Does FIBRINOGEN HUMAN\THROMBIN HUMAN Cause Post procedural complication? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Post procedural complication have been filed in association with FIBRINOGEN HUMAN\THROMBIN HUMAN. This represents 2.6% of all adverse event reports for FIBRINOGEN HUMAN\THROMBIN HUMAN.
26
Reports of Post procedural complication with FIBRINOGEN HUMAN\THROMBIN HUMAN
2.6%
of all FIBRINOGEN HUMAN\THROMBIN HUMAN reports
1
Deaths
8
Hospitalizations
How Dangerous Is Post procedural complication From FIBRINOGEN HUMAN\THROMBIN HUMAN?
Of the 26 reports, 1 (3.8%) resulted in death, 8 (30.8%) required hospitalization, and 3 (11.5%) were considered life-threatening.
Is Post procedural complication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FIBRINOGEN HUMAN\THROMBIN HUMAN. However, 26 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)
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)
Haematoma (23)
What Other Drugs Cause Post procedural complication?
ADALIMUMAB (2,494)
ETANERCEPT (318)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (244)
UPADACITINIB (241)
RISANKIZUMAB-RZAA (232)
INFLIXIMAB (217)
METHOTREXATE (188)
TREPROSTINIL (174)
HUMAN IMMUNOGLOBULIN G (159)
PREDNISONE (157)
Which FIBRINOGEN HUMAN\THROMBIN HUMAN Alternatives Have Lower Post procedural complication 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