Does CABOZANTINIB S-MALATE Cause Ageusia? 603 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 603 reports of Ageusia have been filed in association with CABOZANTINIB S-MALATE (CABOMETYX). This represents 1.5% of all adverse event reports for CABOZANTINIB S-MALATE.
603
Reports of Ageusia with CABOZANTINIB S-MALATE
1.5%
of all CABOZANTINIB S-MALATE reports
12
Deaths
52
Hospitalizations
How Dangerous Is Ageusia From CABOZANTINIB S-MALATE?
Of the 603 reports, 12 (2.0%) resulted in death, 52 (8.6%) required hospitalization, and 2 (0.3%) were considered life-threatening.
Is Ageusia Listed in the Official Label?
Yes, Ageusia is listed as a known adverse reaction in the official FDA drug label for CABOZANTINIB S-MALATE.
What Other Side Effects Does CABOZANTINIB S-MALATE Cause?
Diarrhoea (8,282)
Fatigue (6,819)
Off label use (5,245)
Nausea (4,341)
Decreased appetite (4,076)
Blood pressure increased (2,939)
Malignant neoplasm progression (2,718)
Palmar-plantar erythrodysaesthesia syndrome (2,706)
Weight decreased (2,657)
Stomatitis (2,560)
What Other Drugs Cause Ageusia?
LENALIDOMIDE (1,473)
VISMODEGIB (958)
SUNITINIB MALATE (473)
TERBINAFINE (397)
NIRMATRELVIR\RITONAVIR (354)
DUPILUMAB (311)
FLUTICASONE (293)
PALBOCICLIB (277)
ADALIMUMAB (259)
SECUKINUMAB (258)
Which CABOZANTINIB S-MALATE Alternatives Have Lower Ageusia Risk?
CABOZANTINIB S-MALATE vs CAFFEINE
CABOZANTINIB S-MALATE vs CALASPARGASE PEGOL
CABOZANTINIB S-MALATE vs CALASPARGASE PEGOL-MKNL
CABOZANTINIB S-MALATE vs CALCIFEDIOL
CABOZANTINIB S-MALATE vs CALCIPOTRIENE