ID

41995

Descripción

HIS form from Soarian. Urologie Erlangen" with friendly permission of the urology Erlangen (Prof. Wullich) and the medical informatics department Erlangen (PD Dr. Bürkle)

Palabras clave

Versiones (2)
  1. 7/8/13 7/8/13 -
  2. 15/3/21 15/3/21 - Dr. rer. medic Philipp Neuhaus
Subido en

15 de marzo de 2021

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0 Legacy
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

HIS systemic therapy - form prostate cancer

Alemán Inglés

HIS

1 formularios  
  1. StudyEvent: HIS
    1. HIS
Admininstrative Daten
Descripción

Admininstrative Daten

Patient surname
Descripción

Name

Tipo de datos

string

Alias
UMLS CUI-1
C0421448
SNOMED CT-1
184096005
Patient forename
Descripción

Vorname

Tipo de datos

string

Alias
UMLS CUI-1
C0421447
SNOMED CT-1
184095009
Patient title
Descripción

Titel

Tipo de datos

string

Alias
Code-1
Patient title (observable entity)
UMLS CUI-1
C0421450
SNOMED CT-1
184098006
former Patient name
Descripción

früherer Name

Tipo de datos

string

Alias
Code-1
Previous
UMLS CUI-1
C0205156
SNOMED CT-1
9130008
Code-2
Patient name (observable entity)
UMLS CUI-2
C1299487
SNOMED CT-2
371484003
Patient date of birth
Descripción

Geburtsdatum

Tipo de datos

date

Alias
UMLS CUI-1
C0421451
SNOMED CT-1
184099003
patient age
Descripción

Alter

Tipo de datos

integer

Alias
Code-1
patient age
UMLS CUI-1
CL386174
Ethnicity / related nationality data
Descripción

Nationalität

Tipo de datos

string

Alias
UMLS CUI-1
C0438960
SNOMED CT-1
186034007
Code-2
Patients
UMLS CUI-2
C0030705
SNOMED CT-2
116154003
Street Address
Descripción

Adresse

Tipo de datos

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
Descripción

PLZ

Tipo de datos

integer

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

Stadt

Tipo de datos

string

Alias
UMLS CUI-1
C2316883
SNOMED CT-1
433178008
Code-2
Patient address
UMLS CUI-2
C0421449
SNOMED CT-2
184097001
Case Identifier
Descripción

Fallnummer

Tipo de datos

integer

Alias
Code-1
Case - situation (qualifier value)
UMLS CUI-1
C0868928
SNOMED CT-1
398241000
Code-2
Identifier
UMLS CUI-2
C0600091
SNOMED CT-2
118522005
Tumordiagnose
Descripción

Tumordiagnose

Cancer Diagnosis
Descripción

Tumordiagnose (ICD-10)

Tipo de datos

string

Alias
Code-1
Tumor finding (finding)
UMLS CUI-1
C1274082
SNOMED CT-1
395557000
Code-2
Diagnosis ICD code
UMLS CUI-2
C2598420
Date of diagnosis
Descripción

Diagnose-Datum

Tipo de datos

date

Alias
UMLS CUI-1
C2316983
SNOMED CT-1
432213005
Code-2
Tumor finding (finding)
UMLS CUI-2
C1274082
SNOMED CT-2
395557000
Systemic Therapy
Descripción

Systemic Therapy

Guideline Adherence
Descripción

Systemische Therapie befolgt die Leitlinien:

Tipo de datos

boolean

Alias
Item-Info
must_have
UMLS CUI-1
C0525059
Code-2
Systemic Therapy
UMLS CUI-2
C1515119
Reason for Guidelines Adherence
Descripción

falls nein, Grund

Tipo de datos

string

Alias
Code-1
Indication of (contextual qualifier)
UMLS CUI-1
C0392360
SNOMED CT-1
410666004
LOINC-1
MTHU008862
Code-2
Guideline Adherence
UMLS CUI-2
C0525059
Therapeutic procedure
Descripción

Therapeutic procedure

Therapeutic procedure
Descripción

Therapieart

Tipo de datos

boolean

Alias
Item-Info
must_have
Code-Info
for_compare
UMLS CUI-1
C0087111
SNOMED CT-1
277132007
MedDRA-1
10053757
LOINC-1
MTHU008880
Chemotherapy Regimen
Descripción

Chemotherapie

Tipo de datos

boolean

Alias
UMLS CUI-1
C0392920
SNOMED CT-1
69960004
MedDRA-1
10061758
Endocrine Therapy
Descripción

Hormontherapie

Tipo de datos

boolean

Alias
UMLS CUI-1
C0279025
SNOMED CT-1
169413002
MedDRA-1
10065646
Immunotherapy
Descripción

Immuntherapie

Tipo de datos

boolean

Alias
UMLS CUI-1
C0021083
SNOMED CT-1
76334006
Antibody Therapy
Descripción

Antikörper / Tyrosinkinase-Inhibitör

Tipo de datos

boolean

Alias
UMLS CUI-1
C0281176
Admission status
Descripción

Aufnahmemodus

Tipo de datos

integer

Alias
Code-1
Admission statuses (finding)
UMLS CUI-1
C0586002
SNOMED CT-1
308277006
Intent
Descripción

Intention

Tipo de datos

boolean

Alias
Item-Info
must_have
Code-Info
changed_datatype
UMLS CUI-1
C1283828
SNOMED CT-1
367565008
Code-2
Systemic Therapy
UMLS CUI-2
C1515119
Intent - chemotherapy
Descripción

Intention - Chemotherapie

Tipo de datos

integer

Alias
UMLS CUI-1
C1283828
SNOMED CT-1
367565008
Code-2
Chemotherapy Regimen
UMLS CUI-2
C0392920
SNOMED CT-2
69960004
MedDRA-2
10061758
Chemoradiotherapy
Descripción

Kombination Radio/Chemo

Tipo de datos

boolean

Alias
UMLS CUI-1
C0436307
Intent - endocrine therapy
Descripción

Intention - endokrine Therapie

Tipo de datos

integer

Alias
Code-Info
extended_coding
UMLS CUI-1
C1283828
SNOMED CT-1
367565008
Code-2
Endocrine Therapy
UMLS CUI-2
C0279025
SNOMED CT-2
169413002
MedDRA-2
10065646
Intent - immunotherapy
Descripción

Intention - Immuntherapie

Tipo de datos

integer

Alias
Code-Info
extended_coding
UMLS CUI-1
C1283828
SNOMED CT-1
367565008
Code-2
Immunotherapy
UMLS CUI-2
C0021083
SNOMED CT-2
76334006
Intent - antibody therapy
Descripción

Intention - Antikörpertherapie

Tipo de datos

integer

Alias
Code-Info
extended_coding
UMLS CUI-1
C1283828
SNOMED CT-1
367565008
Code-2
Antibody Therapy
UMLS CUI-2
C0281176
Interruption
Descripción

Interruption

Interruption
Descripción

Unterbrechung

Tipo de datos

boolean

Alias
Code-Info
normalized_coding
Code-1
Interruption
UMLS CUI-1
C1512900
Code-2
Therapeutic procedure
UMLS CUI-2
C0087111
SNOMED CT-2
277132007
MedDRA-2
10053757
LOINC-2
MTHU008880
interruption from
Descripción

von

Tipo de datos

date

Alias
Code-1
Date treatment stopped (observable entity)
UMLS CUI-1
C1531784
SNOMED CT-1
413947000
Code-2
Interruption
UMLS CUI-2
C1512900
interruption until
Descripción

bis

Tipo de datos

date

Alias
Code-1
Date treatment started (observable entity)
UMLS CUI-1
C3173309
SNOMED CT-1
413946009
Code-2
Post
UMLS CUI-2
C0231290
SNOMED CT-2
237679004
Code-3
Interruption
UMLS CUI-3
C1512900
Reason for Treatment Interruption
Descripción

Grund

Tipo de datos

string

Alias
UMLS CUI-1
CL436968
Chemotherapy Protocols, Antineoplastic
Descripción

Chemotherapy Protocols, Antineoplastic

Chemotherapy Protocols, Antineoplastic
Descripción

Protokoll

Tipo de datos

string

Alias
Item-Info
must_have
UMLS CUI-1
C0949219
Chemotherapy cycle (procedure)
Descripción

Chemotherapy cycle (procedure)

Chemotherapy cycle (procedure)
Descripción

Zyklen

Tipo de datos

boolean

Alias
Item-Info
must_have
Code-Info
for_compare
UMLS CUI-1
C1302181
SNOMED CT-1
399042005
planned cycles
Descripción

geplante Zyklen

Tipo de datos

string

Alias
Code-1
Plan
UMLS CUI-1
C1301732
SNOMED CT-1
397943006
Code-2
Chemotherapy cycle (procedure)
UMLS CUI-2
C1302181
SNOMED CT-2
399042005
current cycle
Descripción

aktueller Zyklus

Tipo de datos

string

Alias
Code-1
Current Therapy
UMLS CUI-1
C2827774
Code-2
Chemotherapy cycle (procedure)
UMLS CUI-2
C1302181
SNOMED CT-2
399042005
Date treatment started - chemotherapy
Descripción

Beginn - Chemotherapie

Tipo de datos

date

Alias
Code-1
Date treatment started (observable entity)
UMLS CUI-1
C3173309
SNOMED CT-1
413946009
Code-2
Chemotherapy Regimen
UMLS CUI-2
C0392920
SNOMED CT-2
69960004
MedDRA-2
10061758
Date treatment started - endocrine therapy
Descripción

Beginn - endokrine Therapie

Tipo de datos

date

Alias
Code-Info
extended_coding
Code-1
Date treatment started (observable entity)
UMLS CUI-1
C3173309
SNOMED CT-1
413946009
Code-2
Endocrine Therapy
UMLS CUI-2
C0279025
SNOMED CT-2
169413002
Date treatment started - immunotherapy
Descripción

Beginn - Immuntherapie

Tipo de datos

date

Alias
Code-Info
extended_coding
Code-1
Date treatment started (observable entity)
UMLS CUI-1
C3173309
SNOMED CT-1
413946009
Code-2
Immunotherapy
UMLS CUI-2
C0021083
SNOMED CT-2
76334006
Estimated date of completion
Descripción

voraussichtlich bis

Tipo de datos

date

Alias
UMLS CUI-1
C0806067
Code-2
Systemic Therapy
UMLS CUI-2
C1515119
Pharmacologic Substance
Descripción

Pharmacologic Substance

Chemotherapeutic agent
Descripción

Substanz 1

Tipo de datos

string

Alias
Code-1
Chemotherapeutic agent (product)
UMLS CUI-1
C0729502
SNOMED CT-1
312059006
Chemotherapeutic drug level decreased
Descripción

Dosisreduktion

Tipo de datos

boolean

Alias
UMLS CUI-1
C0861114
Single dose characteristic
Descripción

Einzeldosis

Tipo de datos

string

Alias
Code-1
Single dose characteristic (observable entity)
UMLS CUI-1
C1960417
SNOMED CT-1
426146003
Cumulative Dose
Descripción

Menge der Absolutdosis

Tipo de datos

string

Alias
UMLS CUI-1
C2986497
Unit type (qualifier value)
Descripción

Einheit

Tipo de datos

string

Alias
UMLS CUI-1
C0565912
SNOMED CT-1
288462000
Concomitant Agent
Descripción

Concomitant Agent

Concomitant Agent
Descripción

Begleitmedikation

Tipo de datos

boolean

Alias
Code-Info
normalized_coding
UMLS CUI-1
C2347852
Antihormone Therapy
Descripción

Antihomornelle Therapie

Tipo de datos

integer

Alias
UMLS CUI-1
C2986607
Orchiectomy
Descripción

Orchiektomie

Tipo de datos

boolean

Alias
Code-Info
changed_datatype
UMLS CUI-1
C0029189
SNOMED CT-1
120001005
MedDRA-1
10031060
Antiandrogen Therapy
Descripción

periphere Hormonblockade

Tipo de datos

boolean

Alias
Code-Info
changed_datatype
UMLS CUI-1
C0279492
MedDRA-1
10002730
Supportive Care
Descripción

Supportive Therapie

Tipo de datos

integer

Alias
UMLS CUI-1
C0344211
SNOMED CT-1
243114000
Other
Descripción

andere

Tipo de datos

string

Alias
UMLS CUI-1
C0205395
SNOMED CT-1
74964008
Code-2
Supportive Care
UMLS CUI-2
C0344212
SNOMED CT-2
243114001
Code-3
Free Text Format
UMLS CUI-3
C2348713
Adverse event
Descripción

Adverse event

Adverse event
Descripción

Nebenwirkungen

Tipo de datos

boolean

Alias
Code-Info
normalized_coding
UMLS CUI-1
C0877248
MedDRA-1
10060933
LOINC-1
MTHU014542
Leukocytes
Descripción

Leuko

Tipo de datos

integer

Alias
Code-1
Leukocytes Adverse Event
UMLS CUI-1
C1560219
CTCAE-1
MTHU117099
Hemoglobin
Descripción

HB

Tipo de datos

integer

Alias
Code-1
Hemoglobin Adverse Event
UMLS CUI-1
C2239101
CTCAE-1
MTHU116997
neutrophil
Descripción

Granuloz

Tipo de datos

integer

Alias
Code-1
Neutrophils and Granulocytes Adverse Event
UMLS CUI-1
C1560233
CTCAE-1
MTHU117202
Blood Platelets
Descripción

Thrombos

Tipo de datos

integer

Alias
Code-1
Platelets Adverse Event
UMLS CUI-1
C1963076
CTCAE-1
MTHU117353
Creatinine
Descripción

Kreatinin

Tipo de datos

integer

Alias
Code-1
Creatinine Adverse Event
UMLS CUI-1
C1561535
CTCAE-1
MTHU116842
Proteinuria
Descripción

Proteinurie

Tipo de datos

integer

Alias
Code-1
Proteinuria Adverse Event
UMLS CUI-1
C1962972
CTCAE-1
MTHU117382
Urea
Descripción

Harnstoff

Tipo de datos

integer

Alias
Code-1
Urea
UMLS CUI-1
C0041942
SNOMED CT-1
387092000
LOINC-1
MTHU009413
bilirubin
Descripción

Bilirubin

Tipo de datos

integer

Alias
Code-1
Hyperbilirubinemia Adverse Event
UMLS CUI-1
C1557209
CTCAE-1
MTHU117008
Alkaline Phosphatase
Descripción

AP

Tipo de datos

integer

Alias
Code-1
Alkaline Phosphatase Adverse Event
UMLS CUI-1
C1561546
CTCAE-1
MTHU112158
Alanine Transaminase
Descripción

GPT

Tipo de datos

integer

Alias
Code-1
Serum Glutamic Pyruvic Transaminase Adverse Event
UMLS CUI-1
C1557189
CTCAE-1
MTHU117450
Aspartate Transaminase
Descripción

GOT

Tipo de datos

integer

Alias
Code-1
Serum Glutamic Oxaloacetic Transaminase Adverse Event
UMLS CUI-1
C1557198
CTCAE-1
MTHU117449
Nausea
Descripción

Übelkeit

Tipo de datos

integer

Alias
Code-1
Nausea Adverse Event
UMLS CUI-1
C1963179
CTCAE-1
MTHU117189
Diarrhea
Descripción

Diarrhoe

Tipo de datos

integer

Alias
Code-1
Diarrhea Adverse Event
UMLS CUI-1
C0232708
CTCAE-1
MTHU116856
Mucous Membrane
Descripción

Schleimhäute

Tipo de datos

integer

Alias
Code-1
Mucositis and Stomatitis Adverse Event by Functional and Symptomatic Classification
UMLS CUI-1
C1556411
CTCAE-1
MTHU117173
Erbrechen
Descripción

Erbrechen

Tipo de datos

integer

Alias
Code-1
Vomiting Adverse Event
UMLS CUI-1
C1963281
CTCAE-1
MTHU117700
Obstipation
Descripción

Obstipation

Tipo de datos

integer

Alias
Code-1
Constipation Adverse Event
UMLS CUI-1
C1963087
CTCAE-1
MTHU116803
Peripheral Nerves
Descripción

periphere Nerven

Tipo de datos

integer

Alias
Code-1
Neuralgia and Peripheral Nerve Pain Adverse Event
UMLS CUI-1
C1557517
CTCAE-1
MTHU117196
Conscious
Descripción

Bewusstsein

Tipo de datos

integer

Alias
Code-1
Somnolence and Depressed Level of Consciousness Adverse Event
UMLS CUI-1
C1557290
CTCAE-1
MTHU117503
Dyspnea
Descripción

Dyspnoe

Tipo de datos

integer

Alias
Code-1
Dyspnea Adverse Event
UMLS CUI-1
C1963100
CTCAE-1
MTHU116873
Infection
Descripción

Infektionen

Tipo de datos

integer

Alias
Code-1
Adverse Event Associated with Infection
UMLS CUI-1
C1556682
CTCAE-1
MTHU112135
Heart Rhythm
Descripción

Herzrhythmus

Tipo de datos

integer

Alias
Code-1
Adverse Event Associated with Cardiac Arrhythmia
UMLS CUI-1
C1560249
CTCAE-1
MTHU112127
Cardiac function
Descripción

Herzfunktion

Tipo de datos

integer

Alias
Code-1
Adverse Event Associated with the Heart in General
UMLS CUI-1
C1556247
CTCAE-1
MTHU112147
Pericarditis
Descripción

Perikarditis

Tipo de datos

integer

Alias
Code-1
Pericarditis Adverse Event
UMLS CUI-1
C1963211
CTCAE-1
MTHU117310
Fever
Descripción

Fieber

Tipo de datos

integer

Alias
Code-1
Fever Without Neutropenia Adverse Event
UMLS CUI-1
C1556366
CTCAE-1
MTHU116933
Allergic Reaction
Descripción

Allergie

Tipo de datos

integer

Alias
Code-1
Adverse Event Associated with Allergy and Immunology
UMLS CUI-1
C1560126
CTCAE-1
MTHU112125
Pain
Descripción

Schmerzen

Tipo de datos

integer

Alias
Code-1
Other Pain Adverse Event
UMLS CUI-1
C1557623
CTCAE-1
MTHU117260
Skin
Descripción

Haut

Tipo de datos

integer

Alias
Code-1
Other Dermatology or Skin Adverse Event
UMLS CUI-1
C1559104
CTCAE-1
MTHU117246
Cystitis
Descripción

Zystitis

Tipo de datos

integer

Alias
Code-1
Cystitis Adverse Event
UMLS CUI-1
C1963088
CTCAE-1
MTHU116844
Hematuria
Descripción

Hämaturie

Tipo de datos

integer

Alias
Code-1
Hematuria
UMLS CUI-1
C0018965
SNOMED CT-1
34436003
MedDRA-1
10018867
ICD-10-CM-1
R31.9
ICD-9-CM-1
599.7
CTCAE-1
E13000
Volver a la parte superior de la página

Similar models

HIS

1 formularios
  1. StudyEvent: HIS
    1. HIS
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Admininstrative Daten
Name
Item
Patient surname
string
C0421448 (UMLS CUI-1)
184096005 (SNOMED CT-1)
Vorname
Item
Patient forename
string
C0421447 (UMLS CUI-1)
184095009 (SNOMED CT-1)
Titel
Item
Patient title
string
Patient title (observable entity) (Code-1)
C0421450 (UMLS CUI-1)
184098006 (SNOMED CT-1)
früherer Name
Item
former Patient name
string
Previous (Code-1)
C0205156 (UMLS CUI-1)
9130008 (SNOMED CT-1)
Patient name (observable entity) (Code-2)
C1299487 (UMLS CUI-2)
371484003 (SNOMED CT-2)
Geburtsdatum
Item
Patient date of birth
date
C0421451 (UMLS CUI-1)
184099003 (SNOMED CT-1)
Alter
Item
patient age
integer
patient age (Code-1)
CL386174 (UMLS CUI-1)
Nationalität
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)
Adresse
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)
Stadt
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)
Fallnummer
Item
Case Identifier
integer
Case - situation (qualifier value) (Code-1)
C0868928 (UMLS CUI-1)
398241000 (SNOMED CT-1)
Identifier (Code-2)
C0600091 (UMLS CUI-2)
118522005 (SNOMED CT-2)
Item Group
Tumordiagnose
Tumordiagnose (ICD-10)
Item
Cancer Diagnosis
string
Tumor finding (finding) (Code-1)
C1274082 (UMLS CUI-1)
395557000 (SNOMED CT-1)
Diagnosis ICD code (Code-2)
C2598420 (UMLS CUI-2)
Diagnose-Datum
Item
Date of diagnosis
date
C2316983 (UMLS CUI-1)
432213005 (SNOMED CT-1)
Tumor finding (finding) (Code-2)
C1274082 (UMLS CUI-2)
395557000 (SNOMED CT-2)
Item Group
Systemic Therapy
Systemische Therapie befolgt die Leitlinien:
Item
Guideline Adherence
boolean
must_have (Item-Info)
C0525059 (UMLS CUI-1)
Systemic Therapy (Code-2)
C1515119 (UMLS CUI-2)
falls nein, Grund
Item
Reason for Guidelines Adherence
string
Indication of (contextual qualifier) (Code-1)
C0392360 (UMLS CUI-1)
410666004 (SNOMED CT-1)
MTHU008862 (LOINC-1)
Guideline Adherence (Code-2)
C0525059 (UMLS CUI-2)
Item Group
Therapeutic procedure
Therapieart
Item
Therapeutic procedure
boolean
must_have (Item-Info)
for_compare (Code-Info)
C0087111 (UMLS CUI-1)
277132007 (SNOMED CT-1)
10053757 (MedDRA-1)
MTHU008880 (LOINC-1)
Chemotherapie
Item
Chemotherapy Regimen
boolean
C0392920 (UMLS CUI-1)
69960004 (SNOMED CT-1)
10061758 (MedDRA-1)
Hormontherapie
Item
Endocrine Therapy
boolean
C0279025 (UMLS CUI-1)
169413002 (SNOMED CT-1)
10065646 (MedDRA-1)
Immuntherapie
Item
Immunotherapy
boolean
C0021083 (UMLS CUI-1)
76334006 (SNOMED CT-1)
Antikörper / Tyrosinkinase-Inhibitör
Item
Antibody Therapy
boolean
C0281176 (UMLS CUI-1)
Item
Admission status
integer
Admission statuses (finding) (Code-1)
C0586002 (UMLS CUI-1)
308277006 (SNOMED CT-1)
Aufnahmemodus
Code List
Admission status
CL Item
inpatient  (stationär)
C0021562 (UMLS CUI-1)
416800000 (SNOMED CT-1)
MTHU015923 (LOINC-1)
CL Item
outpatients  (ambulant)
C0029921 (UMLS CUI-1)
373864002 (SNOMED CT-1)
MTHU011902 (LOINC-1)
CL Item
partial hospitalization (teilstationär)
Partial (Code-1)
C0728938 (UMLS CUI-1)
255609007 (SNOMED CT-1)
Hospitalization (Code-2)
C0019993 (UMLS CUI-2)
394656005 (SNOMED CT-2)
10054112 (MedDRA-2)
Intention
Item
Intent
boolean
must_have (Item-Info)
changed_datatype (Code-Info)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Systemic Therapy (Code-2)
C1515119 (UMLS CUI-2)
Item
Intent - chemotherapy
integer
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Chemotherapy Regimen (Code-2)
C0392920 (UMLS CUI-2)
69960004 (SNOMED CT-2)
10061758 (MedDRA-2)
Intention - Chemotherapie
Code List
Intent - chemotherapy
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)
Kombination Radio/Chemo
Item
Chemoradiotherapy
boolean
C0436307 (UMLS CUI-1)
Item
Intent - endocrine therapy
integer
extended_coding (Code-Info)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Endocrine Therapy (Code-2)
C0279025 (UMLS CUI-2)
169413002 (SNOMED CT-2)
10065646 (MedDRA-2)
Intention - endokrine Therapie
Code List
Intent - endocrine therapy
CL Item
Curative - procedure intent  (kurativ)
extended_coding (Code-Info)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
CL Item
Palliative - procedure intent  (palliativ)
extended_coding (Code-Info)
Palliative - procedure intent (qualifier value) (Code-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
CL Item
Adjuvant - intent (adjuvant)
extended_coding (Code-Info)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
CL Item
Neo-adjuvant - intent  (neoadjuvant)
extended_coding (Code-Info)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
Item
Intent - immunotherapy
integer
extended_coding (Code-Info)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Immunotherapy (Code-2)
C0021083 (UMLS CUI-2)
76334006 (SNOMED CT-2)
Intention - Immuntherapie
Code List
Intent - immunotherapy
CL Item
Curative - procedure intent  (kurativ)
extended_coding (Code-Info)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
CL Item
Palliative - procedure intent  (palliativ)
extended_coding (Code-Info)
Palliative - procedure intent (qualifier value) (Code-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
CL Item
Adjuvant - intent (adjuvant)
extended_coding (Code-Info)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
CL Item
Neo-adjuvant - intent  (neoadjuvant)
extended_coding (Code-Info)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
Item
Intent - antibody therapy
integer
extended_coding (Code-Info)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Antibody Therapy (Code-2)
C0281176 (UMLS CUI-2)
Intention - Antikörpertherapie
Code List
Intent - antibody therapy
CL Item
Curative - procedure intent  (kurativ)
extended_coding (Code-Info)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
CL Item
Palliative - procedure intent  (palliativ)
extended_coding (Code-Info)
Palliative - procedure intent (qualifier value) (Code-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
CL Item
Adjuvant - intent (adjuvant)
extended_coding (Code-Info)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
CL Item
Neo-adjuvant - intent  (neoadjuvant)
extended_coding (Code-Info)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
Item Group
Interruption
Unterbrechung
Item
Interruption
boolean
normalized_coding (Code-Info)
Interruption (Code-1)
C1512900 (UMLS CUI-1)
Therapeutic procedure (Code-2)
C0087111 (UMLS CUI-2)
277132007 (SNOMED CT-2)
10053757 (MedDRA-2)
MTHU008880 (LOINC-2)
von
Item
interruption from
date
Date treatment stopped (observable entity) (Code-1)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Interruption (Code-2)
C1512900 (UMLS CUI-2)
bis
Item
interruption until
date
Date treatment started (observable entity) (Code-1)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Post (Code-2)
C0231290 (UMLS CUI-2)
237679004 (SNOMED CT-2)
Interruption (Code-3)
C1512900 (UMLS CUI-3)
Grund
Item
Reason for Treatment Interruption
string
CL436968 (UMLS CUI-1)
Item Group
Chemotherapy Protocols, Antineoplastic
Protokoll
Item
Chemotherapy Protocols, Antineoplastic
string
must_have (Item-Info)
C0949219 (UMLS CUI-1)
Item Group
Chemotherapy cycle (procedure)
Zyklen
Item
Chemotherapy cycle (procedure)
boolean
must_have (Item-Info)
for_compare (Code-Info)
C1302181 (UMLS CUI-1)
399042005 (SNOMED CT-1)
geplante Zyklen
Item
planned cycles
string
Plan (Code-1)
C1301732 (UMLS CUI-1)
397943006 (SNOMED CT-1)
Chemotherapy cycle (procedure) (Code-2)
C1302181 (UMLS CUI-2)
399042005 (SNOMED CT-2)
aktueller Zyklus
Item
current cycle
string
Current Therapy (Code-1)
C2827774 (UMLS CUI-1)
Chemotherapy cycle (procedure) (Code-2)
C1302181 (UMLS CUI-2)
399042005 (SNOMED CT-2)
Beginn - Chemotherapie
Item
Date treatment started - chemotherapy
date
Date treatment started (observable entity) (Code-1)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Chemotherapy Regimen (Code-2)
C0392920 (UMLS CUI-2)
69960004 (SNOMED CT-2)
10061758 (MedDRA-2)
Beginn - endokrine Therapie
Item
Date treatment started - endocrine therapy
date
extended_coding (Code-Info)
Date treatment started (observable entity) (Code-1)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Endocrine Therapy (Code-2)
C0279025 (UMLS CUI-2)
169413002 (SNOMED CT-2)
Beginn - Immuntherapie
Item
Date treatment started - immunotherapy
date
extended_coding (Code-Info)
Date treatment started (observable entity) (Code-1)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Immunotherapy (Code-2)
C0021083 (UMLS CUI-2)
76334006 (SNOMED CT-2)
voraussichtlich bis
Item
Estimated date of completion
date
C0806067 (UMLS CUI-1)
Systemic Therapy (Code-2)
C1515119 (UMLS CUI-2)
Item Group
Pharmacologic Substance
Substanz 1
Item
Chemotherapeutic agent
string
Chemotherapeutic agent (product) (Code-1)
C0729502 (UMLS CUI-1)
312059006 (SNOMED CT-1)
Dosisreduktion
Item
Chemotherapeutic drug level decreased
boolean
C0861114 (UMLS CUI-1)
Einzeldosis
Item
Single dose characteristic
string
Single dose characteristic (observable entity) (Code-1)
C1960417 (UMLS CUI-1)
426146003 (SNOMED CT-1)
Menge der Absolutdosis
Item
Cumulative Dose
string
C2986497 (UMLS CUI-1)
Einheit
Item
Unit type (qualifier value)
string
C0565912 (UMLS CUI-1)
288462000 (SNOMED CT-1)
Item Group
Concomitant Agent
Begleitmedikation
Item
Concomitant Agent
boolean
normalized_coding (Code-Info)
C2347852 (UMLS CUI-1)
Item
Antihormone Therapy
integer
C2986607 (UMLS CUI-1)
Antihomornelle Therapie
Code List
Antihormone Therapy
CL Item
Cyproterone/Luteinizing Hormone-Releasing Factor (LHRH)
C0678022 (UMLS CUI-1)
Orchiektomie
Item
Orchiectomy
boolean
changed_datatype (Code-Info)
C0029189 (UMLS CUI-1)
120001005 (SNOMED CT-1)
10031060 (MedDRA-1)
periphere Hormonblockade
Item
Antiandrogen Therapy
boolean
changed_datatype (Code-Info)
C0279492 (UMLS CUI-1)
10002730 (MedDRA-1)
Item
Supportive Care
integer
C0344211 (UMLS CUI-1)
243114000 (SNOMED CT-1)
Supportive Therapie
Code List
Supportive Care
CL Item
zoledronic acid (Zometa)
C0257685 (UMLS CUI-1)
420124002 (SNOMED CT-1)
CL Item
Prednisone  (Prednison)
C0032952 (UMLS CUI-1)
116602009 (SNOMED CT-1)
CL Item
Estramustine  (Estramustin)
C0014921 (UMLS CUI-1)
386909008 (SNOMED CT-1)
CL Item
Other  (andere)
C0205394 (UMLS CUI-1)
74964007 (SNOMED CT-1)
Supportive Care (Code-2)
C0344211 (UMLS CUI-2)
243114000 (SNOMED CT-2)
andere
Item
Other
string
C0205395 (UMLS CUI-1)
74964008 (SNOMED CT-1)
Supportive Care (Code-2)
C0344212 (UMLS CUI-2)
243114001 (SNOMED CT-2)
Free Text Format (Code-3)
C2348713 (UMLS CUI-3)
Item Group
Adverse event
Nebenwirkungen
Item
Adverse event
boolean
normalized_coding (Code-Info)
C0877248 (UMLS CUI-1)
10060933 (MedDRA-1)
MTHU014542 (LOINC-1)
Item
Leukocytes
integer
Leukocytes Adverse Event (Code-1)
C1560219 (UMLS CUI-1)
MTHU117099 (CTCAE-1)
Leuko
Code List
Leukocytes
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Hemoglobin
integer
Hemoglobin Adverse Event (Code-1)
C2239101 (UMLS CUI-1)
MTHU116997 (CTCAE-1)
HB
Code List
Hemoglobin
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
neutrophil
integer
Neutrophils and Granulocytes Adverse Event (Code-1)
C1560233 (UMLS CUI-1)
MTHU117202 (CTCAE-1)
Granuloz
Code List
neutrophil
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Blood Platelets
integer
Platelets Adverse Event (Code-1)
C1963076 (UMLS CUI-1)
MTHU117353 (CTCAE-1)
Thrombos
Code List
Blood Platelets
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Creatinine
integer
Creatinine Adverse Event (Code-1)
C1561535 (UMLS CUI-1)
MTHU116842 (CTCAE-1)
Kreatinin
Code List
Creatinine
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Proteinuria
integer
Proteinuria Adverse Event (Code-1)
C1962972 (UMLS CUI-1)
MTHU117382 (CTCAE-1)
Proteinurie
Code List
Proteinuria
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Urea
integer
Urea (Code-1)
C0041942 (UMLS CUI-1)
387092000 (SNOMED CT-1)
MTHU009413 (LOINC-1)
Harnstoff
Code List
Urea
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
bilirubin
integer
Hyperbilirubinemia Adverse Event (Code-1)
C1557209 (UMLS CUI-1)
MTHU117008 (CTCAE-1)
Bilirubin
Code List
bilirubin
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Alkaline Phosphatase
integer
Alkaline Phosphatase Adverse Event (Code-1)
C1561546 (UMLS CUI-1)
MTHU112158 (CTCAE-1)
AP
Code List
Alkaline Phosphatase
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Alanine Transaminase
integer
Serum Glutamic Pyruvic Transaminase Adverse Event (Code-1)
C1557189 (UMLS CUI-1)
MTHU117450 (CTCAE-1)
GPT
Code List
Alanine Transaminase
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
CL Item
only_in_connection with GOT (only_in_connection with GOT)
Item
Aspartate Transaminase
integer
Serum Glutamic Oxaloacetic Transaminase Adverse Event (Code-1)
C1557198 (UMLS CUI-1)
MTHU117449 (CTCAE-1)
GOT
Code List
Aspartate Transaminase
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
CL Item
only_in_connection with GPT (only_in_connection with GPT)
Item
Nausea
integer
Nausea Adverse Event (Code-1)
C1963179 (UMLS CUI-1)
MTHU117189 (CTCAE-1)
Übelkeit
Code List
Nausea
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Diarrhea
integer
Diarrhea Adverse Event (Code-1)
C0232708 (UMLS CUI-1)
MTHU116856 (CTCAE-1)
Diarrhoe
Code List
Diarrhea
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Mucous Membrane
integer
Mucositis and Stomatitis Adverse Event by Functional and Symptomatic Classification (Code-1)
C1556411 (UMLS CUI-1)
MTHU117173 (CTCAE-1)
Schleimhäute
Code List
Mucous Membrane
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Erbrechen
integer
Vomiting Adverse Event (Code-1)
C1963281 (UMLS CUI-1)
MTHU117700 (CTCAE-1)
Erbrechen
Code List
Erbrechen
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Obstipation
integer
Constipation Adverse Event (Code-1)
C1963087 (UMLS CUI-1)
MTHU116803 (CTCAE-1)
Obstipation
Code List
Obstipation
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Peripheral Nerves
integer
Neuralgia and Peripheral Nerve Pain Adverse Event (Code-1)
C1557517 (UMLS CUI-1)
MTHU117196 (CTCAE-1)
periphere Nerven
Code List
Peripheral Nerves
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Conscious
integer
Somnolence and Depressed Level of Consciousness Adverse Event (Code-1)
C1557290 (UMLS CUI-1)
MTHU117503 (CTCAE-1)
Bewusstsein
Code List
Conscious
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Dyspnea
integer
Dyspnea Adverse Event (Code-1)
C1963100 (UMLS CUI-1)
MTHU116873 (CTCAE-1)
Dyspnoe
Code List
Dyspnea
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Infection
integer
Adverse Event Associated with Infection (Code-1)
C1556682 (UMLS CUI-1)
MTHU112135 (CTCAE-1)
Infektionen
Code List
Infection
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Heart Rhythm
integer
Adverse Event Associated with Cardiac Arrhythmia (Code-1)
C1560249 (UMLS CUI-1)
MTHU112127 (CTCAE-1)
Herzrhythmus
Code List
Heart Rhythm
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Cardiac function
integer
Adverse Event Associated with the Heart in General (Code-1)
C1556247 (UMLS CUI-1)
MTHU112147 (CTCAE-1)
Herzfunktion
Code List
Cardiac function
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Pericarditis
integer
Pericarditis Adverse Event (Code-1)
C1963211 (UMLS CUI-1)
MTHU117310 (CTCAE-1)
Perikarditis
Code List
Pericarditis
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
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 Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
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 Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Pain
integer
Other Pain Adverse Event (Code-1)
C1557623 (UMLS CUI-1)
MTHU117260 (CTCAE-1)
Schmerzen
Code List
Pain
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
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 Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Cystitis
integer
Cystitis Adverse Event (Code-1)
C1963088 (UMLS CUI-1)
MTHU116844 (CTCAE-1)
Zystitis
Code List
Cystitis
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Item
Hematuria
integer
Hematuria (Code-1)
C0018965 (UMLS CUI-1)
34436003 (SNOMED CT-1)
10018867 (MedDRA-1)
R31.9 (ICD-10-CM-1)
599.7 (ICD-9-CM-1)
E13000 (CTCAE-1)
Hämaturie
Code List
Hematuria
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

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