Does PEGFILGRASTIM Cause Intentional product use issue? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Intentional product use issue have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 0.0% of all adverse event reports for PEGFILGRASTIM.
24
Reports of Intentional product use issue with PEGFILGRASTIM
0.0%
of all PEGFILGRASTIM reports
3
Deaths
19
Hospitalizations
How Dangerous Is Intentional product use issue From PEGFILGRASTIM?
Of the 24 reports, 3 (12.5%) resulted in death, 19 (79.2%) required hospitalization, and 3 (12.5%) were considered life-threatening.
Is Intentional product use issue 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which PEGFILGRASTIM Alternatives Have Lower Intentional product use issue Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA