ID

6193

Description

Schwerwiegendes unerwünschtes Ereignis (SUE) in der Therapie SUE Berichtsformular Bitte ausfüllen und faxen oder senden an: Westfälische Wilhelms-Universität Münster, Institut für Epidemiologie und Sozialmedizin, Albert-Schweitzer-Campus 1, Gebäude 03, 48149 Münster Fax: (0251) 83-55300, E-Mail: regims@uni-muenster.de http://epi.uni-muenster.de

Link

http://epi.uni-muenster.de

Keywords

Versions (8)
  1. 12/15/14 12/15/14 - Martin Dugas
  2. 12/16/14 12/16/14 - Martin Dugas
  3. 12/17/14 12/17/14 - Martin Dugas
  4. 12/17/14 12/17/14 - Martin Dugas
  5. 1/16/15 1/16/15 - Martin Dugas
  6. 2/6/15 2/6/15 -
  7. 6/25/15 6/25/15 - Martin Dugas
  8. 9/27/21 9/27/21 -
Uploaded on

December 17, 2014

DOI

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License

Creative Commons BY-NC 3.0 Legacy
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Multiple Sclerosis - Severe Adverse Events (REGIMS)

German English

Multiple Sclerosis - Severe Adverse Events (REGIMS)

1 forms  
Serious Adverse Event
Description

Serious Adverse Event

Alias
UMLS CUI-1
C1519255
SAE date of report
Description

SAE date of report

Data type

date

Alias
UMLS CUI-1
C1519255
UMLS CUI-2
C1302584
SAE number
Data type

integer

Alias
UMLS CUI-1
C1519255
UMLS CUI-2
C0237753
Report type
Data type

integer

Alias
UMLS CUI-1
C0585733
FB-ID
Data type

text

Age
Data type

integer

Measurement units
  • Jahre
Alias
UMLS CUI-1
C0001779
Jahre
Gender
Data type

text

Alias
UMLS CUI-1
C0079399
Weight
Data type

float

Measurement units
  • kg
Alias
UMLS CUI-1
C0005910
kg
Height
Data type

integer

Measurement units
  • cm
Alias
UMLS CUI-1
C0005890
cm
Pregnancy
Data type

boolean

Alias
UMLS CUI-1
C0549206
Weeks pregnant
Data type

integer

Alias
UMLS CUI-1
C0460089
SAE Description
Data type

text

Alias
UMLS CUI-1
C2699044
SAE Start Date
Data type

date

Alias
UMLS CUI-1
C2697888
SAE End Date
Data type

date

Alias
UMLS CUI-1
C2697886
SAE Category
Data type

integer

Alias
UMLS CUI-1
C2826790
SAE Severity Code
Data type

integer

Alias
UMLS CUI-1
C2985921
SAE Treatment
Data type

integer

Alias
UMLS CUI-1
C2981656
SAE Treatment Description
Data type

text

Alias
UMLS CUI-1
C2981656
SAE Outcome
Data type

integer

Alias
UMLS CUI-1
C1705586
Death date
Data type

date

Alias
UMLS CUI-1
C1148348
Cause of death
Data type

text

Alias
UMLS CUI-1
C0007465
Autopsy
Data type

boolean

Alias
UMLS CUI-1
C0004398
Medication regarding Multiple Sclerosis
Description

Medication regarding Multiple Sclerosis

Alias
UMLS CUI-1
C0013227
UMLS CUI-2
C0026769
Medication MS
Data type

text

Alias
UMLS CUI-1
C0013227
UMLS CUI-2
C0026769
Medication start date
Data type

date

Alias
UMLS CUI-1
C0451613
Medication end date
Data type

date

Alias
UMLS CUI-1
C3483769
Daily dose
Data type

integer

Alias
UMLS CUI-1
C2348070
Unit
Data type

text

Alias
UMLS CUI-1
C1519795
Action
Data type

integer

Alias
UMLS CUI-1
C3266814
Causality
Data type

integer

Alias
UMLS CUI-1
C1314792
Concomitant medication
Description

Concomitant medication

Alias
UMLS CUI-1
C2347852
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Similar models

Multiple Sclerosis - Severe Adverse Events (REGIMS)

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Serious Adverse Event
C1519255 (UMLS CUI-1)
SAE date of report
Item
date
C1519255 (UMLS CUI-1)
C1302584 (UMLS CUI-2)
SAE number
Item
integer
C1519255 (UMLS CUI-1)
C0237753 (UMLS CUI-2)
Item
integer
C0585733 (UMLS CUI-1)
Report type
Code List
Report type
CL Item
 (1)
CL Item
 (2)
FB-ID
Item
text
Age
Item
integer
C0001779 (UMLS CUI-1)
Item
text
C0079399 (UMLS CUI-1)
Gender
Code List
Gender
CL Item
 (m)
CL Item
 (w)
Weight
Item
float
C0005910 (UMLS CUI-1)
Height
Item
integer
C0005890 (UMLS CUI-1)
Pregnancy
Item
boolean
C0549206 (UMLS CUI-1)
Weeks pregnant
Item
integer
C0460089 (UMLS CUI-1)
SAE Description
Item
text
C2699044 (UMLS CUI-1)
SAE Start Date
Item
date
C2697888 (UMLS CUI-1)
SAE End Date
Item
date
C2697886 (UMLS CUI-1)
Item
integer
C2826790 (UMLS CUI-1)
SAE Category
Code List
SAE Category
CL Item
 (1)
CL Item
 (2)
CL Item
 (3)
Item
integer
C2985921 (UMLS CUI-1)
SAE Severity Code
Code List
SAE Severity Code
CL Item
 (1)
CL Item
 (2)
CL Item
 (3)
CL Item
 (4)
CL Item
 (5)
CL Item
 (6)
Item
integer
C2981656 (UMLS CUI-1)
SAE Treatment
Code List
SAE Treatment
CL Item
 (0)
CL Item
 (1)
CL Item
 (2)
SAE Treatment Description
Item
text
C2981656 (UMLS CUI-1)
Item
integer
C1705586 (UMLS CUI-1)
SAE Outcome
Code List
SAE Outcome
CL Item
 (0)
CL Item
 (1)
CL Item
 (2)
CL Item
 (3)
CL Item
 (4)
Death date
Item
date
C1148348 (UMLS CUI-1)
Cause of death
Item
text
C0007465 (UMLS CUI-1)
Autopsy
Item
boolean
C0004398 (UMLS CUI-1)
Item Group
C0013227 (UMLS CUI-1)
C0026769 (UMLS CUI-2)
Medication MS
Item
text
C0013227 (UMLS CUI-1)
C0026769 (UMLS CUI-2)
Medication start date
Item
date
C0451613 (UMLS CUI-1)
Medication end date
Item
date
C3483769 (UMLS CUI-1)
Daily dose
Item
integer
C2348070 (UMLS CUI-1)
Item
text
C1519795 (UMLS CUI-1)
Unit
Code List
Unit
CL Item
 (mg)
CL Item
 (µg)
Item
integer
C3266814 (UMLS CUI-1)
Action
Code List
Action
CL Item
 (0)
CL Item
 (1)
CL Item
 (2)
CL Item
 (3)
CL Item
 (4)
Item
integer
C1314792 (UMLS CUI-1)
Causality
Code List
Causality
CL Item
 (1)
CL Item
 (2)
CL Item
 (3)
CL Item
 (4)
CL Item
 (5)
CL Item
 (6)
Item Group
C2347852 (UMLS CUI-1)
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