{"id":19708,"date":"2021-05-08T23:51:57","date_gmt":"2021-05-08T22:51:57","guid":{"rendered":"https:\/\/radioljubuski.ba\/?p=19708"},"modified":"2021-05-08T23:51:58","modified_gmt":"2021-05-08T22:51:58","slug":"19708","status":"publish","type":"post","link":"https:\/\/radioljubuski.ba\/index.php\/2021\/05\/08\/19708\/","title":{"rendered":""},"content":{"rendered":"\n<p class=\"wp-block-paragraph\"><strong>Europski medicinski regulator objavio je da istra\u017euje rijetke slu\u010dajeve poreme\u0107aja \u017eiv\u010danog sustava kod ljudi koji su primili cjepivo AstraZenece, dok vlasti diljem svijeta te\u017ee transparentnosti oko sigurnosti cjepiva protiv COVID-19.<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Odbor za sigurnost Europske agencije za lijekove (EMA), u sklopu redovitog pregleda sigurnosnih izvje\u0161\u0107a za Vaxzevriu, cjepivo AstraZenece, analizira podatke koje je ta tvrtka dostavila o slu\u010dajevima Guillain-Barreova sindroma (GBS).<br><br>Poja\u010dana pozornost regulatora na rijetko imunolo\u0161ko stanje otvara nova pitanja o potencijalnim nuspojavama cjepiva protiv koronavirusa nakon \u0161to je EMA pro\u0161li mjesec otkrila mogu\u0107u vezu cjepiva AstraZenece te Johnson &amp; Johnsona s pojavom vrlo rijetkih krvnih ugru\u0161aka.<br><br>Iako je EMA objavila da su koristi jeftinih i lako prenosivih cjepiva britansko-\u0161vedskog proizvo\u0111a\u010da u borbi protiv smrtonosne pandemije ve\u0107e od bilo kakvih rizika, nekoliko europskih zemalja ograni\u010dilo je upotrebu cjepiva na starije dobne skupine ili potpuno obustavile uporabu.<br><br>Regulator je tako\u0111er podr\u017eao cjepivo J&amp;J.<br><br>EMA je navela da je GBS identificiran kao mogu\u0107a \u0161tetna pojava koju treba posebno pratiti tijekom uvjetnog odobrenja cjepiva, dodaju\u0107i da je zatra\u017eila od AstraZenece detaljnije podatke o slu\u010dajevima.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Rijetko stanje<\/strong><br><br>GBS je rijetko neurolo\u0161ko stanje u kojemu imunolo\u0161ki sustav napada za\u0161titnu ovojnicu na \u017eiv\u010danim vlaknima. Ve\u0107ina slu\u010dajeva prati bakterijsku ili virusnu infekciju.<br><br>To stanje je ve\u0107 u pro\u0161losti bilo povezano s cijepljenjem &#8211; ponajvi\u0161e s kampanjom cijepljenja tijekom izbijanja svinjske gripe u Sjedinjenim Dr\u017eavama 1976. godine, a desetlje\u0107ima kasnije i s cjepivom kori\u0161tenim tijekom pandemije gripe H1N1 2009. godine.<br><br>No znanstvenici su otkrili da su \u0161anse za razvoj GBS-a nakon cijepljenja izuzetno male.<br><br>EMA je u petak tako\u0111er rekla da istra\u017euje izvje\u0161taje o upali sr\u010danog mi\u0161i\u0107a nakon cijepljenja cjepivom Pfizer-BioNTech, pod nazivom Comirnaty, te cjepivom Moderne. Europski medicinski regulator navodi da trenuta\u010dno nema naznaka da su ti slu\u010dajevi posljedica primanja cjepiva.<br><br>Oba navedena cjepiva koriste novu mRNA tehnologiju za stvaranje imuniteta.<br><br>Ameri\u010dki centar za kontrolu i prevenciju bolesti (CDC) objavio je pro\u0161li tjedan da nije otkrio vezu izme\u0111u upale sr\u010danog mi\u0161i\u0107a i cjepiva protiv COVID-19.<br><br>AstraZeneca, Pfizer, BioNTech i Moderna nisu bili dostupni za komentar.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Izvor:hrt.hr<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Europski medicinski regulator objavio je da istra\u017euje rijetke slu\u010dajeve poreme\u0107aja \u017eiv\u010danog sustava kod ljudi koji su primili cjepivo AstraZenece, dok vlasti diljem svijeta te\u017ee transparentnosti oko sigurnosti cjepiva protiv COVID-19. Odbor za sigurnost Europske agencije za lijekove (EMA), u sklopu redovitog pregleda sigurnosnih izvje\u0161\u0107a za Vaxzevriu, cjepivo AstraZenece, analizira podatke koje je ta tvrtka dostavila [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":10205,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"h5ap_radio_sources":[],"footnotes":""},"categories":[1],"tags":[],"class_list":["post-19708","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-bihiregija"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.7 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>- RADIO LJUBU\u0160KI<\/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:\/\/radioljubuski.ba\/index.php\/2021\/05\/08\/19708\/\" \/>\n<meta property=\"og:locale\" content=\"hr_HR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"- RADIO LJUBU\u0160KI\" \/>\n<meta property=\"og:description\" content=\"Europski medicinski regulator objavio je da istra\u017euje rijetke slu\u010dajeve poreme\u0107aja \u017eiv\u010danog sustava kod ljudi koji su primili cjepivo AstraZenece, dok vlasti diljem svijeta te\u017ee transparentnosti oko sigurnosti cjepiva protiv COVID-19. 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