Does PEGFILGRASTIM Cause Wrong technique in product usage process? 10,217 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10,217 reports of Wrong technique in product usage process have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 12.6% of all adverse event reports for PEGFILGRASTIM.
10,217
Reports of Wrong technique in product usage process with PEGFILGRASTIM
12.6%
of all PEGFILGRASTIM reports
13
Deaths
80
Hospitalizations
How Dangerous Is Wrong technique in product usage process From PEGFILGRASTIM?
Of the 10,217 reports, 13 (0.1%) resulted in death, 80 (0.8%) required hospitalization, and 3 (0.0%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 10,217 reports have been filed with the FAERS database.
What Other Side Effects Does PEGFILGRASTIM Cause?
Device adhesion issue (11,326)
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)
Device occlusion (3,239)
Off label use (3,228)
Bone pain (2,266)
Febrile neutropenia (2,154)
What Other Drugs Cause Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
DICLOFENAC (2,298)
Which PEGFILGRASTIM Alternatives Have Lower Wrong technique in product usage process Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA