Does PEGFILGRASTIM-JMDB Cause Device defective? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Device defective have been filed in association with PEGFILGRASTIM-JMDB. This represents 2.7% of all adverse event reports for PEGFILGRASTIM-JMDB.
8
Reports of Device defective with PEGFILGRASTIM-JMDB
2.7%
of all PEGFILGRASTIM-JMDB reports
2
Deaths
2
Hospitalizations
How Dangerous Is Device defective From PEGFILGRASTIM-JMDB?
Of the 8 reports, 2 (25.0%) resulted in death, 2 (25.0%) required hospitalization.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM-JMDB. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does PEGFILGRASTIM-JMDB Cause?
Death (51)
Product quality issue (21)
Drug ineffective (20)
Device leakage (17)
Hospitalisation (15)
Needle issue (14)
Neutropenia (13)
Febrile neutropenia (12)
Nausea (11)
Off label use (11)
What Other Drugs Cause Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which PEGFILGRASTIM-JMDB Alternatives Have Lower Device defective Risk?
PEGFILGRASTIM-JMDB vs PEGINTERFERON ALFA
PEGFILGRASTIM-JMDB vs PEGINTERFERON ALFA-2A
PEGFILGRASTIM-JMDB vs PEGINTERFERON ALFA-2A OR PEGINTERFERON ALFA-2B
PEGFILGRASTIM-JMDB vs PEGINTERFERON ALFA-2A OR PEGINTERFERON ALFA-2B OR PEGINTERFERON BETA-1A OR PEGINTERFERON LAMBDA-1A
PEGFILGRASTIM-JMDB vs PEGINTERFERON ALFA-2B