Does PEGFILGRASTIM Cause Device failure? 829 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 829 reports of Device failure have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 1.0% of all adverse event reports for PEGFILGRASTIM.
829
Reports of Device failure with PEGFILGRASTIM
1.0%
of all PEGFILGRASTIM reports
1
Deaths
14
Hospitalizations
How Dangerous Is Device failure From PEGFILGRASTIM?
Of the 829 reports, 1 (0.1%) resulted in death, 14 (1.7%) required hospitalization.
Is Device failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 829 reports have been filed with the FAERS database.
What Other Side Effects Does PEGFILGRASTIM Cause?
Device adhesion issue (11,326)
Wrong technique in product usage process (10,217)
Unintentional medical device removal (8,882)
Device malfunction (6,818)
Device use error (6,001)
Device issue (5,071)
Accidental exposure to product (4,967)
Device occlusion (3,239)
Off label use (3,228)
Bone pain (2,266)
What Other Drugs Cause Device failure?
EPINEPHRINE (1,344)
SOMATROPIN (1,141)
TREPROSTINIL (713)
BACLOFEN (691)
BUDESONIDE\FORMOTEROL (686)
ETANERCEPT (576)
GOLIMUMAB (487)
LEVONORGESTREL (332)
ACLIDINIUM (304)
INSULIN ASPART (271)
Which PEGFILGRASTIM Alternatives Have Lower Device failure Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA