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)
Skin exfoliation23.03.07.0030.002642%Not Available
Skin hypopigmentation23.05.02.0030.001007%
Skin irritation23.03.04.0090.001332%Not Available
Skin lesion23.03.03.0100.001310%Not Available
Skin reaction23.03.03.013; 10.01.03.019--Not Available
Skin ulcer23.07.03.003; 24.04.03.007--
Sleep apnoea syndrome22.02.01.013; 19.02.05.002; 17.15.05.0010.000414%
Somnolence19.02.05.003; 17.02.04.006--
Splenomegaly01.09.02.0010.001321%Not Available
Stevens-Johnson syndrome12.03.01.014; 11.07.01.005; 10.01.01.045; 23.03.01.007--
Stomatitis07.05.06.005--
Stress19.06.02.004--Not Available
Subarachnoid haemorrhage24.07.04.004; 17.08.01.010; 12.01.10.011--Not Available
Subdural haematoma24.07.04.005; 17.08.05.002; 12.01.10.003--Not Available
Swelling08.01.03.0150.008786%Not Available
Swelling face08.01.03.100; 23.04.01.018; 10.01.05.0180.004634%Not Available
Syncope17.02.04.008; 02.11.04.015; 24.06.02.012--
Systemic lupus erythematosus rash23.03.13.007; 15.06.02.005; 10.04.03.005--Not Available
T-cell lymphoma16.17.02.001; 11.05.17.006; 01.11.02.0010.000112%Not Available
Tachycardia02.03.02.007--Not Available
Tendonitis15.07.01.003; 12.01.07.007--Not Available
Tension19.06.02.0050.000302%Not Available
Therapeutic response decreased08.06.01.016--Not Available
Thrombocytopenia01.08.01.0020.006503%Not Available
Thrombocytosis01.08.02.0010.000358%Not Available
Thrombophlebitis24.01.02.001--Not Available
Thrombosis24.01.01.006--Not Available
Thrombotic thrombocytopenic purpura24.07.06.014; 23.06.01.011; 01.08.01.0050.000112%
Thyroiditis05.02.04.0010.000112%Not Available
Tinnitus17.04.07.004; 04.04.01.0020.003761%
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ADReCS-Target
Drug Name ADR Term Target
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