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)
Visual acuity reduced06.02.10.012; 17.17.01.0110.000448%
Vitiligo23.05.02.004; 10.04.02.0040.000224%Not Available
Vitreous detachment12.01.04.005; 06.09.01.0020.000112%Not Available
Vitreous haemorrhage24.07.05.005; 06.10.03.0010.000112%
Vocal cord paralysis22.04.01.002; 17.04.06.0020.000302%
Vomiting07.01.07.0030.025229%
Vomiting projectile07.01.07.0120.000381%Not Available
Weight decreased13.15.01.005--
Weight increased13.15.01.006--
White blood cell count decreased13.01.06.012--
Pneumoperitoneum07.07.01.0080.000280%Not Available
Fibromyalgia15.05.02.002--Not Available
Musculoskeletal disorder15.03.05.025--Not Available
Cardiotoxicity02.11.01.009; 12.03.01.0070.001007%Not Available
Hydrothorax22.05.02.0040.000168%Not Available
Hypereosinophilic syndrome01.02.04.0050.000168%Not Available
Acute generalised exanthematous pustulosis11.07.01.018; 10.01.01.034; 23.03.10.002; 12.03.01.005--Not Available
Hypoacusis04.02.01.0060.001948%
Onychoclasis23.02.05.0050.000560%Not Available
Performance status decreased08.01.03.0420.000112%Not Available
Peripheral swelling08.01.03.053; 02.05.04.0150.008932%Not Available
Localised oedema14.05.06.009; 08.01.07.011; 02.05.04.0060.000224%
Brain oedema17.07.02.003; 12.01.10.010--
Acute phase reaction08.01.05.0040.000112%Not Available
Brain death17.02.03.003; 08.04.01.0040.000112%Not Available
Onychomadesis23.02.05.0060.000168%
Sudden cardiac death08.04.01.008; 02.03.04.0160.000224%Not Available
General physical health deterioration08.01.03.018--Not Available
Erythropoiesis abnormal01.07.02.0100.000224%Not Available
Anal haemorrhage07.12.03.004; 24.07.02.0290.000246%
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ADReCS-Target
Drug Name ADR Term Target
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