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 approved
ATC Code L01EA01
DrugBank ID DB00619
KEGG ID D08066
MeSH ID D000068877
PubChem ID 5291
TTD Drug ID D0AZ3C
NDC Product Code 63850-4826; 68554-0034; 43598-345; 65162-795; 42292-044; 0378-2246; 43598-344; 51407-270; 0378-2245; 42292-043; 51407-269; 48087-0143; 65162-794
UNII BKJ8M8G5HI
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
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)
Blindness06.02.10.003; 17.17.01.0030.001735%-
Blindness transient06.02.10.006; 17.17.01.0040.000168%-
Blindness unilateral06.02.10.007; 17.17.01.0160.000358%-
Blister12.01.06.002; 23.03.01.0010.004477%-
Blood bilirubin increased13.03.04.018--
Blood creatine phosphokinase increased13.04.01.001--
Blood creatinine increased13.13.01.004--
Blood lactate dehydrogenase increased13.04.02.002--
Blood uric acid increased13.02.04.001---
Body temperature increased13.15.01.001---
Bone disorder15.02.04.004---
Bone pain15.02.01.0010.005910%
Breast enlargement21.05.04.001---
Breast mass21.05.04.0020.000112%-
Breast swelling21.05.05.0080.000112%-
Burning sensation08.01.09.029; 17.02.06.001---
Cachexia08.01.01.009; 14.03.02.001; 16.32.03.0110.000112%-
Capillary leak syndrome08.01.07.012; 24.06.03.0010.000112%
Cardiac arrest02.03.04.001--
Cardiac failure02.05.01.0010.002574%
Cardiac failure acute02.05.01.0050.000280%-
Cardiac failure congestive02.05.01.0020.002507%-
Cardiac tamponade02.06.01.0010.000504%
Cardiomegaly02.04.02.0010.000224%-
Cardiomyopathy02.04.01.0010.001007%-
Cardiovascular disorder02.11.01.010; 24.03.02.0090.000448%-
Cataract06.06.01.001--
Cellulitis11.02.01.001; 23.11.02.004---
Central nervous system neoplasm16.30.01.001; 17.20.01.0010.000112%-
Cerebral haemorrhage17.08.01.003; 24.07.04.001---
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ADReCS-Target
Drug Name ADR Term Target
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