Does PEGFILGRASTIM Cause Device use error? 6,001 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6,001 reports of Device use error have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 7.4% of all adverse event reports for PEGFILGRASTIM.
6,001
Reports of Device use error with PEGFILGRASTIM
7.4%
of all PEGFILGRASTIM reports
4
Deaths
20
Hospitalizations
How Dangerous Is Device use error From PEGFILGRASTIM?
Of the 6,001 reports, 4 (0.1%) resulted in death, 20 (0.3%) required hospitalization, and 1 (0.0%) were considered life-threatening.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 6,001 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 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 use error?
ALBUTEROL (5,215)
ALBIGLUTIDE (4,056)
EVOLOCUMAB (4,002)
SOMATROPIN (2,801)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
TREPROSTINIL (563)
Which PEGFILGRASTIM Alternatives Have Lower Device use error Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA