Table 2. Summary of adverse events.
No. participants with AEs, n (%) | Empagliflozin | Placebo (n = 21) | |||
---|---|---|---|---|---|
1 mg (n = 19) | 5 mg (n = 21) | 10 mg (n = 20) | 25 mg (n = 19) | ||
Any AE | 6 (31.6) | 4 (19.0) | 6 (30.0) | 7 (36.8) | 2 (9.5) |
Most frequently reported AEs by preferred term† | |||||
Nasopharyngitis | 2 (10.5) | 1 (4.8) | 0 (0.0) | 1 (5.3) | 0 (0.0) |
Constipation | 0 (0.0) | 1 (4.8) | 2 (10.0) | 1 (5.3) | 1 (4.8) |
Upper abdominal pain | 0 (0.0) | 0 (0.0) | 2 (10.0) | 0 (0.0) | 0 (0.0) |
Drug‐related AEs‡ | 2 (10.5) | 0 (0.0) | 4 (20.0) | 3 (15.8) | 1 (4.8) |
†Reported by ≥10% of subjects in ≥1 group. ‡Investigator defined. AEs, adverse events.