FHIR IG Statistics: ValueSet/MedDRATransfusionAdverseEventVS

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{
  "resourceType": "ValueSet",
  "id": "MedDRATransfusionAdverseEventVS",
  "text": {
    "status": "additional",
    "div": "<!-- snip (see above) -->"
  },
  "url": "http://hl7.org/fhir/us/icsr-ae-reporting/ValueSet/MedDRATransfusionAdverseEventVS",
  "version": "1.0.1",
  "name": "MedDRATransfusionAdverseEventVS",
  "title": "Transfusion-related Adverse Events",
  "status": "draft",
  "experimental": false,
  "date": "2023-08-30T17:02:44+00:00",
  "publisher": "Biomedical Research & Regulation WG",
  "contact": [
    {
      "name": "Biomedical Research & Regulation WG",
      "telecom": [
        {
          "system": "url",
          "value": "http://hl7.org/Special/committees/rcrim"
        }
      ]
    },
    {
      "name": "Jean Duteau",
      "telecom": [
        {
          "system": "email",
          "value": "mailto:jean.duteau@ibm.com"
        }
      ]
    }
  ],
  "description": "MedDRA codes that represent the specific transfusion adverse events that are considered by this Implementation Guide",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "urn:iso:std:iso:3166",
          "code": "US",
          "display": "United States of America"
        }
      ]
    }
  ],
  "copyright": "MedDRA® is a registered trademark of the International Federation of Pharmaceutical Manufacturers and Associations.  All rights reserved."
}