ID

22055

Descripción

Study part: Previous/ Concomitant medications. A phase III multinational, randomized, single-blind study of recombinant humanized anti-p185HER2 monoclonal antibody (rhuMAb HER2) in patients with HER2/neu overexpression who have not received prior cytotoxic chemotherapy for metastatic breast cancer. "Terms of use: You may not use this document or the information contained herein to a regulatory authority in connection with an application for a marketing authorization or any other regulatory submission without the express written consent of Roche"

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Versiones (2)
  1. 16/5/17 16/5/17 -
  2. 15/3/21 15/3/21 - Dr. rer. medic Philipp Neuhaus
Titular de derechos de autor

Roche

Subido en

16 de mayo de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0
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PREVIOUS/ CONCOMITANT MEDICATIONS Roche H0650g Breast Cancer

Inglés

PREVIOUS/ CONCOMITANT MEDICATIONS

1 formularios  
PREVIOUS/ CONCOMITANT MEDICATIONS
Descripción

PREVIOUS/ CONCOMITANT MEDICATIONS

Alias
UMLS CUI-1
C2347852
PATIENT INT.
Descripción

Patient initial

Tipo de datos

text

Alias
UMLS CUI [1]
C2986440
PATIENT NUMBER
Descripción

Patient id

Tipo de datos

integer

Alias
UMLS CUI [1]
C2348585
DRUG NAME
Descripción

concomitant medication

Tipo de datos

text

Alias
UMLS CUI [1]
C2347852
INDICATION- PROPHYLAXIS ?
Descripción

Prophylaxis Indication medication

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0199176
UMLS CUI [1,2]
C3146298
UMLS CUI [1,3]
C0013227
INDICATION
Descripción

Indication medication

Tipo de datos

text

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0013227
TOTAL DAILY DOSE- PRN ?
Descripción

TOTAL DAILY DOSE

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348070
TOTAL DAILY DOSE (units)
Descripción

TOTAL DAILY DOSE

Tipo de datos

float

Alias
UMLS CUI [1]
C2348070
DATE OF FIRST DOSE
Descripción

therapy start date

Tipo de datos

date

Alias
UMLS CUI [1]
C1531783
DATE OF FINAL DOSE- ONGOING?
Descripción

CONCOMITANT MEDICATIONS

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2347852
DATE OF FINAL DOSE
Descripción

therapy end date

Tipo de datos

date

Alias
UMLS CUI [1]
C1531784
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Similar models

PREVIOUS/ CONCOMITANT MEDICATIONS

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
PREVIOUS/ CONCOMITANT MEDICATIONS
C2347852 (UMLS CUI-1)
Patient initial
Item
PATIENT INT.
text
C2986440 (UMLS CUI [1])
Patient id
Item
PATIENT NUMBER
integer
C2348585 (UMLS CUI [1])
concomitant medication
Item
DRUG NAME
text
C2347852 (UMLS CUI [1])
Prophylaxis Indication medication
Item
INDICATION- PROPHYLAXIS ?
boolean
C0199176 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
Indication medication
Item
INDICATION
text
C3146298 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
TOTAL DAILY DOSE
Item
TOTAL DAILY DOSE- PRN ?
boolean
C2348070 (UMLS CUI [1])
TOTAL DAILY DOSE
Item
TOTAL DAILY DOSE (units)
float
C2348070 (UMLS CUI [1])
therapy start date
Item
DATE OF FIRST DOSE
date
C1531783 (UMLS CUI [1])
CONCOMITANT MEDICATIONS
Item
DATE OF FINAL DOSE- ONGOING?
boolean
C2347852 (UMLS CUI [1])
therapy end date
Item
DATE OF FINAL DOSE
date
C1531784 (UMLS CUI [1])
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