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%-
Neutrophilic dermatosis01.02.01.013; 23.03.03.0590.000414%-
Troponin increased13.04.01.004---
Enterocolitis infectious07.19.01.005; 11.01.07.009--
Disturbance in sexual arousal19.08.04.003---
Hepatic vein occlusion09.01.06.011; 24.04.07.0050.000112%-
Gastrointestinal toxicity07.08.03.006; 12.03.01.0190.000280%-
Ventricular dysfunction02.04.02.005---
Intestinal haemorrhage07.12.03.005; 24.07.02.0310.000224%-
Angiopathy24.03.02.0070.000168%-
Protein-losing gastroenteropathy07.11.01.013; 14.03.02.015---
Pleuropericarditis02.06.02.003; 22.05.01.002---
Skin toxicity12.03.01.020; 23.03.03.0320.000504%-
Drug resistance08.06.01.0050.002194%-
Hot flush08.01.03.027; 21.02.02.001; 24.03.01.0050.003862%
Neurological symptom17.02.05.0100.000112%-
Adverse event08.06.01.0100.056334%-
Bacterial infection11.02.01.005---
Pneumonia bacterial11.02.01.009; 22.07.06.004---
Ventricular failure02.05.01.007---
Appetite disorder14.03.01.004; 19.09.01.0020.000437%-
Breast disorder21.05.04.004---
Cardiac disorder02.11.01.0030.003895%-
Connective tissue disorder10.04.04.026; 15.06.01.006---
Embolism24.01.01.009--
Haematotoxicity01.05.01.007; 12.03.01.0250.000750%-
Infestation11.09.01.001; 23.11.01.002---
Inflammation08.01.05.007; 10.02.01.089---
Malnutrition14.03.02.004---
Mediastinal disorder22.09.03.001---
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ADReCS-Target
Drug Name ADR Term Target
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