Does ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT Cause Device defective? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Device defective have been filed in association with ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT. This represents 0.1% of all adverse event reports for ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT.
8
Reports of Device defective with ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT
0.1%
of all ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device defective From ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT?
Of the 8 reports.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT Cause?
Haemarthrosis (3,360)
Haemorrhage (2,925)
Fall (709)
Arthralgia (561)
Muscle haemorrhage (554)
Limb injury (525)
Drug ineffective (513)
Joint injury (511)
Contusion (496)
Pain (484)
What Other Drugs Cause Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT Alternatives Have Lower Device defective Risk?
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT vs ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT RESIDUES 743-1636 DELETED
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT vs ANTIHEMOPHILIC FACTOR, PEGYLATED HUMAN SEQUENCE RECOMBINANT
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT vs ANTIHEMOPHILIC FACTOR PORCINE, B-DOMAIN TRUNCATED RECOMBINANT
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT vs APALUTAMIDE
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT vs APATINIB