Does PEGFILGRASTIM-CBQV Cause Device use error? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Device use error have been filed in association with PEGFILGRASTIM-CBQV. This represents 1.0% of all adverse event reports for PEGFILGRASTIM-CBQV.
7
Reports of Device use error with PEGFILGRASTIM-CBQV
1.0%
of all PEGFILGRASTIM-CBQV reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device use error From PEGFILGRASTIM-CBQV?
Of the 7 reports.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM-CBQV. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does PEGFILGRASTIM-CBQV Cause?
Device malfunction (356)
No adverse event (265)
Death (76)
Product dose omission issue (61)
Product label confusion (36)
Accidental exposure to product (29)
Neutrophil count decreased (18)
Bone pain (17)
Device failure (16)
Product packaging confusion (16)
What Other Drugs Cause Device use error?
PEGFILGRASTIM (6,001)
ALBUTEROL (5,215)
ALBIGLUTIDE (4,056)
EVOLOCUMAB (4,002)
SOMATROPIN (2,801)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
Which PEGFILGRASTIM-CBQV Alternatives Have Lower Device use error Risk?
PEGFILGRASTIM-CBQV vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM-CBQV vs PEGINTERFERON ALFA
PEGFILGRASTIM-CBQV vs PEGINTERFERON ALFA-2A
PEGFILGRASTIM-CBQV vs PEGINTERFERON ALFA-2A OR PEGINTERFERON ALFA-2B
PEGFILGRASTIM-CBQV vs PEGINTERFERON ALFA-2A OR PEGINTERFERON ALFA-2B OR PEGINTERFERON BETA-1A OR PEGINTERFERON LAMBDA-1A