Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Imatinib
Drug ID BADD_D01136
Description Imatinib is a small molecule kinase inhibitor used to treat certain types of cancer. It is currently marketed by Novartis as Gleevec (USA) or Glivec (Europe/Australia) as its mesylate salt, imatinib mesilate (INN). It is occasionally referred to as CGP57148B or STI571 (especially in older publications). It is used in treating chronic myelogenous leukemia (CML), gastrointestinal stromal tumors (GISTs) and a number of other malignancies. It is the first member of a new class of agents that act by inhibiting particular tyrosine kinase enzymes, instead of non-specifically inhibiting rapidly dividing cells.
Indications and Usage For the treatment of Philadelphia chromosome positive chronic myeloid leukemia (Ph+ CML), Ph+ acute lymphoblastic leukaemia, myelodysplastic/myeloproliferative diseases, aggressive systemic mastocytosis, hypereosinophilic syndrome and/or chronic eosinophilic leukemia (CEL), dermatofibrosarcoma protuberans, and malignant gastrointestinal stromal tumors (GIST).
Marketing Status Prescription; Discontinued
ATC Code L01EA01
DrugBank ID DB00619
KEGG ID D08066
MeSH ID D000068877
PubChem ID 5291
TTD Drug ID D0AZ3C
NDC Product Code 65162-795; 51407-270; 63850-4826; 68180-391; 65162-794; 42292-043; 0378-2246; 68554-0034; 43598-344; 51407-269; 42292-044; 48087-0143; 43598-345; 0378-2245; 68180-390
Synonyms Imatinib Mesylate | Mesylate, Imatinib | Imatinib Methanesulfonate | Methanesulfonate, Imatinib | STI571 | STI-571 | STI 571 | Gleevec | Glivec | ST 1571 | ST1571 | CGP 57148 | CGP57148B | CGP-57148 | CGP57148 | Imatinib | Alpha-(4-methyl-1-piperazinyl)-3'-((4-(3-pyridyl)-2-pyrimidinyl)amino)-p-tolu-p-toluidide
Chemical Information
Molecular Formula C29H31N7O
CAS Registry Number 152459-95-5
SMILES CC1=C(C=C(C=C1)NC(=O)C2=CC=C(C=C2)CN3CCN(CC3)C)NC4=NC=CC(=N4)C5=CN=CC=C5
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Chronic myeloid leukaemiaLeptinP41159T7948525648025
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Ecchymosis24.07.06.002; 23.06.01.001; 01.01.03.0010.001066%Not Available
Eclampsia24.08.07.001; 20.01.08.001; 18.02.03.001; 17.12.03.0120.000533%Not Available
Eczema23.03.04.0060.001865%
Electrocardiogram QT prolonged13.14.05.004--
Electrolyte imbalance14.05.01.0020.000208%Not Available
Emphysema22.01.02.0020.000347%Not Available
Empyema11.01.08.0200.000533%Not Available
Encephalopathy17.13.02.001--
Enteritis07.08.03.0020.000533%
Enterocolitis07.08.03.0030.000533%
Eosinophil count increased13.01.06.0040.001066%Not Available
Eosinophilia01.02.04.0010.004529%
Epistaxis24.07.01.005; 22.04.03.001--
Eructation07.01.02.0030.000533%
Erysipelas23.09.01.002; 11.02.06.0010.000533%Not Available
Erythema23.03.06.0010.008792%Not Available
Erythema annulare23.03.08.0040.000533%Not Available
Erythema multiforme23.03.01.003; 10.01.03.015--
Erythema nodosum23.07.02.001; 10.02.01.0200.000799%Not Available
Essential thrombocythaemia16.21.03.004; 01.13.03.0030.001332%Not Available
Exomphalos03.04.07.001; 07.16.03.0020.000208%Not Available
Extrasystoles02.03.02.0030.000533%Not Available
Eye discharge06.04.05.0010.000533%Not Available
Eye disorder06.08.03.0010.001598%Not Available
Eye haemorrhage06.07.02.001; 24.07.05.0020.003463%Not Available
Eye infection11.01.06.001; 06.04.05.0070.000799%
Eye irritation06.04.05.003--Not Available
Eye pain06.08.03.0020.001865%
Eye swelling06.08.03.0030.014653%Not Available
Eyelid oedema23.04.01.003; 10.01.05.001; 06.04.04.0040.008259%Not Available
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