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Adverse events
| Intervention group | Control group | |||||
|---|---|---|---|---|---|---|
| Related to ingestion of the study product | Related to ingestion of the study product | |||||
| No | Yes | Unclear | No | Yes | Unclear | |
| Urticaria | 2 | 1 | ||||
| Eczema flares | 2 | 1 | 5 | |||
| Vomiting | 1 | 2a | 3 | |||
| Abdominal Pain | 1 | |||||
| Hospital Admission >24 h | 1 | 2 | ||||
avomiting in both cases was associated with reintroduction of study product after gastroenteritis
