Does PEGFILGRASTIM Cause Device leakage? 1,380 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,380 reports of Device leakage have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 1.7% of all adverse event reports for PEGFILGRASTIM.
1,380
Reports of Device leakage with PEGFILGRASTIM
1.7%
of all PEGFILGRASTIM reports
0
Deaths
12
Hospitalizations
How Dangerous Is Device leakage From PEGFILGRASTIM?
Of the 1,380 reports, 12 (0.9%) required hospitalization.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 1,380 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 leakage?
SOMATROPIN (9,113)
LEUPROLIDE (5,861)
EXENATIDE (5,115)
ALBIGLUTIDE (1,195)
SECUKINUMAB (910)
RISPERIDONE (878)
TREPROSTINIL (874)
DEVICE (795)
GUSELKUMAB (712)
ABATACEPT (671)
Which PEGFILGRASTIM Alternatives Have Lower Device leakage Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA