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Adverse event rates recorded in both study groups during the follow-up period. Data are presented as n (%)
| Adverse events | All patients (N = 31) | No treatment (N = 14) | Exenatide (N = 17) (N = 17) | p-value |
|---|---|---|---|---|
| Gastrointestinal | 9 (29.0) | 0 (0) | 9 (52.9) | < 0.001 |
| Neuropsychiatric | 3 (9.7) | 0 (0) | 3 (17.6) | 0.1 |
| Other | 9(29.0) | 6 (42.8) | 3 (17.6) | 0.12 |
| At least one AE | 18 (58.1) | 6 (42.8) | 12 (70.6) | 0.12 |
