Does FIBRINOGEN HUMAN Cause Haemorrhage? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Haemorrhage have been filed in association with FIBRINOGEN HUMAN (TachoSil). This represents 5.2% of all adverse event reports for FIBRINOGEN HUMAN.
21
Reports of Haemorrhage with FIBRINOGEN HUMAN
5.2%
of all FIBRINOGEN HUMAN reports
3
Deaths
3
Hospitalizations
How Dangerous Is Haemorrhage From FIBRINOGEN HUMAN?
Of the 21 reports, 3 (14.3%) resulted in death, 3 (14.3%) required hospitalization, and 10 (47.6%) were considered life-threatening.
Is Haemorrhage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FIBRINOGEN HUMAN. However, 21 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 Haemorrhage?
RIVAROXABAN (6,571)
APIXABAN (4,770)
EMICIZUMAB-KXWH (3,612)
WARFARIN (2,930)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (2,925)
ASPIRIN (2,878)
ADALIMUMAB (2,681)
IBRUTINIB (1,907)
CLOPIDOGREL BISULFATE (1,762)
INSULIN LISPRO (1,614)
Which FIBRINOGEN HUMAN Alternatives Have Lower Haemorrhage 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