Does PEGFILGRASTIM Cause Product storage error? 862 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 862 reports of Product storage error have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 1.1% of all adverse event reports for PEGFILGRASTIM.
862
Reports of Product storage error with PEGFILGRASTIM
1.1%
of all PEGFILGRASTIM reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product storage error From PEGFILGRASTIM?
Of the 862 reports, 3 (0.3%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 862 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 Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which PEGFILGRASTIM Alternatives Have Lower Product storage error Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA