Does PEGFILGRASTIM Cause Device issue? 5,071 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5,071 reports of Device issue have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 6.3% of all adverse event reports for PEGFILGRASTIM.
5,071
Reports of Device issue with PEGFILGRASTIM
6.3%
of all PEGFILGRASTIM reports
7
Deaths
48
Hospitalizations
How Dangerous Is Device issue From PEGFILGRASTIM?
Of the 5,071 reports, 7 (0.1%) resulted in death, 48 (0.9%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 5,071 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)
Accidental exposure to product (4,967)
Device occlusion (3,239)
Off label use (3,228)
Bone pain (2,266)
Febrile neutropenia (2,154)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
EVOLOCUMAB (1,659)
Which PEGFILGRASTIM Alternatives Have Lower Device issue Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA