Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Varenicline tartrate
Drug ID BADD_D02338
Description Varenicline is a prescription medication used to treat smoking addiction. This medication is the first approved nicotinic receptor partial agonist. Specifically, varenicline is a partial agonist of the alpha4/beta2 subtype of the nicotinic acetylcholine receptor. In addition it acts on alpha3/beta4 and weakly on alpha3beta2 and alpha6-containing receptors. A full agonism was displayed on alpha7-receptors. On March 9, 2015, the U.S. Food and Drug Administration warned that Varenicline, in the form of Pfizer Inc's quit-smoking drug, Chantix, has been associated with seizures and that some patients who drink while taking the drug may become aggressive or black out. Pfizer is conducting an additional safety study of the drug, results of which are expected in late 2015. The FDA said it is keeping the black box in place at least until the results of the trial are announced.
Indications and Usage For use as an aid in smoking cessation.
Marketing Status Prescription
ATC Code N07BA03
DrugBank ID DB01273
KEGG ID D06282
MeSH ID D000068580
PubChem ID 46783232
TTD Drug ID D0LM4A
NDC Product Code 43353-899; 49884-156; 65015-758; 0069-0469; 63539-473; 71205-381; 49884-155; 50090-4481; 50090-4482; 65977-0120; 0069-0468; 65372-1199; 50090-0995; 10829-1469; 42413-0179; 49884-944; 53296-0093; 65085-0073; 75945-040; 15894-0024; 0069-0471; 50090-0998; 10829-1468; 16436-0093; 63187-618; 60687-648
Synonyms Varenicline | 6,7,8,9-Tetrahydro-6,10-methano-6H-pyrazino(2,3-h)benzazepine | Chantix | Varenicline Tartrate | Champix
Chemical Information
Molecular Formula C17H19N3O6
CAS Registry Number 375815-87-5
SMILES C1C2CNCC1C3=CC4=NC=CN=C4C=C23.C(C(C(=O)O)O)(C(=O)O)O
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Myositis15.05.01.001--
Nausea07.01.07.001--
Nephrolithiasis20.04.01.002--
Night blindness14.12.03.001; 06.02.02.003--
Nightmare19.02.03.003--Not Available
Nocturia20.02.03.001--Not Available
Nystagmus17.02.02.006; 06.05.02.006--
Oedema14.05.06.010; 08.01.07.006--Not Available
Oesophagitis07.08.05.001--
Osteoporosis15.02.03.002; 14.04.04.002--
Palpitations02.01.02.003--
Pancreatitis acute07.18.01.002--Not Available
Panic attack19.06.04.001--Not Available
Paranoia19.05.01.005--Not Available
Parosmia17.04.04.002; 22.04.03.007--Not Available
Photophobia06.01.01.004; 17.17.02.006--
Photosensitivity reaction23.03.09.003--
Pleurisy22.05.01.001--Not Available
Polyuria20.02.03.002--Not Available
Pruritus23.03.12.001--
Psoriasis23.03.14.002; 10.02.01.036--Not Available
Psychomotor hyperactivity17.01.02.011; 19.11.02.003--Not Available
Pulmonary embolism24.01.06.001; 22.06.02.001--Not Available
Pyrexia08.05.02.003--
Rash23.03.13.001--Not Available
Renal failure20.01.03.005--Not Available
Respiratory disorder22.02.07.002--Not Available
Rhinorrhoea22.02.05.010--
Seizure17.12.03.001--
Sensory disturbance17.02.07.006--Not Available
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