{"id":20021,"date":"2021-12-16T13:20:32","date_gmt":"2021-12-16T20:20:32","guid":{"rendered":"https:\/\/fuentesfidedignas.com.mx\/?p=20021"},"modified":"2021-12-16T13:20:34","modified_gmt":"2021-12-16T20:20:34","slug":"europa-avala-uso-de-emergencia-de-la-pildora-pfizer-contra-covid-19","status":"publish","type":"post","link":"https:\/\/fuentesfidedignas.com.mx\/index.php\/2021\/12\/16\/europa-avala-uso-de-emergencia-de-la-pildora-pfizer-contra-covid-19\/","title":{"rendered":"Europa avala uso de emergencia de la p\u00edldora Pfizer contra Covid-19"},"content":{"rendered":"\n<p><strong><em><br>La p\u00edldora de Pfizer se podr\u00e1 suministrar a adultos con Covid-19 que no requieran ox\u00edgeno pero con riesgo a padecer una enfermedad grave<\/em><\/strong><\/p>\n\n\n\n<p>Francia.\u2013 La Agencia Europea de Medicamentos (EMA) respald\u00f3 este mediod\u00eda el uso de emergencia de Paxlovid, la pastilla de la farmac\u00e9utica Pfizer, como tratamiento oral de la Covid-19, bajo decisi\u00f3n individual de las autoridades nacionales a la espera de una licencia oficial europea.<\/p>\n\n\n\n<p>La p\u00edldora se puede usar para tratar a adultos con Covid-19 que no requieren ox\u00edgeno suplementario, pero tiene un mayor riesgo de progresar a una enfermedad grave, y debe administrarse lo antes posible despu\u00e9s del diagn\u00f3stico, dentro de los 5 d\u00edas posteriores al inicio de los s\u00edntomas.<\/p>\n\n\n\n<p>Los dos principios activos del medicamento, PF-07321332 y Ritonavir, que est\u00e1n disponibles en comprimidos separados, deben tomarse juntos dos veces al d\u00eda durante cinco d\u00edas.<\/p>\n\n\n\n<p>El consejo se basa en el an\u00e1lisis de los resultados provisionales del estudio principal en pacientes no hospitalizados y no vacunados que ten\u00edan una enfermedad sintom\u00e1tica y al menos una afecci\u00f3n subyacente que los pon\u00eda en riesgo de desarrollar Covid-19 grave.<\/p>\n\n\n\n<p>\u201cEstos datos mostraron que Paxlovid redujo el riesgo de hospitalizaci\u00f3n y muerte cuando el tratamiento se inici\u00f3 dentro de los 5 d\u00edas posteriores al inicio de los s\u00edntomas\u201d, a\u00f1ade.<\/p>\n\n\n\n<p>Ninguno de los pacientes del grupo de 607 personas que recibieron Paxlovid muri\u00f3 en comparaci\u00f3n con 10 pacientes del grupo de 612 que recibieron placebo, mientras que del primer grupo, 6 personas fueron hospitalizadas dentro de los 28 d\u00edas posteriores al inicio del tratamiento, en comparaci\u00f3n con 41 del segundo grupo.<\/p>\n\n\n\n<p>Los efectos secundarios m\u00e1s comunes notificados durante el tratamiento y hasta 34 d\u00edas despu\u00e9s de la \u00faltima dosis fueron disgeusia (alteraci\u00f3n del gusto), diarrea y v\u00f3mitos.<\/p>\n\n\n\n<p>La EMA se\u00f1ala que Paxlovid no debe usarse con determinados medicamentos, puesto que su acci\u00f3n puede provocar aumentos nocivos de sus niveles en sangre o, por el contrario, reducir la actividad de esta p\u00edldora.<\/p>\n\n\n\n<p>Tampoco debe utilizarse en pacientes con insuficiencia renal o hep\u00e1tica grave, ni se recomienda su ingesta durante el embarazo, ni en personas que puedan quedar embarazadas y que no est\u00e9n usando m\u00e9todos anticonceptivos.<\/p>\n\n\n\n<p>La lactancia tambi\u00e9n debe interrumpirse durante el tratamiento.<\/p>\n\n\n\n<p>Los estudios de laboratorio en animales sugieren que altas dosis de Paxlovid pueden afectar el crecimiento del feto.<\/p>\n\n\n\n<p>La EMA ha emitido este consejo cient\u00edfico previo a su decisi\u00f3n final sobre la autorizaci\u00f3n oficial de este f\u00e1rmaco para ayudar a las autoridades nacionales a decidir sobre el posible uso temprano del medicamento, como en entornos de uso de emergencia, debido a las crecientes tasas de contagios y muertes por Covid-19 en la Uni\u00f3n Europea (UE).<\/p>\n\n\n\n<p>La agencia europea tambi\u00e9n anunci\u00f3 que a inicio de semana comenz\u00f3 una revisi\u00f3n continua m\u00e1s completa de esta p\u00edldora para evaluar en tiempo real datos m\u00e1s completos sobre la calidad, seguridad y eficacia del medicamento a medida que est\u00e9n disponibles, una evaluaci\u00f3n que continuar\u00e1 hasta que haya datos suficientes para pedir una licencia europea.<\/p>\n\n\n\n<p>La p\u00edldora \u201cbloquea\u201d la actividad de una enzima espec\u00edfica que el SARS-CoV-2 necesita para replicarse en el cuerpo infectado, un mecanismo similar al de molnupiravir, la pastilla desarrollada por MSD (Merck en EU y Canad\u00e1).<\/p>\n\n\n\n<p>Pfizer anunci\u00f3 este martes que su pastilla reduce en un 89 % de los casos el riesgo de hospitalizaci\u00f3n o muerte en adultos e indic\u00f3 que sus datos m\u00e1s recientes confirman que el medicamento es un \u201cinhibidor potente\u201d ante la variante \u00d3micron del coronavirus.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>La p\u00edldora de Pfizer se podr\u00e1 suministrar a adultos con Covid-19 que no requieran ox\u00edgeno pero con riesgo a padecer una enfermedad grave Francia.\u2013 La Agencia Europea de Medicamentos (EMA) respald\u00f3 este mediod\u00eda el uso de emergencia de Paxlovid, la pastilla de la farmac\u00e9utica Pfizer, como tratamiento oral de la Covid-19, bajo decisi\u00f3n individual de [&hellip;]<\/p>\n","protected":false},"author":22,"featured_media":20022,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"tdm_status":"","tdm_grid_status":"","footnotes":""},"categories":[39],"tags":[],"class_list":{"0":"post-20021","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-noticias-nacionales"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Europa avala uso de emergencia de la p\u00edldora Pfizer contra Covid-19 - Fuentes Fidedignas<\/title>\n<meta name=\"robots\" content=\"index, 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