Does FIBRINOGEN HUMAN Cause Shock haemorrhagic? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Shock haemorrhagic have been filed in association with FIBRINOGEN HUMAN (TachoSil). This represents 3.9% of all adverse event reports for FIBRINOGEN HUMAN.
16
Reports of Shock haemorrhagic with FIBRINOGEN HUMAN
3.9%
of all FIBRINOGEN HUMAN reports
4
Deaths
5
Hospitalizations
How Dangerous Is Shock haemorrhagic From FIBRINOGEN HUMAN?
Of the 16 reports, 4 (25.0%) resulted in death, 5 (31.3%) required hospitalization, and 14 (87.5%) were considered life-threatening.
Is Shock haemorrhagic Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FIBRINOGEN HUMAN. However, 16 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 Shock haemorrhagic?
RIVAROXABAN (906)
ASPIRIN (830)
APIXABAN (476)
ENOXAPARIN (473)
CLOPIDOGREL BISULFATE (403)
DABIGATRAN ETEXILATE (383)
WARFARIN (351)
HEPARIN (291)
TACROLIMUS (241)
FUROSEMIDE (204)
Which FIBRINOGEN HUMAN Alternatives Have Lower Shock haemorrhagic 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