Information:
Fel:
ID
44065
Beskrivning
base-dataset from ADT - systemic therapy, ODM derived from http://www.tumorzentren.de/tl_files/dokumente/adt_basis.pdf
Länk
http://www.tumorzentren.de/tl_files/dokumente/adt_basis.pdf
Nyckelord
Versioner (3)
- 2013-08-01 2013-08-01 -
- 2021-03-15 2021-03-15 - Dr. rer. medic Philipp Neuhaus
- 2021-09-20 2021-09-20 -
Uppladdad den
20 september 2021
DOI
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Licens
Creative Commons BY-NC 3.0 Legacy
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quality management ADT-systemic therapy cancer
quality management
- StudyEvent: quality management
Similar models
quality management
- StudyEvent: quality management
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Patientenidentifikationsnummer
Item
patient number
string
Patients (Code-1)
C0030705 (UMLS CUI-1)
116154003 (SNOMED CT-1)
Identification number (Code-2)
C1300638 (UMLS CUI-2)
396278008 (SNOMED CT-2)
C0030705 (UMLS CUI-1)
116154003 (SNOMED CT-1)
Identification number (Code-2)
C1300638 (UMLS CUI-2)
396278008 (SNOMED CT-2)
Krankenkasse
Item
Health Insurance
string
C0021682 (UMLS CUI-1)
Telefon
Item
Patient telephone number
string
C0421455 (UMLS CUI-1)
184103008 (SNOMED CT-1)
184103008 (SNOMED CT-1)
Name
Item
Patient surname
string
C0421448 (UMLS CUI-1)
184096005 (SNOMED CT-1)
184096005 (SNOMED CT-1)
Geburtsname
Item
Maiden Name
string
C0806887 (UMLS CUI-1)
423203003 (SNOMED CT-1)
MTHU010481 (LOINC-1)
Patients (Code-2)
C0030705 (UMLS CUI-2)
116154003 (SNOMED CT-2)
423203003 (SNOMED CT-1)
MTHU010481 (LOINC-1)
Patients (Code-2)
C0030705 (UMLS CUI-2)
116154003 (SNOMED CT-2)
Vorname
Item
Patient forename
string
C0421447 (UMLS CUI-1)
184095009 (SNOMED CT-1)
184095009 (SNOMED CT-1)
CL Item
Female (weiblich)
C0086287 (UMLS CUI-1)
1086007 (SNOMED CT-1)
1086007 (SNOMED CT-1)
CL Item
Male gender (männlich)
C0086582 (UMLS CUI-1)
10052007 (SNOMED CT-1)
10052007 (SNOMED CT-1)
Geburtsdatum
Item
Patient date of birth
date
C0421451 (UMLS CUI-1)
184099003 (SNOMED CT-1)
184099003 (SNOMED CT-1)
Staatsangehörigkeit
Item
Ethnicity / related nationality data
string
C0438960 (UMLS CUI-1)
186034007 (SNOMED CT-1)
Patients (Code-2)
C0030705 (UMLS CUI-2)
116154003 (SNOMED CT-2)
186034007 (SNOMED CT-1)
Patients (Code-2)
C0030705 (UMLS CUI-2)
116154003 (SNOMED CT-2)
Straße
Item
Street Address
string
C1301826 (UMLS CUI-1)
398099009 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
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)
184102003 (SNOMED CT-1)
Ort
Item
City of residence
string
C2316883 (UMLS CUI-1)
433178008 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
433178008 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
Chemotherapie
Item
Chemotherapy Regimen
boolean
C0392920 (UMLS CUI-1)
69960004 (SNOMED CT-1)
10061758 (MedDRA-1)
69960004 (SNOMED CT-1)
10061758 (MedDRA-1)
Hormontherapie
Item
Endocrine Therapy
boolean
C0279025 (UMLS CUI-1)
169413002 (SNOMED CT-1)
169413002 (SNOMED CT-1)
Antikörper/Immuntherapie
Item
Immunotherapy
boolean
C0021083 (UMLS CUI-1)
76334006 (SNOMED CT-1)
76334006 (SNOMED CT-1)
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)
367565008 (SNOMED CT-1)
Chemotherapy Regimen (Code-2)
C0392920 (UMLS CUI-2)
69960004 (SNOMED CT-2)
10061758 (MedDRA-2)
CL Item
Curative - procedure intent (kurativ)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-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)
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)
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)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-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)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Endocrine Therapy (Code-2)
C0279025 (UMLS CUI-2)
169413002 (SNOMED CT-2)
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)
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)
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)
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)
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)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Immunotherapy (Code-2)
C0021083 (UMLS CUI-2)
76334006 (SNOMED CT-2)
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)
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)
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)
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)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
Protokoll
Item
Chemotherapy Protocols, Antineoplastic
string
C0949219 (UMLS CUI-1)
Zyklen geplant
Item
planned cycles
integer
Plan (Code-1)
C1301732 (UMLS CUI-1)
397943006 (SNOMED CT-1)
Chemotherapy cycle (procedure) (Code-2)
C1302181 (UMLS CUI-2)
399042005 (SNOMED CT-2)
C1301732 (UMLS CUI-1)
397943006 (SNOMED CT-1)
Chemotherapy cycle (procedure) (Code-2)
C1302181 (UMLS CUI-2)
399042005 (SNOMED CT-2)
Zyklen durchgeführt
Item
executed cycles
integer
Execution (Code-1)
C1705848 (UMLS CUI-1)
Chemotherapy cycle (procedure) (Code-2)
C1302181 (UMLS CUI-2)
399042005 (SNOMED CT-2)
C1705848 (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)
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)
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)
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)
Substanzen
Item
Chemotherapeutic agent
string
Chemotherapeutic agent (product) (Code-1)
C0729502 (UMLS CUI-1)
312059006 (SNOMED CT-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
integer
Single dose characteristic (observable entity) (Code-1)
C1960417 (UMLS CUI-1)
426146003 (SNOMED CT-1)
C1960417 (UMLS CUI-1)
426146003 (SNOMED CT-1)
Menge der Absolutdosis
Item
Cumulative Dose
integer
C2986497 (UMLS CUI-1)
Einheit
Item
Unit type
string
Unit type (qualifier value) (Code-1)
C0565912 (UMLS CUI-1)
288462000 (SNOMED CT-1)
C0565912 (UMLS CUI-1)
288462000 (SNOMED CT-1)
Unterbrechung vom:
Item
Date treatment stopped - interruption
date
Date treatment stopped (observable entity) (Code-1)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Interruption (Code-2)
C1512900 (UMLS CUI-2)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Interruption (Code-2)
C1512900 (UMLS CUI-2)
Unterbrechung bis:
Item
Date treatment started after interruption
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)
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)
Gründe der Unterbrechung
Item
Reason for Treatment Interruption
string
CL436968 (UMLS CUI-1)
Therapieende Chemo
Item
Date treatment stopped - chemotherapy
date
Date treatment stopped (observable entity) (Code-1)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Chemotherapy Regimen (Code-2)
C0392920 (UMLS CUI-2)
69960004 (SNOMED CT-2)
10061758 (MedDRA-2)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Chemotherapy Regimen (Code-2)
C0392920 (UMLS CUI-2)
69960004 (SNOMED CT-2)
10061758 (MedDRA-2)
Therapieende endokrine Therape
Item
Date treatment stopped - endocrine therapy
date
Date treatment stopped (observable entity) (Code-1)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Endocrine Therapy (Code-2)
C0279025 (UMLS CUI-2)
169413002 (SNOMED CT-2)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Endocrine Therapy (Code-2)
C0279025 (UMLS CUI-2)
169413002 (SNOMED CT-2)
Therapieende Immuntherapie
Item
Date treatment stopped - immunotherapy
date
Date treatment stopped (observable entity) (Code-1)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Immunotherapy (Code-2)
C0021083 (UMLS CUI-2)
76334006 (SNOMED CT-2)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Immunotherapy (Code-2)
C0021083 (UMLS CUI-2)
76334006 (SNOMED CT-2)
Item
Termination systemic therapy
integer
for_compare (Code-Info)
Termination - action (qualifier value) (Code-1)
C1283212 (UMLS CUI-1)
360239007 (SNOMED CT-1)
Systemic Therapy (Code-2)
C1515119 (UMLS CUI-2)
Termination - action (qualifier value) (Code-1)
C1283212 (UMLS CUI-1)
360239007 (SNOMED CT-1)
Systemic Therapy (Code-2)
C1515119 (UMLS CUI-2)
CL Item
regular End of Therapy (reguläres Ende)
changed_datatype (Code-Info)
Regular (Code-1)
C0449581 (UMLS CUI-1)
17854005 (SNOMED CT-1)
End (Code-2)
C1272693 (UMLS CUI-2)
385656004 (SNOMED CT-2)
Regular (Code-1)
C0449581 (UMLS CUI-1)
17854005 (SNOMED CT-1)
End (Code-2)
C1272693 (UMLS CUI-2)
385656004 (SNOMED CT-2)
CL Item
Discontinue because of adverse effects (Abbruch wegen Nebenwirkung)
changed_datatype (Code-Info)
Adverse effects (Code-1)
C0879626 (UMLS CUI-1)
281647001 (SNOMED CT-1)
10067484 (MedDRA-1)
Discontinue (Code-2)
C1444662 (UMLS CUI-2)
410546004 (SNOMED CT-2)
Indication of (contextual qualifier) (Code-3)
C0392360 (UMLS CUI-3)
230165009 (SNOMED CT-3)
MTHU008319 (LOINC-3)
Adverse effects (Code-1)
C0879626 (UMLS CUI-1)
281647001 (SNOMED CT-1)
10067484 (MedDRA-1)
Discontinue (Code-2)
C1444662 (UMLS CUI-2)
410546004 (SNOMED CT-2)
Indication of (contextual qualifier) (Code-3)
C0392360 (UMLS CUI-3)
230165009 (SNOMED CT-3)
MTHU008319 (LOINC-3)
CL Item
Refusal of Treatment (Patient verweigert Therapie)
changed_datatype (Code-Info)
C0040809 (UMLS CUI-1)
105480006 (SNOMED CT-1)
10056407 (MedDRA-1)
C0040809 (UMLS CUI-1)
105480006 (SNOMED CT-1)
10056407 (MedDRA-1)
sonstige Gründe
Item
other reason
string
Indication of (contextual qualifier) (Code-1)
C0392360 (UMLS CUI-1)
230165009 (SNOMED CT-1)
MTHU008319 (LOINC-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
C0392360 (UMLS CUI-1)
230165009 (SNOMED CT-1)
MTHU008319 (LOINC-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
Item
Tumor Status
integer
for_compare (Code-Info)
C0475752 (UMLS CUI-1)
277058005 (SNOMED CT-1)
C0475752 (UMLS CUI-1)
277058005 (SNOMED CT-1)
CL Item
In complete remission (Vollremission)
changed_datatype (Code-Info)
C0677874 (UMLS CUI-1)
103338009 (SNOMED CT-1)
C0677874 (UMLS CUI-1)
103338009 (SNOMED CT-1)
CL Item
partial response (Teilremission)
changed_datatype (Code-Info)
C1521726 (UMLS CUI-1)
103337004 (SNOMED CT-1)
C1521726 (UMLS CUI-1)
103337004 (SNOMED CT-1)
CL Item
Stable Disease (keine Änderung)
changed_datatype (Code-Info)
C0677946 (UMLS CUI-1)
C0677946 (UMLS CUI-1)
CL Item
Tumor Progression (Progression)
changed_datatype (Code-Info)
C0178874 (UMLS CUI-1)
419835002 (SNOMED CT-1)
C0178874 (UMLS CUI-1)
419835002 (SNOMED CT-1)
CL Item
Cannot Be Assessed (nicht beurteilbar)
Cannot Be Assessed (Code-1)
C1707258 (UMLS CUI-1)
C1707258 (UMLS CUI-1)
CL Item
Unknown (unbekannt)
changed_datatype (Code-Info)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Nebenwirkungen
Item
Adverse event
boolean
Item
Hemoglobin
integer
Hemoglobin Adverse Event (Code-1)
C2239101 (UMLS CUI-1)
MTHU116997 (CTCAE-1)
C2239101 (UMLS CUI-1)
MTHU116997 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
C2699517 (UMLS CUI-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
C1513302 (UMLS CUI-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
C1513374 (UMLS CUI-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
C1519275 (UMLS CUI-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
C1517874 (UMLS CUI-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
Item
Aspartate Transaminase
integer
Serum Glutamic Oxaloacetic Transaminase Adverse Event (Code-1)
C1557198 (UMLS CUI-1)
MTHU117449 (CTCAE-1)
C1557198 (UMLS CUI-1)
MTHU117449 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
only in connection with GPT (only in connection with GPT)
Item
Alanine Transaminase
integer
Serum Glutamic Pyruvic Transaminase Adverse Event (Code-1)
C1557189 (UMLS CUI-1)
MTHU117450 (CTCAE-1)
C1557189 (UMLS CUI-1)
MTHU117450 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
only in connection with GPT (only in connection with GPT)
Item
Creatinine
integer
Creatinine Adverse Event (Code-1)
C1561535 (UMLS CUI-1)
MTHU116842 (CTCAE-1)
C1561535 (UMLS CUI-1)
MTHU116842 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Skin
integer
Other Dermatology or Skin Adverse Event (Code-1)
C1559104 (UMLS CUI-1)
MTHU117246 (CTCAE-1)
C1559104 (UMLS CUI-1)
MTHU117246 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Peripheral Nerves
integer
Neuralgia and Peripheral Nerve Pain Adverse Event (Code-1)
C1557517 (UMLS CUI-1)
MTHU117196 (CTCAE-1)
C1557517 (UMLS CUI-1)
MTHU117196 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Hemorrhage
integer
Other Hemorrhage and Bleeding Adverse Event (Code-1)
C1556642 (UMLS CUI-1)
MTHU117250 (CTCAE-1)
C1556642 (UMLS CUI-1)
MTHU117250 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Bilirubin
integer
Hyperbilirubinemia Adverse Event (Code-1)
C1557209 (UMLS CUI-1)
MTHU117008 (CTCAE-1)
C1557209 (UMLS CUI-1)
MTHU117008 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Leukocytes
integer
Leukocytes Adverse Event (Code-1)
C1560219 (UMLS CUI-1)
MTHU117099 (CTCAE-1)
C1560219 (UMLS CUI-1)
MTHU117099 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Alkaline Phosphatase
integer
Alkaline Phosphatase Adverse Event (Code-1)
C1561546 (UMLS CUI-1)
MTHU112158 (CTCAE-1)
C1561546 (UMLS CUI-1)
MTHU112158 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Proteinuria
integer
Proteinuria Adverse Event (Code-1)
C1962972 (UMLS CUI-1)
MTHU117382 (CTCAE-1)
C1962972 (UMLS CUI-1)
MTHU117382 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Obstipation
integer
Constipation Adverse Event (Code-1)
C1963087 (UMLS CUI-1)
MTHU116803 (CTCAE-1)
C1963087 (UMLS CUI-1)
MTHU116803 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Diarrhea
integer
Diarrhea Adverse Event (Code-1)
C0232708 (UMLS CUI-1)
MTHU116856 (CTCAE-1)
C0232708 (UMLS CUI-1)
MTHU116856 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Urea
integer
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
neutrophil
integer
Neutrophils and Granulocytes Adverse Event (Code-1)
C1560233 (UMLS CUI-1)
MTHU117202 (CTCAE-1)
C1560233 (UMLS CUI-1)
MTHU117202 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Mucous Membrane
integer
Mucositis and Stomatitis Adverse Event by Functional and Symptomatic Classification (Code-1)
C1556411 (UMLS CUI-1)
MTHU117173 (CTCAE-1)
C1556411 (UMLS CUI-1)
MTHU117173 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Hematuria
integer
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)
34436003 (SNOMED CT-1)
10018867 (MedDRA-1)
R31.9 (ICD-10-CM-1)
599.7 (ICD-9-CM-1)
E13000 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Infection
integer
Adverse Event Associated with Infection (Code-1)
C1556682 (UMLS CUI-1)
MTHU112135 (CTCAE-1)
C1556682 (UMLS CUI-1)
MTHU112135 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Fever
integer
Fever Without Neutropenia Adverse Event (Code-1)
C1556366 (UMLS CUI-1)
MTHU116933 (CTCAE-1)
C1556366 (UMLS CUI-1)
MTHU116933 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Allergic Reaction
integer
Adverse Event Associated with Allergy and Immunology (Code-1)
C1560126 (UMLS CUI-1)
MTHU112125 (CTCAE-1)
C1560126 (UMLS CUI-1)
MTHU112125 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Blood Platelets
integer
Platelets Adverse Event (Code-1)
C1963076 (UMLS CUI-1)
MTHU117353 (CTCAE-1)
C1963076 (UMLS CUI-1)
MTHU117353 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Nausea
integer
Nausea Adverse Event (Code-1)
C1963179 (UMLS CUI-1)
MTHU117189 (CTCAE-1)
C1963179 (UMLS CUI-1)
MTHU117189 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Heart Rhythm
integer
Adverse Event Associated with Cardiac Arrhythmia (Code-1)
C1560249 (UMLS CUI-1)
MTHU112127 (CTCAE-1)
C1560249 (UMLS CUI-1)
MTHU112127 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Cardiac function
integer
Adverse Event Associated with the Heart in General (Code-1)
C1556247 (UMLS CUI-1)
MTHU112147 (CTCAE-1)
C1556247 (UMLS CUI-1)
MTHU112147 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Pericarditis
integer
Pericarditis Adverse Event (Code-1)
C1963211 (UMLS CUI-1)
MTHU117310 (CTCAE-1)
C1963211 (UMLS CUI-1)
MTHU117310 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Conscious
integer
Somnolence and Depressed Level of Consciousness Adverse Event (Code-1)
C1557290 (UMLS CUI-1)
MTHU117503 (CTCAE-1)
C1557290 (UMLS CUI-1)
MTHU117503 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Gleichzeitig Strahlentherapie?
Item
Therapeutic radiology procedure
boolean
C1522449 (UMLS CUI-1)
108290001 (SNOMED CT-1)
10037770 (MedDRA-1)
Concurrent (qualifier value) (Code-2)
C0205420 (UMLS CUI-2)
68405009 (SNOMED CT-2)
108290001 (SNOMED CT-1)
10037770 (MedDRA-1)
Concurrent (qualifier value) (Code-2)
C0205420 (UMLS CUI-2)
68405009 (SNOMED CT-2)