Does BRIMONIDINE Cause Dysgeusia? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Dysgeusia have been filed in association with BRIMONIDINE (BRIMONIDINE TARTRATE). This represents 0.2% of all adverse event reports for BRIMONIDINE.
27
Reports of Dysgeusia with BRIMONIDINE
0.2%
of all BRIMONIDINE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Dysgeusia From BRIMONIDINE?
Of the 27 reports, 2 (7.4%) required hospitalization.
Is Dysgeusia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIMONIDINE. However, 27 reports have been filed with the FAERS database.
What Other Side Effects Does BRIMONIDINE Cause?
Treatment failure (2,849)
Drug ineffective (1,402)
Eye irritation (950)
Ocular hyperaemia (917)
Hypersensitivity (629)
Erythema (604)
Eye pain (560)
Vision blurred (542)
Headache (492)
Dry eye (490)
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 BRIMONIDINE Alternatives Have Lower Dysgeusia Risk?
BRIMONIDINE vs BRIMONIDINE\BRINZOLAMIDE
BRIMONIDINE vs BRIMONIDINE\TIMOLOL
BRIMONIDINE vs BRINTELLIX
BRIMONIDINE vs BRINZOLAMIDE
BRIMONIDINE vs BRINZOLAMIDE\TIMOLOL