eHDSI Terminologies
0.1.0 - ci-build
eHDSI Terminologies, published by HL7 Europe. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-eu/EHDSI-Terminology-package/ and changes regularly. See the Directory of published versions
Official URL: http://terminology.ehdsi.eu/ValueSet/eHDSIDisplayLabel | Version: 0.1.0 | |||
Draft as of 2024-11-29 | Computable Name: EHDSIDisplayLabel | |||
Other Identifiers: OID:1.3.6.1.4.1.12559.11.10.1.3.1.42.46 |
The Value Set is used to denominate all the labels and messages adopted for the eHDSI CDA display
References
This value set is not used here; it may be used elsewhere (e.g. specifications and/or implementations that use this content)
Generated Narrative: ValueSet eHDSIDisplayLabel
urn:oid:1.3.6.1.4.1.12559.11.10.1.3.1.44.4
Code | Display |
13 | Country |
23 | Dispensed Package Size |
46 | Organisation Identifier |
54 | Preferred HCP/Legal organization to contact |
58 | Prescription ID |
71 | Substitute |
76 | The History of Procedures section is missing ! |
80 | Vaccination Date |
84 | Observation Value |
114 | Name |
129 | Prescription Details |
142 | There is no information available about the subject's current health problems or disability |
150 | Duration of Treatment |
161 | Performer |
167 | Problem Status Code |
171 | Health Professional Identification |
176 | Status |
187 | Address |
193 | Original |
3 | Address |
6 | at |
30 | Family Name |
35 | Guardian |
55 | Prefix |
70 | Strength |
109 | Translated coded |
115 | Dispensed Number of Packages |
122 | Administered |
128 | Medicinal Product |
132 | Last Update of the Information |
138 | There is no information available regarding implanted or external devices for the subject |
141 | There are no medications for the subject that have to be reported in this record. This can mean either that there are none known, or that those known are not relevant for the purpose of this record |
143 | The subject is not known to have any health problems or disabilities that have to be reported in this record. This can mean either that there are none known, or that those known are not relevant for the purpose of this record |
145 | The subject has no history of procedures that have to be reported in this record. This can mean either that there are none known, or that those known are not relevant for the purpose of this record |
163 | Functional Assessment Date |
166 | Functional Assessment Result |
173 | Medication Reason |
182 | Organization Contact Information |
184 | Medicinal Product Identifier |
197 | No information |
1 | Active Ingredient |
4 | Advise to the dispenser |
19 | Date of Birth |
21 | Device/Implant |
25 | Dose Form |
49 | Other Contacts |
51 | Patient |
56 | Prescriber |
63 | Procedure Date |
69 | Specialty |
78 | Units per Intake |
130 | Dispensation Details |
164 | Functional Assessment |
169 | Batch/Lot Number |
174 | Current Pregnancy Status |
177 | History of Previous Pregnancies |
188 | Telecom |
8 | Authoring Device |
24 | Dispensed Product |
27 | Every |
31 | for |
40 | Legal Authenticator |
41 | National Insurance Number |
72 | The Active Problem section is missing ! |
74 | The Medical Devices and Implants section is missing ! |
110 | Clinical Sections |
112 | Code System |
117 | Original Document Language |
144 | There is no information available about the subject's past history of procedures |
151 | The date of the organizer should match the date of the observations |
155 | Duration |
158 | Certainty |
179 | Number of Children |
189 | Part |
190 | Time(s) per |
192 | Description |
11 | Closed/Inactive Problem |
26 | End Date |
29 | Facility Name |
34 | Given Name |
36 | Implant Date |
38 | Is substitution of brand name allowed? |
62 | Procedure |
66 | Regional/National Health ID |
75 | The Medication Summary section is missing ! |
81 | Yes |
108 | Original narrative |
123 | Severity |
127 | Represented Organization |
131 | Creation Date of the Document |
139 | There are no devices known to be implanted in or used by the subject that have to be reported in this record. This can mean either that there are none known, or that those known are not relevant for the purpose of this record |
148 | Until |
185 | Medicinal Product Package Identifier |
195 | Translated |
196 | Info |
199 | Diagnosis Assertion Status |
2 | Active Problem |
9 | Brand Name |
10 | Clinical Manifestation |
33 | Gender |
37 | Instructions to patient |
44 | Observation Type |
47 | Organisation Name |
68 | See details |
77 | unit(s) |
79 | Vaccination |
85 | Date From |
113 | Code |
124 | Marketing Authorization Holder |
125 | Primary Patient Identifier |
140 | There is no information available about the subject's medication use or administration |
149 | Around |
153 | Unmapped concept. Nationally used concept for which no translations are available and no safe mappings are possible |
154 | Body Site |
156 | Criticality |
175 | Observation Date |
186 | Pharmaceutical Product Identifier |
198 | Rare Diseases |
5 | Agent |
16 | Custodian |
17 | Date |
20 | Date of Prescription |
32 | Frequency of Intakes |
42 | No |
53 | per unit |
116 | 'If substitution of brand name is marked as not allowed, pharmacists may still consider dispensing the national equivalent even though the brand name might be slightly different. This is a known situation: the same pharmaceutical company is marketing the same medicinal product in different countries with slightly different names due to marketing reasons. If the pharmacist is certain that this is the case, the systems allows the input of the new brand name.' |
118 | Diagnostic Date |
119 | Blood Group |
133 | There is no information available regarding the subject's allergy conditions |
147 | From |
159 | Result Type |
162 | Reporter |
170 | Administering Center |
172 | Country of Vaccination |
194 | English |
7 | Author (HCP) |
12 | Contact Information |
18 | Date To |
22 | Dispense |
28 | Facility ID |
43 | Number of Packages |
45 | Onset Date |
50 | Package Size |
64 | Profession |
65 | Reaction Type |
67 | Route of Administration |
73 | The Allergies, Adverse Reactions, Alerts section is missing ! |
126 | Secondary Patient Identifier |
134 | The subject has no known allergy conditions |
146 | Missing Information |
152 | Dose Number in Series |
202 | Mark the checkbox if brand name (when allowed) has been substituted or package size has been changed |
157 | Allergy Status |
160 | Result Value |
178 | Outcome |
180 | Outcome Dates |
191 | Packaging Details |
200 | Related Health Professional |
201 | Related External Resource |
203 | Device ID |
No Expansion for this valueset (Unknown Code System)
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 |