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	<title>Chantix Recall &#187; angiodema</title>
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		<title>FDA monitoring Chantix for serious risks, new safety concerns</title>
		<link>http://www.chantix-legal.com/news/2009/06/09/fda-monitoring-chantix-for-serious-risks-new-safety-concerns/</link>
		<comments>http://www.chantix-legal.com/news/2009/06/09/fda-monitoring-chantix-for-serious-risks-new-safety-concerns/#comments</comments>
		<pubDate>Tue, 09 Jun 2009 13:45:04 +0000</pubDate>
		<dc:creator>Kurt Niland</dc:creator>
				<category><![CDATA[News]]></category>
		<category><![CDATA[adverse event]]></category>
		<category><![CDATA[Adverse Event Reporting System]]></category>
		<category><![CDATA[AERS]]></category>
		<category><![CDATA[angiodema]]></category>
		<category><![CDATA[Chantix]]></category>
		<category><![CDATA[FDA]]></category>
		<category><![CDATA[Food and Drug Administration]]></category>
		<category><![CDATA[psychiatric disorders]]></category>
		<category><![CDATA[psychiatric effects]]></category>
		<category><![CDATA[serious injuries]]></category>
		<category><![CDATA[side effects]]></category>
		<category><![CDATA[test]]></category>
		<category><![CDATA[VA]]></category>

		<guid isPermaLink="false">http://www.chantix-legal.com/?p=592</guid>
		<description><![CDATA[Last week, the Food and Drug Administration released a list of about 20 pharmaceutical drugs that the agency’s researchers are closely monitoring for potential safety concerns. Not surprisingly, Chantix (Varenicline) claimed a spot on the list. According to the FDA, the drug is being watched to determine whether it causes or contributes to angiodema (rapid [...]<p>SOURCE: <a href="http://www.chantix-legal.com">Chantix Recall</a> &rsaquo; <a href="http://www.chantix-legal.com/news/2009/06/09/fda-monitoring-chantix-for-serious-risks-new-safety-concerns/">FDA monitoring Chantix for serious risks, new safety concerns</a></p>
]]></description>
			<content:encoded><![CDATA[<p><img class="alignleft size-thumbnail wp-image-594" title="no-smoking" src="http://www.chantix-legal.com/media/2009/06/no-smoking-100x100.jpg" alt="no smoking 100x100" width="100" height="100" />Last week, the <a href="http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/ucm161063.htm"><strong>Food and Drug Administration</strong></a> released a list of about 20 pharmaceutical drugs that the agency’s researchers are closely monitoring for potential <strong>safety concerns</strong>. Not surprisingly, <strong><a href="http://www.chantix-legal.com/" title="" rel="external">Chantix</a></strong> (Varenicline) claimed a spot on the list. According to the <a href="http://www.chantix-legal.com/tag/fda/" class="st_tag internal_tag" rel="tag" title="Posts tagged with FDA">FDA</a>, the drug is being watched to determine whether it causes or contributes to <strong>angiodema</strong> (rapid and potentially life-threatening swelling of skin and tissue), other <strong>serious skin reactions</strong>, <strong>visual impairment</strong>, and <strong>accidental injury</strong>. <span id="more-592"></span></p>
<p>Data pulled from the <a href="http://www.chantix-legal.com/tag/fda/" class="st_tag internal_tag" rel="tag" title="Posts tagged with FDA">FDA</a>’s <strong><a href="http://www.chantix-legal.com/tag/adverse-event/" class="st_tag internal_tag" rel="tag" title="Posts tagged with adverse event">Adverse Event</a> Reporting System</strong> (AERS) between October and December of 2008 suggested that <a href="http://www.chantix-legal.com/" title="" rel="external">Chantix</a> may be linked to the <a href="http://www.chantix-legal.com/tag/side-effects/" class="st_tag internal_tag" rel="tag" title="Posts tagged with side effects">side effects</a>. The <a href="http://www.chantix-legal.com/tag/fda/" class="st_tag internal_tag" rel="tag" title="Posts tagged with FDA">FDA</a> will continue to monitor <a href="http://www.chantix-legal.com/tag/chantix/" title="" rel="external">Chantix</a> for an unspecified length of time until it determines what, if any, <strong>regulatory action</strong> is needed.</p>
<p>The <a href="http://www.chantix-legal.com/tag/fda/" class="st_tag internal_tag" rel="tag" title="Posts tagged with FDA">FDA</a> does not fully test prescription drugs for safety before allowing them to enter into the market. Why? It’s a matter of logistics more than anything. Typically, <a href="http://www.chantix-legal.com/tag/fda/" class="st_tag internal_tag" rel="tag" title="Posts tagged with FDA">FDA</a> studies are designed to measure a drug’s effectiveness using thousands of patients who willingly participate in pre-market clinical trials. These patients obviously represent a very small slice of U.S. population. The <a href="http://www.chantix-legal.com/tag/fda/" class="st_tag internal_tag" rel="tag" title="Posts tagged with FDA">FDA</a> also relies on studies conducted by the pharmaceutical companies themselves to determine how effective test drugs are. If new drugs that have passed tests for efficacy appear to be <strong>reasonably safe</strong>, then <a href="http://www.chantix-legal.com/tag/fda/" class="st_tag internal_tag" rel="tag" title="Posts tagged with FDA">FDA</a> researchers give them the green light.</p>
<p>The <a href="http://www.chantix-legal.com/tag/fda/" class="st_tag internal_tag" rel="tag" title="Posts tagged with FDA">FDA</a>, incidentally, reviewed Chantix in six months rather than the regular review time of 10 months.</p>
<p>The millions of people in the U.S. and around the world who started taking Chantix when it debuted on the world market in May 2006 became patients in the world’s first mass clinical trial. Most people assume that the <a href="http://www.chantix-legal.com/tag/fda/" class="st_tag internal_tag" rel="tag" title="Posts tagged with FDA">FDA</a> seal of approval means that the drug will be perfectly safe, but the truth is that <strong>most of a drug’s risks are not known until it is prescribed to millions of consumers</strong>.</p>
<p>The first reports of adverse events linked to Chantix emerged just months after the drug was released to the public. On February 1, 2008, the <a href="http://www.chantix-legal.com/tag/fda/" class="st_tag internal_tag" rel="tag" title="Posts tagged with FDA">FDA</a> issued a statement saying “it appears increasingly likely that there is an association between Chantix and <strong>serious neuropsychiatric symptoms</strong>.”</p>
<p>By May 2008, Chantix was linked to more than <strong>3,000</strong> reports of serious <a href="http://www.chantix-legal.com/tag/side-effects/" class="st_tag internal_tag" rel="tag" title="Posts tagged with side effects">side effects</a>. By November of the same year, data from the <a href="http://www.chantix-legal.com/tag/fda/" class="st_tag internal_tag" rel="tag" title="Posts tagged with FDA">FDA</a>’s <a href="http://www.chantix-legal.com/tag/adverse-event/" class="st_tag internal_tag" rel="tag" title="Posts tagged with adverse event">Adverse Event</a> Reporting System showed that <strong>more reported serious injuries</strong> resulted from Chantix than any other prescription drug.</p>
<p>SOURCE: <a href="http://www.chantix-legal.com">Chantix Recall</a> &rsaquo; <a href="http://www.chantix-legal.com/news/2009/06/09/fda-monitoring-chantix-for-serious-risks-new-safety-concerns/">FDA monitoring Chantix for serious risks, new safety concerns</a></p>
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