ID

44642

Descrição

base-dataset from ADT - radiotherapy, ODM derived from http://www.tumorzentren.de/tl_files/dokumente/adt_basis.pdf

Link

http://www.tumorzentren.de/tl_files/dokumente/adt_basis.pdf

Palavras-chave

Versões (2)
  1. 07/08/2013 07/08/2013 -
  2. 27/09/2021 27/09/2021 -
Transferido a

27 de setembro de 2021

DOI

Para um pedido faça login.

Licença

Creative Commons BY-NC 3.0 Legacy
Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Voltar para os comentários do modelo
Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

quality management ADT-radiotherapy cancer

Alemão Inglês

quality management

1 Formulários  
  1. StudyEvent: quality management
    1. quality management
Patient data
Descrição

Patient data

patient number
Descrição

Patientenidentifikationsnummer

Tipo de dados

string

Alias
Code-1
Patients
UMLS CUI-1
C0030705
SNOMED CT-1
116154003
Code-2
Identification number
UMLS CUI-2
C1300638
SNOMED CT-2
396278008
Health Insurance
Descrição

Krankenkasse

Tipo de dados

string

Alias
UMLS CUI-1
C0021682
Patient telephone number
Descrição

Telefon

Tipo de dados

string

Alias
UMLS CUI-1
C0421455
SNOMED CT-1
184103008
Patient surname
Descrição

Name

Tipo de dados

string

Alias
UMLS CUI-1
C0421448
SNOMED CT-1
184096005
Maiden Name
Descrição

Geburtsname

Tipo de dados

string

Alias
UMLS CUI-1
C0806887
SNOMED CT-1
423203003
LOINC-1
MTHU010481
Code-2
Patients
UMLS CUI-2
C0030705
SNOMED CT-2
116154003
Patient forename
Descrição

Vorname

Tipo de dados

string

Alias
UMLS CUI-1
C0421447
SNOMED CT-1
184095009
Patient sex
Descrição

Geschlecht

Tipo de dados

integer

Alias
UMLS CUI-1
C0150831
SNOMED CT-1
184100006
Patient date of birth
Descrição

Geburtsdatum

Tipo de dados

date

Alias
UMLS CUI-1
C0421451
SNOMED CT-1
184099003
Ethnicity / related nationality data
Descrição

Staatsangehörigkeit

Tipo de dados

string

Alias
UMLS CUI-1
C0438960
SNOMED CT-1
186034007
Code-2
Patients
UMLS CUI-2
C0030705
SNOMED CT-2
116154003
Patient address
Descrição

Patient address

Street Address
Descrição

Straße

Tipo de dados

string

Alias
UMLS CUI-1
C1301826
SNOMED CT-1
398099009
Code-2
Patient address
UMLS CUI-2
C0421449
SNOMED CT-2
184097001
Patient postal code
Descrição

PLZ

Tipo de dados

integer

Alias
UMLS CUI-1
C0421454
SNOMED CT-1
184102003
City of residence
Descrição

Ort

Tipo de dados

string

Alias
UMLS CUI-1
C2316883
SNOMED CT-1
433178008
Code-2
Patient address
UMLS CUI-2
C0421449
SNOMED CT-2
184097001
Therapeutic radiology procedure
Descrição

Therapeutic radiology procedure

Organ target(s)
Descrição

Zielgebiet

Tipo de dados

string

Alias
UMLS CUI-1
C0807185
Radiotherapy Technique
Descrição

Applikationsart

Tipo de dados

integer

Alias
Code-1
Technique
UMLS CUI-1
C0449851
SNOMED CT-1
246501002
Code-2
Therapeutic radiology procedure
UMLS CUI-2
C1522449
SNOMED CT-2
108290001
MedDRA-2
10037770
Start Radiotherapy
Descrição

Beginn

Tipo de dados

date

Alias
Code-1
Radiotherapy started (situation)
UMLS CUI-1
C0436382
SNOMED CT-1
168531007
End Radiotherapy
Descrição

Ende

Tipo de dados

date

Alias
Code-1
Radiotherapy completed (situation)
UMLS CUI-1
C0436385
SNOMED CT-1
168534004
total amount of radiation
Descrição

Gesamtdosis (Gy/Gbq)

Tipo de dados

integer

Alias
Code-1
Total radiation dose delivered (observable entity)
UMLS CUI-1
C2919490
SNOMED CT-1
445461008
Intent
Descrição

Intention

Tipo de dados

integer

Alias
UMLS CUI-1
C1283828
SNOMED CT-1
367565008
Code-2
Therapeutic radiology procedure
UMLS CUI-2
C1522449
SNOMED CT-2
108290001
MedDRA-2
10037770
Termination of Radiotherapy
Descrição

Beendigung der Strahlentherapie

Tipo de dados

integer

Alias
Code-1
Radiotherapy stopped (situation)
UMLS CUI-1
C0436384
SNOMED CT-1
168533005
Common Terminology Criteria for Adverse Events
Descrição

Common Terminology Criteria for Adverse Events

Adverse event
Descrição

Nebenwirkungen

Tipo de dados

boolean

Alias
Code-Info
for_compare
UMLS CUI-1
C0877248
MedDRA-1
10060933
LOINC-1
MTHU014542
Laboratory Values
Descrição

Laborwerte

Tipo de dados

integer

Alias
Code-1
Other Metabolic and Laboratory Adverse Event
UMLS CUI-1
C1559945
CTCAE-1
MTHU117254
Genitourinary system
Descrição

Niere/Blase

Tipo de dados

integer

Alias
Code-1
Renal or Genitourinary Other Adverse Event
UMLS CUI-1
C1558061
CTCAE-1
MTHU117419
Skin
Descrição

Haut

Tipo de dados

integer

Alias
Code-1
Other Dermatology or Skin Adverse Event
UMLS CUI-1
C1559104
CTCAE-1
MTHU117246
Allergic Reaction
Descrição

Allergie

Tipo de dados

integer

Alias
Code-1
Adverse Event Associated with Allergy and Immunology
UMLS CUI-1
C1560126
CTCAE-1
MTHU112125
Gastrointestinal system
Descrição

Gastrointestinaltrakt

Tipo de dados

integer

Alias
Code-1
Adverse Event Associated with the Gastrointestinal System
UMLS CUI-1
C1559265
CTCAE-1
MTHU112146
Nervous system structure
Descrição

Nervensystem

Tipo de dados

integer

Alias
Code-1
Adverse Event Associated with the Nervous System
UMLS CUI-1
C1561270
CTCAE-1
MTHU112152
Fever
Descrição

Fieber

Tipo de dados

integer

Alias
Code-1
Fever Without Neutropenia Adverse Event
UMLS CUI-1
C1556366
CTCAE-1
MTHU116933
Infection
Descrição

Infektion

Tipo de dados

integer

Alias
Code-1
Adverse Event Associated with Infection
UMLS CUI-1
C1556682
CTCAE-1
MTHU112135
Systemic circulatory system
Descrição

Herz/Kreislauf

Tipo de dados

integer

Alias
Code-1
Adverse Event Associated with the Heart in General
UMLS CUI-1
C1556247
CTCAE-1
MTHU112147
Entire sensory organ
Descrição

Sinnesorgane

Tipo de dados

integer

Alias
Code-1
Adverse Event Associated with the Ear and Auditory System
UMLS CUI-1
C1560154
CTCAE-1
MTHU112144
General symptom
Descrição

Allgemeinsymptome

Tipo de dados

integer

Alias
Code-1
Adverse Event Associated with Constitutional Symptoms
UMLS CUI-1
C1556354
CTCAE-1
MTHU112129
Lung/Larynx
Descrição

Lunge/Kehlkopf

Tipo de dados

integer

Alias
Code-1
Adverse Event Associated with Pulmonary and Upper Respiratory Systems
UMLS CUI-1
C1557628
CTCAE-1
MTHU112139
Endocrine system
Descrição

Endokrines System

Tipo de dados

integer

Alias
Code-1
Adverse Event Associated with the Endocrine System
UMLS CUI-1
C1559198
CTCAE-1
MTHU112145
general appearance
Descrição

Allgemeinzustand

Tipo de dados

integer

Alias
Code-1
general appearance (physical finding)
UMLS CUI-1
C1148438
LOINC-1
MTHU015040
other adverse event
Descrição

Sonstige

Tipo de dados

integer

Alias
Code-1
Adverse event
UMLS CUI-1
C0877248
MedDRA-1
10060933
LOINC-1
MTHU014542
Code-2
Other
UMLS CUI-2
C0205395
SNOMED CT-2
74964008
Voltar ao início da página

Similar models

quality management

1 Formulários
  1. StudyEvent: quality management
    1. quality management
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Patient data
Patientenidentifikationsnummer
Item
patient number
string
Patients (Code-1)
C0030705 (UMLS CUI-1)
116154003 (SNOMED CT-1)
Identification number (Code-2)
C1300638 (UMLS CUI-2)
396278008 (SNOMED CT-2)
Krankenkasse
Item
Health Insurance
string
C0021682 (UMLS CUI-1)
Telefon
Item
Patient telephone number
string
C0421455 (UMLS CUI-1)
184103008 (SNOMED CT-1)
Name
Item
Patient surname
string
C0421448 (UMLS CUI-1)
184096005 (SNOMED CT-1)
Geburtsname
Item
Maiden Name
string
C0806887 (UMLS CUI-1)
423203003 (SNOMED CT-1)
MTHU010481 (LOINC-1)
Patients (Code-2)
C0030705 (UMLS CUI-2)
116154003 (SNOMED CT-2)
Vorname
Item
Patient forename
string
C0421447 (UMLS CUI-1)
184095009 (SNOMED CT-1)
Item
Patient sex
integer
C0150831 (UMLS CUI-1)
184100006 (SNOMED CT-1)
Geschlecht
Code List
Patient sex
CL Item
Female (weiblich)
C0086287 (UMLS CUI-1)
1086007 (SNOMED CT-1)
CL Item
Male gender (männlich)
C0086582 (UMLS CUI-1)
10052007 (SNOMED CT-1)
Geburtsdatum
Item
Patient date of birth
date
C0421451 (UMLS CUI-1)
184099003 (SNOMED CT-1)
Staatsangehörigkeit
Item
Ethnicity / related nationality data
string
C0438960 (UMLS CUI-1)
186034007 (SNOMED CT-1)
Patients (Code-2)
C0030705 (UMLS CUI-2)
116154003 (SNOMED CT-2)
Item Group
Patient address
Straße
Item
Street Address
string
C1301826 (UMLS CUI-1)
398099009 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
PLZ
Item
Patient postal code
integer
C0421454 (UMLS CUI-1)
184102003 (SNOMED CT-1)
Ort
Item
City of residence
string
C2316883 (UMLS CUI-1)
433178008 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
Item Group
Therapeutic radiology procedure
Zielgebiet
Item
Organ target(s)
string
C0807185 (UMLS CUI-1)
Item
Radiotherapy Technique
integer
Technique (Code-1)
C0449851 (UMLS CUI-1)
246501002 (SNOMED CT-1)
Therapeutic radiology procedure (Code-2)
C1522449 (UMLS CUI-2)
108290001 (SNOMED CT-2)
10037770 (MedDRA-2)
Applikationsart
Code List
Radiotherapy Technique
CL Item
Teleradiotherapy procedure (P = Percutan (Teletherapie))
Teleradiotherapy procedure (procedure) (Code-1)
C0419095 (UMLS CUI-1)
33195004 (SNOMED CT-1)
CL Item
Brachytherapy (P = Percutan (Brachytherapie))
extended_coding (Code-Info)
Brachytherapy (Code-1)
C0006098 (UMLS CUI-1)
399315003 (SNOMED CT-1)
10061018 (MedDRA-1)
CL Item
Intracavity Radiotherapy  (K = endokavitäare Kontakttherapie)
C0021864 (UMLS CUI-1)
384692006 (SNOMED CT-1)
CL Item
Internal radiotherapy - permanent seeds  (I = Interstitielle Kontakttherapie)
Internal radiotherapy - permanent seeds (procedure) (Code-1)
C0436265 (UMLS CUI-1)
169359004 (SNOMED CT-1)
CL Item
Internal metabolic radiotherapy (procedure) (M = Metabolische Therapie (radionuclide))
C0436254 (UMLS CUI-1)
169340001 (SNOMED CT-1)
CL Item
Afterloading cavity radiotherapy (procedure)  (A = afterloading)
C0436298 (UMLS CUI-1)
169387008 (SNOMED CT-1)
Beginn
Item
Start Radiotherapy
date
Radiotherapy started (situation) (Code-1)
C0436382 (UMLS CUI-1)
168531007 (SNOMED CT-1)
Ende
Item
End Radiotherapy
date
Radiotherapy completed (situation) (Code-1)
C0436385 (UMLS CUI-1)
168534004 (SNOMED CT-1)
Gesamtdosis (Gy/Gbq)
Item
total amount of radiation
integer
Total radiation dose delivered (observable entity) (Code-1)
C2919490 (UMLS CUI-1)
445461008 (SNOMED CT-1)
Item
Intent
integer
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Therapeutic radiology procedure (Code-2)
C1522449 (UMLS CUI-2)
108290001 (SNOMED CT-2)
10037770 (MedDRA-2)
Intention
Code List
Intent
CL Item
Curative - procedure intent  (kurativ)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
CL Item
Palliative - procedure intent (palliativ)
Palliative - procedure intent (qualifier value) (Code-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
CL Item
Adjuvant - intent (adjuvant)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
CL Item
Neo-adjuvant - intent  (neoadjuvant)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
Item
Termination of Radiotherapy
integer
Radiotherapy stopped (situation) (Code-1)
C0436384 (UMLS CUI-1)
168533005 (SNOMED CT-1)
Beendigung der Strahlentherapie
Code List
Termination of Radiotherapy
CL Item
Discontinue because of adverse effects (Abbruch wegen Nebenwirkungen)
Adverse effects (Code-1)
C0879626 (UMLS CUI-1)
281647001 (SNOMED CT-1)
10067484 (MedDRA-1)
Discontinue (Code-2)
C1444662 (UMLS CUI-2)
410546004 (SNOMED CT-2)
Indication of (contextual qualifier) (Code-3)
C0392360 (UMLS CUI-3)
230165009 (SNOMED CT-3)
MTHU008319 (LOINC-3)
CL Item
regular End of Therapy (reguläres Ende)
Regular (Code-1)
C0449581 (UMLS CUI-1)
17854005 (SNOMED CT-1)
End (Code-2)
C1272693 (UMLS CUI-2)
385656004 (SNOMED CT-2)
CL Item
Refusal of Treatment (Pat. verw. Therapie)
C0040809 (UMLS CUI-1)
105480006 (SNOMED CT-1)
10056407 (MedDRA-1)
Item Group
Common Terminology Criteria for Adverse Events
Nebenwirkungen
Item
Adverse event
boolean
for_compare (Code-Info)
C0877248 (UMLS CUI-1)
10060933 (MedDRA-1)
MTHU014542 (LOINC-1)
Item
Laboratory Values
integer
Other Metabolic and Laboratory Adverse Event (Code-1)
C1559945 (UMLS CUI-1)
MTHU117254 (CTCAE-1)
Laborwerte
Code List
Laboratory Values
CL Item
no adverse event (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
CL Item
mild adverse event (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
CL Item
moderate adverse event (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
CL Item
strong adverse event (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
CL Item
Life Threatening adverse event (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
CL Item
unknown adverse event (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
Item
Genitourinary system
integer
Renal or Genitourinary Other Adverse Event (Code-1)
C1558061 (UMLS CUI-1)
MTHU117419 (CTCAE-1)
Niere/Blase
Code List
Genitourinary system
CL Item
no adverse event (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
CL Item
mild adverse event (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
CL Item
moderate adverse event (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
CL Item
strong adverse event (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
CL Item
Life Threatening adverse event (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
CL Item
unknown adverse event (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
Item
Skin
integer
Other Dermatology or Skin Adverse Event (Code-1)
C1559104 (UMLS CUI-1)
MTHU117246 (CTCAE-1)
Haut
Code List
Skin
CL Item
no adverse event (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
CL Item
mild adverse event (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
CL Item
moderate adverse event (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
CL Item
strong adverse event (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
CL Item
Life Threatening adverse event (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
CL Item
unknown adverse event (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
CL Item
only in connection with Allergy (only in connection with Allergy)
Item
Allergic Reaction
integer
Adverse Event Associated with Allergy and Immunology (Code-1)
C1560126 (UMLS CUI-1)
MTHU112125 (CTCAE-1)
Allergie
Code List
Allergic Reaction
CL Item
no adverse event (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
CL Item
mild adverse event (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
CL Item
moderate adverse event (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
CL Item
strong adverse event (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
CL Item
Life Threatening adverse event (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
CL Item
unknown adverse event (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
CL Item
only in connection with Skin (only in connection with Skin)
Item
Gastrointestinal system
integer
Adverse Event Associated with the Gastrointestinal System (Code-1)
C1559265 (UMLS CUI-1)
MTHU112146 (CTCAE-1)
Gastrointestinaltrakt
Code List
Gastrointestinal system
CL Item
no adverse event (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
CL Item
mild adverse event (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
CL Item
moderate adverse event (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
CL Item
strong adverse event (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
CL Item
Life Threatening adverse event (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
CL Item
unknown adverse event (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
Item
Nervous system structure
integer
Adverse Event Associated with the Nervous System (Code-1)
C1561270 (UMLS CUI-1)
MTHU112152 (CTCAE-1)
Nervensystem
Code List
Nervous system structure
CL Item
no adverse event (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
CL Item
mild adverse event (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
CL Item
moderate adverse event (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
CL Item
strong adverse event (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
CL Item
Life Threatening adverse event (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
CL Item
unknown adverse event (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
Item
Fever
integer
Fever Without Neutropenia Adverse Event (Code-1)
C1556366 (UMLS CUI-1)
MTHU116933 (CTCAE-1)
Fieber
Code List
Fever
CL Item
no adverse event (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
CL Item
mild adverse event (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
CL Item
moderate adverse event (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
CL Item
strong adverse event (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
CL Item
Life Threatening adverse event (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
CL Item
unknown adverse event (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
CL Item
only in connection with Infection (only in connection with Infection)
Item
Infection
integer
Adverse Event Associated with Infection (Code-1)
C1556682 (UMLS CUI-1)
MTHU112135 (CTCAE-1)
Infektion
Code List
Infection
CL Item
no adverse event (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
CL Item
mild adverse event (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
CL Item
moderate adverse event (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
CL Item
strong adverse event (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
CL Item
Life Threatening adverse event (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
CL Item
unknown adverse event (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
CL Item
only in connection with fever (only in connection with fever)
Item
Systemic circulatory system
integer
Adverse Event Associated with the Heart in General (Code-1)
C1556247 (UMLS CUI-1)
MTHU112147 (CTCAE-1)
Herz/Kreislauf
Code List
Systemic circulatory system
CL Item
no adverse event (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
CL Item
mild adverse event (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
CL Item
moderate adverse event (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
CL Item
strong adverse event (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
CL Item
Life Threatening adverse event (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
CL Item
unknown adverse event (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
Item
Entire sensory organ
integer
Adverse Event Associated with the Ear and Auditory System (Code-1)
C1560154 (UMLS CUI-1)
MTHU112144 (CTCAE-1)
Sinnesorgane
Code List
Entire sensory organ
CL Item
no adverse event (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
CL Item
mild adverse event (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
CL Item
moderate adverse event (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
CL Item
strong adverse event (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
CL Item
Life Threatening adverse event (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
CL Item
unknown adverse event (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
Item
General symptom
integer
Adverse Event Associated with Constitutional Symptoms (Code-1)
C1556354 (UMLS CUI-1)
MTHU112129 (CTCAE-1)
Allgemeinsymptome
Code List
General symptom
CL Item
no adverse event (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
CL Item
mild adverse event (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
CL Item
moderate adverse event (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
CL Item
strong adverse event (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
CL Item
Life Threatening adverse event (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
CL Item
unknown adverse event (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
Item
Lung/Larynx
integer
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-1)
C1557628 (UMLS CUI-1)
MTHU112139 (CTCAE-1)
Lunge/Kehlkopf
Code List
Lung/Larynx
CL Item
no adverse event (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
CL Item
mild adverse event (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
CL Item
moderate adverse event (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
CL Item
strong adverse event (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
CL Item
Life Threatening adverse event (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
CL Item
unknown adverse event (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
Item
Endocrine system
integer
Adverse Event Associated with the Endocrine System (Code-1)
C1559198 (UMLS CUI-1)
MTHU112145 (CTCAE-1)
Endokrines System
Code List
Endocrine system
CL Item
no adverse event (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
CL Item
mild adverse event (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
CL Item
moderate adverse event (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
CL Item
strong adverse event (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
CL Item
Life Threatening adverse event (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
CL Item
unknown adverse event (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
Item
general appearance
integer
general appearance (physical finding) (Code-1)
C1148438 (UMLS CUI-1)
MTHU015040 (LOINC-1)
Allgemeinzustand
Code List
general appearance
CL Item
no adverse event (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
general appearance (physical finding) (Code-2)
C1148438 (UMLS CUI-2)
MTHU015040 (LOINC-2)
CL Item
mild adverse event (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
general appearance (physical finding) (Code-2)
C1148438 (UMLS CUI-2)
MTHU015040 (LOINC-2)
CL Item
moderate adverse event (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
general appearance (physical finding) (Code-2)
C1148438 (UMLS CUI-2)
MTHU015040 (LOINC-2)
CL Item
strong adverse event (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
general appearance (physical finding) (Code-2)
C1148438 (UMLS CUI-2)
MTHU015040 (LOINC-2)
CL Item
Life Threatening adverse event (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
general appearance (physical finding) (Code-2)
C1148438 (UMLS CUI-2)
MTHU015040 (LOINC-2)
CL Item
unknown adverse event (X = Nebenwirkungen unbekannt)
Common Terminology Criteria for Adverse Events (Code-1)
C1516728 (UMLS CUI-1)
Unknown (Code-2)
C0439673 (UMLS CUI-2)
261665006 (SNOMED CT-2)
general appearance (physical finding) (Code-3)
C1148438 (UMLS CUI-3)
MTHU015040 (LOINC-3)
Item
other adverse event
integer
Adverse event (Code-1)
C0877248 (UMLS CUI-1)
10060933 (MedDRA-1)
MTHU014542 (LOINC-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
Sonstige
Code List
other adverse event
CL Item
no adverse event (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
10060933 (MedDRA-2)
MTHU014542 (LOINC-2)
CL Item
mild adverse event (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
10060933 (MedDRA-2)
MTHU014542 (LOINC-2)
CL Item
moderate adverse event (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
10060933 (MedDRA-2)
MTHU014542 (LOINC-2)
CL Item
strong adverse event (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
10060933 (MedDRA-2)
MTHU014542 (LOINC-2)
CL Item
Life Threatening adverse event (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
10060933 (MedDRA-2)
MTHU014542 (LOINC-2)
CL Item
unknown adverse event (X = Nebenwirkungen unbekannt)
Adverse event (Code-1)
C0877248 (UMLS CUI-1)
10060933 (MedDRA-1)
MTHU014542 (LOINC-1)
Unknown (Code-2)
C0439673 (UMLS CUI-2)
261665006 (SNOMED CT-2)
Other (Code-3)
C0205395 (UMLS CUI-3)
74964008 (SNOMED CT-3)
Voltar ao início da página 

Contacto

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

Ajuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial