Conivaptan
File:Conivaptan structure.svg | |
Clinical data | |
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Routes of administration | iv |
Pharmacokinetic data | |
Bioavailability | N/A |
Identifiers | |
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CAS Number | |
PubChem CID | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C32H26N4O2 |
Molar mass | 498.583 |
WikiDoc Resources for Conivaptan |
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Most recent articles on Conivaptan |
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Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Conivaptan at Clinical Trials.gov Clinical Trials on Conivaptan at Google
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Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Conivaptan
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Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Conivaptan Discussion groups on Conivaptan Patient Handouts on Conivaptan Directions to Hospitals Treating Conivaptan Risk calculators and risk factors for Conivaptan
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Healthcare Provider Resources |
Causes & Risk Factors for Conivaptan |
Continuing Medical Education (CME) |
International |
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Business |
Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Conivaptan (vaprisol®, YM 087) 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), and there is some evidence it may be effective in heart failure. It is marketed by Astellas Pharma Inc.
Mechanism of Action
Conivaptan inhibits both isotypes of the vasopressin receptor (V1a and V2). Effectively, it causes iatrogenic nephrogenic diabetes insipidus.
See also
References
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- Hormonal agents
- Diuretics
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