MyHealth@Eu MVC package
9.1.0 - trial-use

MyHealth@Eu MVC package - Local Development build (v9.1.0) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions

CodeSystem: eHDSI Display Label CodeSystem

Official URL: http://terminology.ehdsi.eu/CodeSystem/eHDSIDisplayLabel Version: 9.1.0
Active as of 2026-05-07 Computable Name: EpSOSDisplayLabels
Other Identifiers: OID:1.3.6.1.4.1.12559.11.10.1.3.1.44.4

Display labels used across MyHealth@EU clinical documents

This Code system is referenced in the content logical definition of the following value sets:

This case-sensitive code system http://terminology.ehdsi.eu/CodeSystem/eHDSIDisplayLabel defines the following codes:

CodeDisplay
1 Active Ingredient
2 Active Problem
3 Address
4 Advise to the dispenser
5 Agent
6 at
7 Author (HCP)
8 Authoring Device
9 Brand Name
10 Clinical Manifestation
11 Closed/Inactive Problem
12 Contact Information
13 Country
14 Country A Medicinal Product Code
15 Creation Date
16 Custodian
17 Date
18 Date To
19 Date of Birth
20 Date of Prescription
21 Device/Implant
22 Dispense
23 Dispensed Package Size
24 Dispensed Product
25 Dose Form
26 End Date
27 Every
28 Facility ID
29 Facility Name
30 Family Name
31 for
32 Frequency of Intakes
33 Gender
34 Given Name
35 Guardian
36 Implant Date
37 Instructions to patient
38 Is substitution of brand name allowed?
39 Last Update
40 Legal Authenticator
41 National Insurance Number
42 No
43 Number of Packages
44 Observation Type
45 Onset Date
46 Organisation Identifier
47 Organisation Name
48 Other Active Ingredients
49 Other Contacts
50 Package Size
51 Patient
52 Patient IDs
53 per unit
54 Preferred HCP/Legal organization to contact
55 Prefix
56 Prescriber
57 Prescriber details
58 Prescription ID
59 Prescription Item Details
60 Prescription Item ID
61 Prescription Items List
62 Procedure
63 Procedure Date
64 Profession
65 Reaction Type
66 Regional/National Health ID
67 Route of Administration
68 See details
69 Specialty
70 Strength
71 Substitute
72 The Active Problem section is missing !
73 The Allergies, Adverse Reactions, Alerts section is missing !
74 The Medical Devices and Implants section is missing !
75 The Medication Summary section is missing !
76 The History of Procedures section is missing !
77 unit(s)
78 Units per Intake
79 Vaccination
80 Vaccination Date
81 Yes
82 I have identified the patient-data subject
83 I confirm that the patient 'data subject has consented to the following statement: I agree that my ePrescription may be transferred to a registered Health Professional in [COUNTRY B] for the purposes of providing me with medical care and/or medication'
84 Observation Value
85 Date From
99 Physical Findings
100 +/-
107 I confirm that the patient 'data subject has consented to the following statement: 'I agree that my Patient Summary may be transferred to a registered Health Professional in [COUNTRY B] for the purposes of providing me with medical care and/or medication'
108 Original narrative
109 Translated coded
110 Clinical Sections
111 Prescription and Dispensation details
112 Code System
113 Code
114 Name
115 Dispensed Number of Packages
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.'
117 Original Document Language
118 Diagnostic Date
119 Blood Group
120 Min
121 Max
122 Administered
123 Severity
124 Marketing Authorization Holder
125 Primary Patient Identifier
126 Secondary Patient Identifier
127 Represented Organization
128 Medicinal Product
129 Prescription Details
130 Dispensation Details
131 Creation Date of the Document
132 Last Update of the Information
133 There is no information available regarding the subject's allergy conditions
134 The subject has no known allergy conditions
135 The subject has no known medication allergy conditions
136 The subject has no known environmental allergy conditions
137 The subject has no known food allergy conditions
138 There is no information available regarding implanted or external devices for the subject
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
140 There is no information available about the subject's medication use or administration
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
142 There is no information available about the subject's current health problems or disability
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
144 There is no information available about the subject's past history of procedures
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
146 Missing Information
147 From
148 Until
149 Around
150 Duration of Treatment
151 The date of the organizer should match the date of the observations
152 Dose Number in Series
153 Unmapped concept. Nationally used concept for which no translations are available and no safe mappings are possible
154 Body Site
155 Duration
156 Criticality
157 Allergy Status
158 Certainty
159 Result Type
160 Result Value
161 Performer
162 Reporter
163 Functional Assessment Date
164 Functional Assessment
166 Functional Assessment Result
167 Problem Status
169 Batch/Lot Number
170 Administering Center
171 Health Professional Identification
172 Country of Vaccination
173 Medication Reason
174 Current Pregnancy Status
175 Observation Date
176 Status
177 History of Previous Pregnancies
178 Outcome
179 Number of Children
180 Outcome Dates
182 Organization Contact Information
183 Parts
184 Medicinal Product Identifier
185 Medicinal Product Package Identifier
186 Pharmaceutical Product Identifier
187 Address
188 Telecom
189 Part
190 Time(s) per
191 Packaging Details
192 Description
193 Original
194 English
195 Translated
196 Info
197 No information
198 Rare Diseases
199 Diagnosis Assertion Status
200 Related Health Professional
201 Related External Resource
202 Mark the checkbox if brand name (when allowed) has been substituted or package size has been changed
203 Device ID
204 Product Classification
205 Medicinal Product Package Description
206 Package Type
208 Specimen Information
209 Observation Results
210 Laboratory Result Observations
211 Result Observations
212 Specimen Collections
213 Comment Activities
214 Collection Date
215 Specimen Type
216 Collection Method
217 Collection Site
218 Comment
219 Reference Range