ID

16975

Beskrivning

ODM derived from: http://www.qmcr.ualberta.ca/en/ToolsandTemplates/CaseReportFormCRFTemplates.aspx. Template Name: Adverse Events. University of Alberta, Quality Management in Clinical Research. Copyright: 2002-2016 University of Alberta.

Länk

http://www.qmcr.ualberta.ca/en/ToolsandTemplates/CaseReportFormCRFTemplates.aspx

Nyckelord

  1. 2016-08-17 2016-08-17 -
Uppladdad den

17 augusti 2016

DOI

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Licens

Creative Commons BY-NC 3.0

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Adverse Events: CRF QMCR University of Alberta

Adverse Events: CRF QMCR University of Alberta

General Information
Beskrivning

General Information

Study Name
Beskrivning

Study Name

Datatyp

text

Site Number
Beskrivning

Site Number

Datatyp

integer

Pt_ID
Beskrivning

Pt_ID

Datatyp

integer

Has the participant had any Adverse Events during this Study? (see Description)
Beskrivning

If yes, please list all Adverse Events below.

Datatyp

boolean

Adverse Events
Beskrivning

Adverse Events

Adverse Event
Beskrivning

Adverse Event

Datatyp

text

Start Date
Beskrivning

Start Date

Datatyp

date

Stop Date
Beskrivning

Stop Date

Datatyp

date

Severity
Beskrivning

Severity

Datatyp

text

Relationship to Study Treatment
Beskrivning

Relationship to Study Treatment

Datatyp

text

Action Taken (see Description)
Beskrivning

1= None 2= Discontinued permanently 3= Discontinued temporarily 4= Reduced Dose 5= Increased Dose 6= Delayed Dose

Datatyp

integer

Outcome of AE (see Description)
Beskrivning

1= Resolved, No Sequel 2= AE still present - no treatment 3= AE still present - being treated 4= Residual effects present - not treated 5= Residual effects present - treated 6= Death 7= Unknown

Datatyp

integer

Expected?
Beskrivning

Expected?

Datatyp

boolean

Serious Adverse Event
Beskrivning

Serious Adverse Event

Datatyp

text

Initials
Beskrivning

Initials

Datatyp

text

Similar models

Adverse Events: CRF QMCR University of Alberta

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
General Information
Study Name
Item
Study Name
text
Site Number
Item
Site Number
integer
Pt_ID
Item
Pt_ID
integer
Has the participant had any Adverse Events during this Study? (see Description)
Item
Has the participant had any Adverse Events during this Study? (see Description)
boolean
Item Group
Adverse Events
Adverse Event
Item
Adverse Event
text
Start Date
Item
Start Date
date
Stop Date
Item
Stop Date
date
Item
Severity
text
Code List
Severity
CL Item
Mild (1)
CL Item
Moderate (2)
CL Item
Severe (3)
Item
Relationship to Study Treatment
text
Code List
Relationship to Study Treatment
CL Item
Definitely related (1)
CL Item
Possibly related (2)
CL Item
Not related (3)
Action Taken (see Description)
Item
Action Taken (see Description)
integer
Outcome of AE (see Description)
Item
Outcome of AE (see Description)
integer
Expected?
Item
Expected?
boolean
Item
Serious Adverse Event
text
Code List
Serious Adverse Event
CL Item
Yes (complete SAE form) (1)
CL Item
No (2)
Initials
Item
Initials
text

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