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. 2017 Mar 31;19(6):874–882. doi: 10.1111/dom.12898

Table 3.

Adverse events

T + P (n = 68) T + C (n = 70)
n (%) n (%)
AEs 32 (47.1) 42 (60.0)
Drug‐related AEs 8 (11.8) 7 (10.0)
Serious AEs 2 (2.9) 1 (1.4)
Serious drug‐related AEs 1 (1.5) 0 (0)
AEs leading to discontinuation 2 (2.9) 2 (2.9)
Drug‐related AEs leading to discontinuation 1 (1.5) 1 (1.4)
AEs of special interest
Hypoglycaemia 0 (0) 0 (0)
Urinary tract infection 1 (1.5) 0 (0)
Fracture 0 (0) 1 (1.4)
Blood ketone bodies increased 2 (2.9) 2 (2.9)
Cardiovascular‐related events 2 (2.9) 1 (1.4)
Skin and subcutaneous tissue disorders 2 (2.9) 7 (10.0)
Gastrointestinal disorders 1 (1.5) 10 (14.3)
Hepatic function impairment 2 (2.9) 0 (0)

Abbreviations: AE, adverse event; T + C, teneligliptin plus canagliflozin; T + P, teneligliptin plus placebo.