{
  "value": "adverse_event_report_drafter",
  "label": "Draft Adverse Event Reports",
  "description": "This workflow helps draft comprehensive adverse event narratives for regulatory reporting. Input the patient details, event description, timeline, interventions, and outcome, and the AI will create a properly structured narrative following pharmacovigilance best practices.",
  "name": "AE Report Draft",
  "category": "Pharmaceuticals",
  "type": "Industry",
  "config": {
    "temperature": 5,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "Draft a clear adverse event narrative based on the information provided. Start with patient demographics and relevant medical history. Describe the event chronologically including onset, symptoms, severity, and duration. Detail all interventions taken and their timing. Include relevant concomitant medications, test results, and causality assessment. End with the outcome and any follow-up plans. Use medical terminology appropriately and maintain an objective, factual tone throughout. Ensure all dates and times are clearly stated."
      }
    ]
  }
}