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)
Leukoencephalopathy17.13.02.0030.000112%
Leukopenia01.02.02.0010.000526%Not Available
Liver abscess11.01.18.001; 09.01.11.001--Not Available
Lung consolidation22.01.02.0100.000660%Not Available
Lung disorder22.02.07.0010.000560%Not Available
Lung infiltration22.01.02.0040.000638%Not Available
Lymphadenitis01.09.01.0010.000224%Not Available
Lymphadenopathy01.09.01.0020.000168%Not Available
Maculopathy06.09.03.0070.000112%Not Available
Megacolon07.02.05.0020.000168%Not Available
Melaena24.07.02.013; 07.12.02.0040.000336%Not Available
Metabolic acidosis14.01.01.0030.000560%Not Available
Mouth haemorrhage07.05.02.001; 24.07.02.0140.000112%
Mouth ulceration07.05.06.0040.000168%Not Available
Movement disorder17.01.02.0100.000112%Not Available
Mucosal inflammation08.01.06.0020.002720%Not Available
Muscle necrosis15.05.05.0070.000112%Not Available
Muscular weakness17.05.03.005; 15.05.06.0010.000392%
Myelodysplastic syndrome01.10.04.001; 16.01.04.0010.001455%
Myelofibrosis16.21.03.001; 01.13.03.0050.000112%Not Available
Myelopathy17.10.01.0070.000168%Not Available
Myocarditis02.04.03.0010.000414%
Nausea07.01.07.001--
Neck pain15.03.04.0090.000224%
Necrosis24.04.02.006; 08.03.03.0010.000112%Not Available
Nephrogenic diabetes insipidus20.05.03.010; 14.05.07.0020.000168%Not Available
Nephropathy toxic20.05.03.002; 12.03.01.0100.000224%Not Available
Nervous system disorder17.02.10.0010.000448%Not Available
Neuritis17.09.03.001--Not Available
Neurotoxicity12.03.01.011; 17.02.10.0020.001511%Not Available
The 6th Page    First    Pre   6 7 8 9 10    Next   Last    Total 14 Pages
ADReCS-Target
Drug Name ADR Term Target
Tip:  Drug Name  ADR Term  Protein  Variation  Gene