Does BIVALIRUDIN Cause Haemoglobin decreased? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Haemoglobin decreased have been filed in association with BIVALIRUDIN (BIVALIRUDIN). This represents 1.9% of all adverse event reports for BIVALIRUDIN.
16
Reports of Haemoglobin decreased with BIVALIRUDIN
1.9%
of all BIVALIRUDIN reports
5
Deaths
6
Hospitalizations
How Dangerous Is Haemoglobin decreased From BIVALIRUDIN?
Of the 16 reports, 5 (31.3%) resulted in death, 6 (37.5%) required hospitalization, and 3 (18.8%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BIVALIRUDIN. However, 16 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 Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which BIVALIRUDIN Alternatives Have Lower Haemoglobin decreased 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