Does PEGFILGRASTIM Cause Extra dose administered? 61 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 61 reports of Extra dose administered have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 0.1% of all adverse event reports for PEGFILGRASTIM.
61
Reports of Extra dose administered with PEGFILGRASTIM
0.1%
of all PEGFILGRASTIM reports
1
Deaths
1
Hospitalizations
How Dangerous Is Extra dose administered From PEGFILGRASTIM?
Of the 61 reports, 1 (1.6%) resulted in death, 1 (1.6%) required hospitalization.
Is Extra dose administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 61 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 Extra dose administered?
TIRZEPATIDE (6,774)
DULAGLUTIDE (3,047)
LORATADINE (1,556)
DUPILUMAB (1,422)
FEXOFENADINE (1,413)
NAPROXEN (908)
POLYETHYLENE GLYCOL 3350 (589)
ACETAMINOPHEN (552)
DALFAMPRIDINE (519)
FLUTICASONE\SALMETEROL (499)
Which PEGFILGRASTIM Alternatives Have Lower Extra dose administered Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA