Table 2:
Adverse effects experienced by study participants
| Relamorelin (n=8) |
Placebo (n=12) |
p-value | |
|---|---|---|---|
| Injection site ecchymoses, bruising, erythema | 4 participants (50%) | 4 participants (33.3%) | 0.65 |
| Electrolyte abnormalities | 2 participants (25%) | 4 participants (33.3%) | 0.99 |
| Dizziness | |||
| -All participants | 5 participants (62.5%) | 1 participant (8.3%) | 0.02 |
| -Participants not reporting symptom at baseline | 3 participants (50%) | 0 participants (0%) | 0.03 |
| Fatigue | |||
| -All participants | 7 participants (87.5%) | 5 participants (41.7%) | 0.07 |
| -Participants not reporting symptom at baseline | 2 participants (66.7%) | 2 participants (25%) | 0.49 |
| Abdominal pain/cramping | |||
| -All participants | 7 participants (87.5%) | 9 participants (75%) | 0.62 |
| -Participants not reporting symptom at baseline | 1 participant (50%) | 3 participants (60%) | 0.99 |
| Muscle weakness | |||
| -All participants | 1 participant (12.5%) | 2 participants (16.7%) | 0.99 |
| -Participants not reporting symptom at baseline | 1 participant (12.5%) | 1 participant (9.1%) | 0.99 |
| Hyperhidrosis | |||
| -All participants | 2 participants (25%) | 1 participant (8.3%) | 0.54 |
| -Participants not reporting symptom at baseline | 1 participant (14.3%) | 0 participants (0%) | 0.41 |