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ID

44642

Description

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

Lien

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

Mots-clés

Versions (2)
  1. 07/08/2013 07/08/2013 -
  2. 27/09/2021 27/09/2021 -
Téléchargé le

27 septembre 2021

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0 Legacy
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    quality management ADT-radiotherapy cancer

    Allemand Anglais

    quality management

    1 Formulaires  
    1. StudyEvent: quality management
      1. quality management
    Patient data
    Description

    Patient data

    Patientennummer
    Description

    Patientenidentifikationsnummer

    Type de données

    string

    Alias
    Code-1
    Patients
    UMLS CUI-1
    C0030705
    SNOMED CT-1
    116154003
    Code-2
    Identification number
    UMLS CUI-2
    C1300638
    SNOMED CT-2
    396278008
    Krankenkasse
    Description

    Krankenkasse

    Type de données

    string

    Alias
    UMLS CUI-1
    C0021682
    Patienten-Telefonnummer
    Description

    Telefon

    Type de données

    string

    Alias
    UMLS CUI-1
    C0421455
    SNOMED CT-1
    184103008
    Patienten-Nachname
    Description

    Name

    Type de données

    string

    Alias
    UMLS CUI-1
    C0421448
    SNOMED CT-1
    184096005
    Geburtsname
    Description

    Geburtsname

    Type de données

    string

    Alias
    UMLS CUI-1
    C0806887
    SNOMED CT-1
    423203003
    LOINC-1
    MTHU010481
    Code-2
    Patients
    UMLS CUI-2
    C0030705
    SNOMED CT-2
    116154003
    Patienten-Vorname
    Description

    Vorname

    Type de données

    string

    Alias
    UMLS CUI-1
    C0421447
    SNOMED CT-1
    184095009
    Patienten-Geschlecht
    Description

    Geschlecht

    Type de données

    integer

    Alias
    UMLS CUI-1
    C0150831
    SNOMED CT-1
    184100006
    Patienten-Geburtsdatum
    Description

    Geburtsdatum

    Type de données

    date

    Alias
    UMLS CUI-1
    C0421451
    SNOMED CT-1
    184099003
    Nationalität/Staatsangehörigkeit
    Description

    Staatsangehörigkeit

    Type de données

    string

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

    Patientenadresse

    Straße
    Description

    Straße

    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
    Postleitzahl Patient
    Description

    PLZ

    Type de données

    integer

    Alias
    UMLS CUI-1
    C0421454
    SNOMED CT-1
    184102003
    Wohnort
    Description

    Ort

    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
    Strahlentherapie
    Description

    Strahlentherapie

    Zielorgane
    Description

    Zielgebiet

    Type de données

    string

    Alias
    UMLS CUI-1
    C0807185
    Strahlentherapie - Technik
    Description

    Applikationsart

    Type de données

    integer

    Alias
    Code-1
    Technique
    UMLS CUI-1
    C0449851
    SNOMED CT-1
    246501002
    Code-2
    Therapeutic radiology procedure
    UMLS CUI-2
    C1522449
    SNOMED CT-2
    108290001
    MedDRA-2
    10037770
    Beginn Strahlentherapie
    Description

    Beginn

    Type de données

    date

    Alias
    Code-1
    Radiotherapy started (situation)
    UMLS CUI-1
    C0436382
    SNOMED CT-1
    168531007
    Ende Strahlentherapie
    Description

    Ende

    Type de données

    date

    Alias
    Code-1
    Radiotherapy completed (situation)
    UMLS CUI-1
    C0436385
    SNOMED CT-1
    168534004
    Gesamtdosis
    Description

    Gesamtdosis (Gy/Gbq)

    Type de données

    integer

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

    Intention

    Type de données

    integer

    Alias
    UMLS CUI-1
    C1283828
    SNOMED CT-1
    367565008
    Code-2
    Therapeutic radiology procedure
    UMLS CUI-2
    C1522449
    SNOMED CT-2
    108290001
    MedDRA-2
    10037770
    Beendigung der Strahlentherapie
    Description

    Beendigung der Strahlentherapie

    Type de données

    integer

    Alias
    Code-1
    Radiotherapy stopped (situation)
    UMLS CUI-1
    C0436384
    SNOMED CT-1
    168533005
    Nebenwirkungen nach CTC
    Description

    Nebenwirkungen nach CTC

    Nebenwirkungen
    Description

    Nebenwirkungen

    Type de données

    boolean

    Alias
    Code-Info
    for_compare
    UMLS CUI-1
    C0877248
    MedDRA-1
    10060933
    LOINC-1
    MTHU014542
    Laborwerte
    Description

    Laborwerte

    Type de données

    integer

    Alias
    Code-1
    Other Metabolic and Laboratory Adverse Event
    UMLS CUI-1
    C1559945
    CTCAE-1
    MTHU117254
    Urogenital-System
    Description

    Niere/Blase

    Type de données

    integer

    Alias
    Code-1
    Renal or Genitourinary Other Adverse Event
    UMLS CUI-1
    C1558061
    CTCAE-1
    MTHU117419
    Haut
    Description

    Haut

    Type de données

    integer

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

    Allergie

    Type de données

    integer

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

    Gastrointestinaltrakt

    Type de données

    integer

    Alias
    Code-1
    Adverse Event Associated with the Gastrointestinal System
    UMLS CUI-1
    C1559265
    CTCAE-1
    MTHU112146
    Nervensystem
    Description

    Nervensystem

    Type de données

    integer

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

    Fieber

    Type de données

    integer

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

    Infektion

    Type de données

    integer

    Alias
    Code-1
    Adverse Event Associated with Infection
    UMLS CUI-1
    C1556682
    CTCAE-1
    MTHU112135
    Systemischer Kreislauf
    Description

    Herz/Kreislauf

    Type de données

    integer

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

    Sinnesorgane

    Type de données

    integer

    Alias
    Code-1
    Adverse Event Associated with the Ear and Auditory System
    UMLS CUI-1
    C1560154
    CTCAE-1
    MTHU112144
    Allgemeinsymptome
    Description

    Allgemeinsymptome

    Type de données

    integer

    Alias
    Code-1
    Adverse Event Associated with Constitutional Symptoms
    UMLS CUI-1
    C1556354
    CTCAE-1
    MTHU112129
    Lunge/Kehlkopf
    Description

    Lunge/Kehlkopf

    Type de données

    integer

    Alias
    Code-1
    Adverse Event Associated with Pulmonary and Upper Respiratory Systems
    UMLS CUI-1
    C1557628
    CTCAE-1
    MTHU112139
    Endokrines System
    Description

    Endokrines System

    Type de données

    integer

    Alias
    Code-1
    Adverse Event Associated with the Endocrine System
    UMLS CUI-1
    C1559198
    CTCAE-1
    MTHU112145
    Allgemeinzustand
    Description

    Allgemeinzustand

    Type de données

    integer

    Alias
    Code-1
    general appearance (physical finding)
    UMLS CUI-1
    C1148438
    LOINC-1
    MTHU015040
    andere Nebenwirkung
    Description

    Sonstige

    Type de données

    integer

    Alias
    Code-1
    Adverse event
    UMLS CUI-1
    C0877248
    MedDRA-1
    10060933
    LOINC-1
    MTHU014542
    Code-2
    Other
    UMLS CUI-2
    C0205395
    SNOMED CT-2
    74964008
    Retour au début de la page

    Similar models

    quality management

    1 Formulaires
    1. StudyEvent: quality management
      1. quality management
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Patient data
    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)
    Krankenkasse
    Item
    Krankenkasse
    string
    C0021682 (UMLS CUI-1)
    Telefon
    Item
    Patienten-Telefonnummer
    string
    C0421455 (UMLS CUI-1)
    184103008 (SNOMED CT-1)
    Name
    Item
    Patienten-Nachname
    string
    C0421448 (UMLS CUI-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)
    Vorname
    Item
    Patienten-Vorname
    string
    C0421447 (UMLS CUI-1)
    184095009 (SNOMED CT-1)
    Item
    Patienten-Geschlecht
    integer
    C0150831 (UMLS CUI-1)
    184100006 (SNOMED CT-1)
    Geschlecht
    Code List
    Patienten-Geschlecht
    CL Item
    weiblich (weiblich)
    C0086287 (UMLS CUI-1)
    1086007 (SNOMED CT-1)
    CL Item
    männlich (männlich)
    C0086582 (UMLS CUI-1)
    10052007 (SNOMED CT-1)
    Geburtsdatum
    Item
    Patienten-Geburtsdatum
    date
    C0421451 (UMLS CUI-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)
    Item Group
    Patientenadresse
    Straße
    Item
    Straße
    string
    C1301826 (UMLS CUI-1)
    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)
    Ort
    Item
    Wohnort
    string
    C2316883 (UMLS CUI-1)
    433178008 (SNOMED CT-1)
    Patient address (Code-2)
    C0421449 (UMLS CUI-2)
    184097001 (SNOMED CT-2)
    Item Group
    Strahlentherapie
    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)
    Applikationsart
    Code List
    Strahlentherapie - Technik
    CL Item
    Tele-Radiotherapie (P = Percutan (Teletherapie))
    Teleradiotherapy procedure (procedure) (Code-1)
    C0419095 (UMLS CUI-1)
    33195004 (SNOMED CT-1)
    CL Item
    Brachytherapy (P = Percutan (Brachytherapie))
    extended_coding (Code-Info)
    Brachytherapy (Code-1)
    C0006098 (UMLS CUI-1)
    399315003 (SNOMED CT-1)
    10061018 (MedDRA-1)
    CL Item
    Intrakavitäre Radiotherapie (K = endokavitäare Kontakttherapie)
    C0021864 (UMLS CUI-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)
    CL Item
    Interne metabolische Therapie (M = Metabolische Therapie (radionuclide))
    C0436254 (UMLS CUI-1)
    169340001 (SNOMED CT-1)
    CL Item
    Afterloading (A = afterloading)
    C0436298 (UMLS CUI-1)
    169387008 (SNOMED CT-1)
    Beginn
    Item
    Beginn Strahlentherapie
    date
    Radiotherapy started (situation) (Code-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)
    Gesamtdosis (Gy/Gbq)
    Item
    Gesamtdosis
    integer
    Total radiation dose delivered (observable entity) (Code-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)
    Intention
    Code List
    Intention
    CL Item
    Kurativ (kurativ)
    Curative - procedure intent (qualifier value) (Code-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)
    CL Item
    Adjuvant (adjuvant)
    Adjuvant - intent (qualifier value) (Code-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)
    Item
    Beendigung der Strahlentherapie
    integer
    Radiotherapy stopped (situation) (Code-1)
    C0436384 (UMLS CUI-1)
    168533005 (SNOMED CT-1)
    Beendigung der Strahlentherapie
    Code List
    Beendigung der Strahlentherapie
    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)
    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)
    CL Item
    Verweigerung der Therapie (Pat. verw. Therapie)
    C0040809 (UMLS CUI-1)
    105480006 (SNOMED CT-1)
    10056407 (MedDRA-1)
    Item Group
    Nebenwirkungen nach CTC
    Nebenwirkungen
    Item
    Nebenwirkungen
    boolean
    for_compare (Code-Info)
    C0877248 (UMLS CUI-1)
    10060933 (MedDRA-1)
    MTHU014542 (LOINC-1)
    Item
    Laborwerte
    integer
    Other Metabolic and Laboratory Adverse Event (Code-1)
    C1559945 (UMLS CUI-1)
    MTHU117254 (CTCAE-1)
    Laborwerte
    Code List
    Laborwerte
    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)
    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)
    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)
    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)
    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)
    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)
    Item
    Urogenital-System
    integer
    Renal or Genitourinary Other Adverse Event (Code-1)
    C1558061 (UMLS CUI-1)
    MTHU117419 (CTCAE-1)
    Niere/Blase
    Code List
    Urogenital-System
    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)
    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)
    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)
    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)
    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)
    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)
    Item
    Haut
    integer
    Other Dermatology or Skin Adverse Event (Code-1)
    C1559104 (UMLS CUI-1)
    MTHU117246 (CTCAE-1)
    Haut
    Code List
    Haut
    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)
    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)
    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)
    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)
    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)
    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)
    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)
    Allergie
    Code List
    Allergie
    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)
    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)
    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)
    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)
    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)
    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)
    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)
    Gastrointestinaltrakt
    Code List
    Gastrointestinaltrakt
    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)
    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)
    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)
    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)
    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)
    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)
    Item
    Nervensystem
    integer
    Adverse Event Associated with the Nervous System (Code-1)
    C1561270 (UMLS CUI-1)
    MTHU112152 (CTCAE-1)
    Nervensystem
    Code List
    Nervensystem
    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)
    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)
    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)
    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)
    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)
    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)
    Item
    Fieber
    integer
    Fever Without Neutropenia Adverse Event (Code-1)
    C1556366 (UMLS CUI-1)
    MTHU116933 (CTCAE-1)
    Fieber
    Code List
    Fieber
    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)
    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)
    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)
    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)
    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)
    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)
    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)
    Infektion
    Code List
    Infektion
    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)
    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)
    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)
    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)
    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)
    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)
    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)
    Herz/Kreislauf
    Code List
    Systemischer Kreislauf
    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)
    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)
    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)
    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)
    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)
    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)
    Item
    Sinnesorgane
    integer
    Adverse Event Associated with the Ear and Auditory System (Code-1)
    C1560154 (UMLS CUI-1)
    MTHU112144 (CTCAE-1)
    Sinnesorgane
    Code List
    Sinnesorgane
    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)
    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)
    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)
    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)
    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)
    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)
    Item
    Allgemeinsymptome
    integer
    Adverse Event Associated with Constitutional Symptoms (Code-1)
    C1556354 (UMLS CUI-1)
    MTHU112129 (CTCAE-1)
    Allgemeinsymptome
    Code List
    Allgemeinsymptome
    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)
    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)
    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)
    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)
    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)
    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)
    Item
    Lunge/Kehlkopf
    integer
    Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-1)
    C1557628 (UMLS CUI-1)
    MTHU112139 (CTCAE-1)
    Lunge/Kehlkopf
    Code List
    Lunge/Kehlkopf
    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)
    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)
    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)
    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)
    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)
    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)
    Item
    Endokrines System
    integer
    Adverse Event Associated with the Endocrine System (Code-1)
    C1559198 (UMLS CUI-1)
    MTHU112145 (CTCAE-1)
    Endokrines System
    Code List
    Endokrines System
    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)
    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)
    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)
    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)
    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)
    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)
    Item
    Allgemeinzustand
    integer
    general appearance (physical finding) (Code-1)
    C1148438 (UMLS CUI-1)
    MTHU015040 (LOINC-1)
    Allgemeinzustand
    Code List
    Allgemeinzustand
    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)
    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)
    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)
    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)
    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)
    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)
    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)
    Sonstige
    Code List
    andere Nebenwirkung
    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)
    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)
    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)
    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)
    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)
    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)
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