Does PEGFILGRASTIM Cause Intercepted product preparation error? 1,514 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,514 reports of Intercepted product preparation error have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 1.9% of all adverse event reports for PEGFILGRASTIM.
1,514
Reports of Intercepted product preparation error with PEGFILGRASTIM
1.9%
of all PEGFILGRASTIM reports
1
Deaths
1
Hospitalizations
How Dangerous Is Intercepted product preparation error From PEGFILGRASTIM?
Of the 1,514 reports, 1 (0.1%) resulted in death, 1 (0.1%) required hospitalization.
Is Intercepted product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 1,514 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 Intercepted product preparation error?
LEUPROLIDE (8,621)
DEVICE (1,033)
CARFILZOMIB (367)
BLINATUMOMAB (110)
BEVACIZUMAB-AWWB (54)
ROMIPLOSTIM (48)
TRASTUZUMAB-ANNS (42)
AFLIBERCEPT (39)
TOCILIZUMAB (26)
AVACINCAPTAD PEGOL (20)
Which PEGFILGRASTIM Alternatives Have Lower Intercepted product preparation error Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA