Does FILGRASTIM-AAFI Cause Device mechanical issue? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Device mechanical issue have been filed in association with FILGRASTIM-AAFI. This represents 1.8% of all adverse event reports for FILGRASTIM-AAFI.
8
Reports of Device mechanical issue with FILGRASTIM-AAFI
1.8%
of all FILGRASTIM-AAFI reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device mechanical issue From FILGRASTIM-AAFI?
Of the 8 reports.
Is Device mechanical issue 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 mechanical issue?
SOMATROPIN (6,411)
INSULIN GLARGINE-YFGN (853)
INSULIN GLARGINE (725)
ALBUTEROL (455)
DEVICE (226)
ETANERCEPT (145)
FLUTICASONE\SALMETEROL (127)
GLATIRAMER (124)
EXENATIDE (108)
MEDROXYPROGESTERONE (99)
Which FILGRASTIM-AAFI Alternatives Have Lower Device mechanical issue Risk?
FILGRASTIM-AAFI vs FILGRASTIM-SNDZ
FILGRASTIM-AAFI vs FINASTERIDE
FILGRASTIM-AAFI vs FINASTERIDE\TAMSULOSIN
FILGRASTIM-AAFI vs FINERENONE
FILGRASTIM-AAFI vs FINGOLIMOD