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    <title>topic Re: Analysis of Pharmacovigilance database in SAS Programming</title>
    <link>https://communities.sas.com/t5/SAS-Programming/Analysis-of-Pharmacovigilance-database/m-p/888072#M350880</link>
    <description>&lt;P&gt;This is an &lt;STRONG&gt;old&lt;/STRONG&gt; paper :&lt;/P&gt;
&lt;P&gt;&amp;nbsp;&lt;/P&gt;
&lt;P&gt;SAS Global Forum 2013 -- Pharma and Health Care&lt;BR /&gt;Paper 166-2013&lt;BR /&gt;Identifying and Addressing Post-Marketing Pharmaceutical Safety Surveillance and Spontaneous Reported Events&lt;BR /&gt;Carrie Boorse, Stuart Levine, and Kathy Schaan&lt;BR /&gt;SAS Institute Inc., Cary, NC&lt;BR /&gt;&lt;A href="https://support.sas.com/resources/papers/proceedings13/166-2013.pdf" target="_blank"&gt;https://support.sas.com/resources/papers/proceedings13/166-2013.pdf&lt;/A&gt;&lt;/P&gt;
&lt;P&gt;&amp;nbsp;&lt;/P&gt;
&lt;P&gt;There might be a more recent solution in SAS Viya.&lt;/P&gt;
&lt;P&gt;&amp;nbsp;&lt;/P&gt;
&lt;P&gt;Koen&lt;/P&gt;</description>
    <pubDate>Sun, 06 Aug 2023 16:24:09 GMT</pubDate>
    <dc:creator>sbxkoenk</dc:creator>
    <dc:date>2023-08-06T16:24:09Z</dc:date>
    <item>
      <title>Analysis of Pharmacovigilance database</title>
      <link>https://communities.sas.com/t5/SAS-Programming/Analysis-of-Pharmacovigilance-database/m-p/888041#M350865</link>
      <description>Hi. I’m looking for SAS coding for Reporting Odds Ratios (ROR) and Proportional Reporting Ratios (PRR) analysis in Pharmacovigilance database. Could you help me please?</description>
      <pubDate>Sat, 05 Aug 2023 21:48:24 GMT</pubDate>
      <guid>https://communities.sas.com/t5/SAS-Programming/Analysis-of-Pharmacovigilance-database/m-p/888041#M350865</guid>
      <dc:creator>Jerbaly</dc:creator>
      <dc:date>2023-08-05T21:48:24Z</dc:date>
    </item>
    <item>
      <title>Re: Analysis of Pharmacovigilance database</title>
      <link>https://communities.sas.com/t5/SAS-Programming/Analysis-of-Pharmacovigilance-database/m-p/888072#M350880</link>
      <description>&lt;P&gt;This is an &lt;STRONG&gt;old&lt;/STRONG&gt; paper :&lt;/P&gt;
&lt;P&gt;&amp;nbsp;&lt;/P&gt;
&lt;P&gt;SAS Global Forum 2013 -- Pharma and Health Care&lt;BR /&gt;Paper 166-2013&lt;BR /&gt;Identifying and Addressing Post-Marketing Pharmaceutical Safety Surveillance and Spontaneous Reported Events&lt;BR /&gt;Carrie Boorse, Stuart Levine, and Kathy Schaan&lt;BR /&gt;SAS Institute Inc., Cary, NC&lt;BR /&gt;&lt;A href="https://support.sas.com/resources/papers/proceedings13/166-2013.pdf" target="_blank"&gt;https://support.sas.com/resources/papers/proceedings13/166-2013.pdf&lt;/A&gt;&lt;/P&gt;
&lt;P&gt;&amp;nbsp;&lt;/P&gt;
&lt;P&gt;There might be a more recent solution in SAS Viya.&lt;/P&gt;
&lt;P&gt;&amp;nbsp;&lt;/P&gt;
&lt;P&gt;Koen&lt;/P&gt;</description>
      <pubDate>Sun, 06 Aug 2023 16:24:09 GMT</pubDate>
      <guid>https://communities.sas.com/t5/SAS-Programming/Analysis-of-Pharmacovigilance-database/m-p/888072#M350880</guid>
      <dc:creator>sbxkoenk</dc:creator>
      <dc:date>2023-08-06T16:24:09Z</dc:date>
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