Does FIBRINOGEN HUMAN\THROMBIN HUMAN Cause Seroma? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Seroma have been filed in association with FIBRINOGEN HUMAN\THROMBIN HUMAN. This represents 4.9% of all adverse event reports for FIBRINOGEN HUMAN\THROMBIN HUMAN.
49
Reports of Seroma with FIBRINOGEN HUMAN\THROMBIN HUMAN
4.9%
of all FIBRINOGEN HUMAN\THROMBIN HUMAN reports
0
Deaths
5
Hospitalizations
How Dangerous Is Seroma From FIBRINOGEN HUMAN\THROMBIN HUMAN?
Of the 49 reports, 5 (10.2%) required hospitalization.
Is Seroma Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FIBRINOGEN HUMAN\THROMBIN HUMAN. However, 49 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)
Drug ineffective for unapproved indication (42)
Product physical consistency issue (31)
Wound infection (29)
Post procedural complication (26)
Haematoma (23)
What Other Drugs Cause Seroma?
ADALIMUMAB (101)
BACLOFEN (65)
ASPIRIN (53)
PREDNISOLONE (53)
VALSARTAN (52)
BISOPROLOL (49)
CLOPIDOGREL BISULFATE (48)
DICLOFENAC (48)
PANTOPRAZOLE (46)
FENTANYL (45)
Which FIBRINOGEN HUMAN\THROMBIN HUMAN Alternatives Have Lower Seroma 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