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. 2013 Apr;29(3):290–297. doi: 10.1089/jop.2012.0235

Table 4.

Treatment-Related Adverse Events with an Incidence ≥1%

Treatment-related adverse event BBFC N=221 n (%) Brinzolamide N=234 n (%) Brimonidine N=235 n (%)
Ocular
 Vision blurred 10 (4.5%) 16 (6.8%) 0 (0%)
 Eye irritation 12 (5.4%) 4 (1.7%) 6 (2.6%)
 Eye allergy 10 (4.5%) 0 (0%) 2 (0.9%)
 Eye pain 6 (2.7%) 4 (1.7%) 3 (1.3%)
 Eye pruritus 5 (2.3%) 3 (1.3%) 0 (0%)
 Conjunctivitis 4 (1.8%) 0 (0%) 7 (3.0%)
 Conjunctivitis allergic 4 (1.8%) 1 (0.4%) 5 (2.1%)
 Conjunctival hyperemia 4 (1.8%) 1 (0.4%) 2 (0.9%)
 Dry eye 4 (1.8%) 2 (0.9%) 1 (0.4%)
 Lacrimation increased 3 (1.4%) 1 (0.4%) 1 (0.4%)
 Ocular hyperemia 2 (0.9%) 1 (0.4%) 6 (2.6%)
 Conjunctival follicles 1 (0.5%) 0 (0%) 3 (1.3%)
Non-ocular
 Dysgeusia 9 (4.1%) 24 (10.3%) 1 (0.4%)
 Dry mouth 6 (2.7%) 0 (0%) 5 (2.1%)
 Fatigue 1 (0.5%) 0 (0%) 4 (1.7%)

Adverse events were analyzed using the safety population.