Table 3.

Adverse events (>10% or >2 patients in any ADS‐5102 group)

Adverse Event n (%)	Placebo (n = 22)	260 mg ADS‐5102 (n = 20)	340 mg ADS‐5102 (n = 21)	420 mg ADS‐5102 (n = 20)
Constipation	2 (9.1)	7 (35.0)	5 (23.8)	3 (15.0)
Dizziness	1 (4.5)	3 (15.0)	6 (28.6)	3 (15.0)
Hallucination	0	4 (20.0)	5 (23.8)	4 (20.0)
Dry mouth	0	3 (15.0)	4 (19.0)	2 (10.0)
Fall	3 (13.6)	1 (5.0)	3 (14.3)	3 (15.0)
Confusion	1 (4.5)	1 (5.0)	3 (14.3)	2 (10.0)
Headache	1 (4.5)	1 (5.0)	3 (14.3)	1 (5.0)
Nausea	1 (4.5)	1 (5.0)	3 (14.3)	1 (5.0)
Asthenia	1 (4.5)	0	3 (14.3)	1 (5.0)