Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Sitaxentan
Drug ID BADD_D02031
Description Sitaxentan was marketed under the trade name Thelin for the treatment of pulmonary arterial hypertension (PAH) by Encysive Pharmaceuticals until Pfizer purchased Encysive in February 2008. In 2010, Pfizer voluntarily removed sitaxentan from the market over concerns of hepatotoxicity.
Indications and Usage Investigated for use/treatment in pulmonary hypertension, connective tissue diseases, hypertension, and congestive heart failure.
Marketing Status approved; investigational; withdrawn
ATC Code C02KX03
DrugBank ID DB06268
KEGG ID D07171
MeSH ID C106276
PubChem ID 216235
TTD Drug ID D0T1RG
NDC Product Code Not Available
UNII J9QH779MEM
Synonyms sitaxsentan | N-(4-chloro-3-methyl-5-isoxazolyl)-2-(3,4-(methylenedioxy)-6-methyl)phenylacetyl-3-thiophenesulfonamide | N-(4-chloro-3-methyl-5-isoxazolyl)-2-((4,5-(methylenedioxy)-O-toly)acetyl)-3-thiophenesulfonamide | TBC-11251 | TBC 11251 | TBC11251
Chemical Information
Molecular Formula C18H15ClN2O6S2
CAS Registry Number 184036-34-8
SMILES CC1=CC2=C(C=C1CC(=O)C3=C(C=CS3)S(=O)(=O)NC4=C(C(=NO4)C)Cl)OCO2
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)
Ventricular tachycardia02.03.04.010--
Vertigo17.02.12.002; 04.04.01.003--
Viral infection11.05.04.001--Not Available
Visual impairment06.02.10.013--Not Available
Vitreous floaters06.09.01.005--
Vomiting07.01.07.003--
Weight decreased13.15.01.005--
Wheezing22.03.01.009--
White blood cell count decreased13.01.06.012--
Tubulointerstitial nephritis20.05.02.002--Not Available
Fibromyalgia15.05.02.002--Not Available
Post thrombotic syndrome24.01.01.019--Not Available
Urosepsis11.01.11.005; 20.08.02.002--Not Available
Breast calcifications21.05.04.009--Not Available
Localised oedema02.05.04.006; 14.05.06.009; 08.01.07.011--
Weight fluctuation14.03.02.002--Not Available
Nocturnal dyspnoea02.11.05.009; 22.02.01.019--Not Available
Gastrointestinal fungal infection11.03.05.018; 07.19.02.013--Not Available
Muscle fatigue15.05.03.006--Not Available
Sputum purulent22.02.03.008; 11.01.09.009--Not Available
Blood phosphorus increased13.11.01.016--Not Available
Cerumen impaction04.01.01.001--Not Available
Contusion24.07.06.001; 23.03.11.002; 12.01.06.001; 15.03.05.007--
Musculoskeletal chest pain22.09.01.001; 15.03.04.012--
Post procedural haemorrhage24.07.01.014; 12.02.05.004--
Catheter site haemorrhage24.07.01.003; 12.07.02.002; 08.02.02.002--Not Available
Puncture site haemorrhage24.07.01.034; 08.02.04.007; 12.07.04.006--Not Available
Viral diarrhoea11.05.04.012; 07.19.02.008--Not Available
Large intestine polyp16.05.02.006; 07.20.01.010--Not Available
Acute coronary syndrome24.04.04.011; 02.02.02.015--Not Available
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