Does REPOTRECTINIB Cause Dysgeusia? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Dysgeusia have been filed in association with REPOTRECTINIB (Augtyro). This represents 2.7% of all adverse event reports for REPOTRECTINIB.
5
Reports of Dysgeusia with REPOTRECTINIB
2.7%
of all REPOTRECTINIB reports
0
Deaths
1
Hospitalizations
How Dangerous Is Dysgeusia From REPOTRECTINIB?
Of the 5 reports, 1 (20.0%) required hospitalization.
Is Dysgeusia Listed in the Official Label?
Yes, Dysgeusia is listed as a known adverse reaction in the official FDA drug label for REPOTRECTINIB.
What Other Side Effects Does REPOTRECTINIB Cause?
Dizziness (32)
Death (21)
Nausea (12)
Adverse event (11)
Neuropathy peripheral (11)
Off label use (10)
Paraesthesia (10)
Balance disorder (9)
Pain (9)
Hospitalisation (8)
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 REPOTRECTINIB Alternatives Have Lower Dysgeusia Risk?
REPOTRECTINIB vs REQUIP
REPOTRECTINIB vs RESLIZUMAB
REPOTRECTINIB vs RESMETIROM
REPOTRECTINIB vs RESTASIS
REPOTRECTINIB vs RETINOL