Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Conivaptan
Drug ID BADD_D00526
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 D07748
MeSH ID C106389
PubChem ID 151171
TTD Drug ID D0VU2X
NDC Product Code Not Available
UNII 0NJ98Y462X
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 C32H26N4O2
CAS Registry Number 210101-16-9
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
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)
Oral candidiasis07.05.07.001; 11.03.03.004---
Orthostatic hypotension17.05.01.020; 24.06.03.004---
Pain08.01.08.004--
Phlebitis12.02.01.002; 24.12.03.004--
Pneumonia11.01.09.003; 22.07.01.003---
Pollakiuria20.02.02.007--
Polyuria20.02.03.002---
Pruritus23.03.12.001--
Sepsis11.01.11.003--
Skin disorder23.03.03.007---
Thirst08.01.09.021; 14.03.02.007---
Urethral disorder20.07.01.002---
Urinary tract disorder20.08.01.001---
Urinary tract infection11.01.14.004; 20.08.02.001--
Vomiting07.01.07.003--
Infusion site erythema08.02.05.008; 12.07.05.009; 23.03.06.016---
Lymphatic disorder01.09.01.003---
Infusion site pain08.02.05.014; 12.07.05.002---
Infusion site swelling08.02.05.002; 12.07.05.003---
Infusion site phlebitis08.02.05.003; 12.07.05.004; 24.12.03.002---
Infusion site reaction08.02.05.005; 12.07.05.006---
Post procedural diarrhoea07.02.01.003; 12.02.03.009---
Angiopathy24.03.02.007---
Urine output increased13.13.03.002---
Cardiac disorder02.11.01.003---
Infestation11.09.01.001; 23.11.01.002---
Malnutrition14.03.02.004---
Mediastinal disorder22.09.03.001---
Mental disorder19.07.01.002---
Blood disorder01.05.01.004---
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