US Medication Risk Evaluation and Mitigation Strategies (REMS) FHIR IG
1.0.0 - STU1 United States of America flag

This page is part of the US Medication REMS (v1.0.0: STU1) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions

Artifacts Summary

Contents:

This page provides a list of the FHIR artifacts defined as part of this implementation guide.

Behavior: Capability Statements

The following artifacts define the specific capabilities that different types of systems are expected to have in order to comply with this implementation guide. Systems conforming to this implementation guide are expected to declare conformance to one or more of the following capability statements.

Medication REMS Capability Statement - Provider System

This CapabilityStatement describes the expected capabilities of a Provider System that conforms to the conventions of the Medication REMS FHIR implementation guide.
Medication REMS Capability Statement - REMS Administrator System

This CapabilityStatement describes the expected capabilities of a REMS Administrator System that conforms to the conventions of the Medication REMS FHIR implementation guide.

Structures: Resource Profiles

These define constraints on FHIR resources for systems conforming to this implementation guide.

Medication REMS Task - SMART Launch

This profile defines a Task to be returned in a REMS Administrator's CDS Hooks response - enabling the provider or staff to launch a SMART app from their work queue.

Example: Example Instances

These are example instances that show what data produced and consumed by systems conforming with this implementation guide might look like.

example-patient-123

Example of a US Core patient
example-rems-docref-1

Example of a US Core document reference containing a patient's REMS program information
medication-rems-task-smart-launch-1

Complete patient enrollment using the DRUG-X REMS SMART app