Document Detail

ACS chemical neuroscience molecule spotlight on Potiga (Ezogabine).
MedLine Citation:
PMID:  22896808     Owner:  NLM     Status:  MEDLINE    
On June 10th, 2011, the U.S. Food and Drug Administration approved Potiga (ezogabine) as an add-on medication for the treatment of seizures in adults, and it is being developed by Valeant Pharmaceuticals.
Corey R Hopkins
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Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  ACS chemical neuroscience     Volume:  3     ISSN:  1948-7193     ISO Abbreviation:  ACS Chem Neurosci     Publication Date:  2012 Aug 
Date Detail:
Created Date:  2012-08-16     Completed Date:  2013-04-10     Revised Date:  2013-08-18    
Medline Journal Info:
Nlm Unique ID:  101525337     Medline TA:  ACS Chem Neurosci     Country:  United States    
Other Details:
Languages:  eng     Pagination:  632     Citation Subset:  IM    
Vanderbilt Center for Neuroscience Drug Discovery, Department of Pharmacology and Chemistry, Vanderbilt University Medical Center, Vanderbilt University, Nashville, Tennessee 37232-6600, USA.
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MeSH Terms
Anticonvulsants / pharmacology*,  therapeutic use
Carbamates / pharmacology*,  therapeutic use
Epilepsy / drug therapy
KCNQ Potassium Channels / agonists
Phenylenediamines / pharmacology*,  therapeutic use
Potassium Channels / agonists
Randomized Controlled Trials as Topic
Seizures / prevention & control
United States
United States Food and Drug Administration
Reg. No./Substance:
0/Anticonvulsants; 0/Carbamates; 0/KCNQ Potassium Channels; 0/Phenylenediamines; 0/Potassium Channels; 12G01I6BBU/ezogabine

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

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