<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"><channel rdf:about="http://onlinelibrary.wiley.com/rss/journal/10.1002/(ISSN)1931-2261" xmlns="http://purl.org/rss/1.0/"><title>Future Prescriber</title><description> Wiley Online Library : Future Prescriber</description><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2F%28ISSN%291931-2261</link><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc</dc:publisher><dc:language xmlns:dc="http://purl.org/dc/elements/1.1/">en</dc:language><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/">Copyright © John Wiley &amp; Sons Ltd, The Atrium, Southern Gate, Chichester, West Sussex PO19 8SQ</dc:rights><prism:issn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1468-9871</prism:issn><prism:eIssn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1931-2261</prism:eIssn><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-01T00:00:00-05:00</dc:date><prism:coverDisplayDate xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">December 2012</prism:coverDisplayDate><prism:volume xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">13</prism:volume><prism:number xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">3</prism:number><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">5</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">23</prism:endingPage><image rdf:resource="http://onlinelibrary.wiley.com/store/10.1002/fps.v13.3/asset/cover.gif?v=1&amp;s=581a87bf3156e11fdb640ef50ea2e1e6a289bb09"/><items><rdf:Seq><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.96"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.97"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.98"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.99"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.100"/></rdf:Seq></items></channel><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.96" xmlns="http://purl.org/rss/1.0/"><title>Dexmedetomidine: a unique clinical profile in ICU sedation</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.96</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Dexmedetomidine: a unique clinical profile in ICU sedation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Steve Chaplin</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-16T10:50:54.187711-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/fps.96</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/fps.96</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.96</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Drug Profile</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">5</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">9</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Dexmedetomidine is a sedating agent with a pharmacological and therapeutic profile that is unlike those of the most commonly used sedative agents (midazolam and propofol). In this article, we provide an over view of dexmedetomidine in terms of its pharmacokinetics and pharmacodynamics, and describe its place in the management of patients in intensive care. Copyright © 2013 John Wiley &amp; Sons, Ltd.</p></div>
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Dexmedetomidine is a sedating agent with a pharmacological and therapeutic profile that is unlike those of the most commonly used sedative agents (midazolam and propofol). In this article, we provide an over view of dexmedetomidine in terms of its pharmacokinetics and pharmacodynamics, and describe its place in the management of patients in intensive care. Copyright © 2013 John Wiley &amp; Sons, Ltd.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.97" xmlns="http://purl.org/rss/1.0/"><title>Mirabegron use in the treatment of overactive bladder symptoms</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.97</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Mirabegron use in the treatment of overactive bladder symptoms</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G Alessandro Digesu, Michelle Gore, Vik Khullar</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-16T10:50:54.187711-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/fps.97</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/fps.97</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.97</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Drug Profile</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">13</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Beta-3 adrenoreceptors have been proposed as a target in the treatment of OAB due to their role in the mediation of bladder smooth muscle relaxation. Mirabegron is an oral medication that selectively targets beta-3 adrenoreceptors and has been shown to reduce rhythmic abnormal detrusor contractions in animal models. In this Drug profile the authors present the clinical data relating to its efficacy and adverse effects and discuss its potential place in the treatment of OAB. Copyright © 2013 John Wiley &amp; Sons, Ltd.</p></div>
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Beta-3 adrenoreceptors have been proposed as a target in the treatment of OAB due to their role in the mediation of bladder smooth muscle relaxation. Mirabegron is an oral medication that selectively targets beta-3 adrenoreceptors and has been shown to reduce rhythmic abnormal detrusor contractions in animal models. In this Drug profile the authors present the clinical data relating to its efficacy and adverse effects and discuss its potential place in the treatment of OAB. Copyright © 2013 John Wiley &amp; Sons, Ltd.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.98" xmlns="http://purl.org/rss/1.0/"><title>Linaclotide for irritable bowel syndrome with constipation</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.98</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Linaclotide for irritable bowel syndrome with constipation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Steve Chaplin</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-16T10:50:54.187711-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/fps.98</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/fps.98</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.98</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Drug Profile</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">14</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">16</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Linaclotide is a guanylate cyclase agonist that promotes increased stool water content, which increases bowel movement frequency. It has recently received a positive opinion from the CHMP for the treatment of constipation-predominant IBS. In this Drug profile Steve Chaplin presents the clinical data relating to its efficacy and adverse events. Copyright © 2013 John Wiley &amp; Sons, Ltd.</p></div>
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Linaclotide is a guanylate cyclase agonist that promotes increased stool water content, which increases bowel movement frequency. It has recently received a positive opinion from the CHMP for the treatment of constipation-predominant IBS. In this Drug profile Steve Chaplin presents the clinical data relating to its efficacy and adverse events. Copyright © 2013 John Wiley &amp; Sons, Ltd.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.99" xmlns="http://purl.org/rss/1.0/"><title>Ingenol mebutate: a novel topical agent for actinic keratosis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.99</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ingenol mebutate: a novel topical agent for actinic keratosis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Colin A Morton</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-16T10:50:54.187711-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/fps.99</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/fps.99</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.99</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Drug Profile</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">17</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">19</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Ingenol mebutate is a once-daily topical treatment for actinic keratosis (AK) that is applied for only two or three days depending on body site. It has recently been approved by the FDA for the treatment of AK on the face, scalp, trunk and extremities and recommended for approval by the CHMP in September 2012. In this drug profile, the author reviews its mode of action, efficacy and tolerability and comments on the drug's likely place in practice. Copyright © 2013 John Wiley &amp; Sons, Ltd.</p></div>
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Ingenol mebutate is a once-daily topical treatment for actinic keratosis (AK) that is applied for only two or three days depending on body site. It has recently been approved by the FDA for the treatment of AK on the face, scalp, trunk and extremities and recommended for approval by the CHMP in September 2012. In this drug profile, the author reviews its mode of action, efficacy and tolerability and comments on the drug's likely place in practice. Copyright © 2013 John Wiley &amp; Sons, Ltd.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.100" xmlns="http://purl.org/rss/1.0/"><title>Ruxolitinib: JAK2 inhibitor for treatment of myelofibrosis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.100</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ruxolitinib: JAK2 inhibitor for treatment of myelofibrosis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Adam Mead</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-16T10:50:54.187711-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/fps.100</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/fps.100</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Ffps.100</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Drug Profile</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">20</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">23</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Ruxolitinib is an orally administered JAK2 inhibitor for the treatment of disease-related splenomegaly or symptoms in primary myelofibrosis or myelofibrosis due to polycythaemia vera or essential thrombocythaemia. In our Drug profile Dr Adam Mead presents the clinical data relating to its efficacy and adverse events and comments on its place in therapy. Copyright © 2013 John Wiley &amp; Sons, Ltd.</p></div>
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Ruxolitinib is an orally administered JAK2 inhibitor for the treatment of disease-related splenomegaly or symptoms in primary myelofibrosis or myelofibrosis due to polycythaemia vera or essential thrombocythaemia. In our Drug profile Dr Adam Mead presents the clinical data relating to its efficacy and adverse events and comments on its place in therapy. Copyright © 2013 John Wiley &amp; Sons, Ltd.
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