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Table 3 Discontinuations in double blind, placebo controlled trials of 3–48 months duration Significantly fewer discontinuations with finasteride than with placebo.

From: Finasteride in the treatment of clinical benign prostatic hyperplasia: A systematic review of randomised trials

A. Total number of patients who discontinued

Number of studies

Time point (months)

Discontinued with finasteride 5 mg

Discontinued with placebo

Relative risk (95% CI)

NNT (95% CI)

  

Number

Percent

Number

Percent

  

1

3

No data

  

5

12

553/4098

13

299/1764

17

0.8 (0.7 to 0.9)

29 (18 to 71)

4

24

467/2146

22

507/2140

24

0.9 (0.8 to 1.03)

n/c

1

48

524/1524

34

633/1516

42

0.8 (0.7 to 0.9)

13 (9 to 27)

B. Discontinuations because of lack of efficacy

Number of studies

Time point (months)

Discontinued with finasteride 5 mg

Discontinued with placebo

Relative risk (95% CI)

NNT (95% CI)

  

Number

Percent

Number

Percent

  

1

3

No data

  

4

12

116/3788

3

46/1459

3

0.9 (0.7 to 1.4)

n/c

4

24

81/2146

4

107/2140

5

0.8 (0.6 to 1.0)

n/c

1

48

99/1524

6

104/1516

7

0.9 (0.7 to 1.2)

n/c

C. Discontinuations because of adverse effects

Number of studies

Time point (months)

Discontinued with finasteride 5 mg

Discontinued with placebo

Relative risk (95% CI)

NNT (95% CI)

  

Number

Percent

Number

Percent

  

1

3

No data

  

5

12

251/4098

6

89/1764

5

1.2 (0.9 to 1.5)

n/c

1

18

No data

4

24

178/2146

8

210/2140

14

0.8 (0.7 to 1.02)

n/c

1

48

176/1524

12

166/1516

11

1.0 (0.9 to 1.3)

n/c

  1. NB: Number-needed-to-treat to prevent one discontinuation with finasteride compared with placebo