Table 5.

Treatment-related adverse events

Adverse event	No (%) of patients
	Bimatoprost (n = 131)	Travoprost (n = 133)
Eye pruritus	3 (2.3%)	1 (0.8%)
Conjunctival or ocular hyperaemia	4 (3.1%)	2 (1.5%)
Punctate keratitis	1 (0.8%)	2 (1.5%)
Eye irritation	2 (1.5%)	0 (0.0%)
Growth of eyelashes	2 (1.5%)	0 (0.0%)
Abnormal sensation in eye	1 (0.8%)	0 (0.0%)
Drug hypersensitivity	0 (0.0%)	1 (0.8%)
Dry skin	1 (0.8%)	0 (0.0%)
Foreign-body sensation	0 (0.0%)	1 (0.8%)
Hyperaemia (non-ocular)	0 (0.0%)	1 (0.8%)
Pruritus at instillation site	0 (0.0%)	1 (0.8%)
Skin pigmentation	1 (0.8%)	0 (0.0%)
Visual acuity reduced	0 (0.0%)	1 (0.8%)
Overall*	11 (8.4%)	8 (6.0%)

*Patients reporting any treatment-related adverse event.