ID

41995

Description

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

Mots-clés

Versions (2)
  1. 07/08/2013 07/08/2013 -
  2. 15/03/2021 15/03/2021 - Dr. rer. medic Philipp Neuhaus
Téléchargé le

15 mars 2021

DOI

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HIS systemic therapy - form prostate cancer

Allemand Anglais

HIS

1 Formulaires  
  1. StudyEvent: HIS
    1. HIS
Admininstrative Daten
Description

Admininstrative Daten

Patient surname
Description

Name

Type de données

string

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

Vorname

Type de données

string

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

Titel

Type de données

string

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

früherer Name

Type de données

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
Description

Geburtsdatum

Type de données

date

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

Alter

Type de données

integer

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

Nationalität

Type de données

string

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

Adresse

Type de données

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
Description

PLZ

Type de données

integer

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

Stadt

Type de données

string

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

Fallnummer

Type de données

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
Description

Tumordiagnose

Cancer Diagnosis
Description

Tumordiagnose (ICD-10)

Type de données

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
Description

Diagnose-Datum

Type de données

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
Description

Systemic Therapy

Guideline Adherence
Description

Systemische Therapie befolgt die Leitlinien:

Type de données

boolean

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

falls nein, Grund

Type de données

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
Description

Therapeutic procedure

Therapeutic procedure
Description

Therapieart

Type de données

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
Description

Chemotherapie

Type de données

boolean

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

Hormontherapie

Type de données

boolean

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

Immuntherapie

Type de données

boolean

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

Antikörper / Tyrosinkinase-Inhibitör

Type de données

boolean

Alias
UMLS CUI-1
C0281176
Admission status
Description

Aufnahmemodus

Type de données

integer

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

Intention

Type de données

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
Description

Intention - Chemotherapie

Type de données

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
Description

Kombination Radio/Chemo

Type de données

boolean

Alias
UMLS CUI-1
C0436307
Intent - endocrine therapy
Description

Intention - endokrine Therapie

Type de données

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
Description

Intention - Immuntherapie

Type de données

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
Description

Intention - Antikörpertherapie

Type de données

integer

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

Interruption

Interruption
Description

Unterbrechung

Type de données

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
Description

von

Type de données

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
Description

bis

Type de données

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
Description

Grund

Type de données

string

Alias
UMLS CUI-1
CL436968
Chemotherapy Protocols, Antineoplastic
Description

Chemotherapy Protocols, Antineoplastic

Chemotherapy Protocols, Antineoplastic
Description

Protokoll

Type de données

string

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

Chemotherapy cycle (procedure)

Chemotherapy cycle (procedure)
Description

Zyklen

Type de données

boolean

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

geplante Zyklen

Type de données

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
Description

aktueller Zyklus

Type de données

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
Description

Beginn - Chemotherapie

Type de données

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
Description

Beginn - endokrine Therapie

Type de données

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
Description

Beginn - Immuntherapie

Type de données

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
Description

voraussichtlich bis

Type de données

date

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

Pharmacologic Substance

Chemotherapeutic agent
Description

Substanz 1

Type de données

string

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

Dosisreduktion

Type de données

boolean

Alias
UMLS CUI-1
C0861114
Single dose characteristic
Description

Einzeldosis

Type de données

string

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

Menge der Absolutdosis

Type de données

string

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

Einheit

Type de données

string

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

Concomitant Agent

Concomitant Agent
Description

Begleitmedikation

Type de données

boolean

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

Antihomornelle Therapie

Type de données

integer

Alias
UMLS CUI-1
C2986607
Orchiectomy
Description

Orchiektomie

Type de données

boolean

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

periphere Hormonblockade

Type de données

boolean

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

Supportive Therapie

Type de données

integer

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

andere

Type de données

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
Description

Adverse event

Adverse event
Description

Nebenwirkungen

Type de données

boolean

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

Leuko

Type de données

integer

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

HB

Type de données

integer

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

Granuloz

Type de données

integer

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

Thrombos

Type de données

integer

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

Kreatinin

Type de données

integer

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

Proteinurie

Type de données

integer

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

Harnstoff

Type de données

integer

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

Bilirubin

Type de données

integer

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

AP

Type de données

integer

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

GPT

Type de données

integer

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

GOT

Type de données

integer

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

Übelkeit

Type de données

integer

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

Diarrhoe

Type de données

integer

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

Schleimhäute

Type de données

integer

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

Erbrechen

Type de données

integer

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

Obstipation

Type de données

integer

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

periphere Nerven

Type de données

integer

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

Bewusstsein

Type de données

integer

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

Dyspnoe

Type de données

integer

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

Infektionen

Type de données

integer

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

Herzrhythmus

Type de données

integer

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

Herzfunktion

Type de données

integer

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

Perikarditis

Type de données

integer

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

Fieber

Type de données

integer

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

Allergie

Type de données

integer

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

Schmerzen

Type de données

integer

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

Haut

Type de données

integer

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

Zystitis

Type de données

integer

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

Hämaturie

Type de données

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
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Similar models

HIS

1 Formulaires
  1. StudyEvent: HIS
    1. HIS
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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)
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