Does PEGFILGRASTIM Cause Intercepted product storage error? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Intercepted product storage error have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 0.0% of all adverse event reports for PEGFILGRASTIM.
24
Reports of Intercepted product storage error with PEGFILGRASTIM
0.0%
of all PEGFILGRASTIM reports
0
Deaths
1
Hospitalizations
How Dangerous Is Intercepted product storage error From PEGFILGRASTIM?
Of the 24 reports, 1 (4.2%) required hospitalization.
Is Intercepted product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 24 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 storage error?
TOCILIZUMAB (381)
DUPILUMAB (325)
OMALIZUMAB (256)
ALTEPLASE (227)
INSULIN GLARGINE (129)
DORNASE ALFA (115)
BEVACIZUMAB (113)
RITUXIMAB (105)
OCRELIZUMAB (88)
PERTUZUMAB (84)
Which PEGFILGRASTIM Alternatives Have Lower Intercepted product storage error Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA