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. 2006 Sep 6;91(1):62–68. doi: 10.1136/bjo.2006.096693

Table 3 Adverse events.

Adverse event Number of trials Crude event rate RR (95% CI) RD (95% CI) I2 (%)
Latanoprost Brimonidine
Itch/discomfort 8 62/583 96/532 0.81 (0.40 to 1.61) −0.02 (−0.11 to 0.06) 73.1
Hyperemia 8 66/530 46/482 1.37 (0.84 to 2.25) 0.04 (−0.02 to 0.10) 39.2
Eyelid disorder (swelling, blepharitis, laxity) 5 8/341 5/308 1.61 (0.47 to 5.48) 0.01 (−0.02 to 0.05) 10.4
Visual disturbance (photophobia, blurred vision, floaters, diploplia) 8 53/504 46/468 1.19 (0.88 to 1.61) 0 (−0.02 to 0.02) 0
Conjunctival disorder (including conjunctivitis) 2 9/313 27/260 0.16 (0.01 to 5.09) −0.08 (−0.18 to 0.01) 82.3
Keratopathy 3 10/249 14/213 0.69 (0.24 to 1.96) −0.03 (−0.07 to 0.01) 30.5
Dry eye 4 5/149 7/152 0.76 (0.26 to 2.27) −0.02 (−0.05 to 0.02) 0
Hypertrichosis 1 6/182 0/145 10.37 (0.59 to 182.60) 0.03 (0 to 0.06) NA
Increased iris pigmentation 2 6/268 0/229 5.48 (0.65 to 46.50) 0.03 (−0.04 to 0.10) 0
Fatigue* 3 3/247 11/211 0.27 (0.08 to 0.88) −0.04 (−0.07 to −0.01) 0
Headache 4 6/362 13/327 0.43 (0.17 to 1.11) −0.02 (−0.04 to 0.01) 0

I2, intertrial statistical heterogeneity (Cochran Q test); NA, not available; RD, risk difference.

*Significant.