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	<title>Comments on: FDA urges Pfizer to pull Bextra from shelves, issues Celebrex, Vioxx warning</title>
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	<link>http://blog.lawinfo.com/2005/04/07/fda-urges-pfizer-to-pulls-bextra-from-shelves-issues-celebrex-warning/</link>
	<description>Lawyer Blog &#124; Attorney Blog &#124; Read and Post</description>
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		<title>By: Lindsey</title>
		<link>http://blog.lawinfo.com/2005/04/07/fda-urges-pfizer-to-pulls-bextra-from-shelves-issues-celebrex-warning/comment-page-1/#comment-3542</link>
		<dc:creator>Lindsey</dc:creator>
		<pubDate>Wed, 01 Oct 2008 16:51:19 +0000</pubDate>
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		<description>Pat- it appears Celebrex was not recalled, though the FDA did issue a statement about it and required some additional information.  According to the FDA:  

&quot;FDA ALERT-[4/7/2005]: Celebrex has been linked to an increased risk of serious cardiovascular (CV) events (such as heart attack or stroke) which appears to be a risk shared by all medicines called non-steroidal anti-inflammatory drugs (NSAIDs) (excluding aspirin). FDA has requested that the package insert (labeling) for all NSAIDs, including Celebrex, be revised to include a “boxed” or serious warning to highlight the potential increased risk of CV events, and the well known risk of serious, and potentially life-threatening, stomach bleeding. FDA has also requested that the package insert for all NSAIDs be revised to state that patients who have just had heart surgery should not take these medicines. &quot;

You can learn read the FDA&#039;s statement about Celebrex here:  http://www.fda.gov/bbs/topics/news/2004/new01144.html.    The FDA may take a variety of actions related to certain drugs including safety alerts, withdrawals and recalls.  Not all actions taken by the FDA lead to a recall. See:  http://www.fda.gov/oc/po/firmrecalls/recall_defin.html.</description>
		<content:encoded><![CDATA[<p>Pat- it appears Celebrex was not recalled, though the FDA did issue a statement about it and required some additional information.  According to the FDA:  </p>
<p>&#8220;FDA ALERT-[4/7/2005]: Celebrex has been linked to an increased risk of serious cardiovascular (CV) events (such as heart attack or stroke) which appears to be a risk shared by all medicines called non-steroidal anti-inflammatory drugs (NSAIDs) (excluding aspirin). FDA has requested that the package insert (labeling) for all NSAIDs, including Celebrex, be revised to include a “boxed” or serious warning to highlight the potential increased risk of CV events, and the well known risk of serious, and potentially life-threatening, stomach bleeding. FDA has also requested that the package insert for all NSAIDs be revised to state that patients who have just had heart surgery should not take these medicines. &#8221;</p>
<p>You can learn read the FDA&#8217;s statement about Celebrex here:  <a href="http://www.fda.gov/bbs/topics/news/2004/new01144.html" rel="nofollow" class="liexternal">http://www.fda.gov/bbs/topics/news/2004/new01144.html</a>.    The FDA may take a variety of actions related to certain drugs including safety alerts, withdrawals and recalls.  Not all actions taken by the FDA lead to a recall. See:  <a href="http://www.fda.gov/oc/po/firmrecalls/recall_defin.html." rel="nofollow" class="liexternal">http://www.fda.gov/oc/po/firmrecalls/recall_defin.html.</a></p>
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		<title>By: Pat</title>
		<link>http://blog.lawinfo.com/2005/04/07/fda-urges-pfizer-to-pulls-bextra-from-shelves-issues-celebrex-warning/comment-page-1/#comment-3539</link>
		<dc:creator>Pat</dc:creator>
		<pubDate>Tue, 30 Sep 2008 16:17:27 +0000</pubDate>
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		<description>Was Celebrex also recalled?</description>
		<content:encoded><![CDATA[<p>Was Celebrex also recalled?</p>
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