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<channel>
	<title>Online Pharmacy US &#187; anxiety</title>
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	<link>http://medsnetic.com/blog</link>
	<description>Viagra, Xanax, Cialis, Phentermine, Levitra</description>
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		<title>Sun Pharma receives USFDA nod for anti-anxiety drug</title>
		<link>http://medsnetic.com/blog/2010/08/04/sun-pharma-receives-usfda-nod-for-anti-anxiety-drug/</link>
		<comments>http://medsnetic.com/blog/2010/08/04/sun-pharma-receives-usfda-nod-for-anti-anxiety-drug/#comments</comments>
		<pubDate>Wed, 04 Aug 2010 13:40:14 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[anti]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[Drug]]></category>
		<category><![CDATA[Pharma]]></category>
		<category><![CDATA[Receives]]></category>
		<category><![CDATA[USFDA]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/08/04/sun-pharma-receives-usfda-nod-for-anti-anxiety-drug/</guid>
		<description><![CDATA[ Sun Pharmaceutical Industries today said that it has received the US Food and Drug Administration&#8217;s nod to market a generic version of alprazolam, an anti-anxiety drug, in the US market. (Source: The Economic Times Healthcare and Biotech News)
   MedWorm Message:   Register for MedMatcha, MedWorm&#8217;s medical advertising network, and receive $5 [...]]]></description>
			<content:encoded><![CDATA[<p> Sun Pharmaceutical Industries today said that it has received the US Food and Drug Administration&#8217;s nod to market a generic version of alprazolam, an anti-anxiety drug, in the US market. (Source: The Economic Times Healthcare and Biotech News)
<p>  <i> MedWorm Message: </i>  Register for MedMatcha, MedWorm&#8217;s medical advertising network, and receive $5 free advertising. </p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Despite Known Health Risks Long-Term Use Of Anti-Anxiety Drugs Continues In B.C.</title>
		<link>http://medsnetic.com/blog/2010/06/06/despite-known-health-risks-long-term-use-of-anti-anxiety-drugs-continues-in-b-c-2/</link>
		<comments>http://medsnetic.com/blog/2010/06/06/despite-known-health-risks-long-term-use-of-anti-anxiety-drugs-continues-in-b-c-2/#comments</comments>
		<pubDate>Sun, 06 Jun 2010 00:56:49 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[anti]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[Continues]]></category>
		<category><![CDATA[Despite]]></category>
		<category><![CDATA[Drugs]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[Known]]></category>
		<category><![CDATA[Long]]></category>
		<category><![CDATA[Risks]]></category>
		<category><![CDATA[Term]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/06/06/despite-known-health-risks-long-term-use-of-anti-anxiety-drugs-continues-in-b-c-2/</guid>
		<description><![CDATA[ Drugs to treat anxiety and sleep disorders are still being prescribed for extended periods to British Columbian patients &#8211; and i ncreasingly so for baby boomers &#8211; despite warnings against long-term use, according to a University of British Columbia study. Published online in the journal Health Policy, the study by researchers at UBC&#8217;s Centre [...]]]></description>
			<content:encoded><![CDATA[<p> Drugs to treat anxiety and sleep disorders are still being prescribed for extended periods to British Columbian patients &#8211; and i ncreasingly so for baby boomers &#8211; despite warnings against long-term use, according to a University of British Columbia study. Published online in the journal Health Policy, the study by researchers at UBC&#8217;s Centre for Health Services and Policy Research (CHSPR) is the first of its kind to examine the use of benzodiazepines <span id="more-2581"></span> such as <b>Xanax</b> and Ativan for an entire population over time&#8230; (Source: Health News from Medical News Today)</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>An effect-size analysis of pharmacologic treatments for generalized anxiety disorder</title>
		<link>http://medsnetic.com/blog/2010/05/31/an-effect-size-analysis-of-pharmacologic-treatments-for-generalized-anxiety-disorder-2/</link>
		<comments>http://medsnetic.com/blog/2010/05/31/an-effect-size-analysis-of-pharmacologic-treatments-for-generalized-anxiety-disorder-2/#comments</comments>
		<pubDate>Mon, 31 May 2010 23:53:10 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[analysis]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[Disorder]]></category>
		<category><![CDATA[effect]]></category>
		<category><![CDATA[generalized]]></category>
		<category><![CDATA[pharmacologic]]></category>
		<category><![CDATA[size]]></category>
		<category><![CDATA[treatments]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/05/31/an-effect-size-analysis-of-pharmacologic-treatments-for-generalized-anxiety-disorder-2/</guid>
		<description><![CDATA[ Generalized anxiety disorder (GAD) is a prevalent and impairing disorder, associated with extensive psychiatric and medical comorbidity and usually characterized by a chronic course. Different drugs have been investigated in GAD; among them are the following: 1) SSRIS: paroxetine, sertraline, fluvoxamine and escitalopram; 2) SNRI1S: venlafaxine; 3) benzodiaze pines (BZS): alprazolam, diazepam and lorazepam; [...]]]></description>
			<content:encoded><![CDATA[<p> Generalized anxiety disorder (GAD) is a prevalent and impairing disorder, associated with extensive psychiatric and medical comorbidity and usually characterized by a chronic course. Different drugs have been investigated in GAD; among them are the following: 1) SSRIS: paroxetine, <b>sertraline</b>, fluvoxamine and escitalopram; 2) SNRI1S: venlafaxine; 3) benzodiaze pines (BZS): alprazolam, diazepam and lorazepam; 4) azapirones (AZAS): buspirone; 5) <span id="more-2437"></span> antihistamines (AHS): hydroxyzine; 6) pregabalin (PGB); and 7) complementary/alternative medicine (CAM): kava-kava and homeopathic preparation. We conducted an effect size (ES) analysis of 21 double-blind placebo-controlled tr ials of medications treating DSM-III-R, DSM-IV or ICD-10 GAD using HAM-A change in score from baseline or endpoint score as the &#8230;</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Anxiety Medications</title>
		<link>http://medsnetic.com/blog/2010/05/30/anxiety-medications-2/</link>
		<comments>http://medsnetic.com/blog/2010/05/30/anxiety-medications-2/#comments</comments>
		<pubDate>Sun, 30 May 2010 10:45:00 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[Medications]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/05/30/anxiety-medications-2/</guid>
		<description><![CDATA[ Antianxiety medications help to calm and relax the anxious person and remove the troubling symptoms. There are a number of antianxiety medications currently available. The preferred medications for most anxiety disorders are the benzodiazepines such as Valium, Xanax/Zanex, and Ativan. (Source: About.com Mental Health)
]]></description>
			<content:encoded><![CDATA[<p> Antianxiety medications help to calm and relax the anxious person and remove the troubling symptoms. There are a number of antianxiety medications currently available. The preferred medications for most anxiety disorders are the benzodiazepines such as Valium, <b>Xanax</b>/Zanex, and Ativan. (Source: About.com Mental Health)</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Erratum to: Validating a human model for anxiety using startle potentiated by cue and context: the effects of alprazolam, pregabalin, and diphenhydramine</title>
		<link>http://medsnetic.com/blog/2010/05/29/erratum-to-validating-a-human-model-for-anxiety-using-startle-potentiated-by-cue-and-context-the-effects-of-alprazolam-pregabalin-and-diphenhydramine-2/</link>
		<comments>http://medsnetic.com/blog/2010/05/29/erratum-to-validating-a-human-model-for-anxiety-using-startle-potentiated-by-cue-and-context-the-effects-of-alprazolam-pregabalin-and-diphenhydramine-2/#comments</comments>
		<pubDate>Sat, 29 May 2010 13:10:11 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Cialis]]></category>
		<category><![CDATA[Alprazolam]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[context]]></category>
		<category><![CDATA[diphenhydramine]]></category>
		<category><![CDATA[effects]]></category>
		<category><![CDATA[Erratum]]></category>
		<category><![CDATA[Human]]></category>
		<category><![CDATA[model]]></category>
		<category><![CDATA[potentiated]]></category>
		<category><![CDATA[pregabalin]]></category>
		<category><![CDATA[startle]]></category>
		<category><![CDATA[Using]]></category>
		<category><![CDATA[Validating]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/05/29/erratum-to-validating-a-human-model-for-anxiety-using-startle-potentiated-by-cue-and-context-the-effects-of-alprazolam-pregabalin-and-diphenhydramine-2/</guid>
		<description><![CDATA[ Content Type Journal ArticleCategory ErratumDOI 10.1007/s00213-010-1837-4Authors
		J. M. P. Baas, Utrecht University Department of Experimental Psychology, Faculty of Social Sciences Van Unnik Building, Heidelberglaan 2 3584 CS Ut recht The NetherlandsN. Mol, Utrecht University Department of Experimental Psychology, Faculty of Social Sciences Van Unnik Building, Heidelberglaan 2 3584 CS Utrecht The NetherlandsJ. L. Kenemans, Utrecht [...]]]></description>
			<content:encoded><![CDATA[<p> Content Type Journal ArticleCategory ErratumDOI 10.1007/s00213-010-1837-4Authors<br />
		J. M. P. Baas, Utrecht University Department of Experimental Psychology, Faculty of Social Sciences Van Unnik Building, Heidelberglaan 2 3584 CS Ut recht The NetherlandsN. Mol, Utrecht University Department of Experimental Psychology, Faculty of Social Sciences Van Unnik Building, Heidelberglaan 2 3584 CS Utrecht The NetherlandsJ. L. Kenemans, Utrecht University <span id="more-2304"></span> Department of Experimental Psychology, Faculty of Social Sciences Van Unnik Building, Heidelberglaan 2 3584 CS Utrecht The NetherlandsE. P. Prinssen, CNS Research, F. Hoffmann-La Roche, Clinical Development Basel SwitzerlandI. Niklson, CNS Research, F. Hoffmann-La Roche, Clinical Development Base l SwitzerlandC. Xia-Chen, Centre for Human Drug Resear&#8230;</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Despite Known Health Risks Long-Term Use Of Anti-Anxiety Drugs Continues In B.C.</title>
		<link>http://medsnetic.com/blog/2010/05/28/despite-known-health-risks-long-term-use-of-anti-anxiety-drugs-continues-in-b-c/</link>
		<comments>http://medsnetic.com/blog/2010/05/28/despite-known-health-risks-long-term-use-of-anti-anxiety-drugs-continues-in-b-c/#comments</comments>
		<pubDate>Fri, 28 May 2010 11:13:26 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[anti]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[Continues]]></category>
		<category><![CDATA[Despite]]></category>
		<category><![CDATA[Drugs]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[Known]]></category>
		<category><![CDATA[Long]]></category>
		<category><![CDATA[Risks]]></category>
		<category><![CDATA[Term]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/05/28/despite-known-health-risks-long-term-use-of-anti-anxiety-drugs-continues-in-b-c/</guid>
		<description><![CDATA[ Drugs to treat anxiety and sleep disorders are still being prescribed for extended periods to British Columbian patients &#8211; and increasingly so for baby boomers &#8211; despite warnings against long-term use, according to a University of British Columbi a study. Published online in the journal Health Policy, the study by researchers at UBC&#8217;s Centre [...]]]></description>
			<content:encoded><![CDATA[<p> Drugs to treat anxiety and sleep disorders are still being prescribed for extended periods to British Columbian patients &#8211; and increasingly so for baby boomers &#8211; despite warnings against long-term use, according to a University of British Columbi a study. Published online in the journal Health Policy, the study by researchers at UBC&#8217;s Centre for Health Services and Policy Research (CHSPR) is the first of its kind to examine the use of benzodiazepines <span id="more-2293"></span> such as <b>Xanax</b> and Ativan for an entire population over time&#8230; (Source: Health News from Medical News Today)</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Early onset anxiolytic efficacy after a single dose of pregabalin: double-blind, placebo- and active-comparator controlled evaluation using a dental anxiety model</title>
		<link>http://medsnetic.com/blog/2010/05/26/early-onset-anxiolytic-efficacy-after-a-single-dose-of-pregabalin-double-blind-placebo-and-active-comparator-controlled-evaluation-using-a-dental-anxiety-model-2/</link>
		<comments>http://medsnetic.com/blog/2010/05/26/early-onset-anxiolytic-efficacy-after-a-single-dose-of-pregabalin-double-blind-placebo-and-active-comparator-controlled-evaluation-using-a-dental-anxiety-model-2/#comments</comments>
		<pubDate>Wed, 26 May 2010 15:13:20 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[active]]></category>
		<category><![CDATA[After]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[Anxiolytic]]></category>
		<category><![CDATA[blind]]></category>
		<category><![CDATA[comparator]]></category>
		<category><![CDATA[controlled]]></category>
		<category><![CDATA[dental]]></category>
		<category><![CDATA[dose]]></category>
		<category><![CDATA[double]]></category>
		<category><![CDATA[Early]]></category>
		<category><![CDATA[Efficacy]]></category>
		<category><![CDATA[evaluation]]></category>
		<category><![CDATA[model]]></category>
		<category><![CDATA[onset]]></category>
		<category><![CDATA[placebo]]></category>
		<category><![CDATA[pregabalin]]></category>
		<category><![CDATA[single]]></category>
		<category><![CDATA[Using]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/05/26/early-onset-anxiolytic-efficacy-after-a-single-dose-of-pregabalin-double-blind-placebo-and-active-comparator-controlled-evaluation-using-a-dental-anxiety-model-2/</guid>
		<description><![CDATA[ To evaluate acute onset of anxiolytic activity using a dental anxiety model, 89 patients were randomised to double-blind single dose pregabalin 150 mg, alprazolam 0.5 mg or placebo 4 h before a scheduled dental procedure. A Dental Anxiety Total score &#62;12 (moderate-to-severe) without meeting Diagnostic and Statistical Manual of Mental Di sorders (Fourth edition) [...]]]></description>
			<content:encoded><![CDATA[<p> To evaluate acute onset of anxiolytic activity using a dental anxiety model, 89 patients were randomised to double-blind single dose pregabalin 150 mg, alprazolam 0.5 mg or placebo 4 h before a scheduled dental procedure. A Dental Anxiety Total score &gt;12 (moderate-to-severe) without meeting Diagnostic and Statistical Manual of Mental Di sorders (Fourth edition) (DSM-IV) anxiety disorder criteria was required. Efficacy and safety, assessed <span id="more-2143"></span> 2, 2.5, 3, 3.5 and 4 h postdose, included 100 mm Visual Analogue Scale for Anxiety (VAS -Anxiety; primary outcome), 100 mm VAS-Sedation and Time-to-Onset of Action Scale (TOAS), a patient-rated anti-anxiety drug-benefit scale (no [0] to full benefit [10]). Mixed model analysis found significantly greater VAS-A improvement slopes for pregabalin (t = &#038;ndas&#8230;</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Validating a human model for anxiety using startle potentiated by cue and context: the effects of alprazolam, pregabalin, and diphenhydramine</title>
		<link>http://medsnetic.com/blog/2010/05/22/validating-a-human-model-for-anxiety-using-startle-potentiated-by-cue-and-context-the-effects-of-alprazolam-pregabalin-and-diphenhydramine-2/</link>
		<comments>http://medsnetic.com/blog/2010/05/22/validating-a-human-model-for-anxiety-using-startle-potentiated-by-cue-and-context-the-effects-of-alprazolam-pregabalin-and-diphenhydramine-2/#comments</comments>
		<pubDate>Sat, 22 May 2010 20:05:08 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Cialis]]></category>
		<category><![CDATA[Alprazolam]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[context]]></category>
		<category><![CDATA[diphenhydramine]]></category>
		<category><![CDATA[effects]]></category>
		<category><![CDATA[Human]]></category>
		<category><![CDATA[model]]></category>
		<category><![CDATA[potentiated]]></category>
		<category><![CDATA[pregabalin]]></category>
		<category><![CDATA[startle]]></category>
		<category><![CDATA[Using]]></category>
		<category><![CDATA[Validating]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/05/22/validating-a-human-model-for-anxiety-using-startle-potentiated-by-cue-and-context-the-effects-of-alprazolam-pregabalin-and-diphenhydramine-2/</guid>
		<description><![CDATA[ Conclusion&#160;&#160;Even though fear-potentiated startle may be used to translate preclini cal evidence to human populations, methodological issues
 still hamper the application of this model to early screening of putative anxiolytic drugs.
	Content Type Journal ArticleCategory Original InvestigationDOI 10.1007/s00213-009-1516-5Authors
		J. M. P. Baas, Utrecht University Department of Experimental Psychology, Faculty of Social Sciences  Van Unnik Building, [...]]]></description>
			<content:encoded><![CDATA[<p> Conclusion&nbsp;&nbsp;Even though fear-potentiated startle may be used to translate preclini cal evidence to human populations, methodological issues<br />
 still hamper the application of this model to early screening of putative anxiolytic drugs.</p>
<p>	Content Type Journal ArticleCategory Original InvestigationDOI 10.1007/s00213-009-1516-5Authors<br />
		J. M. P. Baas, Utrecht University Department of Experimental Psychology, Faculty of Social Sciences <span id="more-2027"></span> Van Unnik Building, Heidelberglaan 2 3584 CS Utrecht The NetherlandsN. Mol, Utrecht Univer sity Department of Experimental Psychology, Faculty of Social Sciences Van Unnik Building, Heidelberglaan 2 3584 CS Utrecht The NetherlandsJ. L. Kenemans, Utrecht University Department of Experimental Psychology, Faculty of Social Sciences Van Unnik Building, Hei&#8230;</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>A comparison of the effects of a subtype selective and non-selective benzodiazepine receptor agonist in two CO2 models of experimental human anxiety</title>
		<link>http://medsnetic.com/blog/2010/05/21/a-comparison-of-the-effects-of-a-subtype-selective-and-non-selective-benzodiazepine-receptor-agonist-in-two-co2-models-of-experimental-human-anxiety-2/</link>
		<comments>http://medsnetic.com/blog/2010/05/21/a-comparison-of-the-effects-of-a-subtype-selective-and-non-selective-benzodiazepine-receptor-agonist-in-two-co2-models-of-experimental-human-anxiety-2/#comments</comments>
		<pubDate>Fri, 21 May 2010 14:51:22 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[Agonist]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[benzodiazepine]]></category>
		<category><![CDATA[Comparison]]></category>
		<category><![CDATA[effects]]></category>
		<category><![CDATA[experimental]]></category>
		<category><![CDATA[Human]]></category>
		<category><![CDATA[models]]></category>
		<category><![CDATA[Receptor]]></category>
		<category><![CDATA[Selective]]></category>
		<category><![CDATA[subtype]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/05/21/a-comparison-of-the-effects-of-a-subtype-selective-and-non-selective-benzodiazepine-receptor-agonist-in-two-co2-models-of-experimental-human-anxiety-2/</guid>
		<description><![CDATA[ In conclusion, our results show that zolpidem shows some anxiolytic efficacy in the 7.5% CO2 model, similar to alprazolam, and this is the first report of such an effect of zolpidem in a model of a nxiety. These and other studies of benzodiazepines in clinical and volunteer studies suggest a definite role of the [...]]]></description>
			<content:encoded><![CDATA[<p> In conclusion, our results show that zolpidem shows some anxiolytic efficacy in the 7.5% CO2 model, similar to alprazolam, and this is the first report of such an effect of zolpidem in a model of a nxiety. These and other studies of benzodiazepines in clinical and volunteer studies suggest a definite role of the GABA-A receptor in CO2-induced anxiety, and it would be of interest to examine other GABA-A receptor subtype selective drugs, which <span id="more-1950"></span> are now in early phase clinical studies and are showing selective efficacy in pharmacodynamic studies. (Source: Journal of Psychopharmacology)
<p>  <i> MedWorm Message: </i>  Register for MedMatcha, MedWorm&#8217;s medical advertising netw ork, and receive $5 free advertising. </p>
]]></content:encoded>
			<wfw:commentRss>http://medsnetic.com/blog/2010/05/21/a-comparison-of-the-effects-of-a-subtype-selective-and-non-selective-benzodiazepine-receptor-agonist-in-two-co2-models-of-experimental-human-anxiety-2/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Review: Benzodiazepines in generalized anxiety disorder: heterogeneity of         outcomes based on a systematic review and meta-analysis of clinical trials</title>
		<link>http://medsnetic.com/blog/2010/05/21/review-benzodiazepines-in-generalized-anxiety-disorder-heterogeneity-of-outcomes-based-on-a-systematic-review-and-meta-analysis-of-clinical-trials-2/</link>
		<comments>http://medsnetic.com/blog/2010/05/21/review-benzodiazepines-in-generalized-anxiety-disorder-heterogeneity-of-outcomes-based-on-a-systematic-review-and-meta-analysis-of-clinical-trials-2/#comments</comments>
		<pubDate>Fri, 21 May 2010 01:33:33 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[analysis]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[Based]]></category>
		<category><![CDATA[benzodiazepines]]></category>
		<category><![CDATA[Clinical]]></category>
		<category><![CDATA[Disorder]]></category>
		<category><![CDATA[generalized]]></category>
		<category><![CDATA[heterogeneity]]></category>
		<category><![CDATA[meta]]></category>
		<category><![CDATA[outcomes]]></category>
		<category><![CDATA[Review]]></category>
		<category><![CDATA[systematic]]></category>
		<category><![CDATA[trials]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/05/21/review-benzodiazepines-in-generalized-anxiety-disorder-heterogeneity-of-outcomes-based-on-a-systematic-review-and-meta-analysis-of-clinical-trials-2/</guid>
		<description><![CDATA[ The objective of         this study was to assess the effectiveness and efficacy of benzodiazepines in the         treatment of GAD based on trial drop-out rates. We used a systematic review of         [...]]]></description>
			<content:encoded><![CDATA[<p> The objective of         this study was to assess the effectiveness and efficacy of benzodiazepines in the         treatment of GAD based on trial drop-out rates. We used a systematic review of         randomized controlled trials that compared any of the thr ee best established         benzodiazepines (diazepam, Lorazepam and aLprazolam) against placebo. Our primary         outcome for effectiveness was withdrawal for any reason. Our secondary <span id="more-1931"></span> outcome         tapping efficacy was withdrawal due to lack of efficacy, and that tapping side         effects was withdrawals due to adverse events.We included 23 trials. Pooled analysis indicated less risk of treatment         discontin uation due to lack of efficacy for benzodiazepines, compared to placebo,         relative risk (RR) 0.29 (95% CI 0&#8230;</p>
]]></content:encoded>
			<wfw:commentRss>http://medsnetic.com/blog/2010/05/21/review-benzodiazepines-in-generalized-anxiety-disorder-heterogeneity-of-outcomes-based-on-a-systematic-review-and-meta-analysis-of-clinical-trials-2/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Treatments for Anxiety</title>
		<link>http://medsnetic.com/blog/2010/05/20/treatments-for-anxiety-2/</link>
		<comments>http://medsnetic.com/blog/2010/05/20/treatments-for-anxiety-2/#comments</comments>
		<pubDate>Thu, 20 May 2010 11:05:46 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[treatments]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/05/20/treatments-for-anxiety-2/</guid>
		<description><![CDATA[ Anxiety is a well-understood and readily treated condition. There are many different kinds of specific anxiety disorders, ranging from generalized anxiety disorder (GAD) to panic attacks. The below treatment options cover general anxiety disorders and are usually recomme nded in some combination.
	Medications
	The medications most often used to treat anxiety are a class of drugs [...]]]></description>
			<content:encoded><![CDATA[<p> Anxiety is a well-understood and readily treated condition. There are many different kinds of specific anxiety disorders, ranging from generalized anxiety disorder (GAD) to panic attacks. The below treatment options cover general anxiety disorders and are usually recomme nded in some combination.<br />
	Medications<br />
	The medications most often used to treat anxiety are a class of drugs known as benzodiazepines (also called &#8220;minor tranquilizers&#8221;). <span id="more-1906"></span> These include Xana x, Ativan and Klonopin. The primary concern with these substances is their potential for tolerance, physical dependence, and the likely recurrence of panic and anxiety symptoms when the medication is stopped. Hence, they are best used for treating short-term anxiety and panic. Because anxiety is so often associated with depre&#8230;
<p>  <i> MedWorm Message: </i>  Register for MedMatcha, MedWorm&#8217;s medical advertising network, and receive $5 free advertising. </p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Chimpanzee Was On Anti-Anxiety Drug Xanax</title>
		<link>http://medsnetic.com/blog/2010/05/18/chimpanzee-was-on-anti-anxiety-drug-xanax-2/</link>
		<comments>http://medsnetic.com/blog/2010/05/18/chimpanzee-was-on-anti-anxiety-drug-xanax-2/#comments</comments>
		<pubDate>Tue, 18 May 2010 20:35:02 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[anti]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[Chimpanzee]]></category>
		<category><![CDATA[Drug]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/05/18/chimpanzee-was-on-anti-anxiety-drug-xanax-2/</guid>
		<description><![CDATA[ Travis the chimpanzee &#8212; whose presence in a Stamford home had been called an &#8220;accident waiting to happen&#8221; months before he attacked Charla Nash &#8212; had the anti-anxiety drug Xanax in his system, according to the state&#8217;s attorney&#8217;s office.
It is&#8230; (Source: OrlandoSentinel: Medical Research)
]]></description>
			<content:encoded><![CDATA[<p> Travis the chimpanzee &#8212; whose presence in a Stamford home had been called an &#8220;accident waiting to happen&#8221; months before he attacked Charla Nash &#8212; had the anti-anxiety drug <b>Xanax</b> in his system, according to the state&#8217;s attorney&#8217;s office.</p>
<p>It is&#8230; (Source: OrlandoSentinel: Medical Research)</p>
]]></content:encoded>
			<wfw:commentRss>http://medsnetic.com/blog/2010/05/18/chimpanzee-was-on-anti-anxiety-drug-xanax-2/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Erratum to: Validating a human model for anxiety using startle potentiated by cue and context: the effects of alprazolam, pregabalin, and diphenhydramine</title>
		<link>http://medsnetic.com/blog/2010/04/26/erratum-to-validating-a-human-model-for-anxiety-using-startle-potentiated-by-cue-and-context-the-effects-of-alprazolam-pregabalin-and-diphenhydramine/</link>
		<comments>http://medsnetic.com/blog/2010/04/26/erratum-to-validating-a-human-model-for-anxiety-using-startle-potentiated-by-cue-and-context-the-effects-of-alprazolam-pregabalin-and-diphenhydramine/#comments</comments>
		<pubDate>Mon, 26 Apr 2010 13:44:17 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Cialis]]></category>
		<category><![CDATA[Alprazolam]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[context]]></category>
		<category><![CDATA[diphenhydramine]]></category>
		<category><![CDATA[effects]]></category>
		<category><![CDATA[Erratum]]></category>
		<category><![CDATA[Human]]></category>
		<category><![CDATA[model]]></category>
		<category><![CDATA[potentiated]]></category>
		<category><![CDATA[pregabalin]]></category>
		<category><![CDATA[startle]]></category>
		<category><![CDATA[Using]]></category>
		<category><![CDATA[Validating]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/04/26/erratum-to-validating-a-human-model-for-anxiety-using-startle-potentiated-by-cue-and-context-the-effects-of-alprazolam-pregabalin-and-diphenhydramine/</guid>
		<description><![CDATA[ Content Type Journal ArticleCategory ErratumDOI 10.1007/s00213-010-1837-4Authors
		J. M. P. Baas, Utrecht University Department of Experimental Psychology, Faculty of Social S ciences Van Unnik Building, Heidelberglaan 2 3584 CS Utrecht The NetherlandsN. Mol, Utrecht University Department of Experimental Psychology, Faculty of Social Sciences Van Unnik Building, Heidelberglaan 2 3584 CS Utrecht The NetherlandsJ. L. Kenemans, Utrecht [...]]]></description>
			<content:encoded><![CDATA[<p> Content Type Journal ArticleCategory ErratumDOI 10.1007/s00213-010-1837-4Authors<br />
		J. M. P. Baas, Utrecht University Department of Experimental Psychology, Faculty of Social S ciences Van Unnik Building, Heidelberglaan 2 3584 CS Utrecht The NetherlandsN. Mol, Utrecht University Department of Experimental Psychology, Faculty of Social Sciences Van Unnik Building, Heidelberglaan 2 3584 CS Utrecht The NetherlandsJ. L. Kenemans, Utrecht University <span id="more-1251"></span> Department of Experimental Psychology, Faculty of Social Sciences Van Unnik Building, Heidelberglaan 2 3584 CS Utrecht The NetherlandsE. P. Prinssen, CNS Research, F. Hoffmann-La Roche, Clinical Development Basel SwitzerlandI. Niklson, CNS Research, F. Hoffmann-La Roch e, Clinical Development Basel SwitzerlandC. Xia-Chen, Centre for Human Drug Resear&#8230;</p>
]]></content:encoded>
			<wfw:commentRss>http://medsnetic.com/blog/2010/04/26/erratum-to-validating-a-human-model-for-anxiety-using-startle-potentiated-by-cue-and-context-the-effects-of-alprazolam-pregabalin-and-diphenhydramine/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Medications for Anxiety</title>
		<link>http://medsnetic.com/blog/2010/03/06/medications-for-anxiety/</link>
		<comments>http://medsnetic.com/blog/2010/03/06/medications-for-anxiety/#comments</comments>
		<pubDate>Sat, 06 Mar 2010 02:03:40 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[Medications]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/03/06/medications-for-anxiety/</guid>
		<description><![CDATA[ Medications for anxiet y benzodiazepines clonazepam Klonopin alprazolam Xanax diazepam Valium lorazepam Ativan buspirone buspar propranolol Inderal Inderide (Source: About.com Mental Health)
   MedWorm Message:   Get the very latest Swine Flu news via the MedWorm Swine Flu RSS news feed &#8211;  updated hourly from thousands of authoritative health and news [...]]]></description>
			<content:encoded><![CDATA[<p> Medications for anxiet y benzodiazepines clonazepam Klonopin alprazolam <b>Xanax</b> diazepam Valium lorazepam Ativan buspirone buspar propranolol Inderal Inderide (Source: About.com Mental Health)
<p>  <i> MedWorm Message: </i>  Get the very latest Swine Flu news via the MedWorm Swine Flu RSS news feed &#8211;  updated hourly from thousands of authoritative health and news sources. </p>
]]></content:encoded>
			<wfw:commentRss>http://medsnetic.com/blog/2010/03/06/medications-for-anxiety/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Anxiety Medications</title>
		<link>http://medsnetic.com/blog/2010/03/02/anxiety-medications/</link>
		<comments>http://medsnetic.com/blog/2010/03/02/anxiety-medications/#comments</comments>
		<pubDate>Tue, 02 Mar 2010 23:13:15 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[Medications]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/03/02/anxiety-medications/</guid>
		<description><![CDATA[ Antianxiety medications help to calm and relax the anxious person and remove the troubling symptoms. There are a n umber of antianxiety medications currently available. The preferred medications for most anxiety disorders are the benzodiazepines such as Valium, Xanax/Zanex, and Ativan. (Source: About.com Mental Health)
   MedWorm Message:   Get the very [...]]]></description>
			<content:encoded><![CDATA[<p> Antianxiety medications help to calm and relax the anxious person and remove the troubling symptoms. There are a n umber of antianxiety medications currently available. The preferred medications for most anxiety disorders are the benzodiazepines such as Valium, <b>Xanax</b>/Zanex, and Ativan. (Source: About.com Mental Health)
<p>  <i> MedWorm Message: </i>  Get the very latest Swine Flu news via the MedWorm Swine Flu RSS news feed &#8211;  updated hourly from <span id="more-336"></span> thousands of authoritative health and news sources. </p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Chimpanzee Was On Anti-Anxiety Drug Xanax</title>
		<link>http://medsnetic.com/blog/2010/03/01/chimpanzee-was-on-anti-anxiety-drug-xanax/</link>
		<comments>http://medsnetic.com/blog/2010/03/01/chimpanzee-was-on-anti-anxiety-drug-xanax/#comments</comments>
		<pubDate>Mon, 01 Mar 2010 23:51:20 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[anti]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[Chimpanzee]]></category>
		<category><![CDATA[Drug]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/03/01/chimpanzee-was-on-anti-anxiety-drug-xanax/</guid>
		<description><![CDATA[ Travis the chimpanzee &#8212; whose presence in a Stamford home had been called an &#8220;accident waiting to happen&#8221; months before he attacked Charla Nash &#8212; had the anti-anxiety drug Xanax in his system, according to the state&#8217;s attorney&#8217;s office.
It is&#8230; (Source: OrlandoSentinel: Medical Research)
]]></description>
			<content:encoded><![CDATA[<p> Travis the chimpanzee &#8212; whose presence in a Stamford home had been called an &#8220;accident waiting to happen&#8221; months before he attacked Charla Nash &#8212; had the anti-anxiety drug <b>Xanax</b> in his system, according to the state&#8217;s attorney&#8217;s office.</p>
<p>It is&#8230; (Source: OrlandoSentinel: Medical Research)</p>
]]></content:encoded>
			<wfw:commentRss>http://medsnetic.com/blog/2010/03/01/chimpanzee-was-on-anti-anxiety-drug-xanax/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Treatments for Anxiety</title>
		<link>http://medsnetic.com/blog/2010/02/20/treatments-for-anxiety/</link>
		<comments>http://medsnetic.com/blog/2010/02/20/treatments-for-anxiety/#comments</comments>
		<pubDate>Sat, 20 Feb 2010 01:24:58 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[treatments]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/02/20/treatments-for-anxiety/</guid>
		<description><![CDATA[ Anxiety is a well-understood and readily treated condition. T here are many different kinds of specific anxiety disorders, ranging from generalized anxiety disorder (GAD) to panic attacks. The below treatment options cover general anxiety disorders and are usually recommended in some combination.
	Medications
	The medications most often used to treat anxiety are a class of drugs [...]]]></description>
			<content:encoded><![CDATA[<p> Anxiety is a well-understood and readily treated condition. T here are many different kinds of specific anxiety disorders, ranging from generalized anxiety disorder (GAD) to panic attacks. The below treatment options cover general anxiety disorders and are usually recommended in some combination.<br />
	Medications<br />
	The medications most often used to treat anxiety are a class of drugs known as benzodiazepines (also called &#8220;minor tranquilizers&#8221;). <span id="more-267"></span> These include <b>Xanax</b>, Ativan and Klonopin. The primary concern with these substances is their potential for tolerance, physical dependence, and the likely recurrence of panic and anxiety symptoms when the medication is stopped. Hence, they are best used for treating short-term anxiety and panic. Because an xiety is so often associated with depre&#8230;</p>
]]></content:encoded>
			<wfw:commentRss>http://medsnetic.com/blog/2010/02/20/treatments-for-anxiety/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Validating a human model for anxiety using startle potentiated by cue and context: the effects of alprazolam, pregabalin, and diphenhydramine</title>
		<link>http://medsnetic.com/blog/2010/02/17/validating-a-human-model-for-anxiety-using-startle-potentiated-by-cue-and-context-the-effects-of-alprazolam-pregabalin-and-diphenhydramine/</link>
		<comments>http://medsnetic.com/blog/2010/02/17/validating-a-human-model-for-anxiety-using-startle-potentiated-by-cue-and-context-the-effects-of-alprazolam-pregabalin-and-diphenhydramine/#comments</comments>
		<pubDate>Wed, 17 Feb 2010 17:49:05 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Cialis]]></category>
		<category><![CDATA[Alprazolam]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[context]]></category>
		<category><![CDATA[diphenhydramine]]></category>
		<category><![CDATA[effects]]></category>
		<category><![CDATA[Human]]></category>
		<category><![CDATA[model]]></category>
		<category><![CDATA[potentiated]]></category>
		<category><![CDATA[pregabalin]]></category>
		<category><![CDATA[startle]]></category>
		<category><![CDATA[Using]]></category>
		<category><![CDATA[Validating]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/02/17/validating-a-human-model-for-anxiety-using-startle-potentiated-by-cue-and-context-the-effects-of-alprazolam-pregabalin-and-diphenhydramine/</guid>
		<description><![CDATA[ Conclusion&#160;&#160;Even though fear-potentiated startle may be used to translate preclinical evidence to human populations, methodological issues
 still hamper the application of this model to early screening of putative anxiolytic drugs.
	Content Type Journal ArticleCategory Original InvestigationDOI 10.1007/s00213-009-1516-5Authors
		J. M. P. Baas, Utrecht University Department of Experimental Psychology, Faculty of Social Sciences  Van Unnik Building, Heidelberglaan [...]]]></description>
			<content:encoded><![CDATA[<p> Conclusion&nbsp;&nbsp;Even though fear-potentiated startle may be used to translate preclinical evidence to human populations, methodological issues<br />
 still hamper the application of this model to early screening of putative anxiolytic drugs.</p>
<p>	Content Type Journal ArticleCategory Original InvestigationDOI 10.1007/s00213-009-1516-5Authors<br />
		J. M. P. Baas, Utrecht University Department of Experimental Psychology, Faculty of Social Sciences <span id="more-240"></span> Van Unnik Building, Heidelberglaan 2 3584 CS Utrecht The NetherlandsN. Mol, Utrecht Univ ersity Department of Experimental Psychology, Faculty of Social Scien ces Van Unnik Building, Heidelberglaan 2 3584 CS Utrecht The NetherlandsJ. L. Kenemans, Utrecht University Department of Experimental Psychology, Faculty of Social Sciences Van Unnik Building, Hei&#8230;</p>
]]></content:encoded>
			<wfw:commentRss>http://medsnetic.com/blog/2010/02/17/validating-a-human-model-for-anxiety-using-startle-potentiated-by-cue-and-context-the-effects-of-alprazolam-pregabalin-and-diphenhydramine/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>A comparison of the effects of a subtype selective and non-selective benzodiazepine receptor agonist in two CO2 models of experimental human anxiety</title>
		<link>http://medsnetic.com/blog/2010/02/16/a-comparison-of-the-effects-of-a-subtype-selective-and-non-selective-benzodiazepine-receptor-agonist-in-two-co2-models-of-experimental-human-anxiety/</link>
		<comments>http://medsnetic.com/blog/2010/02/16/a-comparison-of-the-effects-of-a-subtype-selective-and-non-selective-benzodiazepine-receptor-agonist-in-two-co2-models-of-experimental-human-anxiety/#comments</comments>
		<pubDate>Tue, 16 Feb 2010 08:55:34 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[Agonist]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[benzodiazepine]]></category>
		<category><![CDATA[Comparison]]></category>
		<category><![CDATA[effects]]></category>
		<category><![CDATA[experimental]]></category>
		<category><![CDATA[Human]]></category>
		<category><![CDATA[models]]></category>
		<category><![CDATA[Receptor]]></category>
		<category><![CDATA[Selective]]></category>
		<category><![CDATA[subtype]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/02/16/a-comparison-of-the-effects-of-a-subtype-selective-and-non-selective-benzodiazepine-receptor-agonist-in-two-co2-models-of-experimental-human-anxiety/</guid>
		<description><![CDATA[ In conclusion, our results show that zolpidem shows some anxiolytic efficacy in the 7.5% CO2 model, similar to alprazolam, and this is the first report of such an effect of zolpidem in a model of anxiety. These and other studies of benzodiazepines in clinical and volunteer studies suggest a definite role of the GABA-A [...]]]></description>
			<content:encoded><![CDATA[<p> In conclusion, our results show that zolpidem shows some anxiolytic efficacy in the 7.5% CO2 model, similar to alprazolam, and this is the first report of such an effect of zolpidem in a model of anxiety. These and other studies of benzodiazepines in clinical and volunteer studies suggest a definite role of the GABA-A rec eptor in CO2-induced anxiety, and it would be of interest to examine other GABA-A receptor subtype selective drugs, which <span id="more-226"></span> are now in early phase clinical studies and are showing selective efficacy in pharmacodynamic studies. (Source: Journal of Psychopharmacology)</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Early onset anxiolytic efficacy after a single dose of pregabalin: double-blind, placebo- and active-comparator controlled evaluation using a dental anxiety model</title>
		<link>http://medsnetic.com/blog/2010/02/14/early-onset-anxiolytic-efficacy-after-a-single-dose-of-pregabalin-double-blind-placebo-and-active-comparator-controlled-evaluation-using-a-dental-anxiety-model/</link>
		<comments>http://medsnetic.com/blog/2010/02/14/early-onset-anxiolytic-efficacy-after-a-single-dose-of-pregabalin-double-blind-placebo-and-active-comparator-controlled-evaluation-using-a-dental-anxiety-model/#comments</comments>
		<pubDate>Sun, 14 Feb 2010 05:00:35 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[active]]></category>
		<category><![CDATA[After]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[Anxiolytic]]></category>
		<category><![CDATA[blind]]></category>
		<category><![CDATA[comparator]]></category>
		<category><![CDATA[controlled]]></category>
		<category><![CDATA[dental]]></category>
		<category><![CDATA[dose]]></category>
		<category><![CDATA[double]]></category>
		<category><![CDATA[Early]]></category>
		<category><![CDATA[Efficacy]]></category>
		<category><![CDATA[evaluation]]></category>
		<category><![CDATA[model]]></category>
		<category><![CDATA[onset]]></category>
		<category><![CDATA[placebo]]></category>
		<category><![CDATA[pregabalin]]></category>
		<category><![CDATA[single]]></category>
		<category><![CDATA[Using]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/02/14/early-onset-anxiolytic-efficacy-after-a-single-dose-of-pregabalin-double-blind-placebo-and-active-comparator-controlled-evaluation-using-a-dental-anxiety-model/</guid>
		<description><![CDATA[ To evaluate acute onset of anxiolytic activity using a dental anxiety model, 89 patients were randomised to double-blind single dose pregabalin 150 mg, alprazolam 0.5 mg or placebo 4 h before a scheduled dental procedure. A Dental Anxiety Total score &#62;12 (moderate-to-severe) without meeting Diagnostic and Statistical Manual of Mental Disorders (Fourth edition) (DSM-IV) [...]]]></description>
			<content:encoded><![CDATA[<p> To evaluate acute onset of anxiolytic activity using a dental anxiety model, 89 patients were randomised to double-blind single dose pregabalin 150 mg, alprazolam 0.5 mg or placebo 4 h before a scheduled dental procedure. A Dental Anxiety Total score &gt;12 (moderate-to-severe) without meeting Diagnostic and Statistical Manual of Mental Disorders (Fourth edition) (DSM-IV) anxiety disorder criteria was required. Efficacy and safety, asse ssed <span id="more-199"></span> 2, 2.5, 3, 3.5 and 4 h postdose, included 100 mm Visual Analogue Scale for Anxiety (VAS-Anxiety; primary outcome), 100 mm VAS-Sedation and Time-to-Onset of Action Scale (TOAS), a patient-rated anti-anxiety drug-benefit scale (no [0] to full benefit [10]). Mixed model analysis found significantly greater V AS-A improvement slopes for pregabalin (t = &#038;ndas&#8230;
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]]></content:encoded>
			<wfw:commentRss>http://medsnetic.com/blog/2010/02/14/early-onset-anxiolytic-efficacy-after-a-single-dose-of-pregabalin-double-blind-placebo-and-active-comparator-controlled-evaluation-using-a-dental-anxiety-model/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>An effect-size analysis of pharmacologic treatments for generalized anxiety disorder</title>
		<link>http://medsnetic.com/blog/2010/02/12/an-effect-size-analysis-of-pharmacologic-treatments-for-generalized-anxiety-disorder/</link>
		<comments>http://medsnetic.com/blog/2010/02/12/an-effect-size-analysis-of-pharmacologic-treatments-for-generalized-anxiety-disorder/#comments</comments>
		<pubDate>Fri, 12 Feb 2010 23:00:18 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[analysis]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[Disorder]]></category>
		<category><![CDATA[effect]]></category>
		<category><![CDATA[generalized]]></category>
		<category><![CDATA[pharmacologic]]></category>
		<category><![CDATA[size]]></category>
		<category><![CDATA[treatments]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/02/12/an-effect-size-analysis-of-pharmacologic-treatments-for-generalized-anxiety-disorder/</guid>
		<description><![CDATA[ Generalized anxiety disorder (GAD) is a prevalent and impairing disorder, associated with extensive psychiatric and medical comorbidity and usually characterized by a chronic course. Different drugs have been investigated in GAD; among them are the followin g: 1) SSRIS: paroxetine, sertraline, fluvoxamine and escitalopram; 2) SNRI1S: venlafaxine; 3) benzodiazepines (BZS): alprazolam, diazepam and lorazepam; [...]]]></description>
			<content:encoded><![CDATA[<p> Generalized anxiety disorder (GAD) is a prevalent and impairing disorder, associated with extensive psychiatric and medical comorbidity and usually characterized by a chronic course. Different drugs have been investigated in GAD; among them are the followin g: 1) SSRIS: paroxetine, <b>sertraline</b>, fluvoxamine and escitalopram; 2) SNRI1S: venlafaxine; 3) benzodiazepines (BZS): alprazolam, diazepam and lorazepam; 4) azapirones (AZAS): buspirone; 5) <span id="more-189"></span> antihistamines (AH S): hydroxyzine; 6) pregabalin (PGB); and 7) complementary/alternative medicine (CAM): kava-kava and homeopathic preparation. We conducted an effect size (ES) analysis of 21 double-blind placebo-controlled trials of medications treating DSM-III-R, DSM-IV or ICD-10 GAD using HAM-A change in score from baseline or endpoint score as the &#8230;</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Review: Benzodiazepines in generalized anxiety disorder: heterogeneity of         outcomes based on a systematic review and meta-analysis of clinical trials</title>
		<link>http://medsnetic.com/blog/2010/02/10/review-benzodiazepines-in-generalized-anxiety-disorder-heterogeneity-of-outcomes-based-on-a-systematic-review-and-meta-analysis-of-clinical-trials/</link>
		<comments>http://medsnetic.com/blog/2010/02/10/review-benzodiazepines-in-generalized-anxiety-disorder-heterogeneity-of-outcomes-based-on-a-systematic-review-and-meta-analysis-of-clinical-trials/#comments</comments>
		<pubDate>Wed, 10 Feb 2010 23:29:10 +0000</pubDate>
		<dc:creator>drugs</dc:creator>
				<category><![CDATA[Xanax]]></category>
		<category><![CDATA[analysis]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[Based]]></category>
		<category><![CDATA[benzodiazepines]]></category>
		<category><![CDATA[Clinical]]></category>
		<category><![CDATA[Disorder]]></category>
		<category><![CDATA[generalized]]></category>
		<category><![CDATA[heterogeneity]]></category>
		<category><![CDATA[meta]]></category>
		<category><![CDATA[outcomes]]></category>
		<category><![CDATA[Review]]></category>
		<category><![CDATA[systematic]]></category>
		<category><![CDATA[trials]]></category>

		<guid isPermaLink="false">http://medsnetic.com/blog/2010/02/10/review-benzodiazepines-in-generalized-anxiety-disorder-heterogeneity-of-outcomes-based-on-a-systematic-review-and-meta-analysis-of-clinical-trials/</guid>
		<description><![CDATA[ The objective of         this study was to assess the effectiveness and efficacy of benzodiazepines in the         treatment of GAD based on trial drop-out rates. We used a systematic review of         [...]]]></description>
			<content:encoded><![CDATA[<p> The objective of         this study was to assess the effectiveness and efficacy of benzodiazepines in the         treatment of GAD based on trial drop-out rates. We used a systematic review of         randomized controlled tr ials that compared any of the three best established         benzodiazepines (diazepam, Lorazepam and aLprazolam) against placebo. Our primary         outcome for effectiveness was withdrawal for any reason. Our secondary <span id="more-158"></span> outcome         tapping efficacy was withdrawal due to lack of efficacy, and that tapping side         effects was withdrawals due to adverse events.We included 23 trials. Pooled analysis indicated less risk of treatment         discontinuation due to lack of efficacy for benzodiazepines, compared to placebo,         relative risk (RR) 0.29 (95% CI 0&#8230;
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		<slash:comments>0</slash:comments>
		</item>
	</channel>
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