Does PEGFILGRASTIM-CBQV Cause Device failure? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Device failure have been filed in association with PEGFILGRASTIM-CBQV. This represents 2.2% of all adverse event reports for PEGFILGRASTIM-CBQV.
16
Reports of Device failure with PEGFILGRASTIM-CBQV
2.2%
of all PEGFILGRASTIM-CBQV reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device failure From PEGFILGRASTIM-CBQV?
Of the 16 reports, 1 (6.3%) required hospitalization.
Is Device failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM-CBQV. However, 16 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)
Product packaging confusion (16)
Product quality issue (15)
What Other Drugs Cause Device failure?
EPINEPHRINE (1,344)
SOMATROPIN (1,141)
PEGFILGRASTIM (829)
TREPROSTINIL (713)
BACLOFEN (691)
BUDESONIDE\FORMOTEROL (686)
ETANERCEPT (576)
GOLIMUMAB (487)
LEVONORGESTREL (332)
ACLIDINIUM (304)
Which PEGFILGRASTIM-CBQV Alternatives Have Lower Device failure 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