Does FIBRINOGEN HUMAN\THROMBIN HUMAN Cause Device dislocation? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device dislocation have been filed in association with FIBRINOGEN HUMAN\THROMBIN HUMAN. This represents 0.5% of all adverse event reports for FIBRINOGEN HUMAN\THROMBIN HUMAN.
5
Reports of Device dislocation with FIBRINOGEN HUMAN\THROMBIN HUMAN
0.5%
of all FIBRINOGEN HUMAN\THROMBIN HUMAN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device dislocation From FIBRINOGEN HUMAN\THROMBIN HUMAN?
Of the 5 reports.
Is Device dislocation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FIBRINOGEN HUMAN\THROMBIN HUMAN. However, 5 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)
Post procedural complication (26)
What Other Drugs Cause Device dislocation?
LEVONORGESTREL (13,757)
COPPER (6,955)
CARBIDOPA\LEVODOPA (2,937)
ETONOGESTREL (2,909)
TREPROSTINIL (1,626)
MIRENA (677)
BACLOFEN (492)
PARAGARD 380A (479)
ADALIMUMAB (372)
EPOPROSTENOL (358)
Which FIBRINOGEN HUMAN\THROMBIN HUMAN Alternatives Have Lower Device dislocation 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