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)
Temperature intolerance08.01.09.0220.000437%Not Available
Neutrophilic dermatosis23.03.03.059; 01.02.01.0130.000414%Not Available
Troponin increased13.04.01.004--Not Available
Enterocolitis infectious07.19.01.005; 11.01.07.009--
Disturbance in sexual arousal19.08.04.003--Not Available
Hepatic vein occlusion24.04.07.005; 09.01.06.0110.000112%Not Available
Gastrointestinal toxicity12.03.01.019; 07.08.03.0060.000280%Not Available
Ventricular dysfunction02.04.02.005--Not Available
Intestinal haemorrhage24.07.02.031; 07.12.03.0050.000224%Not Available
Angiopathy24.03.02.0070.000168%Not Available
Protein-losing gastroenteropathy14.03.02.015; 07.11.01.013--Not Available
Pleuropericarditis02.06.02.003; 22.05.01.002--Not Available
Skin toxicity23.03.03.032; 12.03.01.0200.000504%Not Available
Drug resistance08.06.01.0050.002194%Not Available
Hot flush21.02.02.001; 08.01.03.027; 24.03.01.0050.003862%
Neurological symptom17.02.05.0100.000112%Not Available
Adverse event08.06.01.0100.056334%Not Available
Bacterial infection11.02.01.005--Not Available
Pneumonia bacterial22.07.06.004; 11.02.01.009--Not Available
Ventricular failure02.05.01.007--Not Available
Appetite disorder19.09.01.002; 14.03.01.0040.000437%Not Available
Breast disorder21.05.04.004--Not Available
Cardiac disorder02.11.01.0030.003895%Not Available
Connective tissue disorder15.06.01.006; 10.04.04.026--Not Available
Embolism24.01.01.009--
Haematotoxicity12.03.01.025; 01.05.01.0070.000750%Not Available
Infestation23.11.01.002; 11.09.01.001--Not Available
Inflammation10.02.01.089; 08.01.05.007--Not Available
Malnutrition14.03.02.004--Not Available
Mediastinal disorder22.09.03.001--Not Available
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ADReCS-Target
Drug Name ADR Term Target
Tip:  Drug Name  ADR Term  Protein  Variation  Gene