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. 2017 Aug 16;83(12):2778–2788. doi: 10.1111/bcp.13379

Table 3.

Summary of adverse events (AEs) reported during part I by frequency

Treatment A (n = 20) Treatment B1 (n = 20) Treatment B2 (n = 20) Overall (n = 20)
Preferred term AEs n % AEs n % AEs n % AEs n %
Number of subjects with at least one AE 15 75 3 15 20 100 20 100
Number of different AEs 3 2 11 12
Total number of AEs 17 3 74 94
Headache 15 14 70 1 1 5 20 18 90 36 18 90
Nausea 18 15 75 18 15 75
Vomiting 23 12 60 23 12 60
Pain in extremity 1 1 5 4 3 15 5 3 15
Diarrhoea 2 2 10 1 1 5 3 3 15
Myalgia 2 2 10 2 2 10
Pain in jaw 2 2 10 2 2 10
Presyncope 1 1 5 1 1 5
Dyspepsia 1 1 5 1 1 5
Arthralgia 1 1 5 1 1 5
Neck pain 1 1 5 1 1 5
Nasopharyngitis 1 1 5 1 1 5

Treatments: A = selexipag; B1 = gemfibrozil; B2 = gemfibrozil + selexipag. Data are expressed as AE (number of adverse events), n (number of subjects experiencing at least one AE) and % (percentage of subjects with at least one AE)