HDR Version 7 HL7 Version 3 Messaging Conformance Specification

5.18 A_ObservationEventReaction (universal) - COCT_RM120600HT02

This section contains the following topics:

5.18.1 Introduction
5.18.2 RMIM
5.18.3 Referenced CMETs
5.18.4 Links to Artifacts

5.18.1 Introduction

The A_ObservationEventReaction (universal) CMET represents an observation made on a patient about a reaction that occurred. A reaction is the consequence, perhaps strongly indicated or only possibly related, of an adverse event, potential adverse event, or intolerance. It constitutes the core of the individual case safety report since without a reaction there will be no perception of an adverse event and no report at all. This CMET also serves to provide reaction information caused by an intolerance. It includes information about a clinical trial protocol, if relevant for adverse events.

5.18.2 RMIM

The following figure shows the A_ObservationEventReaction (universal) RMIM:

Figure: 5.18.2-1 A_ObservationEventReaction (universal) RMIM

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5.18.3 Referenced CMETs

• 5.14 A_Encounter (universal) - COCT_RM010100HT02
  
• 5.20 A_ObservationGeneral (universal) - COCT_RM120500HT04
  
• 5.24 A_ObservationOrder (universal) - COCT_RM970000HT04
  
• 5.26 A_ObservationSupportingCodedValue (minimal) - COCT_RM120214HT02
  
• 5.32 A_ProcedureEvent (universal) - COCT_RM951000HT02
  
• 5.34 A_ProcedureOrder (universal) - COCT_RM950000HT04
  
• 5.37 A_SpecimenObservationEvent (universal) - COCT_RM121500HT03
  
• 5.39 A_SpecimenObservationOrder (universal) - COCT_RM971000HT03
  
• 5.41 A_SubstanceAdminEvent (universal) - COCT_RM920100HT02
  
• 5.43 A_SubstanceAdminOrder (universal) - COCT_RM920000HT02
  
• 5.57 R_AssignedPersonOrganization (universal) - COCT_RM090400HT02
  
• 5.58 R_ClinicalTrialResearchSubject (minimal) - COCT_RM100004HT02
  
• 5.64 R_EmploymentStaff (universal) - COCT_RM410000HT02
  
• 5.69 R_LocationServiceDelivery (universal) - COCT_RM240000HT02
  
• 5.76 R_Patient (universal) - COCT_RM050000HT04
  

5.18.4 Links to Artifacts

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