Does FIBRINOGEN HUMAN\HUMAN THROMBIN Cause Post procedural infection? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Post procedural infection have been filed in association with FIBRINOGEN HUMAN\HUMAN THROMBIN. This represents 7.7% of all adverse event reports for FIBRINOGEN HUMAN\HUMAN THROMBIN.
8
Reports of Post procedural infection with FIBRINOGEN HUMAN\HUMAN THROMBIN
7.7%
of all FIBRINOGEN HUMAN\HUMAN THROMBIN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Post procedural infection From FIBRINOGEN HUMAN\HUMAN THROMBIN?
Of the 8 reports.
Is Post procedural infection Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FIBRINOGEN HUMAN\HUMAN THROMBIN. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does FIBRINOGEN HUMAN\HUMAN THROMBIN Cause?
Drug ineffective (26)
Off label use (19)
Blood pressure increased (13)
Haemorrhage (11)
Adverse reaction (8)
Anaphylactic reaction (8)
Anaphylactic shock (8)
Angiopathy (8)
Back pain (8)
Cerebrospinal fluid leakage (8)
What Other Drugs Cause Post procedural infection?
ADALIMUMAB (1,109)
ETANERCEPT (362)
METHOTREXATE (226)
INFLIXIMAB (223)
UPADACITINIB (188)
TOFACITINIB (184)
GOLIMUMAB (177)
VEDOLIZUMAB (166)
RISANKIZUMAB-RZAA (157)
USTEKINUMAB (150)
Which FIBRINOGEN HUMAN\HUMAN THROMBIN Alternatives Have Lower Post procedural infection Risk?
FIBRINOGEN HUMAN\HUMAN THROMBIN vs FIBRINOGEN HUMAN\THROMBIN HUMAN
FIBRINOGEN HUMAN\HUMAN THROMBIN vs FIDAXOMICIN
FIBRINOGEN HUMAN\HUMAN THROMBIN vs FILGOTINIB
FIBRINOGEN HUMAN\HUMAN THROMBIN vs FILGRASTIM
FIBRINOGEN HUMAN\HUMAN THROMBIN vs FILGRASTIM-AAFI