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)
Hypercholesterolaemia14.08.01.001--Not Available
Hyperhidrosis08.01.03.028; 23.02.03.004--
Hyperplasia08.03.04.0080.000806%Not Available
Hypersensitivity10.01.03.003--
Hypersensitivity vasculitis24.12.04.013; 23.06.02.005; 10.02.02.017; 01.01.04.008--Not Available
Hypertension24.08.02.001--
Hypertensive encephalopathy24.08.05.001; 17.13.02.0020.000112%Not Available
Hypertensive heart disease02.11.02.001; 24.08.05.0020.000112%Not Available
Hyperthyroidism14.11.01.011; 05.02.02.001--
Hyperuricaemia14.09.01.0030.000246%
Hypervolaemia02.05.04.019; 14.05.06.0030.000414%Not Available
Hypoaesthesia23.03.03.081; 17.02.06.0230.009637%Not Available
Hypoalbuminaemia14.10.01.002; 09.01.02.0030.000168%
Hypocalcaemia14.04.01.004--
Hypogammaglobulinaemia10.03.02.0070.000224%Not Available
Hypokalaemia14.05.03.002--
Hypophosphataemia14.04.03.001--
Hypotension24.06.03.002--
Hypothyroidism14.11.01.012; 05.02.03.001--
Ileus07.13.01.001--
Immune system disorder10.02.01.0010.000627%Not Available
Increased tendency to bruise24.07.06.012; 23.06.01.009; 01.01.03.0050.000571%Not Available
Infection11.01.08.002--Not Available
Influenza like illness08.01.03.0100.002239%
Initial insomnia17.15.03.005; 19.02.01.0050.000381%Not Available
Insomnia19.02.01.002; 17.15.03.002--
Intermittent claudication24.04.03.0010.000224%Not Available
Interstitial lung disease10.02.01.033; 22.01.02.003--Not Available
Intestinal ulcer07.04.06.0030.000112%Not Available
Intracranial pressure increased17.07.02.0020.000168%Not Available
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ADReCS-Target
Drug Name ADR Term Target
Tip:  Drug Name  ADR Term  Protein  Variation  Gene