Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Cytarabine
Drug ID BADD_D00560
Description A pyrimidine nucleoside analog that is used mainly in the treatment of leukemia, especially acute non-lymphoblastic leukemia. Cytarabine is an antimetabolite antineoplastic agent that inhibits the synthesis of DNA. Its actions are specific for the S phase of the cell cycle. It also has antiviral and immunosuppressant properties. (From Martindale, The Extra Pharmacopoeia, 30th ed, p472)
Indications and Usage For the treatment of acute non-lymphocytic leukemia, acute lymphocytic leukemia and blast phase of chronic myelocytic leukemia. Cytarabine is indicated in combination with [daunorubicin] for the treatment of newly-diagnosed therapy-related acute myeloid leukemia (t-AML) or AML with myelodysplasia-related changes (AML-MRC) in adults and pediatric patients 1 year and older.[L32843]
Marketing Status approved; investigational
ATC Code L01BC01
DrugBank ID DB00987
KEGG ID D00168
MeSH ID D003561
PubChem ID 6253
TTD Drug ID D07XSN
NDC Product Code 71288-168; 61703-304; 55512-0026; 25021-229; 61703-319; 68083-343; 71288-108; 12848-1003; 71288-109; 71288-169; 58623-0026; 61703-303; 63323-120; 68083-337; 61703-305; 67430-075; 25021-223
UNII 04079A1RDZ
Synonyms Cytarabine | Arabinosylcytosine | Cytosine Arabinoside | Arabinoside, Cytosine | Arabinofuranosylcytosine | Aracytidine | beta-Ara C | beta Ara C | Cytarabine Hydrochloride | Cytosar | Cytosar-U | Cytosar U | Ara-C | Ara C | Aracytine | Cytonal
Chemical Information
Molecular Formula C9H13N3O5
CAS Registry Number 147-94-4
SMILES C1=CN(C(=O)N=C1N)C2C(C(C(O2)CO)O)O
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Toxic leukoencephalopathy17.13.02.012; 12.03.01.0590.000112%Not Available
Gastrointestinal wall thickening07.01.06.0320.000168%Not Available
Catheter site oedema12.07.02.024; 08.02.02.0240.000112%Not Available
Corneal toxicity12.03.01.061; 06.11.03.0030.000112%Not Available
Differentiation syndrome08.01.07.016; 22.02.01.036; 16.32.03.037; 12.03.01.0630.000280%Not Available
Disease complication08.01.03.0870.000112%Not Available
Gelatinous transformation of the bone marrow01.03.03.0140.000112%Not Available
Haemoperitoneum12.01.17.007; 07.07.02.007; 24.07.02.0650.000112%Not Available
Haemophagocytic lymphohistiocytosis16.32.03.038; 10.02.01.077; 01.05.01.0260.000392%Not Available
Hepatic cytolysis09.01.07.0360.000112%Not Available
Hyperleukocytosis01.02.01.0180.000280%Not Available
Intra-abdominal fluid collection21.07.04.014; 07.07.01.0140.000112%Not Available
Lung opacity22.12.01.0060.000112%Not Available
Mucosal disorder08.01.06.0290.000112%Not Available
Myelodysplastic syndrome with excess blasts16.01.04.010; 01.10.04.0100.000112%Not Available
Myelosuppression01.03.03.0150.001959%Not Available
Oesophagobronchial fistula22.03.02.015; 07.11.05.0220.000112%Not Available
Orbital space occupying lesion06.09.05.0050.000112%Not Available
Therapy non-responder08.06.01.0630.000839%Not Available
Toxic erythema of chemotherapy23.03.05.013; 17.02.07.0300.000112%Not Available
Vocal cord dysfunction22.04.01.0180.000112%Not Available
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ADReCS-Target
Drug Name ADR Term Target
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