Does IBRUTINIB Cause Post procedural haemorrhage? 269 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 269 reports of Post procedural haemorrhage have been filed in association with IBRUTINIB (Imbruvica). This represents 0.4% of all adverse event reports for IBRUTINIB.
269
Reports of Post procedural haemorrhage with IBRUTINIB
0.4%
of all IBRUTINIB reports
6
Deaths
95
Hospitalizations
How Dangerous Is Post procedural haemorrhage From IBRUTINIB?
Of the 269 reports, 6 (2.2%) resulted in death, 95 (35.3%) required hospitalization, and 5 (1.9%) were considered life-threatening.
Is Post procedural haemorrhage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IBRUTINIB. However, 269 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 Post procedural haemorrhage?
LEVONORGESTREL (1,106)
RIVAROXABAN (930)
ASPIRIN (618)
APIXABAN (539)
ADALIMUMAB (476)
CLOPIDOGREL BISULFATE (235)
HEPARIN (174)
WARFARIN (170)
DABIGATRAN ETEXILATE (121)
COPPER (106)
Which IBRUTINIB Alternatives Have Lower Post procedural haemorrhage Risk?
IBRUTINIB vs IBUPROFEN
IBRUTINIB vs IBUPROFEN LYSINE
IBRUTINIB vs IBUPROFEN UNKNOWN PRODUCT
IBRUTINIB vs IBUPROFEN\IBUPROFEN
IBRUTINIB vs IBUPROFEN\PHENYLEPHRINE