Does PEGFILGRASTIM Cause Device delivery system issue? 323 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 323 reports of Device delivery system issue have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 0.4% of all adverse event reports for PEGFILGRASTIM.
323
Reports of Device delivery system issue with PEGFILGRASTIM
0.4%
of all PEGFILGRASTIM reports
0
Deaths
10
Hospitalizations
How Dangerous Is Device delivery system issue From PEGFILGRASTIM?
Of the 323 reports, 10 (3.1%) required hospitalization.
Is Device delivery system issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 323 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 delivery system issue?
ALBUTEROL (9,509)
SOMATROPIN (1,848)
EXENATIDE (1,533)
BUDESONIDE\FORMOTEROL (1,260)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (1,181)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (523)
LEVALBUTEROL (459)
MOMETASONE FUROATE\OLOPATADINE (347)
ABATACEPT (342)
ALBUTEROL\BUDESONIDE (244)
Which PEGFILGRASTIM Alternatives Have Lower Device delivery system issue Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA