{"id":8637,"date":"2023-09-12T12:00:54","date_gmt":"2023-09-12T09:00:54","guid":{"rendered":"https:\/\/urbancare.clinic\/fda-approves-updated-covid-vaccines-heres-what-you-need-to-know\/"},"modified":"2023-09-12T12:00:54","modified_gmt":"2023-09-12T09:00:54","slug":"die-fda-genehmigt-aktualisierte-covid-impfstoffe-hier-ist-was-sie-wissen-mussen","status":"publish","type":"post","link":"https:\/\/urbancare.clinic\/de\/die-fda-genehmigt-aktualisierte-covid-impfstoffe-hier-ist-was-sie-wissen-mussen\/","title":{"rendered":"FDA genehmigt aktualisierte COVID-Impfstoffe; Folgendes m\u00fcssen Sie wissen:"},"content":{"rendered":"
<\/div>\n

Die Food and Drug Administration hat am Montag aktualisierte COVID-Impfstoffe von Pfizer und Moderna genehmigt, die auf die neuen Untervarianten des Coronavirus, einschlie\u00dflich XBB.1.5, abzielen, da F\u00e4lle und Krankenhausaufenthalte in den USA zunehmen<\/p>\n

\u201eDie aktualisierten mRNA-Impfstoffe sind jeweils f\u00fcr Personen ab 12 Jahren zugelassen und im Notfall f\u00fcr Personen im Alter von 6 Monaten bis 11 Jahren zugelassen\u201c, sagte die FDA in einem Pressemitteilung<\/a>.<\/p>\n

Jeder ab f\u00fcnf Jahren kann unabh\u00e4ngig von seinem Impfstatus die aktualisierte Auffrischungsimpfung erhalten, sagte die FDA. Wer geimpft ist, sollte nach der letzten Impfung gegen COVID-19 mindestens zwei Monate warten.<\/p>\n

Der Beratende Ausschuss f\u00fcr Impfpraktiken des Centers for Disease Control and Prevention wird nach einer Sitzung am Dienstag die klinischen Empfehlungen zur Verwendung der Impfstoffe ver\u00f6ffentlichen. Nach der CDC-Genehmigung werden die Impfungen bis Ende der Woche in Apotheken, Kliniken und anderen Vertriebszentren f\u00fcr den \u00f6ffentlichen Gebrauch verf\u00fcgbar sein.<\/p>\n

Der aktualisierte Novavax-Impfstoff, der im Gegensatz zur mRNA-Technologie von Pfizer und Moderna eine proteinbasierte Technologie nutzt, befindet sich noch in der FDA-Pr\u00fcfung.<\/p>\n

Die Gesundheitsbeh\u00f6rden hoffen, dass die aktualisierten Impfstoffe einen besseren Schutz vor schwerwiegenden Folgen von COVID-19, einschlie\u00dflich Krankenhausaufenthalten und Todesf\u00e4llen, bieten.<\/p>\n

\u201eImpfungen bleiben f\u00fcr die \u00f6ffentliche Gesundheit und den anhaltenden Schutz vor schwerwiegenden Folgen von COVID-19, einschlie\u00dflich Krankenhausaufenthalten und Todesf\u00e4llen, von entscheidender Bedeutung\u201c, sagte Peter Marks, Direktor des Center for Biologics Evaluation and Research der FDA, in der Pressemitteilung. \u201eDie \u00d6ffentlichkeit kann sicher sein, dass diese aktualisierten Impfstoffe den strengen wissenschaftlichen Standards der Beh\u00f6rde f\u00fcr Sicherheit, Wirksamkeit und Herstellungsqualit\u00e4t entsprechen. Wir ermutigen diejenigen, die dazu in Frage kommen, nachdr\u00fccklich, \u00fcber eine Impfung nachzudenken.\u201c<\/p>\n

Die FDA forderte die Arzneimittelhersteller im Juni auf, ihre Impfstoffe auf XBB.1.5 zu aktualisieren, als es sich um eine dominante Variante handelte. Laut einer CDC Bericht<\/a> Ab der ersten Septemberwoche macht XBB.1.5 nur noch etwa 3% der neuen COVID-19-F\u00e4lle aus. Andere im Umlauf befindliche Subvarianten, darunter EG.5, auf die 21,5 % neuer F\u00e4lle entfallen, und FL.1.5.1, auf die etwa 14,15 % neuer F\u00e4lle entfallen, sind jedoch alle Teil der XBB-Subvariantenfamilie und jetzt zugelassen Booster<\/a> gegen sie arbeiten.<\/p>\n

Die neueste Omicron-Subvariante, BA.2.86<\/a>, auch bekannt als \u201ePirola\u201c, gab aufgrund seiner erheblichen Anzahl an Mutationen zun\u00e4chst Anlass zur Sorge. Labortests zeigten jedoch, dass es m\u00f6glicherweise nicht so resistent gegen Immunit\u00e4t ist wie urspr\u00fcnglich bef\u00fcrchtet. Sowohl Moderna als auch Pfizer gaben letzte Woche bekannt, dass ihre Booster stark wirken k\u00f6nnen Antik\u00f6rper<\/a> Antwort gegen die Variante.<\/p>\n

Ver\u00f6ffentlicht von Medicaldaily.com<\/p>\n

Medizinische t\u00e4gliche Quelle<\/a><\/p>\n

","protected":false},"excerpt":{"rendered":"

<\/div>\n

Die Food and Drug Administration hat am Montag aktualisierte COVID-Impfstoffe von Pfizer und Moderna genehmigt, die auf die neuen Untervarianten des Coronavirus, einschlie\u00dflich XBB.1.5, abzielen, da F\u00e4lle und Krankenhausaufenthalte in den USA zunehmen<\/p>\n

\u201eDie aktualisierten mRNA-Impfstoffe sind jeweils f\u00fcr Personen ab 12 Jahren zugelassen und im Notfall f\u00fcr Personen im Alter von 6 Monaten bis 11 Jahren zugelassen\u201c, sagte die FDA in einem Pressemitteilung<\/a>.<\/p>\n

Jeder ab f\u00fcnf Jahren kann unabh\u00e4ngig von seinem Impfstatus die aktualisierte Auffrischungsimpfung erhalten, sagte die FDA. Wer geimpft ist, sollte nach der letzten Impfung gegen COVID-19 mindestens zwei Monate warten.<\/p>\n

Der Beratende Ausschuss f\u00fcr Impfpraktiken des Centers for Disease Control and Prevention wird nach einer Sitzung am Dienstag die klinischen Empfehlungen zur Verwendung der Impfstoffe ver\u00f6ffentlichen. Nach der CDC-Genehmigung werden die Impfungen bis Ende der Woche in Apotheken, Kliniken und anderen Vertriebszentren f\u00fcr den \u00f6ffentlichen Gebrauch verf\u00fcgbar sein.<\/p>\n

Der aktualisierte Novavax-Impfstoff, der im Gegensatz zur mRNA-Technologie von Pfizer und Moderna eine proteinbasierte Technologie nutzt, befindet sich noch in der FDA-Pr\u00fcfung.<\/p>\n

Die Gesundheitsbeh\u00f6rden hoffen, dass die aktualisierten Impfstoffe einen besseren Schutz vor schwerwiegenden Folgen von COVID-19, einschlie\u00dflich Krankenhausaufenthalten und Todesf\u00e4llen, bieten.<\/p>\n

\u201eImpfungen bleiben f\u00fcr die \u00f6ffentliche Gesundheit und den anhaltenden Schutz vor schwerwiegenden Folgen von COVID-19, einschlie\u00dflich Krankenhausaufenthalten und Todesf\u00e4llen, von entscheidender Bedeutung\u201c, sagte Peter Marks, Direktor des Center for Biologics Evaluation and Research der FDA, in der Pressemitteilung. \u201eDie \u00d6ffentlichkeit kann sicher sein, dass diese aktualisierten Impfstoffe den strengen wissenschaftlichen Standards der Beh\u00f6rde f\u00fcr Sicherheit, Wirksamkeit und Herstellungsqualit\u00e4t entsprechen. Wir ermutigen diejenigen, die dazu in Frage kommen, nachdr\u00fccklich, \u00fcber eine Impfung nachzudenken.\u201c<\/p>\n

Die FDA forderte die Arzneimittelhersteller im Juni auf, ihre Impfstoffe auf XBB.1.5 zu aktualisieren, als es sich um eine dominante Variante handelte. Laut einer CDC Bericht<\/a> Ab der ersten Septemberwoche macht XBB.1.5 nur noch etwa 3% der neuen COVID-19-F\u00e4lle aus. Andere im Umlauf befindliche Subvarianten, darunter EG.5, auf die 21,5 % neuer F\u00e4lle entfallen, und FL.1.5.1, auf die etwa 14,15 % neuer F\u00e4lle entfallen, sind jedoch alle Teil der XBB-Subvariantenfamilie und jetzt zugelassen Booster<\/a> gegen sie arbeiten.<\/p>\n

Die neueste Omicron-Subvariante, BA.2.86<\/a>, auch bekannt als \u201ePirola\u201c, gab aufgrund seiner erheblichen Anzahl an Mutationen zun\u00e4chst Anlass zur Sorge. Labortests zeigten jedoch, dass es m\u00f6glicherweise nicht so resistent gegen Immunit\u00e4t ist wie urspr\u00fcnglich bef\u00fcrchtet. Sowohl Moderna als auch Pfizer gaben letzte Woche bekannt, dass ihre Booster stark wirken k\u00f6nnen Antik\u00f6rper<\/a> Antwort gegen die Variante.<\/p>\n

Ver\u00f6ffentlicht von Medicaldaily.com<\/p>","protected":false},"author":2,"featured_media":8638,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"Default","format":"standard","meta":{"fifu_image_url":"https:\/\/urbancare.clinic\/wp-content\/uploads\/2023\/09\/fda-approves-updated-covid-vaccines-heres-what-you-need-to-know.jpg","fifu_image_alt":"","footnotes":""},"categories":[27],"tags":[],"class_list":["post-8637","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-blog"],"yoast_head":"\nFDA Approves Updated COVID Vaccines; Here's What You Need To Know - Urban Care Clinic<\/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:\/\/urbancare.clinic\/de\/die-fda-genehmigt-aktualisierte-covid-impfstoffe-hier-ist-was-sie-wissen-mussen\/\" \/>\n<meta property=\"og:locale\" content=\"de_DE\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"FDA Approves Updated COVID Vaccines; Here's What You Need To Know - Urban Care Clinic\" \/>\n<meta property=\"og:description\" content=\"The Food and Drug Administration on Monday approved updated COVID vaccines from Pfizer and Moderna that target the new subvariants of coronavirus, including XBB.1.5, as cases and hospitalizations surge in the U.S."The updated mRNA vaccines are each approved for individuals 12 years of age and older and are authorized under emergency use for individuals 6 months through 11 years of age," the FDA said in a news release.Everyone aged five and older can get the updated booster shot irrespective of their vaccination status, the FDA said. Those who are vaccinated should wait at least two months after their last COVID-19 shot.The Centers for Disease Control and Prevention's Advisory Committee on Immunization Practices will release the clinical recommendations regarding the use of the vaccines after a meeting Tuesday. After the CDC approval, the shots will be available for public use through pharmacies, health clinics and other distribution centers by the end of the week.The updated Novavax vaccine that uses protein-based technology, unlike the mRNA technology used in Pfizer and Moderna, is still under FDA review.Health authorities hope the updated vaccines will provide better protection against serious consequences of COVID-19, including hospitalization and death."Vaccination remains critical to public health and continued protection against serious consequences of COVID-19, including hospitalization and death," Peter Marks, director of the FDA's Center for Biologics Evaluation and Research, said in the release. "The public can be assured that these updated vaccines have met the agency's rigorous scientific standards for safety, effectiveness, and manufacturing quality. We very much encourage those who are eligible to consider getting vaccinated."The FDA asked the drugmakers to update their vaccines to target XBB.1.5 in June when it was a dominant variant. According to a CDC report from the first week of September, XBB.1.5 accounts for only about 3% of new COVID-19 cases. However, other subvariants in circulation, including EG.5, which accounts for 21.5 % of new cases, and FL.1.5.1, which accounts for about 14.15 % of new cases, are all part of the XBB subvariant family and the now approved boosters work against them.The latest omicron subvariant, BA.2.86, also known as "Pirola," initially raised concerns due to its significant number of mutations. However, laboratory tests showed it may not be as resistant to immunity as originally feared. Both Moderna and Pfizer announced last week that their boosters can trigger strong antibody response against the variant.Published by Medicaldaily.com\" \/>\n<meta property=\"og:url\" content=\"https:\/\/urbancare.clinic\/de\/die-fda-genehmigt-aktualisierte-covid-impfstoffe-hier-ist-was-sie-wissen-mussen\/\" \/>\n<meta property=\"og:site_name\" content=\"Urban Care Clinic\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/urbancarezanzibar\" \/>\n<meta property=\"article:published_time\" content=\"2023-09-12T09:00:54+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/urbancare.clinic\/wp-content\/uploads\/2023\/09\/fda-approves-updated-covid-vaccines-heres-what-you-need-to-know.jpg\" \/>\n<meta name=\"author\" content=\"Urban Care Clinic\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:image\" content=\"https:\/\/urbancare.clinic\/wp-content\/uploads\/2023\/09\/fda-approves-updated-covid-vaccines-heres-what-you-need-to-know.jpg\" \/>\n<meta name=\"twitter:label1\" content=\"Verfasst von\" \/>\n\t<meta name=\"twitter:data1\" content=\"Urban Care Clinic\" \/>\n\t<meta name=\"twitter:label2\" content=\"Gesch\u00e4tzte Lesezeit\" \/>\n\t<meta name=\"twitter:data2\" content=\"2\u00a0Minuten\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\/\/urbancare.clinic\/fda-approves-updated-covid-vaccines-heres-what-you-need-to-know\/#article\",\"isPartOf\":{\"@id\":\"https:\/\/urbancare.clinic\/fda-approves-updated-covid-vaccines-heres-what-you-need-to-know\/\"},\"author\":{\"name\":\"Urban Care Clinic\",\"@id\":\"https:\/\/urbancare.clinic\/#\/schema\/person\/f286c4d84be896d302aceda3ed7e789c\"},\"headline\":\"FDA Approves Updated COVID Vaccines; 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Those who are vaccinated should wait at least two months after their last COVID-19 shot.The Centers for Disease Control and Prevention's Advisory Committee on Immunization Practices will release the clinical recommendations regarding the use of the vaccines after a meeting Tuesday. After the CDC approval, the shots will be available for public use through pharmacies, health clinics and other distribution centers by the end of the week.The updated Novavax vaccine that uses protein-based technology, unlike the mRNA technology used in Pfizer and Moderna, is still under FDA review.Health authorities hope the updated vaccines will provide better protection against serious consequences of COVID-19, including hospitalization and death.\"Vaccination remains critical to public health and continued protection against serious consequences of COVID-19, including hospitalization and death,\" Peter Marks, director of the FDA's Center for Biologics Evaluation and Research, said in the release. \"The public can be assured that these updated vaccines have met the agency's rigorous scientific standards for safety, effectiveness, and manufacturing quality. We very much encourage those who are eligible to consider getting vaccinated.\"The FDA asked the drugmakers to update their vaccines to target XBB.1.5 in June when it was a dominant variant. According to a CDC report from the first week of September, XBB.1.5 accounts for only about 3% of new COVID-19 cases. However, other subvariants in circulation, including EG.5, which accounts for 21.5 % of new cases, and FL.1.5.1, which accounts for about 14.15 % of new cases, are all part of the XBB subvariant family and the now approved boosters work against them.The latest omicron subvariant, BA.2.86, also known as \"Pirola,\" initially raised concerns due to its significant number of mutations. However, laboratory tests showed it may not be as resistant to immunity as originally feared. 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