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Adverse events reported by the study subjects (no. [%] of study subjects) during the 6-week supplementation period.
| Treatment Group (n = 11) | Placebo Group (n = 11) | |
|---|---|---|
| Constipation | 1 (9.1) | 0 |
| Headache | 1 (9.1) | 0 |
| Indigestion | 1 (9.1) | 0 |
| Dry mouth | 0 | 1 (9.1) |
| Irritability | 0 | 1 (9.1) |
| Nausea | 0 | 1 (9.1) |
| Total events | 3 | 3 |
