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

ValueSet: eHDSI Display Label

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)

Logical Definition (CLD)

Generated Narrative: ValueSet eHDSIDisplayLabel

  • Include these codes as defined in urn:oid:1.3.6.1.4.1.12559.11.10.1.3.1.44.4
    CodeDisplay
    13Country
    23Dispensed Package Size
    46Organisation Identifier
    54Preferred HCP/Legal organization to contact
    58Prescription ID
    71Substitute
    76The History of Procedures section is missing !
    80Vaccination Date
    84Observation Value
    114Name
    129Prescription Details
    142There is no information available about the subject's current health problems or disability
    150Duration of Treatment
    161Performer
    167Problem Status Code
    171Health Professional Identification
    176Status
    187Address
    193Original
    3Address
    6at
    30Family Name
    35Guardian
    55Prefix
    70Strength
    109Translated coded
    115Dispensed Number of Packages
    122Administered
    128Medicinal Product
    132Last Update of the Information
    138There is no information available regarding implanted or external devices for the subject
    141There 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
    143The 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
    145The 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
    163Functional Assessment Date
    166Functional Assessment Result
    173Medication Reason
    182Organization Contact Information
    184Medicinal Product Identifier
    197No information
    1Active Ingredient
    4Advise to the dispenser
    19Date of Birth
    21Device/Implant
    25Dose Form
    49Other Contacts
    51Patient
    56Prescriber
    63Procedure Date
    69Specialty
    78Units per Intake
    130Dispensation Details
    164Functional Assessment
    169Batch/Lot Number
    174Current Pregnancy Status
    177History of Previous Pregnancies
    188Telecom
    8Authoring Device
    24Dispensed Product
    27Every
    31for
    40Legal Authenticator
    41National Insurance Number
    72The Active Problem section is missing !
    74The Medical Devices and Implants section is missing !
    110Clinical Sections
    112Code System
    117Original Document Language
    144There is no information available about the subject's past history of procedures
    151The date of the organizer should match the date of the observations
    155Duration
    158Certainty
    179Number of Children
    189Part
    190Time(s) per
    192Description
    11Closed/Inactive Problem
    26End Date
    29Facility Name
    34Given Name
    36Implant Date
    38Is substitution of brand name allowed?
    62Procedure
    66Regional/National Health ID
    75The Medication Summary section is missing !
    81Yes
    108Original narrative
    123Severity
    127Represented Organization
    131Creation Date of the Document
    139There 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
    148Until
    185Medicinal Product Package Identifier
    195Translated
    196Info
    199Diagnosis Assertion Status
    2Active Problem
    9Brand Name
    10Clinical Manifestation
    33Gender
    37Instructions to patient
    44Observation Type
    47Organisation Name
    68See details
    77unit(s)
    79Vaccination
    85Date From
    113Code
    124Marketing Authorization Holder
    125Primary Patient Identifier
    140There is no information available about the subject's medication use or administration
    149Around
    153Unmapped concept. Nationally used concept for which no translations are available and no safe mappings are possible
    154Body Site
    156Criticality
    175Observation Date
    186Pharmaceutical Product Identifier
    198Rare Diseases
    5Agent
    16Custodian
    17Date
    20Date of Prescription
    32Frequency of Intakes
    42No
    53per 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.'
    118Diagnostic Date
    119Blood Group
    133There is no information available regarding the subject's allergy conditions
    147From
    159Result Type
    162Reporter
    170Administering Center
    172Country of Vaccination
    194English
    7Author (HCP)
    12Contact Information
    18Date To
    22Dispense
    28Facility ID
    43Number of Packages
    45Onset Date
    50Package Size
    64Profession
    65Reaction Type
    67Route of Administration
    73The Allergies, Adverse Reactions, Alerts section is missing !
    126Secondary Patient Identifier
    134The subject has no known allergy conditions
    146Missing Information
    152Dose Number in Series
    202Mark the checkbox if brand name (when allowed) has been substituted or package size has been changed
    157Allergy Status
    160Result Value
    178Outcome
    180Outcome Dates
    191Packaging Details
    200Related Health Professional
    201Related External Resource
    203Device ID

 

Expansion

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