| Level/ Type |
Code |
Display Name |
Code System |
| 0‑L |
1
|
Active Ingredient
|
epSOSDisplayLabel |
| 0‑L |
10
|
Clinical Manifestation
|
epSOSDisplayLabel |
| 0‑L |
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’
|
epSOSDisplayLabel |
| 0‑L |
11
|
Closed/Inactive Problem
|
epSOSDisplayLabel |
| 0‑L |
12
|
Contact Information
|
epSOSDisplayLabel |
| 0‑L |
13
|
Country
|
epSOSDisplayLabel |
| 0‑L |
14
|
Country A Medicinal Product Code
|
epSOSDisplayLabel |
| 0‑L |
15
|
Creation Date
|
epSOSDisplayLabel |
| 0‑L |
16
|
Custodian
|
epSOSDisplayLabel |
| 0‑L |
17
|
Date
|
epSOSDisplayLabel |
| 0‑L |
18
|
Date To
|
epSOSDisplayLabel |
| 0‑L |
19
|
Date of Birth
|
epSOSDisplayLabel |
| 0‑L |
2
|
Active Problem
|
epSOSDisplayLabel |
| 0‑L |
20
|
Date of Prescription
|
epSOSDisplayLabel |
| 0‑L |
21
|
Device/Implant
|
epSOSDisplayLabel |
| 0‑L |
22
|
Dispense
|
epSOSDisplayLabel |
| 0‑L |
23
|
Dispensed Package Size
|
epSOSDisplayLabel |
| 0‑L |
24
|
Dispensed Product
|
epSOSDisplayLabel |
| 0‑L |
25
|
Dose Form
|
epSOSDisplayLabel |
| 0‑L |
26
|
End Date
|
epSOSDisplayLabel |
| 0‑L |
27
|
Every
|
epSOSDisplayLabel |
| 0‑L |
28
|
Facility ID
|
epSOSDisplayLabel |
| 0‑L |
29
|
Facility Name
|
epSOSDisplayLabel |
| 0‑L |
3
|
Address
|
epSOSDisplayLabel |
| 0‑L |
30
|
Family Name
|
epSOSDisplayLabel |
| 0‑L |
31
|
for
|
epSOSDisplayLabel |
| 0‑L |
32
|
Frequency of Intakes
|
epSOSDisplayLabel |
| 0‑L |
33
|
Gender
|
epSOSDisplayLabel |
| 0‑L |
34
|
Given Name
|
epSOSDisplayLabel |
| 0‑L |
35
|
Guardian
|
epSOSDisplayLabel |
| 0‑L |
36
|
Implant Date
|
epSOSDisplayLabel |
| 0‑L |
37
|
Instructions to patient
|
epSOSDisplayLabel |
| 0‑L |
38
|
Is substitution of brand name allowed?
|
epSOSDisplayLabel |
| 0‑L |
39
|
Last Update
|
epSOSDisplayLabel |
| 0‑L |
4
|
Advise to the dispenser
|
epSOSDisplayLabel |
| 0‑L |
40
|
Legal Authenticator
|
epSOSDisplayLabel |
| 0‑L |
41
|
National Insurance Number
|
epSOSDisplayLabel |
| 0‑L |
42
|
No
|
epSOSDisplayLabel |
| 0‑L |
43
|
Number of packages
|
epSOSDisplayLabel |
| 0‑L |
44
|
Observation Type
|
epSOSDisplayLabel |
| 0‑L |
45
|
Onset Date
|
epSOSDisplayLabel |
| 0‑L |
46
|
Organisation Identifier
|
epSOSDisplayLabel |
| 0‑L |
47
|
Organisation Name
|
epSOSDisplayLabel |
| 0‑L |
48
|
Other Active Ingredients
|
epSOSDisplayLabel |
| 0‑L |
49
|
Other Contacts
|
epSOSDisplayLabel |
| 0‑L |
5
|
Agent
|
epSOSDisplayLabel |
| 0‑L |
50
|
Package Size
|
epSOSDisplayLabel |
| 0‑L |
51
|
Patient
|
epSOSDisplayLabel |
| 0‑L |
52
|
Patient IDs
|
epSOSDisplayLabel |
| 0‑L |
53
|
per unit
|
epSOSDisplayLabel |
| 0‑L |
54
|
Preferred HP/Legal organization to contact
|
epSOSDisplayLabel |
| 0‑L |
55
|
Prefix
|
epSOSDisplayLabel |
| 0‑L |
56
|
Prescriber
|
epSOSDisplayLabel |
| 0‑L |
57
|
Prescriber details
|
epSOSDisplayLabel |
| 0‑L |
58
|
Prescription ID
|
epSOSDisplayLabel |
| 0‑L |
59
|
Prescription Item Details
|
epSOSDisplayLabel |
| 0‑L |
6
|
at
|
epSOSDisplayLabel |
| 0‑L |
60
|
Prescription Item ID
|
epSOSDisplayLabel |
| 0‑L |
61
|
Prescription Items List
|
epSOSDisplayLabel |
| 0‑L |
62
|
Procedure
|
epSOSDisplayLabel |
| 0‑L |
63
|
Procedure Date
|
epSOSDisplayLabel |
| 0‑L |
64
|
Profession
|
epSOSDisplayLabel |
| 0‑L |
65
|
Reaction Type
|
epSOSDisplayLabel |
| 0‑L |
66
|
Regional/National Health ID
|
epSOSDisplayLabel |
| 0‑L |
67
|
Route of Administration
|
epSOSDisplayLabel |
| 0‑L |
68
|
See details
|
epSOSDisplayLabel |
| 0‑L |
69
|
Specialty
|
epSOSDisplayLabel |
| 0‑L |
7
|
Author (HP)
|
epSOSDisplayLabel |
| 0‑L |
70
|
Strength
|
epSOSDisplayLabel |
| 0‑L |
71
|
Substitute
|
epSOSDisplayLabel |
| 0‑L |
72
|
The Active Problem section is missing !
|
epSOSDisplayLabel |
| 0‑L |
73
|
The Allergies, adverse reactions, alerts section is missing !
|
epSOSDisplayLabel |
| 0‑L |
74
|
The Medical Devices and implants section is missing !
|
epSOSDisplayLabel |
| 0‑L |
75
|
The Medication Summary section is missing !
|
epSOSDisplayLabel |
| 0‑L |
76
|
The History of Procedures section is missing !
|
epSOSDisplayLabel |
| 0‑L |
77
|
unit(s)
|
epSOSDisplayLabel |
| 0‑L |
78
|
Units per intake
|
epSOSDisplayLabel |
| 0‑L |
79
|
Vaccination
|
epSOSDisplayLabel |
| 0‑L |
8
|
Authoring Device
|
epSOSDisplayLabel |
| 0‑L |
80
|
Vaccination Date
|
epSOSDisplayLabel |
| 0‑L |
81
|
Yes
|
epSOSDisplayLabel |
| 0‑L |
82
|
I have identified the patient-data subject
|
epSOSDisplayLabel |
| 0‑L |
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’
|
epSOSDisplayLabel |
| 0‑L |
84
|
Observation Value
|
epSOSDisplayLabel |
| 0‑L |
85
|
Date From
|
epSOSDisplayLabel |
| 0‑L |
9
|
Brand Name
|
epSOSDisplayLabel |
| 0‑L |
99
|
Physical Findings
|
epSOSDisplayLabel |
|
Value Set epSOSDisplayLabel 2013‑06‑03
Draft
