{description: 'Additional codes found on https://www.fda.gov/safety/reporting-serious-problems-fda/what-serious-adverse-event#:~:text=Required%20Intervention%20to%20Prevent%20Permanent%20Impairment%20or%20Damage%20(Devices),use%20of%20a%20medical%20product. Typically used in reporting for Clinical Research, post-market surveillance (e.g. Form FDA 3500A MedWatch).', package_name: hl7.fhir.uv.ae-research-ig, name: FDAaddSeriousnessCriteriaCS, type: null, package_version: 1.0.0-ballot, class: unknown, kind: null, url: 'http://hl7.org/fhir/uv/ae-research-ig/CodeSystem/fda-add-seriousness-criteria-cs', version: 1.0.0-ballot}