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. 2017 Jul 7;19(12):1681–1687. doi: 10.1111/dom.12987

Table 2.

Incidence of adverse events (AEs) reported in the 2 groups during 24 weeks of treatment

Placebo (n = 80) Evogliptin (n = 78)
Number of patients with AEs, n (%) 28 (35.0) 26 (33.3)
Drug‐related AEs, n (%) 0 (0.0) 4 (5.1)
Serious AEs, n (%) 1 (1.3) 0 (0.0)
Drug‐related serious AEs, n (%) 0 (0.0) 0 (0.0)
AEs reported in ≥ 3%
Nasopharyngitis, n (%) 5 (6.3) 5 (6.4)
Arthralgia, n (%) 0 (0.0) 3 (3.8)
Gastrointestinal disorders, n (%) 7 (8.8) 4 (5.1)