Does PEGFILGRASTIM Cause Dysgeusia? 180 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 180 reports of Dysgeusia have been filed in association with PEGFILGRASTIM (ZIEXTENZO). This represents 0.2% of all adverse event reports for PEGFILGRASTIM.
180
Reports of Dysgeusia with PEGFILGRASTIM
0.2%
of all PEGFILGRASTIM reports
8
Deaths
43
Hospitalizations
How Dangerous Is Dysgeusia From PEGFILGRASTIM?
Of the 180 reports, 8 (4.4%) resulted in death, 43 (23.9%) required hospitalization, and 3 (1.7%) were considered life-threatening.
Is Dysgeusia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGFILGRASTIM. However, 180 reports have been filed with the FAERS database.
What Other Side Effects Does PEGFILGRASTIM Cause?
Device adhesion issue (11,326)
Wrong technique in product usage process (10,217)
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)
What Other Drugs Cause Dysgeusia?
NIRMATRELVIR\RITONAVIR (7,381)
SUNITINIB MALATE (1,226)
SODIUM (1,216)
LENALIDOMIDE (1,180)
LIFITEGRAST (1,067)
CABOZANTINIB S-MALATE (777)
CLARITHROMYCIN (717)
VISMODEGIB (706)
ADALIMUMAB (674)
PALBOCICLIB (620)
Which PEGFILGRASTIM Alternatives Have Lower Dysgeusia Risk?
PEGFILGRASTIM vs PEGFILGRASTIM-APGF
PEGFILGRASTIM vs PEGFILGRASTIM-BMEZ
PEGFILGRASTIM vs PEGFILGRASTIM-CBQV
PEGFILGRASTIM vs PEGFILGRASTIM-JMDB
PEGFILGRASTIM vs PEGINTERFERON ALFA