Does PEGFILGRASTIM Cause Unevaluable event? 382 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 382 reports of Unevaluable event have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 0.5% of all adverse event reports for PEGFILGRASTIM.
382
Reports of Unevaluable event with PEGFILGRASTIM
0.5%
of all PEGFILGRASTIM reports
32
Deaths
117
Hospitalizations
How Dangerous Is Unevaluable event From PEGFILGRASTIM?
Of the 382 reports, 32 (8.4%) resulted in death, 117 (30.6%) required hospitalization, and 13 (3.4%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 382 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 Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which PEGFILGRASTIM Alternatives Have Lower Unevaluable event Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA