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Dose Reduction

1 forms  
  1. StudyEvent: ODM
    1. Dose Reduction
Dose Reduction Due to Adverse Experiences
Description

Dose Reduction Due to Adverse Experiences

Alias
UMLS CUI-1
C1707814
Date of decision to reduce the dose
Description

Dose Reduced, Decision, Date in time

Data type

date

Alias
UMLS CUI [1,1]
C1707814
UMLS CUI [1,2]
C0679006
UMLS CUI [1,3]
C0011008
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Similar models

Dose Reduction

1 forms
  1. StudyEvent: ODM
    1. Dose Reduction
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Dose Reduction Due to Adverse Experiences
C1707814 (UMLS CUI-1)
Dose Reduced, Decision, Date in time
Item
Date of decision to reduce the dose
date
C1707814 (UMLS CUI [1,1])
C0679006 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
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