FHIR Cross-Version Extensions package for FHIR R5 from FHIR R4B - Version 0.0.1-snapshot-2. See the Directory of published versions
| Official URL: http://hl7.org/fhir/4.3/ValueSet/R4B-adverse-event-causality-assess-for-R5 | Version: 0.0.1-snapshot-2 | |||
| Standards status: Informative | Maturity Level: 1 | Responsible: Patient Care | Computable Name: R4B_adverse_event_causality_assess_for_R5 | |
| This cross-version ValueSet represents concepts from http://hl7.org/fhir/ValueSet/adverse-event-causality-assess | 4.3.0 for use in FHIR R5. Concepts not present here have direct equivalent mappings crossing all versions from R4B to R5. |
References
http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess version 4.3.0| Code | Display | Definition |
| Certain | Certain | i) Event or laboratory test abnormality, with plausible time relationship to drug intake; ii) Cannot be explained by disease or other drugs; iii) Response to withdrawal plausible (pharmacologically, pathologically); iv) Event definitive pharmacologically or phenomenologically (i.e. an objective and specific medical disorder or a recognized pharmacological phenomenon); or v) Re-challenge satisfactory, if necessary. |
| Probably-Likely | Probably/Likely | i) Event or laboratory test abnormality, with reasonable time relationship to drug intake; ii) Unlikely to be attributed to disease or other drugs; iii) Response to withdrawal clinically reasonable; or iv) Re-challenge not required. |
| Possible | Possible | i) Event or laboratory test abnormality, with reasonable time relationship to drug intake; ii) Could also be explained by disease or other drugs; or iii) Information on drug withdrawal may be lacking or unclear. |
| Unlikely | Unlikely | i) Event or laboratory test abnormality, with a time to drug intake that makes a relationship improbable (but not impossible); or ii) Disease or other drugs provide plausible explanations. |
| Conditional-Classified | Conditional/Classified | i) Event or laboratory test abnormality; ii) More data for proper assessment needed; or iii) Additional data under examination. |
| Unassessable-Unclassifiable | Unassessable/Unclassifiable | i) Report suggesting an adverse reaction; ii) Cannot be judged because information is insufficient or contradictory; or iii) Data cannot be supplemented or verified. |
This value set expansion contains 6 concepts.
| Code | System | Display | Definition |
| Certain | http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess | Certain | i) Event or laboratory test abnormality, with plausible time relationship to drug intake; ii) Cannot be explained by disease or other drugs; iii) Response to withdrawal plausible (pharmacologically, pathologically); iv) Event definitive pharmacologically or phenomenologically (i.e. an objective and specific medical disorder or a recognized pharmacological phenomenon); or v) Re-challenge satisfactory, if necessary. |
| Probably-Likely | http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess | Probably/Likely | i) Event or laboratory test abnormality, with reasonable time relationship to drug intake; ii) Unlikely to be attributed to disease or other drugs; iii) Response to withdrawal clinically reasonable; or iv) Re-challenge not required. |
| Possible | http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess | Possible | i) Event or laboratory test abnormality, with reasonable time relationship to drug intake; ii) Could also be explained by disease or other drugs; or iii) Information on drug withdrawal may be lacking or unclear. |
| Unlikely | http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess | Unlikely | i) Event or laboratory test abnormality, with a time to drug intake that makes a relationship improbable (but not impossible); or ii) Disease or other drugs provide plausible explanations. |
| Conditional-Classified | http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess | Conditional/Classified | i) Event or laboratory test abnormality; ii) More data for proper assessment needed; or iii) Additional data under examination. |
| Unassessable-Unclassifiable | http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess | Unassessable/Unclassifiable | i) Report suggesting an adverse reaction; ii) Cannot be judged because information is insufficient or contradictory; or iii) Data cannot be supplemented or verified. |
Explanation of the columns that may appear on this page:
| Level | A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies |
| System | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
| Code | The code (used as the code in the resource instance) |
| Display | The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application |
| Definition | An explanation of the meaning of the concept |
| Comments | Additional notes about how to use the code |