Does PEGFILGRASTIM-CBQV Cause Device malfunction? 356 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 356 reports of Device malfunction have been filed in association with PEGFILGRASTIM-CBQV. This represents 48.6% of all adverse event reports for PEGFILGRASTIM-CBQV.
356
Reports of Device malfunction with PEGFILGRASTIM-CBQV
48.6%
of all PEGFILGRASTIM-CBQV reports
1
Deaths
3
Hospitalizations
How Dangerous Is Device malfunction From PEGFILGRASTIM-CBQV?
Of the 356 reports, 1 (0.3%) resulted in death, 3 (0.8%) required hospitalization.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM-CBQV. However, 356 reports have been filed with the FAERS database.
What Other Side Effects Does PEGFILGRASTIM-CBQV Cause?
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)
Product quality issue (15)
What Other Drugs Cause Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which PEGFILGRASTIM-CBQV Alternatives Have Lower Device malfunction 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