Does FILGRASTIM-AAFI 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 FILGRASTIM-AAFI. This represents 1.8% of all adverse event reports for FILGRASTIM-AAFI.
8
Reports of Device defective with FILGRASTIM-AAFI
1.8%
of all FILGRASTIM-AAFI reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device defective From FILGRASTIM-AAFI?
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 FILGRASTIM-AAFI. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does FILGRASTIM-AAFI Cause?
Death (63)
Off label use (63)
White blood cell count decreased (28)
Hospitalisation (17)
Bone pain (15)
Malaise (15)
Needle issue (15)
Pyrexia (15)
Pain (14)
Device leakage (11)
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 FILGRASTIM-AAFI Alternatives Have Lower Device defective Risk?
FILGRASTIM-AAFI vs FILGRASTIM-SNDZ
FILGRASTIM-AAFI vs FINASTERIDE
FILGRASTIM-AAFI vs FINASTERIDE\TAMSULOSIN
FILGRASTIM-AAFI vs FINERENONE
FILGRASTIM-AAFI vs FINGOLIMOD