Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Dasatinib
Drug ID BADD_D00589
Description Dasatinib is an oral dual BCR/ABL and Src family tyrosine kinase inhibitor approved for use in patients with chronic myelogenous leukemia (CML). The main targets of Dasatinib, are BCRABL, SRC, Ephrins and GFR.
Indications and Usage For the treatment of adults with chronic, accelerated, or myeloid or lymphoid blast phase chronic myeloid leukemia with resistance or intolerance to prior therapy. Also indicated for the treatment of adults with Philadelphia chromosome-positive acute lymphoblastic leukemia with resistance or intolerance to prior therapy.
Marketing Status approved; investigational
ATC Code L01EA02
DrugBank ID DB01254
KEGG ID D03658; D06414
MeSH ID D000069439
PubChem ID 3062316
TTD Drug ID D0E6XR
NDC Product Code 0003-0857; 53104-7725; 0003-0852; 68554-0070; 0003-0528; 59651-468; 54893-0015; 62207-973; 63285-863; 63285-866; 0003-0855; 63285-867; 0003-0527; 14778-1313; 50193-0524; 54893-0047; 63285-862; 0003-0524; 63285-864; 63285-865
UNII RBZ1571X5H
Synonyms Dasatinib | N-(2-chloro-6-methylphenyl)-2-(6-(4-(2-hydroxyethyl)piperazin-1-yl)-2-methylpyrimidin-4-ylamino)thiazole-5-carboxamide | Sprycel | (18F)-N-(2-chloro-6-methylphenyl)-2-(6-(4-(2-hydroxyethyl)piperazin-1-yl)-2-methylpyrimidin-4-ylamino)thiazole-5-carboxamide | BMS 354825 | 354825, BMS | BMS354825 | BMS-354825
Chemical Information
Molecular Formula C22H26ClN7O2S
CAS Registry Number 302962-49-8
SMILES CC1=C(C(=CC=C1)Cl)NC(=O)C2=CN=C(S2)NC3=CC(=NC(=N3)C)N4CCN(CC4)CCO
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)
Cytokine release syndrome10.02.01.0100.000392%
Ear discomfort04.03.01.0050.000381%Not Available
Eye oedema06.08.03.013--Not Available
Eye pruritus06.04.05.0060.001007%Not Available
Circumoral oedema23.04.01.012; 10.01.05.0130.000381%Not Available
Respiratory tract congestion22.02.07.0030.002048%Not Available
Lymphatic disorder01.09.01.003--Not Available
Diastolic dysfunction02.04.02.022--Not Available
Nasal discomfort22.12.03.0120.000437%Not Available
Paranasal sinus discomfort22.12.03.0180.000381%Not Available
Deafness bilateral04.02.01.0070.000112%Not Available
Drug tolerance decreased08.06.01.0240.001007%Not Available
Cardiac flutter02.03.02.0120.000437%Not Available
Musculoskeletal stiffness15.03.05.027--Not Available
Protein urine present13.13.02.006--Not Available
Epigastric discomfort07.01.02.0040.000381%Not Available
Musculoskeletal discomfort15.03.04.0010.000627%Not Available
Skin swelling23.03.03.039--Not Available
Vascular occlusion24.04.02.0150.000168%Not Available
Electrocardiogram PR prolongation13.14.05.012--Not Available
Blast cell crisis16.01.02.002; 01.10.02.0020.000224%Not Available
Growth retardation14.03.02.031; 05.03.02.007; 15.03.05.0160.000280%
Cerebral haematoma24.07.04.006; 17.08.01.014--Not Available
Affect lability19.04.01.001--Not Available
Haemorrhoidal haemorrhage24.10.02.001; 07.15.03.0020.000571%
Cerebral disorder17.02.10.0170.000246%Not Available
Haemorrhage24.07.01.002--Not Available
Pulmonary mass22.02.07.0040.000224%Not Available
Intra-abdominal haematoma24.07.02.034; 07.12.02.005--Not Available
Erythrosis01.05.01.014; 23.03.03.055--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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