Does FIBRINOGEN HUMAN Cause No adverse event? 38 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 38 reports of No adverse event have been filed in association with FIBRINOGEN HUMAN (TachoSil). This represents 9.3% of all adverse event reports for FIBRINOGEN HUMAN.
38
Reports of No adverse event with FIBRINOGEN HUMAN
9.3%
of all FIBRINOGEN HUMAN reports
3
Deaths
9
Hospitalizations
How Dangerous Is No adverse event From FIBRINOGEN HUMAN?
Of the 38 reports, 3 (7.9%) resulted in death, 9 (23.7%) required hospitalization, and 3 (7.9%) were considered life-threatening.
Is No adverse event Listed in the Official Label?
Yes, No adverse event is listed as a known adverse reaction in the official FDA drug label for FIBRINOGEN HUMAN.
What Other Side Effects Does FIBRINOGEN HUMAN Cause?
Foetal exposure during pregnancy (40)
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)
Haemorrhage foetal (24)
What Other Drugs Cause No adverse event?
OMALIZUMAB (9,736)
ALBUTEROL (8,971)
ETONOGESTREL (8,827)
TOCILIZUMAB (6,492)
RITUXIMAB (5,915)
METHYLPHENIDATE (4,197)
MOMETASONE FUROATE (3,717)
HUMAN IMMUNOGLOBULIN G (3,064)
ETHINYL ESTRADIOL\NORELGESTROMIN (3,014)
VEDOLIZUMAB (2,477)
Which FIBRINOGEN HUMAN Alternatives Have Lower No adverse event 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