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)
Abdominal adhesions07.07.03.001; 12.02.03.0060.000112%Not Available
Abdominal distension07.01.04.0010.000504%
Abdominal pain07.01.05.0020.001836%
Abdominal tenderness07.01.05.0040.000414%Not Available
Acidosis14.01.03.0020.000392%
Acute febrile neutrophilic dermatosis23.03.03.033; 01.02.01.0060.000616%Not Available
Acute hepatic failure09.01.03.0010.000392%Not Available
Acute leukaemia16.01.02.001; 01.10.02.0010.000112%Not Available
Acute myeloid leukaemia16.01.05.001; 01.10.05.0010.002295%Not Available
Acute myocardial infarction24.04.04.001; 02.02.02.0010.000224%Not Available
Acute respiratory distress syndrome24.03.02.034; 10.02.01.067; 22.01.03.0010.002373%
Acute respiratory failure22.02.06.001; 14.01.04.0040.000974%Not Available
Adrenal insufficiency14.11.01.004; 05.01.02.0010.000280%
Agranulocytosis01.02.03.0010.000280%Not Available
Alopecia23.02.02.001--
Anaemia01.03.02.0010.001533%
Anaemia megaloblastic14.12.01.003; 01.03.02.003--Not Available
Anal fistula07.11.05.0020.000168%
Anaphylactic reaction24.06.03.006; 10.01.07.001--
Anuria20.01.03.0020.000224%Not Available
Aortic aneurysm rupture24.02.03.0030.000112%Not Available
Arteriosclerosis coronary artery24.04.04.012; 02.02.01.0110.000246%Not Available
Ascites09.01.05.003; 07.07.01.001; 02.05.04.0020.000168%
Ataxia17.02.02.001; 08.01.02.0040.000504%
Atelectasis22.01.02.0010.000672%
Atrial fibrillation02.03.03.0020.002384%
Atrial flutter02.03.03.0030.000716%
Atrioventricular block complete02.03.01.0030.000168%
Blindness unilateral06.02.10.007; 17.17.01.0160.000112%Not Available
Capillary leak syndrome24.06.03.001; 08.01.07.0120.000224%
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ADReCS-Target
Drug Name ADR Term Target
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