| Source | hl7.fhir.us.ctcae#current:HL7 FHIR Implementation Guide: Common Terminology Criteria (CTC) Adverse Events Release 1 - DRAFT (v4.0.1) |
| resourceType | ValueSet |
| id | adverse-event-seriousness-value-set |
| canonical | http://hl7.org/fhir/us/ctcae/ValueSet/adverse-event-seriousness-value-set |
| version | 0.0.1 |
| status | draft |
| publisher | HL7 International Clinical Interoperability Council |
| name | AdverseEventSeriousnessVS |
| title | Adverse Event Seriousness Value Set |
| date | 2023-07-20T15:24:06+00:00 |
| description | An adverse event is classified as serious or non-serious. It is considered serious if it results in any of the following outcomes: (1) Death, (2) Life-threatening experience, 3) Inpatient hospitalization or prolongation of existing hospitalization (for > 24 hours), (4) Persistent or significant incapacity or substantial disruption of the ability to conduct normal life functions, (5) Congenital anomaly/birth defect, or (6) Important Medical Event (IME) that may jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the outcomes listed in this definition (reference: https://crawb.crab.org/txwb/CRA_MANUAL/Vol1/chapter%2013_Serious%20Adverse%20Events.pdf). |
| jurisdictions | us |
| Usages | |