Does PEGFILGRASTIM Cause Product communication issue? 333 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 333 reports of Product communication issue have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 0.4% of all adverse event reports for PEGFILGRASTIM.
333
Reports of Product communication issue with PEGFILGRASTIM
0.4%
of all PEGFILGRASTIM reports
2
Deaths
0
Hospitalizations
How Dangerous Is Product communication issue From PEGFILGRASTIM?
Of the 333 reports, 2 (0.6%) resulted in death.
Is Product communication issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 333 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 communication issue?
EVOLOCUMAB (2,341)
SEMAGLUTIDE (842)
ERENUMAB-AOOE (598)
SOMATROPIN (350)
ETANERCEPT (122)
ALBUTEROL (121)
NIRMATRELVIR\RITONAVIR (70)
DENOSUMAB (68)
LEVODOPA (61)
TREPROSTINIL (58)
Which PEGFILGRASTIM Alternatives Have Lower Product communication issue Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA