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	<title>The eDrugSearch Blog &#187; Ketek</title>
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	<description>Helping Americans Buy Prescription Drugs Online from Canada</description>
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		<title>New &#8220;black box&#8221; warning on controversial antibiotic</title>
		<link>/edsblog/new-%e2%80%9cblack-box%e2%80%9d-warning-on-controversial-antibiotic/</link>
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		<pubDate>Wed, 14 Feb 2007 06:25:50 +0000</pubDate>
		<dc:creator>Cary Byrd</dc:creator>
				<category><![CDATA[Ketek]]></category>
		<category><![CDATA[Prescription drugs]]></category>
		<category><![CDATA[Sanofi-Aventis]]></category>

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	<category>sanofi</category>
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		<description><![CDATA[The FDA announced that the antibiotic Ketek, used to treat pneumonia, must come with a new &#8220;black box label&#8221; &#8212; the strongest warning the agency can impose on a drug. Additionally, Ketek can no longer be recommended for treating milder conditions such as sinusitis and bronchitis. The changes come after the medication was found to [...]]]></description>
			<content:encoded><![CDATA[<p>The <a target="_blank" href="http://www.fda.gov/medwatch/safety/2007/safety07.htm#Ketek">FDA announced </a>that the antibiotic Ketek, used to treat pneumonia, must come with a new &#8220;black box label&#8221; &#8212; the strongest warning the agency can impose on a drug.  Additionally, Ketek can no longer be recommended for treating milder conditions such as sinusitis and bronchitis.  The changes come after the medication was found to cause serious liver damage in studies.  </p>
<p><a target="_blank" href="http://www.forbes.com/health/feeds/hscout/2007/02/12/hscout601848.html">Forbes.com</a> states:</p>
<blockquote><p>The drug and the related approval process have been dogged by criticism &#8230; Last June, Sanofi-Aventis agreed to update Ketek&#8217;s labeling to reflect the possibility of severe liver damage. And last month, a European Medicines Agency panel recommended that Ketek not be given to patients with a history of such liver conditions as hepatitis or jaundice.</p></blockquote>
<p>Sanofi-Aventis is currently under investigation by both the U.S. House and Senate for irregularities during the approval process.</p>
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