{"id":7507,"date":"2023-01-30T13:32:09","date_gmt":"2023-01-30T10:32:09","guid":{"rendered":"https:\/\/urbancare.clinic\/fda-revokes-emergency-use-authorization-of-covid-drug-ineffective-against-new-variants\/"},"modified":"2023-01-30T13:32:09","modified_gmt":"2023-01-30T10:32:09","slug":"la-fda-revoque-lautorisation-dutilisation-durgence-dun-medicament-covid-inefficace-contre-les-nouvelles-variantes","status":"publish","type":"post","link":"https:\/\/urbancare.clinic\/fr\/la-fda-revoque-lautorisation-dutilisation-durgence-dun-medicament-covid-inefficace-contre-les-nouvelles-variantes\/","title":{"rendered":"La FDA r\u00e9voque l\u2019autorisation d\u2019utilisation d\u2019urgence d\u2019un m\u00e9dicament Covid inefficace contre les nouvelles variantes"},"content":{"rendered":"<div><img decoding=\"async\" src=\"https:\/\/urbancare.clinic\/wp-content\/uploads\/2023\/01\/fda-revokes-emergency-use-authorization-of-covid-drug-ineffective-against-new-variants.jpg\" class=\"ff-og-image-inserted\" style=\"display:none\"><\/div>\n<p>La Food and Drug Administration (FDA) des \u00c9tats-Unis a annonc\u00e9 jeudi qu&#039;elle retirait l&#039;autorisation d&#039;utilisation d&#039;urgence d&#039;un m\u00e9dicament contre le Covid-19, car il est peu probable qu&#039;il soit efficace contre les nouveaux variants circulant dans la population.<\/p>\n<p>Le m\u00e9dicament en question est l\u2019Evusheld, fabriqu\u00e9 par la soci\u00e9t\u00e9 pharmaceutique et biotechnologique anglo-su\u00e9doise AstraZeneca. Il a \u00e9t\u00e9 autoris\u00e9 pour la premi\u00e8re fois en d\u00e9cembre 2021 comme prophylaxie pr\u00e9-exposition contre le SRAS-COV-2 pour les personnes immunod\u00e9prim\u00e9es, car elles sont moins susceptibles de produire des anticorps suite \u00e0 la vaccination, selon <a href=\"https:\/\/abcnews.go.com\/Health\/fda-withdraws-authorization-covid-drug-effective-new-variants\/story?id=96715718\" rel=\"nofollow noopener\" target=\"_blank\">ABCActualit\u00e9s<\/a>.<\/p>\n<p>C&#039;est un type de <a href=\"https:\/\/www.medicaldaily.com\/how-does-covid-19-prevention-drug-evusheld-work-and-who-should-receive-it-465508\">traitement par anticorps monoclonaux<\/a>, contenant des anticorps produits en laboratoire qui imitent ceux que le corps g\u00e9n\u00e8re naturellement lorsqu\u2019il rencontre le virus. Il s\u2019agit d\u2019une combinaison de deux anticorps, le tixagevimab et le cilgavimab, qui se lient \u00e0 la prot\u00e9ine de pointe du virus responsable du COVID-19 et l\u2019emp\u00eachent de p\u00e9n\u00e9trer et d\u2019infecter les cellules.<\/p>\n<p>Evusheld ne neutralise pas plusieurs sous-variantes d&#039;omicrons, notamment BQ.1, BQ.1.1, BF.7, BF.11, BA.5.2.6, BA.4.6, BA.2.75.2, XBB et XBB.1.5, a d\u00e9clar\u00e9 la FDA. dans un <a href=\"https:\/\/www.fda.gov\/drugs\/drug-safety-and-availability\/fda-announces-evusheld-not-currently-authorized-emergency-use-us\" rel=\"nofollow noopener\" target=\"_blank\">communiqu\u00e9 de presse<\/a>.<\/p>\n<div id=\"dfp-ad-oop2\" class=\"dfp-tag-wrapper\"> <\/div>\n<p>Ces sous-variantes seraient \u00e0 l&#039;origine de 90% de cas aux \u00c9tats-Unis, selon le&nbsp; <a href=\"https:\/\/covid.cdc.gov\/covid-data-tracker\/#variant-proportions\" rel=\"nofollow noopener\" target=\"_blank\"> Centres pour le Contr\u00f4le et la Pr\u00e9vention des catastrophes<\/a>.<\/p>\n<p>&quot;Cela signifie qu&#039;Evusheld ne devrait pas fournir de protection contre le d\u00e9veloppement du COVID-19 s&#039;il est expos\u00e9 \u00e0 ces variantes&quot;, a d\u00e9clar\u00e9 la FDA dans le communiqu\u00e9 de presse.<\/p>\n<p>&quot;L&#039;action d&#039;aujourd&#039;hui visant \u00e0 limiter l&#039;utilisation d&#039;Evusheld \u00e9vite d&#039;exposer les patients \u00e0 d&#039;\u00e9ventuels effets secondaires d&#039;Evusheld tels que des r\u00e9actions allergiques, qui peuvent \u00eatre potentiellement graves, \u00e0 un moment o\u00f9 moins de 10% des variantes en circulation aux \u00c9tats-Unis provoquant une infection sont sensibles au produit&quot;, \u00bb, poursuit le communiqu\u00e9.<\/p>\n<p>La FDA avait d\u00e9j\u00e0 abord\u00e9 ce sujet. Le 6 janvier, la FDA a d\u00e9clar\u00e9 qu&#039;elle \u00e9tait sceptique quant \u00e0 la capacit\u00e9 d&#039;Evusheld \u00e0 neutraliser la sous-variante XBB.1.5 &quot;en raison de sa similitude avec des variantes qui ne sont pas neutralis\u00e9es par Evusheld&quot;, a rapport\u00e9 le m\u00e9dia.<\/p>\n<p>Pendant ce temps, AstraZeneca a d\u00e9clar\u00e9 dans un <a href=\"https:\/\/www.astrazeneca-us.com\/content\/az-us\/media\/press-releases\/2023\/update-on-us-food-and-drug-administration-emergency-use-authorization-of-evusheld.html\" rel=\"nofollow noopener\" target=\"_blank\">d\u00e9claration<\/a> qu&#039;elle continuera \u00e0 coop\u00e9rer avec les d\u00e9cisions de la FDA.<\/p>\n<p>&quot;AstraZeneca continuera \u00e0 travailler avec la FDA et d&#039;autres autorit\u00e9s sanitaires pour collecter, \u00e9valuer et partager des donn\u00e9es pertinentes concernant les variantes Evusheld et du SRAS-CoV-2&quot;, indique le communiqu\u00e9. &quot;Evusheld reste actuellement autoris\u00e9 dans d&#039;autres pays o\u00f9 il est approuv\u00e9 pour la prophylaxie et le traitement pr\u00e9-exposition au COVID-19, notamment dans l&#039;UE et au Japon.&quot;<\/p>\n<p>Malgr\u00e9 la r\u00e9vocation du statut d&#039;autorisation d&#039;utilisation d&#039;urgence du m\u00e9dicament, la FDA a conseill\u00e9 aux fournisseurs du m\u00e9dicament de ne pas jeter leurs produits pour l&#039;instant.<\/p>\n<p>&quot;Le gouvernement am\u00e9ricain recommande que les installations et les fournisseurs d&#039;Evusheld conservent tous leurs produits au cas o\u00f9 les variantes du SRAS-CoV-2 neutralis\u00e9es par Evusheld deviendraient plus r\u00e9pandues aux \u00c9tats-Unis \u00e0 l&#039;avenir&quot;, a d\u00e9clar\u00e9 la FDA dans son communiqu\u00e9 de presse.<\/p>\n<p><a href=\"https:\/\/www.medicaldaily.com\/fda-revokes-emergency-use-authorization-covid-drug-ineffective-against-new-467903?utm_source=Public&#038;utm_medium=Feed&#038;utm_campaign=Distribution\">Source quotidienne m\u00e9dicale<\/a><\/p>\n<p>","protected":false},"excerpt":{"rendered":"<p>Evusheld ne neutralise pas plusieurs sous-variantes d&#039;omicrons, notamment BQ.1, BQ.1.1, BF.7, BF.11, BA.5.2.6, BA.4.6, BA.2.75.2, XBB et XBB.1.5, a d\u00e9clar\u00e9 la FDA dans un communiqu\u00e9 de presse.<\/p>","protected":false},"author":2,"featured_media":7508,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"Default","format":"standard","meta":{"fifu_image_url":"https:\/\/urbancare.clinic\/wp-content\/uploads\/2023\/01\/fda-revokes-emergency-use-authorization-of-covid-drug-ineffective-against-new-variants.jpg","fifu_image_alt":"","footnotes":""},"categories":[27],"tags":[],"class_list":["post-7507","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-blog"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.6 - 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