Does PEGFILGRASTIM Cause Device power source issue? 486 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 486 reports of Device power source issue have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 0.6% of all adverse event reports for PEGFILGRASTIM.
486
Reports of Device power source issue with PEGFILGRASTIM
0.6%
of all PEGFILGRASTIM reports
1
Deaths
0
Hospitalizations
How Dangerous Is Device power source issue From PEGFILGRASTIM?
Of the 486 reports, 1 (0.2%) resulted in death.
Is Device power source issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 486 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 power source issue?
SOMATROPIN (1,219)
TREPROSTINIL (299)
CARBIDOPA\LEVODOPA (62)
ETANERCEPT (54)
BACLOFEN (50)
GLYCOPYRROLATE (39)
DEVICE (20)
FOSCARBIDOPA\FOSLEVODOPA (14)
INTERFERON BETA-1B (13)
LECITHIN\POLOXAMER 407 (11)
Which PEGFILGRASTIM Alternatives Have Lower Device power source issue Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA