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)
Tongue disorder07.14.01.002---
Tongue neoplasm malignant stage unspecified07.21.07.003; 16.13.07.0030.000112%-
Tongue oedema07.14.02.007; 10.01.05.008; 23.04.01.009---
Tooth disorder07.09.05.0010.001388%-
Toothache07.09.06.0010.001007%
Transient ischaemic attack17.08.04.001; 24.04.06.005--
Tremor17.01.06.002--
Tricuspid valve incompetence02.07.05.0010.000224%-
Trigeminal neuralgia17.04.08.0010.000112%-
Tumour lysis syndrome14.05.01.004; 16.32.03.0020.000448%
Ulcer08.03.06.0010.000414%-
Upper respiratory tract infection11.01.13.009; 22.07.03.011--
Urethral disorder20.07.01.002---
Urinary tract disorder20.08.01.0010.000246%-
Urticaria10.01.06.001; 23.04.02.001--
Urticaria vesiculosa10.01.06.008; 23.04.02.008---
Uterine haemorrhage21.07.01.005; 24.07.03.0040.000224%
Uveitis06.04.03.003; 10.02.01.0230.000302%
Vaginal haemorrhage21.08.01.001; 24.07.03.005--
Ventricular arrhythmia02.03.04.006--
Ventricular tachycardia02.03.04.010--
Vertigo04.04.01.003; 17.02.12.002--
Viral infection11.05.04.001---
Vision blurred06.02.06.007; 17.17.01.010--
Visual acuity reduced06.02.10.012; 17.17.01.011--
Visual impairment06.02.10.013---
Vitreous haemorrhage06.10.03.001; 24.07.05.0050.000112%
Vomiting07.01.07.003--
Weight decreased13.15.01.005--
Weight increased13.15.01.006--
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ADReCS-Target
Drug Name ADR Term Target
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