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. 2012 May 18;12:9. doi: 10.1186/1471-2415-12-9

Table 6.

Adverse events reported by ≥ 2% of subjects in any treatment group (ITT population), n (%)

Latanoprost concentration (μg/mL)
 
50
75
100
125
N
71
70
72
69
Eye disorders
 Abnormal sensation in eye
3 (4.2)
4 (5.7)
7 (9.7)
4 (5.8)
 Anterior chamber disorder NOS
0 (0.0)
2 (2.9)
2 (2.8)
1 (1.4)
 Conjunctival disorder NOS
2 (2.8)
1 (1.4)
0 (0.0)
0 (0.0)
 Conjunctival edema
0 (0.0)
2 (2.9)
2 (2.8)
0 (0.0)
 Conjunctival hyperemia
12 (16.9)
13 (18.6)
15 (20.8)
11 (15.9)
 Dry eye NEC
1 (1.4)
2 (2.9)
4 (5.6)
0 (0)
 Eye irritation
5 (7.0)
7 (10.0)
6 (8.3)
8 (11.6)
 Eye pain
2 (2.8)
6 (8.6)
3 (4.2)
4 (5.8)
 Eyelid disorder NOS
0 (0.0)
2 (2.9)
0 (0.0)
0 (0.0)
 Keratitis NEC
2 (2.8)
4 (5.7)
3 (4.2)
3 (4.3)
 Ocular hyperemia*
5 (7.0)
4 (5.7)
5 (6.9)
2 (2.9)
 Red eye
3 (4.2)
5 (7.1)
6 (8.3)
2 (2.9)
 Vision blurred
1 (1.4)
0 (0.0)
2 (2.8)
3 (4.3)
Musculoskeletal, connective tissue and bone disorders
 Arthralgia
1 (1.4)
0 (0.0)
2 (2.8)
1 (1.4)
Nervous system disorders
 Headache NOS 4 (5.6) 4 (5.7) 3 (4.2) 4 (5.8)

ITT intention-to-treat, NEC not elsewhere classified, NOS not otherwise specified.

*Includes conjunctival hyperemia where investigator specified it as bulbar or palpebral.