{"id":65288,"date":"2021-03-16T03:00:57","date_gmt":"2021-03-16T02:00:57","guid":{"rendered":"https:\/\/www.cde.ual.es\/?p=65288"},"modified":"2021-09-15T10:37:47","modified_gmt":"2021-09-15T08:37:47","slug":"covid-19-vaccine-astrazeneca-prac-investigating-cases-of-thromboembolic-events","status":"publish","type":"post","link":"https:\/\/www.cde.ual.es\/en\/covid-19-vaccine-astrazeneca-prac-investigating-cases-of-thromboembolic-events\/","title":{"rendered":"COVID-19 Vaccine AstraZeneca: PRAC investigating cases of thromboembolic events"},"content":{"rendered":"<p><a href=\"https:\/\/www.cde.ual.es\/wp-content\/uploads\/2021\/03\/robina-weermeijer-z8_-Fmfz06c-unsplash-scaled.jpg\"><img decoding=\"async\" class=\"wp-image-65293 aligncenter\" src=\"https:\/\/www.cde.ual.es\/wp-content\/uploads\/2021\/03\/robina-weermeijer-z8_-Fmfz06c-unsplash-scaled.jpg\" alt=\"\" width=\"372\" height=\"248\" srcset=\"https:\/\/www.cde.ual.es\/wp-content\/uploads\/2021\/03\/robina-weermeijer-z8_-Fmfz06c-unsplash-scaled.jpg 2560w, https:\/\/www.cde.ual.es\/wp-content\/uploads\/2021\/03\/robina-weermeijer-z8_-Fmfz06c-unsplash-300x200.jpg 300w, https:\/\/www.cde.ual.es\/wp-content\/uploads\/2021\/03\/robina-weermeijer-z8_-Fmfz06c-unsplash-1024x683.jpg 1024w, https:\/\/www.cde.ual.es\/wp-content\/uploads\/2021\/03\/robina-weermeijer-z8_-Fmfz06c-unsplash-768x512.jpg 768w, https:\/\/www.cde.ual.es\/wp-content\/uploads\/2021\/03\/robina-weermeijer-z8_-Fmfz06c-unsplash-1536x1024.jpg 1536w, https:\/\/www.cde.ual.es\/wp-content\/uploads\/2021\/03\/robina-weermeijer-z8_-Fmfz06c-unsplash-2048x1365.jpg 2048w\" sizes=\"(max-width: 372px) 100vw, 372px\" \/><\/a><\/p>\n<p>EMA is aware that the Danish Health Authority has paused its vaccination campaign with COVID-19 Vaccine AstraZeneca. This was decided as a precautionary measure while a full investigation is ongoing into reports of blood clots in people who received the vaccine, including one case in Denmark where a person died. Some other Member States have also paused vaccination with this vaccine.<\/p>\n<p>There is currently no\u00a0indication\u00a0that vaccination has caused these conditions, which are not listed as side effects with this vaccine. The position of EMA\u2019s safety committee\u00a0PRAC\u00a0is that the vaccine\u2019s benefits continue to outweigh its risks and the vaccine can continue to be administered while investigation of cases of thromboembolic events is ongoing.\u00a0PRAC\u00a0is already\u00a0reviewing\u00a0all cases of thromboembolic events, and other conditions related to blood clots, reported post-vaccination with COVID-19 Vaccine AstraZeneca.<\/p>\n<p>The number of thromboembolic events in vaccinated people is no higher than the number seen in the general population. As of 10 March 2021, 30 cases<sup>1<\/sup>\u00a0of thromboembolic events had been reported among close to 5 million people vaccinated with COVID-19 Vaccine AstraZeneca in the European Economic Area.<\/p>\n<p>EMA will further communicate as the assessment progresses.<\/p>\n<h3>More about the medicine<\/h3>\n<p>COVID-19 Vaccine AstraZeneca is a vaccine for preventing coronavirus disease 2019 (COVID-19) in people aged 18 years and older. COVID-19 is caused by SARS-CoV-2 virus. COVID-19 Vaccine AstraZeneca is made up of another virus (of the adenovirus family) that has been modified to contain the gene for making a protein from SARS-CoV-2. COVID-19 Vaccine AstraZeneca does not contain the virus itself and cannot cause COVID-19.<\/p>\n<p>The most common side effects with COVID-19 Vaccine AstraZeneca are usually mild or moderate and improve within a few days after vaccination.<\/p>\n<h3>More about the procedure<\/h3>\n<p>The review of thromboembolic events with COVID-19 Vaccine AstraZeneca is being carried out in the context of a\u00a0safety signal, under an accelerated timetable. A\u00a0safety signal\u00a0is information on a new or incompletely documented\u00a0adverse event\u00a0that is potentially caused by a medicine and that warrants further investigation.<\/p>\n<p>The review is being carried out by EMA&#8217;s\u00a0Pharmacovigilance Risk Assessment Committee\u00a0(PRAC), the Committee responsible for the evaluation of safety issues for human medicines. Once the review is completed,\u00a0PRAC\u00a0will make any recommendations necessary to minimise risks and protect patients&#8217; health.<\/p>\n<h3>More information<\/h3>\n<p><a href=\"https:\/\/www.ema.europa.eu\/en\/news\/covid-19-vaccine-astrazeneca-prac-investigating-cases-thromboembolic-events-vaccines-benefits\" target=\"_blank\" rel=\"noopener\">European Medicines Agency &#8211; Press Release<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>EMA is aware that the Danish Health Authority has paused its vaccination campaign with COVID-19 Vaccine AstraZeneca. This was decided as a precautionary measure while a full investigation is ongoing into reports of blood clots in people who received the vaccine, including one case in Denmark where a person died. Some other Member States have [&hellip;]<\/p>\n","protected":false},"author":101012,"featured_media":65293,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"_genesis_hide_title":false,"_genesis_hide_breadcrumbs":false,"_genesis_hide_singular_image":false,"_genesis_hide_footer_widgets":false,"_genesis_custom_body_class":"","_genesis_custom_post_class":"","_genesis_layout":"","footnotes":""},"categories":[4093,346,4094],"tags":[2598,2448,2843,700],"class_list":{"0":"post-65288","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-diseases","8":"category-eu-news","9":"category-farmac","10":"tag-astrazeneca-en","11":"tag-covid","12":"tag-thrombosis","13":"tag-vaccine-en","14":"entry"},"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>COVID-19 Vaccine AstraZeneca: PRAC investigating cases of thromboembolic events | CDE Almer\u00eda - Centro de Documentaci\u00f3n Europea - Universidad de Almer\u00eda<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.cde.ual.es\/en\/covid-19-vaccine-astrazeneca-prac-investigating-cases-of-thromboembolic-events\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"COVID-19 Vaccine AstraZeneca: PRAC investigating cases of thromboembolic events | CDE Almer\u00eda - Centro de Documentaci\u00f3n Europea - Universidad de Almer\u00eda\" \/>\n<meta property=\"og:description\" content=\"EMA is aware that the Danish Health Authority has paused its vaccination campaign with COVID-19 Vaccine AstraZeneca. This was decided as a precautionary measure while a full investigation is ongoing into reports of blood clots in people who received the vaccine, including one case in Denmark where a person died. 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