| Source | hl7.fhir.uv.ae-research-backport-ig#current:Adverse Event Clinical Research R4 Backport (v4.0.1) |
| resourceType | StructureDefinition |
| id | supporting-info |
| canonical | http://hl7.org/fhir/uv/ae-research-backport-ig/StructureDefinition/supporting-info |
| version | 1.0.0-ballot |
| status | draft |
| publisher | HL7 International - Biomedical Research and Regulation, Vulcan AdverseEvent groups |
| name | SupportingInfo |
| title | Supporting information relevant to the event |
| date | 2023-07-28T19:26:02+00:00 |
| description | Relevant past history for the subject. In a clinical care context, an example being a patient had an adverse event following a penicillin administration and the patient had a previously documented penicillin allergy. In a clinical trials context, an example is a bunion or rash that was present prior to the study. Additionally, the supporting item can be a document that is relevant to this instance of the adverse event that is not part of the subject's medical history. For example, a clinical note, staff list, or material safety data sheet (MSDS). Supporting information is not a contributing factor, preventive action, or mitigating action. |
| jurisdictions | uv |
| fhirVersion | 4.0.1 |
| kind | complex-type |
| abstract | false |
| sdTtype | Extension |
| derivation | constraint |
| base | http://hl7.org/fhir/StructureDefinition/Extension |
| contexts | element:AdverseEvent |
| Usages | |
Extension
extension
extension:item
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