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    <title>Danish Medicines Agency</title>
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      <title>EMA warns Ozempic linked to ‘very rare’ side effect</title>
      <description>The EMA’s safety committee has issued a warning that the GLP-1 receptor agonist Ozempic (semaglutide, Novo Nordisk A/S) can cause an acute eye condition in which the optic nerve is damaged by a sudden loss of blood supply. After reviewing several large epidemiological studies, clinical trial and in-market data, EMA’s Pharmacovigilance Risk Assessment Committee has concluded non-anterior ischemic optic neuropathy is a “very rare” side effect of Ozempic, that “may affect up to one in 10,000 people taking semaglutide.</description>
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        <![CDATA[The EMA’s safety committee has issued a warning that the GLP-1 receptor agonist Ozempic (semaglutide, Novo Nordisk A/S) can cause an acute eye condition in which the optic nerve is damaged by a sudden loss of blood supply. After reviewing several large epidemiological studies, clinical trial and in-market data, EMA’s Pharmacovigilance Risk Assessment Committee has concluded non-anterior ischemic optic neuropathy is a “very rare” side effect of Ozempic, that “may affect up to one in 10,000 people taking semaglutide.]]>
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      <guid>http://www.bioworld.com/articles/720950</guid>
      <pubDate>Fri, 06 Jun 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/720950-ema-warns-ozempic-linked-to-very-rare-side-effect</link>
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        <media:title type="plain">Ozempic pen and packaging </media:title>
        <media:description type="plain">Credit: Novo Nordisk A/S</media:description>
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      <title>EMA investigating potential semaglutide link to eye disease</title>
      <description>The EMA has started a review of Novo Nordisk A/S’ GLP-1 receptor agonist, semaglutide, after the Danish regulatory agency raised the possibility it causes an increased risk of suffering from an acute eye condition. After the first report in July 2024, the Danish regulator had received, by Dec. 10, 2024, a total of 19 reports of non-arteric anterior ischemic neuropathy, a rare condition that affects the small blood vessels at the front of the optic nerve. This can lead on to sudden vision loss and visual field defects.</description>
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        <![CDATA[The EMA has started a review of Novo Nordisk A/S’ GLP-1 receptor agonist, semaglutide, after the Danish regulatory agency raised the possibility it causes an increased risk of suffering from an acute eye condition. After the first report in July 2024, the Danish regulator had received, by Dec. 10, 2024, a total of 19 reports of non-arteric anterior ischemic neuropathy, a rare condition that affects the small blood vessels at the front of the optic nerve. This can lead on to sudden vision loss and visual field defects.]]>
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      <guid>http://www.bioworld.com/articles/716383</guid>
      <pubDate>Fri, 17 Jan 2025 12:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/716383-ema-investigating-potential-semaglutide-link-to-eye-disease</link>
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      <title>Danish regulators question possible Ozempic link to rare eye condition</title>
      <description>The Danish Medicines Agency is to ask the EMA’s pharmacovigilance committee to investigate a potential increased risk of an acute eye condition in diabetic patients being treated with the glucagon-like peptide-1 receptor agonist Ozempic (semaglutide).</description>
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        <![CDATA[The Danish Medicines Agency is to ask the EMA’s pharmacovigilance committee to investigate a potential increased risk of an acute eye condition in diabetic patients being treated with the glucagon-like peptide-1 receptor agonist Ozempic (semaglutide).]]>
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      <guid>http://www.bioworld.com/articles/715438</guid>
      <pubDate>Tue, 17 Dec 2024 16:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/715438-danish-regulators-question-possible-ozempic-link-to-rare-eye-condition</link>
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        <media:title type="plain">Ozempic pen and packaging </media:title>
        <media:description type="plain">Credit: Novo Nordisk A/S</media:description>
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      <title>Danish Medicines Agency approves AJ Vaccines' polio vaccine</title>
      <description></description>
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        <![CDATA[]]>
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      <guid>http://www.bioworld.com/articles/672504</guid>
      <pubDate>Mon, 01 Jul 2019 00:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/672504-danish-medicines-agency-approves-aj-vaccines-polio-vaccine</link>
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      <title>Danish clearance for Oncology Venture's study of APO-010 in multiple myeloma</title>
      <description></description>
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      <guid>http://www.bioworld.com/articles/658130</guid>
      <pubDate>Thu, 23 Mar 2017 00:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/658130-danish-clearance-for-oncology-venture-s-study-of-apo-010-in-multiple-myeloma</link>
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      <title>Avexxin cleared to conduct study of AVX-001 in Denmark</title>
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        <![CDATA[]]>
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      <guid>http://www.bioworld.com/articles/631919</guid>
      <pubDate>Fri, 08 Feb 2013 00:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/631919-avexxin-cleared-to-conduct-study-of-avx-001-in-denmark</link>
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      <title>Almirall launches aclidinium in Europe</title>
      <description></description>
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        <![CDATA[]]>
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      <guid>http://www.bioworld.com/articles/629516</guid>
      <pubDate>Fri, 21 Sep 2012 00:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/629516-almirall-launches-aclidinium-in-europe</link>
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      <title>First European approval granted for Sumavel DosePro for migraine</title>
      <description></description>
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        <![CDATA[]]>
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      <guid>http://www.bioworld.com/articles/618222</guid>
      <pubDate>Thu, 09 Dec 2010 00:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/618222-first-european-approval-granted-for-sumavel-dosepro-for-migraine</link>
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