This
page
is
part
of
the
FHIR
Specification
(v3.0.2:
(v4.0.1:
R4
-
Mixed
Normative
and
STU
3).
)
in
it's
permanent
home
(it
will
always
be
available
at
this
URL).
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:
R5
R4B
R4
R3
R4
R3
Work
Group
|
Maturity Level : 1 |
|
Use Context : Any |
This is a value set defined by the FHIR project.
Summary
| Defining URL: | http://hl7.org/fhir/ValueSet/adverse-event-causality-assess |
| Version: | 4.0.1 |
| Name: | AdverseEventCausalityAssessment |
| Title: | AdverseEventCausalityAssessment |
| Definition: |
Codes for the assessment of whether the entity caused the event. |
| Committee: |
Work
Group
|
| OID: |
|
| Source Resource | XML / JSON |
This value set is used in the following places:
This value set includes codes from the following code systems:
This
expansion
generated
19
Apr
2017
01
Nov
2019
This
value
set
contains
2
6
concepts
Expansion
based
on
http://hl7.org/fhir/adverse-event-causality-assess
http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess
version
3.0.2
4.0.1
All
codes
from
system
http://hl7.org/fhir/adverse-event-causality-assess
http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess
| 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. |
|
|
|
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. |
|
|
|
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. |
See the full registry of value sets defined as part of FHIR.
Explanation of the columns that may appear on this page:
|
|
A
few
code
lists
that
FHIR
defines
are
hierarchical
-
each
code
is
assigned
a
level.
|
| Source | 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). If the code is in italics, this indicates that the code is not selectable ('Abstract') |
| 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 |