Table 2.
TEAEs by treatment
| Vericiguat + sildenafil (n = 16) | Placebo + sildenafil (n = 16) | Total (N = 32) | |
|---|---|---|---|
| Number (%) with at least one TEAE | 16 (100.0) | 7 (43.8) | 23 (71.9) |
| Vericiguat-related TEAE | 10 (62.5) | 1 (6.3) | 11 (34.4) |
| Sildenafil-related TEAE | 14 (87.5) | 6 (37.5) | 20 (62.5) |
| Maximum TEAE intensity | |||
| Mild | 13 (81.3) | 7 (43.8) | 20 (62.5) |
| Moderate | 3 (18.8) | 0 | 3 (9.4) |
| Maximum intensity of vericiguat-related TEAE | |||
| Mild | 7 (43.8) | 1 (6.3) | 8 (25.0) |
| Moderate | 3 (18.8) | 0 | 3 (9.4) |
| Maximum intensity of sildenafil-related TEAE | |||
| Mild | 11 (68.8) | 6 (37.5) | 17 (53.1) |
| Moderate | 3 (18.8) | 0 | 3 (9.4) |
| Discontinuation of vericiguat due to AE | 1 (6.3) | 0 | 1 (3.1) |
| Discontinuation of sildenafil due to AE | 1 (6.3) | 0 | 1 (3.1) |
AE adverse event, TEAE treatment-emergent adverse event