Information:
Fel:
ID
44642
Beskrivning
base-dataset from ADT - radiotherapy, 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 (2)
- 2013-08-07 2013-08-07 -
- 2021-09-27 2021-09-27 -
Uppladdad den
27 september 2021
DOI
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Licens
Creative Commons BY-NC 3.0 Legacy
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quality management ADT-radiotherapy cancer
quality management
- StudyEvent: quality management
Similar models
quality management
- StudyEvent: quality management
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Patientenidentifikationsnummer
Item
Patientennummer
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
Krankenkasse
string
C0021682 (UMLS CUI-1)
Telefon
Item
Patienten-Telefonnummer
string
C0421455 (UMLS CUI-1)
184103008 (SNOMED CT-1)
184103008 (SNOMED CT-1)
Name
Item
Patienten-Nachname
string
C0421448 (UMLS CUI-1)
184096005 (SNOMED CT-1)
184096005 (SNOMED CT-1)
Geburtsname
Item
Geburtsname
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
Patienten-Vorname
string
C0421447 (UMLS CUI-1)
184095009 (SNOMED CT-1)
184095009 (SNOMED CT-1)
CL Item
weiblich (weiblich)
C0086287 (UMLS CUI-1)
1086007 (SNOMED CT-1)
1086007 (SNOMED CT-1)
CL Item
männlich (männlich)
C0086582 (UMLS CUI-1)
10052007 (SNOMED CT-1)
10052007 (SNOMED CT-1)
Geburtsdatum
Item
Patienten-Geburtsdatum
date
C0421451 (UMLS CUI-1)
184099003 (SNOMED CT-1)
184099003 (SNOMED CT-1)
Staatsangehörigkeit
Item
Nationalität/Staatsangehörigkeit
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
Straße
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
Postleitzahl Patient
integer
C0421454 (UMLS CUI-1)
184102003 (SNOMED CT-1)
184102003 (SNOMED CT-1)
Ort
Item
Wohnort
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)
Zielgebiet
Item
Zielorgane
string
C0807185 (UMLS CUI-1)
Item
Strahlentherapie - Technik
integer
Technique (Code-1)
C0449851 (UMLS CUI-1)
246501002 (SNOMED CT-1)
Therapeutic radiology procedure (Code-2)
C1522449 (UMLS CUI-2)
108290001 (SNOMED CT-2)
10037770 (MedDRA-2)
C0449851 (UMLS CUI-1)
246501002 (SNOMED CT-1)
Therapeutic radiology procedure (Code-2)
C1522449 (UMLS CUI-2)
108290001 (SNOMED CT-2)
10037770 (MedDRA-2)
CL Item
Tele-Radiotherapie (P = Percutan (Teletherapie))
Teleradiotherapy procedure (procedure) (Code-1)
C0419095 (UMLS CUI-1)
33195004 (SNOMED CT-1)
C0419095 (UMLS CUI-1)
33195004 (SNOMED CT-1)
CL Item
Brachytherapy (P = Percutan (Brachytherapie))
extended_coding (Code-Info)
Brachytherapy (Code-1)
C0006098 (UMLS CUI-1)
399315003 (SNOMED CT-1)
10061018 (MedDRA-1)
Brachytherapy (Code-1)
C0006098 (UMLS CUI-1)
399315003 (SNOMED CT-1)
10061018 (MedDRA-1)
CL Item
Intrakavitäre Radiotherapie (K = endokavitäare Kontakttherapie)
C0021864 (UMLS CUI-1)
384692006 (SNOMED CT-1)
384692006 (SNOMED CT-1)
CL Item
Interne Radiotherapie - permanente Seeds (I = Interstitielle Kontakttherapie)
Internal radiotherapy - permanent seeds (procedure) (Code-1)
C0436265 (UMLS CUI-1)
169359004 (SNOMED CT-1)
C0436265 (UMLS CUI-1)
169359004 (SNOMED CT-1)
CL Item
Interne metabolische Therapie (M = Metabolische Therapie (radionuclide))
C0436254 (UMLS CUI-1)
169340001 (SNOMED CT-1)
169340001 (SNOMED CT-1)
CL Item
Afterloading (A = afterloading)
C0436298 (UMLS CUI-1)
169387008 (SNOMED CT-1)
169387008 (SNOMED CT-1)
Beginn
Item
Beginn Strahlentherapie
date
Radiotherapy started (situation) (Code-1)
C0436382 (UMLS CUI-1)
168531007 (SNOMED CT-1)
C0436382 (UMLS CUI-1)
168531007 (SNOMED CT-1)
Ende
Item
Ende Strahlentherapie
date
Radiotherapy completed (situation) (Code-1)
C0436385 (UMLS CUI-1)
168534004 (SNOMED CT-1)
C0436385 (UMLS CUI-1)
168534004 (SNOMED CT-1)
Gesamtdosis (Gy/Gbq)
Item
Gesamtdosis
integer
Total radiation dose delivered (observable entity) (Code-1)
C2919490 (UMLS CUI-1)
445461008 (SNOMED CT-1)
C2919490 (UMLS CUI-1)
445461008 (SNOMED CT-1)
Item
Intention
integer
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Therapeutic radiology procedure (Code-2)
C1522449 (UMLS CUI-2)
108290001 (SNOMED CT-2)
10037770 (MedDRA-2)
367565008 (SNOMED CT-1)
Therapeutic radiology procedure (Code-2)
C1522449 (UMLS CUI-2)
108290001 (SNOMED CT-2)
10037770 (MedDRA-2)
CL Item
Kurativ (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
Palliativ (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 (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
Neoadjuvant (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
Beendigung der Strahlentherapie
integer
Radiotherapy stopped (situation) (Code-1)
C0436384 (UMLS CUI-1)
168533005 (SNOMED CT-1)
C0436384 (UMLS CUI-1)
168533005 (SNOMED CT-1)
CL Item
Abbruch wegen Nebenwirkungen (Abbruch wegen Nebenwirkungen)
Adverse effects (Code-1)
C0879626 (UMLS CUI-1)
281647001 (SNOMED CT-1)
10067484 (MedDRA-1)
Discontinue (Code-2)
C1444662 (UMLS CUI-2)
410546004 (SNOMED CT-2)
Indication of (contextual qualifier) (Code-3)
C0392360 (UMLS CUI-3)
230165009 (SNOMED CT-3)
MTHU008319 (LOINC-3)
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
reguläres Ende der Therapie (reguläres Ende)
Regular (Code-1)
C0449581 (UMLS CUI-1)
17854005 (SNOMED CT-1)
End (Code-2)
C1272693 (UMLS CUI-2)
385656004 (SNOMED CT-2)
C0449581 (UMLS CUI-1)
17854005 (SNOMED CT-1)
End (Code-2)
C1272693 (UMLS CUI-2)
385656004 (SNOMED CT-2)
CL Item
Verweigerung der Therapie (Pat. verw. Therapie)
C0040809 (UMLS CUI-1)
105480006 (SNOMED CT-1)
10056407 (MedDRA-1)
105480006 (SNOMED CT-1)
10056407 (MedDRA-1)
Nebenwirkungen
Item
Nebenwirkungen
boolean
Item
Laborwerte
integer
Other Metabolic and Laboratory Adverse Event (Code-1)
C1559945 (UMLS CUI-1)
MTHU117254 (CTCAE-1)
C1559945 (UMLS CUI-1)
MTHU117254 (CTCAE-1)
CL Item
keine Nebenwirkungen (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
C2699517 (UMLS CUI-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
CL Item
leichte Nebenwirkungen (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
C1513302 (UMLS CUI-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
CL Item
mäßige Nebenwirkungen (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
C1513374 (UMLS CUI-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
CL Item
starke Nebenwirkungen (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
C1519275 (UMLS CUI-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
CL Item
lebensbedrohliche Nebenwirkungen (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
C1517874 (UMLS CUI-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
CL Item
Nebenwirkungen unbekannt (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Other Metabolic and Laboratory Adverse Event (Code-2)
C1559945 (UMLS CUI-2)
MTHU117254 (CTCAE-2)
Item
Urogenital-System
integer
Renal or Genitourinary Other Adverse Event (Code-1)
C1558061 (UMLS CUI-1)
MTHU117419 (CTCAE-1)
C1558061 (UMLS CUI-1)
MTHU117419 (CTCAE-1)
CL Item
keine Nebenwirkungen (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
C2699517 (UMLS CUI-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
CL Item
leichte Nebenwirkungen (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
C1513302 (UMLS CUI-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
CL Item
mäßige Nebenwirkungen (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
C1513374 (UMLS CUI-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
CL Item
starke Nebenwirkungen (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
C1519275 (UMLS CUI-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
CL Item
lebensbedrohliche Nebenwirkungen (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
C1517874 (UMLS CUI-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
CL Item
Nebenwirkungen unbekannt (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Renal or Genitourinary Other Adverse Event (Code-2)
C1558061 (UMLS CUI-2)
MTHU117419 (CTCAE-2)
Item
Haut
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
keine Nebenwirkungen (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
C2699517 (UMLS CUI-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
CL Item
leichte Nebenwirkungen (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
C1513302 (UMLS CUI-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
CL Item
mäßige Nebenwirkungen (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
C1513374 (UMLS CUI-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
CL Item
starke Nebenwirkungen (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
C1519275 (UMLS CUI-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
CL Item
lebensbedrohliche Nebenwirkungen (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
C1517874 (UMLS CUI-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
CL Item
Nebenwirkungen unbekannt (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Other Dermatology or Skin Adverse Event (Code-2)
C1559104 (UMLS CUI-2)
MTHU117246 (CTCAE-2)
CL Item
only in connection with Allergy (only in connection with Allergy)
Item
Allergie
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
keine Nebenwirkungen (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
C2699517 (UMLS CUI-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
CL Item
leichte Nebenwirkungen (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
C1513302 (UMLS CUI-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
CL Item
mäßige Nebenwirkungen (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
C1513374 (UMLS CUI-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
CL Item
starke Nebenwirkungen (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
C1519275 (UMLS CUI-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
CL Item
lebensbedrohliche Nebenwirkungen (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
C1517874 (UMLS CUI-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
CL Item
Nebenwirkungen unbekannt (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with Allergy and Immunology (Code-2)
C1560126 (UMLS CUI-2)
MTHU112125 (CTCAE-2)
CL Item
only in connection with Skin (only in connection with Skin)
Item
Gastrointestinaltrakt
integer
Adverse Event Associated with the Gastrointestinal System (Code-1)
C1559265 (UMLS CUI-1)
MTHU112146 (CTCAE-1)
C1559265 (UMLS CUI-1)
MTHU112146 (CTCAE-1)
CL Item
keine Nebenwirkungen (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
C2699517 (UMLS CUI-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
CL Item
leichte Nebenwirkungen (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
C1513302 (UMLS CUI-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
CL Item
mäßige Nebenwirkungen (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
C1513374 (UMLS CUI-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
CL Item
starke Nebenwirkungen (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
C1519275 (UMLS CUI-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
CL Item
lebensbedrohliche Nebenwirkungen (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
C1517874 (UMLS CUI-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
CL Item
Nebenwirkungen unbekannt (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with the Gastrointestinal System (Code-2)
C1559265 (UMLS CUI-2)
MTHU112146 (CTCAE-2)
Item
Nervensystem
integer
Adverse Event Associated with the Nervous System (Code-1)
C1561270 (UMLS CUI-1)
MTHU112152 (CTCAE-1)
C1561270 (UMLS CUI-1)
MTHU112152 (CTCAE-1)
CL Item
keine Nebenwirkungen (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
C2699517 (UMLS CUI-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
CL Item
leichte Nebenwirkungen (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
C1513302 (UMLS CUI-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
CL Item
mäßige Nebenwirkungen (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
C1513374 (UMLS CUI-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
CL Item
starke Nebenwirkungen (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
C1519275 (UMLS CUI-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
CL Item
lebensbedrohliche Nebenwirkungen (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
C1517874 (UMLS CUI-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
CL Item
Nebenwirkungen unbekannt (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with the Nervous System (Code-2)
C1561270 (UMLS CUI-2)
MTHU112152 (CTCAE-2)
Item
Fieber
integer
Fever Without Neutropenia Adverse Event (Code-1)
C1556366 (UMLS CUI-1)
MTHU116933 (CTCAE-1)
C1556366 (UMLS CUI-1)
MTHU116933 (CTCAE-1)
CL Item
keine Nebenwirkungen (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
C2699517 (UMLS CUI-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
CL Item
leichte Nebenwirkungen (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
C1513302 (UMLS CUI-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
CL Item
mäßige Nebenwirkungen (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
C1513374 (UMLS CUI-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
CL Item
starke Nebenwirkungen (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
C1519275 (UMLS CUI-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
CL Item
lebensbedrohliche Nebenwirkungen (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
C1517874 (UMLS CUI-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
CL Item
Nebenwirkungen unbekannt (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Fever Without Neutropenia Adverse Event (Code-2)
C1556366 (UMLS CUI-2)
MTHU116933 (CTCAE-2)
CL Item
only in connection with Infection (only in connection with Infection)
Item
Infektion
integer
Adverse Event Associated with Infection (Code-1)
C1556682 (UMLS CUI-1)
MTHU112135 (CTCAE-1)
C1556682 (UMLS CUI-1)
MTHU112135 (CTCAE-1)
CL Item
keine Nebenwirkungen (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
C2699517 (UMLS CUI-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
CL Item
leichte Nebenwirkungen (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
C1513302 (UMLS CUI-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
CL Item
mäßige Nebenwirkungen (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
C1513374 (UMLS CUI-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
CL Item
starke Nebenwirkungen (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
C1519275 (UMLS CUI-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
CL Item
lebensbedrohliche Nebenwirkungen (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
C1517874 (UMLS CUI-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
CL Item
Nebenwirkungen unbekannt (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with Infection (Code-2)
C1556682 (UMLS CUI-2)
MTHU112135 (CTCAE-2)
CL Item
only in connection with fever (only in connection with fever)
Item
Systemischer Kreislauf
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
keine Nebenwirkungen (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
C2699517 (UMLS CUI-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
CL Item
leichte Nebenwirkungen (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
C1513302 (UMLS CUI-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
CL Item
mäßige Nebenwirkungen (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
C1513374 (UMLS CUI-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
CL Item
starke Nebenwirkungen (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
C1519275 (UMLS CUI-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
CL Item
lebensbedrohliche Nebenwirkungen (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
C1517874 (UMLS CUI-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
CL Item
Nebenwirkungen unbekannt (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with the Heart in General (Code-2)
C1556247 (UMLS CUI-2)
MTHU112147 (CTCAE-2)
Item
Sinnesorgane
integer
Adverse Event Associated with the Ear and Auditory System (Code-1)
C1560154 (UMLS CUI-1)
MTHU112144 (CTCAE-1)
C1560154 (UMLS CUI-1)
MTHU112144 (CTCAE-1)
CL Item
keine Nebenwirkungen (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
C2699517 (UMLS CUI-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
CL Item
leichte Nebenwirkungen (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
C1513302 (UMLS CUI-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
CL Item
mäßige Nebenwirkungen (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
C1513374 (UMLS CUI-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
CL Item
starke Nebenwirkungen (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
C1519275 (UMLS CUI-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
CL Item
lebensbedrohliche Nebenwirkungen (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
C1517874 (UMLS CUI-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
CL Item
Nebenwirkungen unbekannt (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with the Ear and Auditory System (Code-2)
C1560154 (UMLS CUI-2)
MTHU112144 (CTCAE-2)
Item
Allgemeinsymptome
integer
Adverse Event Associated with Constitutional Symptoms (Code-1)
C1556354 (UMLS CUI-1)
MTHU112129 (CTCAE-1)
C1556354 (UMLS CUI-1)
MTHU112129 (CTCAE-1)
CL Item
keine Nebenwirkungen (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
C2699517 (UMLS CUI-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
CL Item
leichte Nebenwirkungen (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
C1513302 (UMLS CUI-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
CL Item
mäßige Nebenwirkungen (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
C1513374 (UMLS CUI-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
CL Item
starke Nebenwirkungen (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
C1519275 (UMLS CUI-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
CL Item
lebensbedrohliche Nebenwirkungen (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
C1517874 (UMLS CUI-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
CL Item
Nebenwirkungen unbekannt (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with Constitutional Symptoms (Code-2)
C1556354 (UMLS CUI-2)
MTHU112129 (CTCAE-2)
Item
Lunge/Kehlkopf
integer
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-1)
C1557628 (UMLS CUI-1)
MTHU112139 (CTCAE-1)
C1557628 (UMLS CUI-1)
MTHU112139 (CTCAE-1)
CL Item
keine Nebenwirkungen (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
C2699517 (UMLS CUI-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
CL Item
leichte Nebenwirkungen (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
C1513302 (UMLS CUI-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
CL Item
mäßige Nebenwirkungen (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
C1513374 (UMLS CUI-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
CL Item
starke Nebenwirkungen (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
C1519275 (UMLS CUI-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
CL Item
lebensbedrohliche Nebenwirkungen (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
C1517874 (UMLS CUI-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
CL Item
Nebenwirkungen unbekannt (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-2)
C1557628 (UMLS CUI-2)
MTHU112139 (CTCAE-2)
Item
Endokrines System
integer
Adverse Event Associated with the Endocrine System (Code-1)
C1559198 (UMLS CUI-1)
MTHU112145 (CTCAE-1)
C1559198 (UMLS CUI-1)
MTHU112145 (CTCAE-1)
CL Item
keine Nebenwirkungen (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
C2699517 (UMLS CUI-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
CL Item
leichte Nebenwirkungen (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
C1513302 (UMLS CUI-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
CL Item
mäßige Nebenwirkungen (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
C1513374 (UMLS CUI-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
CL Item
starke Nebenwirkungen (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
C1519275 (UMLS CUI-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
CL Item
lebensbedrohliche Nebenwirkungen (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
C1517874 (UMLS CUI-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
CL Item
Nebenwirkungen unbekannt (X = Nebenwirkungen unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Adverse Event Associated with the Endocrine System (Code-2)
C1559198 (UMLS CUI-2)
MTHU112145 (CTCAE-2)
Item
Allgemeinzustand
integer
CL Item
keine Nebenwirkungen (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
general appearance (physical finding) (Code-2)
C1148438 (UMLS CUI-2)
MTHU015040 (LOINC-2)
C2699517 (UMLS CUI-1)
general appearance (physical finding) (Code-2)
C1148438 (UMLS CUI-2)
MTHU015040 (LOINC-2)
CL Item
leichte Nebenwirkungen (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
general appearance (physical finding) (Code-2)
C1148438 (UMLS CUI-2)
MTHU015040 (LOINC-2)
C1513302 (UMLS CUI-1)
general appearance (physical finding) (Code-2)
C1148438 (UMLS CUI-2)
MTHU015040 (LOINC-2)
CL Item
mäßige Nebenwirkungen (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
general appearance (physical finding) (Code-2)
C1148438 (UMLS CUI-2)
MTHU015040 (LOINC-2)
C1513374 (UMLS CUI-1)
general appearance (physical finding) (Code-2)
C1148438 (UMLS CUI-2)
MTHU015040 (LOINC-2)
CL Item
starke Nebenwirkungen (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
general appearance (physical finding) (Code-2)
C1148438 (UMLS CUI-2)
MTHU015040 (LOINC-2)
C1519275 (UMLS CUI-1)
general appearance (physical finding) (Code-2)
C1148438 (UMLS CUI-2)
MTHU015040 (LOINC-2)
CL Item
lebensbedrohliche Nebenwirkungen (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
general appearance (physical finding) (Code-2)
C1148438 (UMLS CUI-2)
MTHU015040 (LOINC-2)
C1517874 (UMLS CUI-1)
general appearance (physical finding) (Code-2)
C1148438 (UMLS CUI-2)
MTHU015040 (LOINC-2)
CL Item
Nebenwirkungen unbekannt (X = Nebenwirkungen unbekannt)
Common Terminology Criteria for Adverse Events (Code-1)
C1516728 (UMLS CUI-1)
Unknown (Code-2)
C0439673 (UMLS CUI-2)
261665006 (SNOMED CT-2)
general appearance (physical finding) (Code-3)
C1148438 (UMLS CUI-3)
MTHU015040 (LOINC-3)
C1516728 (UMLS CUI-1)
Unknown (Code-2)
C0439673 (UMLS CUI-2)
261665006 (SNOMED CT-2)
general appearance (physical finding) (Code-3)
C1148438 (UMLS CUI-3)
MTHU015040 (LOINC-3)
Item
andere Nebenwirkung
integer
Adverse event (Code-1)
C0877248 (UMLS CUI-1)
10060933 (MedDRA-1)
MTHU014542 (LOINC-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
C0877248 (UMLS CUI-1)
10060933 (MedDRA-1)
MTHU014542 (LOINC-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
CL Item
keine Nebenwirkungen (0 = keine)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
10060933 (MedDRA-2)
MTHU014542 (LOINC-2)
C2699517 (UMLS CUI-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
10060933 (MedDRA-2)
MTHU014542 (LOINC-2)
CL Item
leichte Nebenwirkungen (1 = gering/leicht)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
10060933 (MedDRA-2)
MTHU014542 (LOINC-2)
C1513302 (UMLS CUI-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
10060933 (MedDRA-2)
MTHU014542 (LOINC-2)
CL Item
mäßige Nebenwirkungen (2 = mäßig/deutlich)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
10060933 (MedDRA-2)
MTHU014542 (LOINC-2)
C1513374 (UMLS CUI-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
10060933 (MedDRA-2)
MTHU014542 (LOINC-2)
CL Item
starke Nebenwirkungen (3 = stark/ausgeprägt)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
10060933 (MedDRA-2)
MTHU014542 (LOINC-2)
C1519275 (UMLS CUI-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
10060933 (MedDRA-2)
MTHU014542 (LOINC-2)
CL Item
lebensbedrohliche Nebenwirkungen (4 = lebensbedrohlich)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
10060933 (MedDRA-2)
MTHU014542 (LOINC-2)
C1517874 (UMLS CUI-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
10060933 (MedDRA-2)
MTHU014542 (LOINC-2)
CL Item
Nebenwirkungen unbekannt (X = Nebenwirkungen unbekannt)
Adverse event (Code-1)
C0877248 (UMLS CUI-1)
10060933 (MedDRA-1)
MTHU014542 (LOINC-1)
Unknown (Code-2)
C0439673 (UMLS CUI-2)
261665006 (SNOMED CT-2)
Other (Code-3)
C0205395 (UMLS CUI-3)
74964008 (SNOMED CT-3)
C0877248 (UMLS CUI-1)
10060933 (MedDRA-1)
MTHU014542 (LOINC-1)
Unknown (Code-2)
C0439673 (UMLS CUI-2)
261665006 (SNOMED CT-2)
Other (Code-3)
C0205395 (UMLS CUI-3)
74964008 (SNOMED CT-3)