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. 2009 Aug;63(8):1198–1204. doi: 10.1111/j.1742-1241.2009.02108.x

Table 2.

Subject characteristics

Placebo
TOL ER
< 65 years (n = 1171) 65–74 years (n = 477) ≥ 75 years (n = 288) < 65 years (n = 1360) 65–74 years (n = 582) ≥ 75 years (n = 285)
Discontinuations, n (%)
Total* 126 (11) 49 (10) 43 (15) 115 (9) 45 (8) 35 (12)
Owing to an AE* 37 (3) 22 (5) 16 (6) 33 (2) 14 (2) 14 (5)
Men, n (%) 265 (23) 168 (35) 118 (41) 259 (19) 180 (31) 93 (33)
Mean (SD) age, years 50.8 (9.9) 69.0 (2.8) 79.1 (4.0) 50.7 (10.1) 69.1 (2.8) 78.9 (3.4)
Range 19–64 65–74 75–93 18–64 65–74 75–90
Race, n (%)
White 1034 (88) 452 (95) 278 (97) 1224 (90) 555 (95) 278 (98)
Black 73 (6) 15 (3) 6 (2) 71 (5) 13 (2) 4 (1)
Asian 17 (2) 4 (1) 1 (< 1) 18 (1) 4 (1) 2 (1)
Other 47 (4) 6 (1) 3 (1) 47 (3)† 10 (2) 1 (< 1)
Mean (SD) body mass index, kg/m2 29.1 (6.9) 29.0 (5.9) 26.6 (4.5) 29.1 (9.0) 28.9 (5.7) 27.7 (12.4)
Range 15.1–63.9 16.8–49.9 15.7–47.2 16.5–211.5 17.1–60.3 15.8–198.8

TOL ER, tolterodine extended release; AE, adverse event; *Discontinuations and AEs include those related to and those not related to the study drug; †Includes 1 subject who did not specify race.