Does IBRUTINIB Cause International normalised ratio increased? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of International normalised ratio increased have been filed in association with IBRUTINIB (Imbruvica). This represents 0.1% of all adverse event reports for IBRUTINIB.
43
Reports of International normalised ratio increased with IBRUTINIB
0.1%
of all IBRUTINIB reports
13
Deaths
27
Hospitalizations
How Dangerous Is International normalised ratio increased From IBRUTINIB?
Of the 43 reports, 13 (30.2%) resulted in death, 27 (62.8%) required hospitalization.
Is International normalised ratio increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IBRUTINIB. However, 43 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 International normalised ratio increased?
WARFARIN (5,622)
RIVAROXABAN (863)
ACETAMINOPHEN (533)
ASPIRIN (448)
APIXABAN (317)
CLOPIDOGREL BISULFATE (314)
FLUINDIONE (286)
AMIODARONE (277)
FUROSEMIDE (277)
DABIGATRAN ETEXILATE (223)
Which IBRUTINIB Alternatives Have Lower International normalised ratio increased Risk?
IBRUTINIB vs IBUPROFEN
IBRUTINIB vs IBUPROFEN LYSINE
IBRUTINIB vs IBUPROFEN UNKNOWN PRODUCT
IBRUTINIB vs IBUPROFEN\IBUPROFEN
IBRUTINIB vs IBUPROFEN\PHENYLEPHRINE