CTCAE
Common Terminology Criteria for Adverse Events
Blood and lymphatic system disorders
Cardiac disorders
Congenital, familial and genetic disorders
Ear and labyrinth disorders
Endocrine disorders
Eye disorders
Gastrointestinal disorders
General disorders and administration site conditions
Hepatobiliary disorders
Immune system disorders
Infections and infestations
Injury, poisoning and procedural complications
Investigations
Metabolism and nutrition disorders
Musculoskeletal and connective tissue disorders
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Nervous system disorders
Pregnancy, puerperium and perinatal conditions
Psychiatric disorders
Renal and urinary disorders
Reproductive system and breast disorders
Respiratory, thoracic and mediastinal disorders
Skin and subcutaneous tissue disorders
Social circumstances
Surgical and medical procedures
Vascular disorders
Ďalšie informácie
Upozornenie
Tento nástroj je určený iba na vzdelávacie účely, pričom nepredstavuje odbornú lekársku pomoc a ani ju nenahrádza. Nemal by byť používaný na lekársku diagnostiku a/alebo liečbu.
Instructions for use
General description
The Common Terminology Criteria for Adverse Events (CTCAE) is a standardized classification system developed by the National Cancer Institute (NCI) to describe the severity of adverse events. It provides a common language to report and analyze adverse events (AEs), ensuring consistency and comparability across different studies and treatments.
AEs are categorized by system organ classes. Each AE is graded on a scale from 1 to 5. In general, grade 1 represents a mild AE, grade 2 a moderate AE, grade 3 a severe AE, grade 4 a life-threatening or disabling AE and grade 5 death related to the AE.
The tool enables a user to browse or search through the CTCAE classification using relevant keywords.
The Common Terminology Criteria for Adverse Events (CTCAE) is a standardized classification system developed by the National Cancer Institute (NCI) to describe the severity of adverse events. It provides a common language to report and analyze adverse events (AEs), ensuring consistency and comparability across different studies and treatments.
AEs are categorized by system organ classes. Each AE is graded on a scale from 1 to 5. In general, grade 1 represents a mild AE, grade 2 a moderate AE, grade 3 a severe AE, grade 4 a life-threatening or disabling AE and grade 5 death related to the AE.
The tool enables a user to browse or search through the CTCAE classification using relevant keywords.
References
Verzia
1
O tomto nástroji
The Common Terminology Criteria for Adverse Events (CTCAE) is a standardized classification system developed by the National Cancer Institute (NCI) to describe the severity of adverse events. It provides a common language to report and analyze adverse events (AEs), ensuring consistency and comparability across different studies and treatments.
AEs are categorized by system organ classes. Each AE is graded on a scale from 1 to 5. In general, grade 1 represents a mild AE, grade 2 a moderate AE, grade 3 a severe AE, grade 4 a life-threatening or disabling AE and grade 5 death related to the AE.
The tool enables a user to browse or search through the CTCAE classification using relevant keywords.
AEs are categorized by system organ classes. Each AE is graded on a scale from 1 to 5. In general, grade 1 represents a mild AE, grade 2 a moderate AE, grade 3 a severe AE, grade 4 a life-threatening or disabling AE and grade 5 death related to the AE.
The tool enables a user to browse or search through the CTCAE classification using relevant keywords.
