Does PEGFILGRASTIM Cause Device occlusion? 3,239 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,239 reports of Device occlusion have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 4.0% of all adverse event reports for PEGFILGRASTIM.
3,239
Reports of Device occlusion with PEGFILGRASTIM
4.0%
of all PEGFILGRASTIM reports
3
Deaths
13
Hospitalizations
How Dangerous Is Device occlusion From PEGFILGRASTIM?
Of the 3,239 reports, 3 (0.1%) resulted in death, 13 (0.4%) required hospitalization.
Is Device occlusion Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 3,239 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)
Off label use (3,228)
Bone pain (2,266)
Febrile neutropenia (2,154)
What Other Drugs Cause Device occlusion?
CARBIDOPA\LEVODOPA (1,464)
SOMATROPIN (823)
LEUPROLIDE (786)
EPOPROSTENOL (580)
TREPROSTINIL (458)
ALBUTEROL (431)
MEDROXYPROGESTERONE (284)
BACLOFEN (254)
LEVODOPA (224)
RISPERIDONE (182)
Which PEGFILGRASTIM Alternatives Have Lower Device occlusion Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA