Does PEGFILGRASTIM Cause Device malfunction? 6,818 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6,818 reports of Device malfunction have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 8.4% of all adverse event reports for PEGFILGRASTIM.
6,818
Reports of Device malfunction with PEGFILGRASTIM
8.4%
of all PEGFILGRASTIM reports
3
Deaths
53
Hospitalizations
How Dangerous Is Device malfunction From PEGFILGRASTIM?
Of the 6,818 reports, 3 (0.0%) resulted in death, 53 (0.8%) required hospitalization, and 23 (0.3%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 6,818 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 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)
Febrile neutropenia (2,154)
What Other Drugs Cause Device malfunction?
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
ACLIDINIUM (1,325)
Which PEGFILGRASTIM Alternatives Have Lower Device malfunction Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA