{"id":16278,"date":"2021-11-04T15:21:59","date_gmt":"2021-11-04T18:21:59","guid":{"rendered":"https:\/\/portaldasaudenews.com\/?p=16278"},"modified":"2021-11-04T15:21:59","modified_gmt":"2021-11-04T18:21:59","slug":"reino-unido-e-o-1o-pais-a-aprovar-comprimido-experimental-contra-covid","status":"publish","type":"post","link":"https:\/\/portaldasaudenews.com\/?p=16278","title":{"rendered":"Reino Unido \u00e9 o 1\u00ba pa\u00eds a aprovar comprimido experimental contra Covid"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">A ag\u00eancia regulat\u00f3ria do Reino Unido concedeu, nesta quinta-feira (4), autoriza\u00e7\u00e3o condicional para o comprimido contra a Covid-19 desenvolvido pela farmac\u00eautica Merck, conhecida no Brasil como MSD.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">A autoriza\u00e7\u00e3o \u00e9 a primeira do mundo a ser dada ao medicamento, que ainda est\u00e1 sendo avaliado pelas ag\u00eancias regulat\u00f3rias dos Estados Unidos e da Uni\u00e3o Europeia.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Ainda n\u00e3o est\u00e1 claro se o comprimido ser\u00e1 vendido em farm\u00e1cias. Segundo a ag\u00eancia brit\u00e2nica, o Servi\u00e7o Nacional de Sa\u00fade (NHS) do pa\u00eds ir\u00e1 confirmar como o medicamento ser\u00e1 destinado aos pacientes. O medicamento, o molnupiravir, leva o nome comercial de Lagevrio no pa\u00eds.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">O rem\u00e9dio n\u00e3o deve ser utilizado como substituto da vacina\u00e7\u00e3o contra a Covid-19.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">O molnupiravir foi autorizado para uso em pessoas com Covid-19 leve a moderada e pelo menos um fator de risco para o desenvolvimento de doen\u00e7a grave, incluindo obesidade, idade avan\u00e7ada (acima de 60 anos), diabetes ou doen\u00e7as card\u00edacas.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">A recomenda\u00e7\u00e3o da ag\u00eancia regulat\u00f3ria \u00e9 de que o medicamento seja usado o mais rapidamente poss\u00edvel ap\u00f3s um diagn\u00f3stico positivo de Covid-19 e, ao mesmo tempo, dentro de 5 dias ap\u00f3s o in\u00edcio dos sintomas.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">No in\u00edcio de outubro, a farmac\u00eautica americana Merck anunciou que seu rem\u00e9dio experimental contra a Covid-19, o molnupiravir, reduziu as hospitaliza\u00e7\u00f5es e mortes em pessoas no in\u00edcio da infec\u00e7\u00e3o com o coronav\u00edrus.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Nos testes, pacientes que receberam o molnupiravir em at\u00e9 5 dias ap\u00f3s o in\u00edcio dos sintomas da Covid tiveram cerca de metade da taxa de hospitaliza\u00e7\u00e3o e morte em rela\u00e7\u00e3o aos pacientes que receberam um comprimido inativo.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">O medicamento n\u00e3o funciona em pacientes com quadros graves de Covid-19.<\/span><\/p>\n<h2><strong><span style=\"color: #008000;\">Autoriza\u00e7\u00e3o condicional<\/span><\/strong><\/h2>\n<p><span style=\"font-weight: 400;\">A ag\u00eancia regulat\u00f3ria brit\u00e2nica introduziu um esquema nacional de Autoriza\u00e7\u00e3o de Comercializa\u00e7\u00e3o Condicional (CMA, na sigla em ingl\u00eas) para novos medicamentos na Gr\u00e3-Bretanha (Inglaterra, Pa\u00eds de Gales e Esc\u00f3cia), que est\u00e1 em vigor desde 1\u00ba de janeiro deste ano.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Uma autoriza\u00e7\u00e3o de uso de emerg\u00eancia do molnupiravir foi concedida \u00e0 Irlanda do Norte para garantir o acesso em todo o Reino Unido.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">O esquema de autoriza\u00e7\u00e3o condicional se destina a medicamentos que atendem a uma necessidade m\u00e9dica ainda n\u00e3o contemplada, como doen\u00e7as graves e com risco de vida para as quais n\u00e3o h\u00e1 m\u00e9todos de tratamento satisfat\u00f3rios dispon\u00edveis ou em que o produto oferece uma vantagem terap\u00eautica importante.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">A ag\u00eancia pode conceder uma autoriza\u00e7\u00e3o desse tipo quando os dados cl\u00ednicos ainda n\u00e3o estiverem completos, mas quando considera que esses dados estar\u00e3o dispon\u00edveis em breve. (Fonte: G1)<\/span><\/p>\n<p>&nbsp;<\/p>\n<p>*Foto: <span style=\"font-weight: 400;\">Merck &amp; Co.via AP<\/span><\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>A ag\u00eancia regulat\u00f3ria do Reino Unido concedeu, nesta quinta-feira (4), autoriza\u00e7\u00e3o condicional para o comprimido<\/p>\n","protected":false},"author":1,"featured_media":16279,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false,"_monsterinsights_skip_tracking":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":""},"categories":[16,31],"tags":[],"class_list":["post-16278","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-mundo","category-saude-mundo"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Reino Unido \u00e9 o 1\u00ba pa\u00eds a aprovar comprimido experimental contra Covid - 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