adverseevent.json

{
   "resource": "AdverseEvent",
   "toolName": "adverseevent",
   "title": "Adverse Event",
   "description": "Search for or read a FHIR AdverseEvent resource tracking harmful events in research contexts. For direct read, provide _id alone. IMPORTANT: Patient-only search is NOT supported — you MUST provide subject + study together, subject + research-subject, or research-subject alone. Do NOT attempt this resource unless you have a ResearchStudy or ResearchSubject FHIR ID. All ID values are raw FHIR IDs (not prefixed with resource type).",
   "supportsDirectRead": true,
   "searchParams": {
      "_id": "AdverseEvent resource ID — performs direct read when provided alone",
      "actuality": "Whether event is actual or potential",
      "category": "Event category (e.g. product-problem, wrong-dose)",
      "date": "When the event occurred",
      "event": "Type of adverse event (coded)",
      "location": "Location where the event occurred",
      "recorder": "Who recorded the adverse event (user who first recorded it)",
      "research-subject": "ResearchSubject FHIR ID (raw ID, no prefix)",
      "resultingcondition": "Resulting Condition reference",
      "seriousness": "Seriousness of the event: Serious or Non-Serious",
      "severity": "Severity: mild, moderate, severe",
      "study": "ResearchStudy FHIR ID (raw ID, no prefix)",
      "subject": "Patient FHIR ID (raw ID, no Patient/ prefix)",
      "substance": "Suspected causal substance or product"
   },
   "requireOneOf": [
      [
         "subject",
         "study"
      ],
      [
         "subject",
         "research-subject"
      ],
      [
         "research-subject"
      ]
   ]
}