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. 2019 Nov 12;13:3845–3853. doi: 10.2147/DDDT.S215170

Table 5.

Adverse events

System Organ Class/ Preferred Term Placebo (N=6)
n (%)
AZD7594
200 μg (N=7),
n (%)
AZD7594
400 μg (N=7),
n (%)
AZD7594
1600 μg (N=7),
n (%)
Total AZD7594 (N=21),
n (%)
All subjects (N=27), n (%)
Subjects with any AE 1 (16.7) 3 (42.9) 1 (14.3) 1 (14.3) 5 (23.8) 6 (22.2)
Respiratory, thoracic and mediastinal disorders 0 3 (42.9) 0 0 3 (42.9) 3 (11.1)
 Dry throat 0 1 (14.3) 0 0 1 (4.8) 1 (3.7)
 Nasal congestion 0 1 (14.3) 0 0 1 (4.8) 1 (3.7)
 Oropharyngeal pain 0 1 (14.3) 0 0 1 (4.8) 1 (3.7)
Infections and infestations 0 0 1 (14.3) 0 1 (4.8) 1 (3.7)
 Folliculitis 0 0 1 (14.3) 0 1 (4.8) 1 (3.7)
Metabolism and nutritional disorders 1 (16.7) 0 0 0 0 1 (3.7)
 Gout 1 (16.7) 0 0 0 0 1 (3.7)
Nervous system disorders 0 0 0 1 (14.3) 1 (4.8) 1 (3.7)
 Presyncope 0 0 0 1 (14.3) 1 (4.8) 1 (3.7)

Abbreviations: AE, adverse event; N, number of subjects randomized to each treatment or overall; n (%), number of subjects in each category expressed as a percentage of N.