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	<title>Cardiology Product Guide &#187; Uncategorized</title>
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	<link>http://blog.cardiologyproductguide.com</link>
	<description>A comprehensive guide to cardiology products for medical professionals </description>
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		<title>Telmisartan helps in reducing cardiovascular risk</title>
		<link>http://blog.cardiologyproductguide.com/2008/09/02/telmisartan-helps-in-reducing-cardiovascular-risk/</link>
		<comments>http://blog.cardiologyproductguide.com/2008/09/02/telmisartan-helps-in-reducing-cardiovascular-risk/#comments</comments>
		<pubDate>Tue, 02 Sep 2008 18:35:43 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[ACE inhibitors]]></category>
		<category><![CDATA[cardiovascular events]]></category>
		<category><![CDATA[Hamilton Health Sciences]]></category>
		<category><![CDATA[telmisartan]]></category>
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		<description><![CDATA[The TRANSCEND study authored by Dr Salim Yusuf, Hamilton Health Sciences and McMaster University, Hamilton (Ontario, Canada) concluded that the angiotensin-receptor blocker (ARB) telmisartan, when added to other reliable therapies,  proves to be of an additional advantage in treating patients who are unable to tolerate the standard treatment of angiotensin-converting enzyme (ACE) inhibitors. The researchers [...]]]></description>
			<content:encoded><![CDATA[<p><img vspace="5" align="left" width="200" src="http://blog.cardiologyproductguide.com/files/2008/09/hamilton-health-sc.png" hspace="5" height="109" />The TRANSCEND study authored by Dr Salim Yusuf, <a href="http://www.hamiltonhealthsciences.ca/">Hamilton Health Sciences and McMaster University</a>, Hamilton (Ontario, Canada) concluded that the angiotensin-receptor blocker (ARB) telmisartan, when added to other reliable therapies,  proves to be of an additional advantage in treating patients who are unable to tolerate the standard treatment of angiotensin-converting enzyme (ACE) inhibitors. The researchers found in a trial that mean blood pressure was lower in the patients given a dose of telmisartan. Major adverse cardiovascular events such as death, heart attack or stroke were 13% less likely in telmisartan patients as against the placebo group.</p>
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		<title>FDA to continue regulating Vasogen Celacade system</title>
		<link>http://blog.cardiologyproductguide.com/2008/03/06/fda-to-continue-regulating-vasogen-celacade-system/</link>
		<comments>http://blog.cardiologyproductguide.com/2008/03/06/fda-to-continue-regulating-vasogen-celacade-system/#comments</comments>
		<pubDate>Thu, 06 Mar 2008 16:32:07 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Diagnostics & Theraputics]]></category>
		<category><![CDATA[FDA]]></category>
		<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[CBER]]></category>
		<category><![CDATA[Celacade]]></category>
		<category><![CDATA[Center for Biologics Evaluation and Research]]></category>
		<category><![CDATA[heart failure]]></category>
		<category><![CDATA[Vasogen]]></category>
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		<description><![CDATA[The FDA has decided to continue to regulate Vasogen’s Celacade system as a medical device. The Celacade system is a treatment for patients with New York Heart Association (NYHA) Class II heart failure. The FDA&#8217;s Center for Biologics Evaluation and Research (CBER) is to take over as the lead reviewer of the programme. The CBER has [...]]]></description>
			<content:encoded><![CDATA[<p><img border="1" vspace="5" align="left" width="231" src="http://blog.cardiologyproductguide.com/files/2008/03/celacade-logo.jpg" hspace="5" alt="Celacade logo" height="96" />The FDA has decided to continue to regulate <a href="http://www.vasogen.com">Vasogen</a>’s Celacade system as a medical device. The Celacade system is a treatment for patients with New York Heart Association (NYHA) Class II heart failure. The FDA&#8217;s <a href="http://www.fda.gov/Cber/">Center for Biologics Evaluation and Research</a> (CBER) is to take over as the lead reviewer of the programme. The CBER has informed Vasogen that it does not agree with the use of a Bayesian approach in the ACCLAIM II study of the system. The FDA had earlier recommended the design.</p>
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