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Avanafil for treatment of erectile dysfunction: review of its potential
Avanafil is a medication that was recently approved by the US Food and Drug Administration for the management of erectile dysfunction. Avanafil is a new phosphodiesterase type 5 inhibitor similar to sildenafil and tadalafil. Avanafil was studied in over 1300 patients during clinical trials, includin...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3433322/ https://www.ncbi.nlm.nih.gov/pubmed/22973106 http://dx.doi.org/10.2147/VHRM.S26712 |
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author | Burke, Ryan M Evans, Jeffery D |
author_facet | Burke, Ryan M Evans, Jeffery D |
author_sort | Burke, Ryan M |
collection | PubMed |
description | Avanafil is a medication that was recently approved by the US Food and Drug Administration for the management of erectile dysfunction. Avanafil is a new phosphodiesterase type 5 inhibitor similar to sildenafil and tadalafil. Avanafil was studied in over 1300 patients during clinical trials, including patients with diabetes mellitus and those who had undergone radical prostatectomy, and was found to be more effective than placebo in all men who were randomized to the drug. The medication was studied with on-demand dosing that may occur after food and/or alcohol. Avanafil is dosed as 50 mg, 100 mg, or 200 mg tablets. Avanafil may differentiate itself from the other phosphodiesterase type 5 inhibitors with its quicker onset and higher specificity for phosphodiesterase type 5 versus other phosphodiesterase subtypes, but may lead to complications of therapy. |
format | Online Article Text |
id | pubmed-3433322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-34333222012-09-12 Avanafil for treatment of erectile dysfunction: review of its potential Burke, Ryan M Evans, Jeffery D Vasc Health Risk Manag Original Research Avanafil is a medication that was recently approved by the US Food and Drug Administration for the management of erectile dysfunction. Avanafil is a new phosphodiesterase type 5 inhibitor similar to sildenafil and tadalafil. Avanafil was studied in over 1300 patients during clinical trials, including patients with diabetes mellitus and those who had undergone radical prostatectomy, and was found to be more effective than placebo in all men who were randomized to the drug. The medication was studied with on-demand dosing that may occur after food and/or alcohol. Avanafil is dosed as 50 mg, 100 mg, or 200 mg tablets. Avanafil may differentiate itself from the other phosphodiesterase type 5 inhibitors with its quicker onset and higher specificity for phosphodiesterase type 5 versus other phosphodiesterase subtypes, but may lead to complications of therapy. Dove Medical Press 2012 2012-08-29 /pmc/articles/PMC3433322/ /pubmed/22973106 http://dx.doi.org/10.2147/VHRM.S26712 Text en © 2012 Burke and Evans, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Burke, Ryan M Evans, Jeffery D Avanafil for treatment of erectile dysfunction: review of its potential |
title | Avanafil for treatment of erectile dysfunction: review of its potential |
title_full | Avanafil for treatment of erectile dysfunction: review of its potential |
title_fullStr | Avanafil for treatment of erectile dysfunction: review of its potential |
title_full_unstemmed | Avanafil for treatment of erectile dysfunction: review of its potential |
title_short | Avanafil for treatment of erectile dysfunction: review of its potential |
title_sort | avanafil for treatment of erectile dysfunction: review of its potential |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3433322/ https://www.ncbi.nlm.nih.gov/pubmed/22973106 http://dx.doi.org/10.2147/VHRM.S26712 |
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