{"id":1268,"date":"2022-02-16T15:49:56","date_gmt":"2022-02-16T18:49:56","guid":{"rendered":"https:\/\/jornalpontomais.com\/site\/?p=1268"},"modified":"2022-02-16T15:52:20","modified_gmt":"2022-02-16T18:52:20","slug":"covid-19-anvisa-analisa-uso-emergencial-de-medicacao-da-pfizer","status":"publish","type":"post","link":"https:\/\/jornalpontomais.com\/site\/2022\/02\/16\/covid-19-anvisa-analisa-uso-emergencial-de-medicacao-da-pfizer\/","title":{"rendered":"Covid-19: Anvisa analisa uso emergencial de medica\u00e7\u00e3o da Pfizer"},"content":{"rendered":"\n<p>A Ag\u00eancia Nacional de Vigil\u00e2ncia Sanit\u00e1ria (Anvisa) recebeu, nesta quarta-feira (16), em Bras\u00edlia, pedido da Pfizer para uso emergencial do medicamento contra covid-19 Paxlovid (nirmatrelvir +ritonavir). Segundo a farmac\u00eautica, os estudos demonstram que, quando administrado no in\u00edcio da infec\u00e7\u00e3o, o Paxlovid, que \u00e9 do tipo antiviral e de uso oral, tem a capacidade de reduzir os casos de hospitaliza\u00e7\u00e3o e mortes. Os dados ser\u00e3o analisados pela Anvisa.<img decoding=\"async\" src=\"https:\/\/agenciabrasil.ebc.com.br\/ebc.png?id=1442489&amp;o=node\"><img decoding=\"async\" src=\"https:\/\/agenciabrasil.ebc.com.br\/ebc.gif?id=1442489&amp;o=node\"><\/p>\n\n\n\n<p><br><\/p>\n\n\n\n<p><\/p>\n\n\n\n<p>\u201cO prazo de avalia\u00e7\u00e3o para o uso emergencial e tempor\u00e1rio de medicamento contra a covid-19 \u00e9 de at\u00e9 30 dias. A an\u00e1lise n\u00e3o considera o tempo do processo em\u00a0<em>status<\/em>\u00a0de exig\u00eancia t\u00e9cnica, que \u00e9 quando o laborat\u00f3rio precisa responder quest\u00f5es t\u00e9cnicas feitas pela ag\u00eancia no processo\u201d, explicou a Anvisa, em nota \u00e0 imprensa.<\/p>\n\n\n\n<p><br><\/p>\n\n\n\n<p><\/p>\n\n\n\n<p>As primeiras 24 horas de an\u00e1lise ser\u00e3o utilizadas para uma triagem do processo e verificar se os documentos necess\u00e1rios est\u00e3o dispon\u00edveis. Se houver informa\u00e7\u00f5es importantes faltando, a ag\u00eancia pode solicit\u00e1-las ao laborat\u00f3rio. No \u00faltimo dia 19 de janeiro, a Anvisa e o laborat\u00f3rio j\u00e1 haviam realizado reuni\u00e3o de pr\u00e9-submiss\u00e3o do produto, etapa anterior ao envio formal do pedido pela empresa.<\/p>\n\n\n\n<p><br>Fonte: Ag\u00eancia Brasil<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Para farmac\u00eautica, antiviral de uso oral pode reduzir mortes<\/p>\n","protected":false},"author":2,"featured_media":1273,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false,"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"categories":[3],"tags":[310,175,308,309],"class_list":["post-1268","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-saude","tag-anvisa","tag-covid","tag-covid-19","tag-pfizer"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - 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