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. 2021 Oct 28;21:375. doi: 10.1186/s12905-021-01475-2

Table 2.

Summary of treatment-emergent adverse events

Relugolix Placebo
10 mg
(n = 48)
20 mg
(n = 55)
40 mg
(n = 54)
(n = 57)
TEAEs, n 105 143 145 99
Patients with any TEAEs 41 (85.4) 53 (96.4) 48 (88.9) 40 (70.2)
Patients with drug-related TEAEs 33 (68.8) 50 (90.9) 44 (81.5) 23 (40.4)
Intensity of TEAEs
  Mild 36 (75.0) 46 (83.6) 45 (83.3) 34 (59.6)
  Moderate 5 (10.4) 7 (12.7) 2 (3.7) 6 (10.5)
  Severe 0 (0.0) 0 (0.0) 1 (1.9) 0 (0.0)
TEAEs leading to study drug discontinuation 0 (0.0) 1 (1.8) 0 (0.0) 1 (1.8)
Serious TEAEs (%) 0 (0.0) 1 (1.8) 1 (1.9) 1 (1.8)
TEAEs occurring in ≥ 10% of patients in any group
  Nasopharyngitis 9 (18.8) 4 (7.3) 7 (13.0) 16 (28.1)
  Hot flushes 2 (4.2) 16 (29.1) 21 (38.9) 2 (3.5)
  Irregular uterine bleeding 13 (27.1) 17 (30.9) 15 (27.8) 10 (17.5)
  Heavy menstrual bleeding 6 (12.5) 13 (23.6) 12 (22.2) 4 (7.0)
  Headache 1 (2.1) 8 (14.5) 7 (13.0) 1 (1.8)
  Genital hemorrhage 2 (4.2) 6 (10.9) 6 (11.1) 2 (3.5)
  Menstruation irregular 12 (25.0) 8 (14.5) 3 (5.6) 0 (0.0)

Data are n (%) unless stated otherwise

TEAEs treatment-emergent adverse events