Section Investigational Products

Investigational product: AZD6140/placebo
Descripción

Investigational product: AZD6140/placebo

Alias
UMLS CUI-1
C1608718
First dose
Descripción

AZD6140 first dose

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C3173975
UMLS CUI [1,2]
C1608718
Last dose
Descripción

AZD6140 last dose

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C3173975
UMLS CUI [1,2]
C1608718
Investigational product: Clopidogrel/placebo
Descripción

Investigational product: Clopidogrel/placebo

Alias
UMLS CUI-1
C0070166
First dose
Descripción

Clopidogrel first dose

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C3173975
UMLS CUI [1,2]
C0070166
Last dose
Descripción

Clopidogrel last dose

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C3173975
UMLS CUI [1,2]
C0070166
Additional Dose of Investigational Products
Descripción

Additional Dose of Investigational Products

Interruption of Investigational Products
Descripción

Interruption of Investigational Products

Subject Drug Accountability
Descripción

Subject Drug Accountability

Similar models

Section Investigational Products

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Investigational product: AZD6140/placebo
C1608718 (UMLS CUI-1)
AZD6140 first dose
Item
First dose
datetime
C3173975 (UMLS CUI [1,1])
C1608718 (UMLS CUI [1,2])
AZD6140 last dose
Item
Last dose
datetime
C3173975 (UMLS CUI [1,1])
C1608718 (UMLS CUI [1,2])
Item Group
Investigational product: Clopidogrel/placebo
C0070166 (UMLS CUI-1)
Clopidogrel first dose
Item
First dose
datetime
C3173975 (UMLS CUI [1,1])
C0070166 (UMLS CUI [1,2])
Clopidogrel last dose
Item
Last dose
datetime
C3173975 (UMLS CUI [1,1])
C0070166 (UMLS CUI [1,2])
Item Group
Additional Dose of Investigational Products
Item Group
Interruption of Investigational Products
Item Group
Subject Drug Accountability