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)
Scrotal disorder21.12.02.0090.000381%-
Renal impairment20.01.03.010---
Poor quality sleep17.15.04.002; 19.02.05.0050.000951%-
Peripheral arterial occlusive disease24.04.03.0100.000336%-
Increased upper airway secretion22.12.03.0070.000246%-
Neutropenic colitis01.02.03.010; 07.08.01.014---
Effusion08.01.03.0520.000112%-
Bowel movement irregularity07.02.03.0030.000761%-
Lipoedema14.08.04.021---
Gastrointestinal inflammation07.08.03.0070.000168%-
Exfoliative rash23.03.07.006---
Pulmonary arterial hypertension22.06.01.002; 24.08.03.0030.003123%-
Bone marrow failure01.03.03.005--
Incision site oedema12.02.05.038---
Chronic graft versus host disease10.02.01.029; 12.02.09.0030.000112%-
Cytopenia01.03.03.0120.001589%-
Haematological malignancy01.13.01.003; 16.21.01.0020.000112%-
Penile oedema21.12.01.007---
Liver injury09.01.07.022; 12.01.17.0120.000504%-
Oral disorder07.05.01.005---
Genital swelling21.10.01.010---
Vulvovaginal burning sensation21.08.02.0070.000381%-
Focal segmental glomerulosclerosis20.05.01.0030.000112%-
Oropharyngeal pain07.05.05.004; 22.12.03.0160.003571%
Epstein-Barr virus associated lymphoproliferative disorder01.13.02.002; 11.05.10.001; 16.21.02.0020.000224%-
Upper-airway cough syndrome22.12.03.0360.000437%
Gastrointestinal tract irritation07.08.03.0080.000246%-
Toxicity to various agents12.03.01.046---
Posterior reversible encephalopathy syndrome17.13.02.007--
Peripheral artery stenosis24.04.03.0170.000224%-
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ADReCS-Target
Drug Name ADR Term Target
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