Does IBRUTINIB Cause Post procedural complication? 91 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 91 reports of Post procedural complication have been filed in association with IBRUTINIB (Imbruvica). This represents 0.1% of all adverse event reports for IBRUTINIB.
91
Reports of Post procedural complication with IBRUTINIB
0.1%
of all IBRUTINIB reports
11
Deaths
37
Hospitalizations
How Dangerous Is Post procedural complication From IBRUTINIB?
Of the 91 reports, 11 (12.1%) resulted in death, 37 (40.7%) required hospitalization.
Is Post procedural complication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IBRUTINIB. However, 91 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 complication?
ADALIMUMAB (2,494)
ETANERCEPT (318)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (244)
UPADACITINIB (241)
RISANKIZUMAB-RZAA (232)
INFLIXIMAB (217)
METHOTREXATE (188)
TREPROSTINIL (174)
HUMAN IMMUNOGLOBULIN G (159)
PREDNISONE (157)
Which IBRUTINIB Alternatives Have Lower Post procedural complication Risk?
IBRUTINIB vs IBUPROFEN
IBRUTINIB vs IBUPROFEN LYSINE
IBRUTINIB vs IBUPROFEN UNKNOWN PRODUCT
IBRUTINIB vs IBUPROFEN\IBUPROFEN
IBRUTINIB vs IBUPROFEN\PHENYLEPHRINE