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Table 3 Reasons for discontinuation during the study

From: Predictors and impact of non-adherence in adults with attention-deficit/hyperactivity disorder receiving OROS methylphenidate: results from a randomized, placebo-controlled trial

Reason for discontinuation, n(%)

Placebo

OROS MPH

(n= 97)

54 mg/day

72 mg/day

(n= 87)

(n= 92)

Discontinued

29 (29.9)

32 (36.8)

37 (40.2)

 Adverse event

2 (2.1)

15 (17.2)

19 (20.7)

 Lack of efficacy

14 (14.4)

1 (1.1)

4 (4.3)

 Noncompliance

3 (3.1)

5 (5.7)

5 (5.4)

 Consent withdrawal

4 (4.1)

2 (2.3)

3 (3.3)

 Loss to follow-up

5 (5.2)

1 (1.1)

0

 Sponsor’s decision

0

2 (2.3)

0

 Ineligibility to continue the study

0

1 (1.1)

1 (1.1)

 Other

1 (1.0)

5 (5.7)

5 (5.4)