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	<title>Comments on: FDA Riled over Approving Glaxo’s Flu Vaccine after EU Reports of Narcolepsy</title>
	<atom:link href="http://www.jdjournal.com/2013/03/08/fda-riled-over-approving-glaxos-flu-vaccine-after-eu-reports-of-narcolepsy/feed/" rel="self" type="application/rss+xml" />
	<link>http://www.jdjournal.com/2013/03/08/fda-riled-over-approving-glaxos-flu-vaccine-after-eu-reports-of-narcolepsy/</link>
	<description>Legal Industry News</description>
	<lastBuildDate>Wed, 19 Jun 2013 16:40:00 +0000</lastBuildDate>
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		<title>By: Mr. Pube</title>
		<link>http://www.jdjournal.com/2013/03/08/fda-riled-over-approving-glaxos-flu-vaccine-after-eu-reports-of-narcolepsy/comment-page-1/#comment-395999</link>
		<dc:creator>Mr. Pube</dc:creator>
		<pubDate>Wed, 08 May 2013 16:30:10 +0000</pubDate>
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		<description>Kill two birds with one stone, induce ailments in children that can be fed off in the long run and make big profits in the short term, you&#039;ve never had it so good my children, next please.</description>
		<content:encoded><![CDATA[<p>Kill two birds with one stone, induce ailments in children that can be fed off in the long run and make big profits in the short term, you&#8217;ve never had it so good my children, next please.</p>
]]></content:encoded>
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		<title>By: MERYL NASS, MD</title>
		<link>http://www.jdjournal.com/2013/03/08/fda-riled-over-approving-glaxos-flu-vaccine-after-eu-reports-of-narcolepsy/comment-page-1/#comment-238549</link>
		<dc:creator>MERYL NASS, MD</dc:creator>
		<pubDate>Fri, 08 Mar 2013 21:07:14 +0000</pubDate>
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		<description>FDA framed its charge to the advisory committee carefully.  They were not sked to comment on safety.  Their charge was to comment on immunogenicity.  FDA could have made the immunogenicity determination on its own.  But probably sensing a controversy ahead, the vaccine advisory panel was used to gain a sela of approval--that ignored all safety questions.

MN</description>
		<content:encoded><![CDATA[<p>FDA framed its charge to the advisory committee carefully.  They were not sked to comment on safety.  Their charge was to comment on immunogenicity.  FDA could have made the immunogenicity determination on its own.  But probably sensing a controversy ahead, the vaccine advisory panel was used to gain a sela of approval&#8211;that ignored all safety questions.</p>
<p>MN</p>
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