Does FIBRINOGEN HUMAN\THROMBIN HUMAN Cause Product use in unapproved indication? 95 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 95 reports of Product use in unapproved indication have been filed in association with FIBRINOGEN HUMAN\THROMBIN HUMAN. This represents 9.5% of all adverse event reports for FIBRINOGEN HUMAN\THROMBIN HUMAN.
95
Reports of Product use in unapproved indication with FIBRINOGEN HUMAN\THROMBIN HUMAN
9.5%
of all FIBRINOGEN HUMAN\THROMBIN HUMAN reports
3
Deaths
10
Hospitalizations
How Dangerous Is Product use in unapproved indication From FIBRINOGEN HUMAN\THROMBIN HUMAN?
Of the 95 reports, 3 (3.2%) resulted in death, 10 (10.5%) required hospitalization, and 2 (2.1%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FIBRINOGEN HUMAN\THROMBIN HUMAN. However, 95 reports have been filed with the FAERS database.
What Other Side Effects Does FIBRINOGEN HUMAN\THROMBIN HUMAN Cause?
Off label use (225)
Drug ineffective (132)
Cerebrospinal fluid leakage (57)
Haemorrhage (50)
Seroma (49)
Drug ineffective for unapproved indication (42)
Product physical consistency issue (31)
Wound infection (29)
Post procedural complication (26)
Haematoma (23)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which FIBRINOGEN HUMAN\THROMBIN HUMAN Alternatives Have Lower Product use in unapproved indication Risk?
FIBRINOGEN HUMAN\THROMBIN HUMAN vs FIDAXOMICIN
FIBRINOGEN HUMAN\THROMBIN HUMAN vs FILGOTINIB
FIBRINOGEN HUMAN\THROMBIN HUMAN vs FILGRASTIM
FIBRINOGEN HUMAN\THROMBIN HUMAN vs FILGRASTIM-AAFI
FIBRINOGEN HUMAN\THROMBIN HUMAN vs FILGRASTIM-SNDZ