Does BRIMONIDINE Cause Ocular hyperaemia? 917 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 917 reports of Ocular hyperaemia have been filed in association with BRIMONIDINE (BRIMONIDINE TARTRATE). This represents 7.8% of all adverse event reports for BRIMONIDINE.
917
Reports of Ocular hyperaemia with BRIMONIDINE
7.8%
of all BRIMONIDINE reports
0
Deaths
10
Hospitalizations
How Dangerous Is Ocular hyperaemia From BRIMONIDINE?
Of the 917 reports, 10 (1.1%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Ocular hyperaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIMONIDINE. However, 917 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)
Hypersensitivity (629)
Erythema (604)
Eye pain (560)
Vision blurred (542)
Headache (492)
Dry eye (490)
Condition aggravated (445)
What Other Drugs Cause Ocular hyperaemia?
DUPILUMAB (6,938)
CYCLOSPORINE (1,508)
BIMATOPROST (1,447)
CENEGERMIN-BKBJ (1,226)
ADALIMUMAB (714)
LATANOPROST (587)
DORZOLAMIDE\TIMOLOL (581)
LIFITEGRAST (570)
TRAVOPROST (478)
POLYETHYLENE GLYCOL 400\PROPYLENE GLYCOL (454)
Which BRIMONIDINE Alternatives Have Lower Ocular hyperaemia Risk?
BRIMONIDINE vs BRIMONIDINE\BRINZOLAMIDE
BRIMONIDINE vs BRIMONIDINE\TIMOLOL
BRIMONIDINE vs BRINTELLIX
BRIMONIDINE vs BRINZOLAMIDE
BRIMONIDINE vs BRINZOLAMIDE\TIMOLOL