Does BIVALIRUDIN Cause Thrombosis in device? 63 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 63 reports of Thrombosis in device have been filed in association with BIVALIRUDIN (BIVALIRUDIN). This represents 7.5% of all adverse event reports for BIVALIRUDIN.
63
Reports of Thrombosis in device with BIVALIRUDIN
7.5%
of all BIVALIRUDIN reports
9
Deaths
8
Hospitalizations
How Dangerous Is Thrombosis in device From BIVALIRUDIN?
Of the 63 reports, 9 (14.3%) resulted in death, 8 (12.7%) required hospitalization, and 9 (14.3%) were considered life-threatening.
Is Thrombosis in device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BIVALIRUDIN. However, 63 reports have been filed with the FAERS database.
What Other Side Effects Does BIVALIRUDIN Cause?
Drug ineffective (148)
Haemorrhage (79)
Off label use (73)
Vascular stent thrombosis (63)
Heparin-induced thrombocytopenia (61)
Thrombosis (61)
Coagulation time abnormal (42)
Gastrointestinal haemorrhage (40)
Coronary artery thrombosis (33)
Cardiac arrest (28)
What Other Drugs Cause Thrombosis in device?
TREPROSTINIL (186)
TICAGRELOR (154)
EPOPROSTENOL (135)
HEPARIN (111)
CLOPIDOGREL BISULFATE (87)
ASPIRIN (79)
FERRIC PYROPHOSPHATE (76)
AMBRISENTAN (59)
BRILINTA (50)
PRASUGREL (48)
Which BIVALIRUDIN Alternatives Have Lower Thrombosis in device 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