Does COAGULATION FACTOR VIIA RECOMBINANT HUMAN Cause Condition aggravated? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Condition aggravated have been filed in association with COAGULATION FACTOR VIIA RECOMBINANT HUMAN (Sevenfact). This represents 2.4% of all adverse event reports for COAGULATION FACTOR VIIA RECOMBINANT HUMAN.
23
Reports of Condition aggravated with COAGULATION FACTOR VIIA RECOMBINANT HUMAN
2.4%
of all COAGULATION FACTOR VIIA RECOMBINANT HUMAN reports
8
Deaths
11
Hospitalizations
How Dangerous Is Condition aggravated From COAGULATION FACTOR VIIA RECOMBINANT HUMAN?
Of the 23 reports, 8 (34.8%) resulted in death, 11 (47.8%) required hospitalization, and 2 (8.7%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for COAGULATION FACTOR VIIA RECOMBINANT HUMAN. However, 23 reports have been filed with the FAERS database.
What Other Side Effects Does COAGULATION FACTOR VIIA RECOMBINANT HUMAN Cause?
Off label use (169)
Haemorrhage (129)
Drug ineffective (117)
Death (85)
Pre-existing disease (78)
Therapy partial responder (78)
Acquired haemophilia (72)
Haemarthrosis (47)
Haematoma (30)
Therapy responder (30)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which COAGULATION FACTOR VIIA RECOMBINANT HUMAN Alternatives Have Lower Condition aggravated Risk?
COAGULATION FACTOR VIIA RECOMBINANT HUMAN vs COBAMAMIDE
COAGULATION FACTOR VIIA RECOMBINANT HUMAN vs COBICISTAT
COAGULATION FACTOR VIIA RECOMBINANT HUMAN vs COBICISTAT\DARUNAVIR ETHANOLATE
COAGULATION FACTOR VIIA RECOMBINANT HUMAN vs COBICISTAT\DARUNAVIR\EMTRICITABINE\TENOFOVIR ALAFENAMIDE
COAGULATION FACTOR VIIA RECOMBINANT HUMAN vs COBICISTAT\ELVITEGRAVIR\EMTRICITABINE\TENOFOVIR