Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Conivaptan hydrochloride
Drug ID BADD_D00527
Description Conivaptan is a non-peptide inhibitor of antidiuretic hormone (vasopressin). It was approved in 2004 for hyponatremia (low blood sodium levels) caused by syndrome of inappropriate antidiuretic hormone (SIADH). Conivaptan inhibits both isotypes of the vasopressin receptor (V1a and V2).
Indications and Usage For the treatment of euvolemic or hypervolemic hyponatremia (e.g. the syndrome of inappropriate secretion of antidiuretic hormone, or in the setting of hypothyroidism, adrenal insufficiency, pulmonary disorders, etc.) in hospitalized patients.
Marketing Status approved; investigational
ATC Code C03XA02
DrugBank ID DB00872
KEGG ID D01236
MeSH ID C106389
PubChem ID 216322
TTD Drug ID D0VU2X
NDC Product Code Not Available
UNII 75L57R6X36
Synonyms conivaptan | 4''-((4,5-dihydro-2-methylimidazo(4,5-D)(1)benzazepin-6(1H)-yl)carbonyl)-2-biphenylcarboxanilide | (1,1'-biphenyl)-2-carboxamide, N-(4-((4,5-dihydro-2-methylimidazo(4,5-D)(1)benzazepin-6(1H)-yl)carbonyl)phenyl)- | YM 087 | YM087 | conivaptan hydrochloride | (1,1'-biphenyl)-2-carboxamide, N-(4-((4,5-dihydro-2-methylimidazo(4,5-D)(1)benzazepin-6(1H)-yl)carbonyl)phenyl)-, monohydrochloride | Vaprisol
Chemical Information
Molecular Formula C32H27ClN4O2
CAS Registry Number 168626-94-6
SMILES CC1=NC2=C(N1)CCN(C3=CC=CC=C32)C(=O)C4=CC=C(C=C4)NC(=O)C5=CC=CC=C5C6=CC=CC=C6.Cl
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)
Anaemia01.03.02.001--
Atrial fibrillation02.03.03.002--
Confusional state19.13.01.001; 17.02.03.005--
Constipation07.02.02.001--
Diarrhoea07.02.01.001--
Electrocardiogram ST segment depression13.14.05.005--Not Available
Headache17.14.01.001--
Hypertension24.08.02.001--
Hypokalaemia14.05.03.002--
Hypomagnesaemia14.04.02.001--
Hyponatraemia14.05.04.002--
Hypotension24.06.03.002--
Insomnia19.02.01.002; 17.15.03.002--
Laryngeal pain22.12.03.010--
Nausea07.01.07.001--
Oedema peripheral14.05.06.011; 08.01.07.007; 02.05.04.007--
Orthostatic hypotension24.06.03.004; 17.05.01.020--Not Available
Pneumonia22.07.01.003; 11.01.09.003--Not Available
Pruritus23.03.12.001--
Pyrexia08.05.02.003--
Thirst14.03.02.007; 08.01.09.021--Not Available
Urinary tract infection20.08.02.001; 11.01.14.004--
Vomiting07.01.07.003--
Infusion site erythema23.03.06.016; 12.07.05.009; 08.02.05.008--Not Available
Infusion site pain08.02.05.014; 12.07.05.002--Not Available
Infusion site phlebitis24.12.03.002; 12.07.05.004; 08.02.05.003--Not Available
Infusion site reaction12.07.05.006; 08.02.05.005--Not Available
Post procedural diarrhoea07.02.01.003; 12.02.03.009--Not Available
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