Does BIVALIRUDIN Cause International normalised ratio increased? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of International normalised ratio increased have been filed in association with BIVALIRUDIN (BIVALIRUDIN). This represents 0.8% of all adverse event reports for BIVALIRUDIN.
7
Reports of International normalised ratio increased with BIVALIRUDIN
0.8%
of all BIVALIRUDIN reports
0
Deaths
1
Hospitalizations
How Dangerous Is International normalised ratio increased From BIVALIRUDIN?
Of the 7 reports, 1 (14.3%) required hospitalization, and 1 (14.3%) were considered life-threatening.
Is International normalised ratio increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BIVALIRUDIN. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does BIVALIRUDIN Cause?
Drug ineffective (148)
Haemorrhage (79)
Off label use (73)
Thrombosis in device (63)
Vascular stent thrombosis (63)
Heparin-induced thrombocytopenia (61)
Thrombosis (61)
Coagulation time abnormal (42)
Gastrointestinal haemorrhage (40)
Coronary artery thrombosis (33)
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 BIVALIRUDIN Alternatives Have Lower International normalised ratio increased Risk?
BIVALIRUDIN vs BLEOMYCIN
BIVALIRUDIN vs BLINATUMOMAB
BIVALIRUDIN vs BLONANSERIN
BIVALIRUDIN vs --BLOOD-COAGULATION FACTOR VIII FUSION PROTEIN WITH IMMUNOGLOBULIN G1 , ,-BIS WITH IMMUNOGLOBULIN G1
BIVALIRUDIN vs BOCEPREVIR