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. 2008 Nov;62(11):1675–1683. doi: 10.1111/j.1742-1241.2008.01898.x

Table 4.

Incidence rates of adverse events after medication

Solifenacin succinate
Adverse events* 5 mg qd (N= 118), n (%) 10 mg qd (N= 118), n (%) Tolterodine 2 mg bid (N = 118), n (%)
Gastrointestinal disorders 22 (18.64) 42 (35.59) 30 (25.42)
Dry mouth 9 (7.63) 23 (19.49) 22 (18.64)
Constipation 8 (6.78) 17 (14.41) 3 (2.54)
Dyspepsia 3 (2.54) 4 (3.39) 2 (1.69)
Abdominal pain upper 2 (1.69) 4 (3.39) 1 (0.85)
Eye disorders 17 (14.41) 25 (21.19) 18 (15.25)
Vision blurred 16 (13.56) 19 (16.10) 12 (10.17)
Dry eye NOS 0 (0.00) 1 (0.85) 3 (2.54)
Renal and urinary disorders 6 (5.08) 10 (8.47) 14 (11.86)
Difficulty in micturition 1 (0.85) 6 (5.08) 6 (5.08)
Urine flow decreased 3 (2.54) 3 (2.54) 3 (2.54)
Vesical tenesmus 1 (0.85) 1 (0.85) 3 (2.54)
Infections and infestations 7 (5.93) 5 (4.24) 6 (5.08)
Cystitis NOS 3 (2.54) 2 (1.69) 2 (1.69)
Nasopharyngitis 1 (0.85) 1 (0.85) 3 (2.54)
Nervous system disorders 2 (1.69) 3 (2.54) 3 (2.54)
Injury, poisoning and procedural complications 0 (0.00) 5 (4.24) 2 (1.69)
General disorders and administration site conditions 0 (0.00) 1 (0.85) 4 (3.39)
Skin and subcutaneous tissue disorders 1 (0.85) 3 (2.54) 1 (0.85)

*Dictionary: MedDRA 5.0 (incidence of AEs ≥ 2.0%). NOS, not otherwise specified; AEs, adverse events.