Sparked Logical Models, published by CSIRO. This guide is not an authorized publication; it is the continuous build for version 0.0.1 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/aehrc/logical-model-web/ and changes regularly. See the Directory of published versions

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Logical Model: Adverse Reaction Event AUCDI

Official URL: https://aehrc.csiro.au/fhir/logical-models/AdverseReactionEventAUCDI				Version: 0.0.1
Draft as of 2023-09-11				Computable Name: AdverseReactionEventAUCDI
Keywords: core, erequest

The Adverse Reaction Event AUCDI Logical Model Mindmap is shown below.

Information about a specific adverse reaction event caused by exposure to a specific substance.

Purpose

To record information about a specific adverse reaction event caused by exposure to a specific substance.

Misuse

Not to be used to record adverse events, including failures of clinical process, interventions or products. For example: abnormal use or mistakes/errors made in maladministration of an agent or substance; incorrect dosage; mislabelling; harm or injury caused by an intervention or procedure; overdose/poisoning etc. Use a specific model for this purpose.

Considerations

Use to record information about a specific adverse reaction event caused by exposure to a specific substance. The substance may be recorded in the 'Specific substance' element in this archetype, or in an appropriate element in the parent in which this is nested.

Roadmap

Usage:

• Refer to this Logical Model Profile: Adverse Reaction Risk AUCDI

Formal Views of Profile Content

Description of Profiles, Differentials, Snapshots and how the different presentations work.

 

​Other representations of profile: CSV, Excel