Does PEGFILGRASTIM Cause Device deployment issue? 163 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 163 reports of Device deployment issue have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 0.2% of all adverse event reports for PEGFILGRASTIM.
163
Reports of Device deployment issue with PEGFILGRASTIM
0.2%
of all PEGFILGRASTIM reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device deployment issue From PEGFILGRASTIM?
Of the 163 reports, 2 (1.2%) required hospitalization.
Is Device deployment issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 163 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 deployment issue?
ETONOGESTREL (3,621)
GOLIMUMAB (1,265)
GUSELKUMAB (778)
COPPER (768)
LEVONORGESTREL (718)
USTEKINUMAB (639)
SUMATRIPTAN (292)
ABATACEPT (131)
SOMATROPIN (130)
CARBIDOPA\LEVODOPA (88)
Which PEGFILGRASTIM Alternatives Have Lower Device deployment issue Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA