Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Zafirlukast
Drug ID BADD_D02377
Description Zafirlukast is an oral leukotriene receptor antagonist (LTRA) for the maintenance treatment of asthma, often used in conjunction with an inhaled steroid and/or long-acting bronchodilator. It is available as a tablet and is usually dosed twice daily. Another leukotriene receptor antagonist is montelukast (Singulair), which is usually taken just once daily. Zafirlukast blocks the action of the cysteinyl leukotrienes on the CysLT1 receptors, thus reducing constriction of the airways, build-up of mucus in the lungs and inflammation of the breathing passages.
Indications and Usage For the prophylaxis and chronic treatment of asthma.
Marketing Status Prescription
ATC Code R03DC01
DrugBank ID DB00549
KEGG ID D00411
MeSH ID C062735
PubChem ID 5717
TTD Drug ID D05DVP
NDC Product Code 55111-626; 49884-549; 55111-625; 68084-059; 49884-590; 49884-554; 0904-6646; 31722-007; 31722-008; 50370-0008; 63629-2102; 49884-589; 52562-800; 65977-0113; 52562-801; 55111-886
Synonyms zafirlukast | 4-(5-cyclopentyloxycarbonylamino-2-methylindol-3-yl-methyl)-3-methoxy-N-O-tolylsulfonylbenzamide | Olmoran | ICI 204,219 | ICI-204219 | ICI 204219 | Accolate | Aeronix
Chemical Information
Molecular Formula C31H33N3O6S
CAS Registry Number 107753-78-6
SMILES CC1=CC=CC=C1S(=O)(=O)NC(=O)C2=CC(=C(C=C2)CC3=CN(C4=C3C=C(C=C4)NC(=O)OC5CCCC5)C)O C
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Drug level decreasedCytochrome P450 2C9P11712T19244806430; 5458032; 1109248
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abdominal discomfort07.01.06.001--Not Available
Abdominal pain07.01.05.002--
Agranulocytosis01.02.03.001--Not Available
Alanine aminotransferase increased13.03.01.003--
Angioedema23.04.01.001; 10.01.05.009--Not Available
Arthralgia15.01.02.001--
Asthenia08.01.01.001--Not Available
Back pain15.03.04.005--
Blister23.03.01.001; 12.01.06.002--Not Available
Blood caffeine increased13.17.02.004--Not Available
Body temperature increased13.15.01.001--Not Available
Death08.04.01.001--
Depression19.15.01.001--
Dermatitis23.03.04.002--Not Available
Dermatitis bullous23.03.01.002--
Diarrhoea07.02.01.001--
Discomfort08.01.08.003--Not Available
Dizziness24.06.02.007; 17.02.05.003; 02.01.02.004--
Dyspepsia07.01.02.001--
Eosinophilia01.02.04.001--
Eosinophilic pneumonia22.01.01.004; 01.02.04.003--Not Available
Fatigue08.01.01.002--
Feeling abnormal08.01.09.014--Not Available
Gastrointestinal disorder07.11.01.001--Not Available
Gastrointestinal pain07.01.05.005--
Haematemesis24.07.02.011; 07.12.02.002--Not Available
Haemoglobin13.01.05.018--Not Available
Haemoptysis24.07.01.006; 22.02.03.004; 02.01.02.006--Not Available
Headache17.14.01.001--
Hepatic failure09.01.03.002--
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