated with IBRUTINIB
0.3%
of all IBRUTINIB reports
26
Deaths
66
Hospitalizations
How Dangerous Is Condition aggravated From IBRUTINIB?
Of the 201 reports, 26 (12.9%) resulted in death, 66 (32.8%) required hospitalization, and 16 (8.0%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IBRUTINIB. However, 201 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which IBRUTINIB Alternatives Have Lower Condition aggravated Risk?
IBRUTINIB vs IBUPROFEN
IBRUTINIB vs IBUPROFEN LYSINE
IBRUTINIB vs IBUPROFEN UNKNOWN PRODUCT
IBRUTINIB vs IBUPROFEN\IBUPROFEN
IBRUTINIB vs IBUPROFEN\PHENYLEPHRINE