This page is part of the FHIR Specification (v4.2.0: R5 Preview #1). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions . Page versions: R4B R4 R3
Patient Care Work Group | Maturity Level: N/A | Standards Status: Informative |
Raw XML (canonical form + also see XML Format Specification)
Definition for Code System AdverseEventCategory
<?xml version="1.0" encoding="UTF-8"?> <CodeSystem xmlns="http://hl7.org/fhir"> <id value="adverse-event-category"/> <meta> <lastUpdated value="2019-12-31T21:03:40.621+11:00"/> </meta> <text> <status value="generated"/> <div xmlns="http://www.w3.org/1999/xhtml"> <h2> AdverseEventCategory</h2> <div> <p> Overall categorization of the event, e.g. product-related or situational.</p> </div> <p> This code system http://terminology.hl7.org/CodeSystem/adverse-event-category defines the following codes:</p> <table class="codes"> <tr> <td> <b> Lvl</b> </td> <td style="white-space:nowrap"> <b> Code</b> </td> <td> <b> Display</b> </td> <td> <b> Definition</b> </td> </tr> <tr> <td> 1</td> <td style="white-space:nowrap">product-problem <a name="adverse-event-category-product-problem"> </a> </td> <td> Product Problem</td> <td> The adverse event pertains to a product problem.</td> </tr> <tr> <td> 1</td> <td style="white-space:nowrap">product-quality <a name="adverse-event-category-product-quality"> </a> </td> <td> Product Quality</td> <td> The adverse event pertains to product quality.</td> </tr> <tr> <td> 1</td> <td style="white-space:nowrap">product-use-error <a name="adverse-event-category-product-use-error"> </a> </td> <td> Product Use Error</td> <td> The adverse event pertains to a product use error.</td> </tr> <tr> <td> 2</td> <td style="white-space:nowrap">Â Â wrong-dose <a name="adverse-event-category-wrong-dose"> </a> </td> <td> Wrong Dose</td> <td> The adverse event pertains to a wrong dose.</td> </tr> <tr> <td> 2</td> <td style="white-space:nowrap">Â Â incorrect-prescribing-information <a name="adverse-event-category-incorrect-prescribing-information"> </a> </td> <td> Incorrect Prescribing Information</td> <td> The adverse event pertains to incorrect perscribing information.</td> </tr> <tr> <td> 2</td> <td style="white-space:nowrap">Â Â wrong-technique <a name="adverse-event-category-wrong-technique"> </a> </td> <td> Wrong Technique</td> <td> The adverse event pertains to a wrong technique.</td> </tr> <tr> <td> 2</td> <td style="white-space:nowrap">Â Â wrong-route-of-administration <a name="adverse-event-category-wrong-route-of-administration"> </a> </td> <td> Wrong Route of Administration</td> <td> The adverse event pertains to a wrong route of administration.</td> </tr> <tr> <td> 2</td> <td style="white-space:nowrap">Â Â wrong-rate <a name="adverse-event-category-wrong-rate"> </a> </td> <td> Wrong Rate</td> <td> The adverse event pertains to a wrong rate.</td> </tr> <tr> <td> 2</td> <td style="white-space:nowrap">Â Â wrong-duration <a name="adverse-event-category-wrong-duration"> </a> </td> <td> Wrong Duration</td> <td> The adverse event pertains to a wrong duration.</td> </tr> <tr> <td> 2</td> <td style="white-space:nowrap">Â Â wrong-time <a name="adverse-event-category-wrong-time"> </a> </td> <td> Wrong Time</td> <td> The adverse event pertains to a wrong time.</td> </tr> <tr> <td> 2</td> <td style="white-space:nowrap">Â Â expired-drug <a name="adverse-event-category-expired-drug"> </a> </td> <td> Expired Drug</td> <td> The adverse event pertains to an expired drug.</td> </tr> <tr> <td> 1</td> <td style="white-space:nowrap">medical-device-use-error <a name="adverse-event-category-medical-device-use-error"> </a> </td> <td> Medical Device Use Error</td> <td> The adverse event pertains to a medical device use error.</td> </tr> <tr> <td> 1</td> <td style="white-space:nowrap">problem-different-manufacturer <a name="adverse-event-category-problem-different-manufacturer"> </a> </td> <td> Problem with Different Manufacturer of Same Medicine</td> <td> The adverse event pertains to a problem with a different manufacturer of the same medication.</td> </tr> <tr> <td> 1</td> <td style="white-space:nowrap">unsafe-physical-environment <a name="adverse-event-category-unsafe-physical-environment"> </a> </td> <td> Unsafe Physical Environment</td> <td> The adverse event pertains to an unsafe physical environment.</td> </tr> </table> </div> </text> <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-wg"> <valueCode value="pc"/> </extension> <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status"> <valueCode value="trial-use"/> </extension> <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm"> <valueInteger value="0"/> </extension> <url value="http://terminology.hl7.org/CodeSystem/adverse-event-category"/> <identifier> <system value="urn:ietf:rfc:3986"/> <value value="urn:oid:2.16.840.1.113883.4.642.1.1251"/> </identifier> <version value="4.2.0"/> <name value="AdverseEventCategory"/> <title value="AdverseEventCategory"/> <status value="draft"/> <experimental value="false"/> <date value="2019-12-31T21:03:40+11:00"/> <publisher value="HL7 (FHIR Project)"/> <contact> <telecom> <system value="url"/> <value value="http://hl7.org/fhir"/> </telecom> <telecom> <system value="email"/> <value value="fhir@lists.hl7.org"/> </telecom> </contact> <description value="Overall categorization of the event, e.g. product-related or situational."/> <caseSensitive value="true"/> <valueSet value="http://hl7.org/fhir/ValueSet/adverse-event-category"/> <content value="complete"/> <concept> <code value="product-problem"/> <display value="Product Problem"/> <definition value="The adverse event pertains to a product problem."/> </concept> <concept> <code value="product-quality"/> <display value="Product Quality"/> <definition value="The adverse event pertains to product quality."/> </concept> <concept> <code value="product-use-error"/> <display value="Product Use Error"/> <definition value="The adverse event pertains to a product use error."/> <concept> <code value="wrong-dose"/> <display value="Wrong Dose"/> <definition value="The adverse event pertains to a wrong dose."/> </concept> <concept> <code value="incorrect-prescribing-information"/> <display value="Incorrect Prescribing Information"/> <definition value="The adverse event pertains to incorrect perscribing information."/> </concept> <concept> <code value="wrong-technique"/> <display value="Wrong Technique"/> <definition value="The adverse event pertains to a wrong technique."/> </concept> <concept> <code value="wrong-route-of-administration"/> <display value="Wrong Route of Administration"/> <definition value="The adverse event pertains to a wrong route of administration."/> </concept> <concept> <code value="wrong-rate"/> <display value="Wrong Rate"/> <definition value="The adverse event pertains to a wrong rate."/> </concept> <concept> <code value="wrong-duration"/> <display value="Wrong Duration"/> <definition value="The adverse event pertains to a wrong duration."/> </concept> <concept> <code value="wrong-time"/> <display value="Wrong Time"/> <definition value="The adverse event pertains to a wrong time."/> </concept> <concept> <code value="expired-drug"/> <display value="Expired Drug"/> <definition value="The adverse event pertains to an expired drug."/> </concept> </concept> <concept> <code value="medical-device-use-error"/> <display value="Medical Device Use Error"/> <definition value="The adverse event pertains to a medical device use error."/> </concept> <concept> <code value="problem-different-manufacturer"/> <display value="Problem with Different Manufacturer of Same Medicine"/> <definition value="The adverse event pertains to a problem with a different manufacturer of the same medication."/> </concept> <concept> <code value="unsafe-physical-environment"/> <display value="Unsafe Physical Environment"/> <definition value="The adverse event pertains to an unsafe physical environment."/> </concept> </CodeSystem>
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.