Does FIBRINOGEN HUMAN\THROMBIN HUMAN Cause Off label use? 225 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 225 reports of Off label use have been filed in association with FIBRINOGEN HUMAN\THROMBIN HUMAN. This represents 22.4% of all adverse event reports for FIBRINOGEN HUMAN\THROMBIN HUMAN.
225
Reports of Off label use with FIBRINOGEN HUMAN\THROMBIN HUMAN
22.4%
of all FIBRINOGEN HUMAN\THROMBIN HUMAN reports
11
Deaths
30
Hospitalizations
How Dangerous Is Off label use From FIBRINOGEN HUMAN\THROMBIN HUMAN?
Of the 225 reports, 11 (4.9%) resulted in death, 30 (13.3%) required hospitalization, and 4 (1.8%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FIBRINOGEN HUMAN\THROMBIN HUMAN. However, 225 reports have been filed with the FAERS database.
What Other Side Effects Does FIBRINOGEN HUMAN\THROMBIN HUMAN Cause?
Drug ineffective (132)
Product use in unapproved indication (95)
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 Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which FIBRINOGEN HUMAN\THROMBIN HUMAN Alternatives Have Lower Off label use 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