{
  "value": "adverse_event_reporter",
  "label": "Document Adverse Events",
  "description": "Create detailed adverse event reports for regulatory compliance. Provide event details, patient information, and outcomes to generate comprehensive incident documentation.",
  "name": "Adverse Event Report",
  "category": "Clinical Operations (healthcare)",
  "type": "Business Department",
  "config": {
    "temperature": 5,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "Help me document an adverse event. I'll provide details about what happened, when it occurred, patient impact, and any immediate actions taken. Create a structured adverse event report including event description, contributing factors, patient outcome, corrective actions implemented, and recommendations for prevention. Ensure all regulatory reporting requirements are addressed."
      }
    ]
  }
}