Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Bosentan
Drug ID BADD_D00285
Description Bosentan is a dual endothelin receptor antagonist marketed under the trade name Tracleer by Actelion Pharmaceuticals. Bosentan is used to treat pulmonary hypertension by blocking the action of endothelin molecules that would otherwise promote narrowing of the blood vessels and lead to high blood pressure.
Indications and Usage Used in the treatment of pulmonary arterial hypertension (PAH), to improve exercise ability and to decrease the rate of clinical worsening (in patients with WHO Class III or IV symptoms).
Marketing Status Prescription
ATC Code C02KX01
DrugBank ID DB00559
KEGG ID D01227
MeSH ID D000077300
PubChem ID 104865
TTD Drug ID D0U4CE
NDC Product Code 68382-447; 68180-387; 46708-881; 65162-873; 49884-058; 66215-103; 0054-0521; 65162-874; 0591-2512; 47781-271; 65015-770; 66215-101; 68382-446; 49884-059; 53104-7703; 47335-039; 0054-0520; 82245-0104; 0591-2511; 14501-0041; 66215-232; 47335-038; 70771-1018; 66215-102; 70771-1017; 66039-870; 47781-270; 68180-386; 65015-753
Synonyms Bosentan | 4-t-Butyl-N-(6-(2-hydroxyethoxy)-5-(2-methoxyphenoxy)-2,2'-bipyrimidin-4-yl)benzenesulfonamide | Bosentan Monohydrate | Tracleer | Bosentan Anhydrous | Ro 47-0203 | Ro 47 0203 | Ro 470203 | Ro-47-0203
Chemical Information
Molecular Formula C27H29N5O6S
CAS Registry Number 147536-97-8
SMILES CC(C)(C)C1=CC=C(C=C1)S(=O)(=O)NC2=C(C(=NC(=N2)C3=NC=CC=N3)OCCO)OC4=CC=CC=C4OC
Chemical Structure
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Blood sodium decreased13.11.01.0120.001341%Not Available
Blood sodium increased13.11.01.0130.000447%Not Available
Blood urea increased13.13.01.0060.001788%Not Available
Body temperature increased13.15.01.001--Not Available
Bone disorder15.02.04.004--Not Available
Bradycardia02.03.02.002--Not Available
Brain abscess11.01.03.003; 17.06.07.0010.000117%Not Available
Breast cancer16.10.01.001; 21.05.01.0030.005365%Not Available
Bronchiolitis11.05.04.008; 22.03.02.0040.000671%Not Available
Bronchitis11.01.09.001; 22.07.01.0010.013413%
Bronchopulmonary dysplasia18.04.10.001; 22.11.01.0010.000292%Not Available
Bronchospasm10.01.03.012; 22.03.01.004--
C-reactive protein increased13.09.01.007--Not Available
Cachexia08.01.01.009; 14.03.02.001; 16.32.03.0110.000117%Not Available
Carbon dioxide increased13.02.01.0110.002012%Not Available
Cardiac arrest02.03.04.0010.003732%
Cardiac failure02.05.01.0010.007173%
Cardiac failure acute02.05.01.0050.000642%Not Available
Cardiac failure congestive02.05.01.0020.007931%Not Available
Cardiac murmur13.14.01.0010.000671%Not Available
Cardiac output decreased13.14.02.0010.000175%Not Available
Cardiac tamponade02.06.01.001--
Cardio-respiratory arrest02.03.04.002; 22.02.06.0070.001575%Not Available
Cardiogenic shock02.05.01.003; 24.06.02.0060.001341%Not Available
Cardiomegaly02.04.02.0010.000408%Not Available
Cardiomyopathy02.04.01.001--Not Available
Cataract06.06.01.001--
Cellulitis11.02.01.001; 23.09.01.0010.010731%Not Available
Cerebral haemorrhage17.08.01.003; 24.07.04.001--Not Available
Cerebral infarction17.08.01.004; 24.04.06.002--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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