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Table 6 Adverse events reported by ≥ 2% of subjects in any treatment group (ITT population), n (%)

From: A 4-week, dose-ranging study comparing the efficacy, safety and tolerability of latanoprost 75, 100 and 125 μg/mL to latanoprost 50 μg/mL (xalatan) in the treatment of primary open-angle glaucoma and ocular hypertension

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)

  1. ITT intention-to-treat, NEC not elsewhere classified, NOS not otherwise specified.
  2. *Includes conjunctival hyperemia where investigator specified it as bulbar or palpebral.