Does FIBRINOGEN HUMAN Cause Infusion site thrombosis? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Infusion site thrombosis have been filed in association with FIBRINOGEN HUMAN (TachoSil). This represents 3.7% of all adverse event reports for FIBRINOGEN HUMAN.
15
Reports of Infusion site thrombosis with FIBRINOGEN HUMAN
3.7%
of all FIBRINOGEN HUMAN reports
0
Deaths
15
Hospitalizations
How Dangerous Is Infusion site thrombosis From FIBRINOGEN HUMAN?
Of the 15 reports, 15 (100.0%) required hospitalization.
Is Infusion site thrombosis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FIBRINOGEN HUMAN. However, 15 reports have been filed with the FAERS database.
What Other Side Effects Does FIBRINOGEN HUMAN Cause?
Foetal exposure during pregnancy (40)
No adverse event (38)
Off label use (38)
Drug ineffective (34)
Hypotension (31)
Foetal anaemia (27)
Foetal growth restriction (27)
Haemorrhage in pregnancy (26)
Anaphylactic shock (25)
Maternal exposure during pregnancy (25)
What Other Drugs Cause Infusion site thrombosis?
TREPROSTINIL (21)
MESALAMINE (16)
AZATHIOPRINE (15)
RANITIDINE (15)
ESOMEPRAZOLE (14)
HUMAN IMMUNOGLOBULIN G (13)
AMLODIPINE (12)
GEMCITABINE (10)
SODIUM (9)
ASPIRIN (8)
Which FIBRINOGEN HUMAN Alternatives Have Lower Infusion site thrombosis Risk?
FIBRINOGEN HUMAN vs FIBRINOGEN HUMAN\HUMAN THROMBIN
FIBRINOGEN HUMAN vs FIBRINOGEN HUMAN\THROMBIN HUMAN
FIBRINOGEN HUMAN vs FIDAXOMICIN
FIBRINOGEN HUMAN vs FILGOTINIB
FIBRINOGEN HUMAN vs FILGRASTIM