Does PEGFILGRASTIM Cause Device adhesion issue? 11,326 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11,326 reports of Device adhesion issue have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 14.0% of all adverse event reports for PEGFILGRASTIM.
11,326
Reports of Device adhesion issue with PEGFILGRASTIM
14.0%
of all PEGFILGRASTIM reports
9
Deaths
12
Hospitalizations
How Dangerous Is Device adhesion issue From PEGFILGRASTIM?
Of the 11,326 reports, 9 (0.1%) resulted in death, 12 (0.1%) required hospitalization.
Is Device adhesion issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 11,326 reports have been filed with the FAERS database.
What Other Side Effects Does PEGFILGRASTIM Cause?
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)
Febrile neutropenia (2,154)
What Other Drugs Cause Device adhesion issue?
ESTRADIOL (678)
ROTIGOTINE (383)
METHYLPHENIDATE (302)
ESTRADIOL\LEVONORGESTREL (195)
FENTANYL\FENTANYL (190)
FENTANYL (149)
TREPROSTINIL (128)
BUPRENORPHINE (42)
ESTRADIOL\NORETHINDRONE (37)
SUMATRIPTAN (28)
Which PEGFILGRASTIM Alternatives Have Lower Device adhesion issue Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA