Does CRIZOTINIB Cause Dysgeusia? 157 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 157 reports of Dysgeusia have been filed in association with CRIZOTINIB (Xalkori). This represents 1.6% of all adverse event reports for CRIZOTINIB.
157
Reports of Dysgeusia with CRIZOTINIB
1.6%
of all CRIZOTINIB reports
13
Deaths
31
Hospitalizations
How Dangerous Is Dysgeusia From CRIZOTINIB?
Of the 157 reports, 13 (8.3%) resulted in death, 31 (19.7%) required hospitalization, and 6 (3.8%) were considered life-threatening.
Is Dysgeusia Listed in the Official Label?
Yes, Dysgeusia is listed as a known adverse reaction in the official FDA drug label for CRIZOTINIB.
What Other Side Effects Does CRIZOTINIB Cause?
Death (2,028)
Neoplasm progression (1,161)
Nausea (820)
Disease progression (677)
Diarrhoea (631)
Vomiting (600)
Fatigue (419)
Off label use (353)
Dyspnoea (352)
Visual impairment (315)
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 CRIZOTINIB Alternatives Have Lower Dysgeusia Risk?
CRIZOTINIB vs CROFELEMER
CRIZOTINIB vs CROMOLYN
CRIZOTINIB vs CROTALIDAE POLYVALENT IMMUNE FAB
CRIZOTINIB vs CUBICIN
CRIZOTINIB vs CUPRIC