{"id":12612,"date":"2021-04-13T18:40:46","date_gmt":"2021-04-13T17:40:46","guid":{"rendered":"https:\/\/radioljubuski.ba\/?p=12612"},"modified":"2021-04-13T18:40:47","modified_gmt":"2021-04-13T17:40:47","slug":"ema-zatrazila-hitan-sastanak-s-predstavnicima-johnson-johnsona","status":"publish","type":"post","link":"https:\/\/radioljubuski.ba\/index.php\/2021\/04\/13\/ema-zatrazila-hitan-sastanak-s-predstavnicima-johnson-johnsona\/","title":{"rendered":"EMA zatra\u017eila hitan sastanak s predstavnicima Johnson &#038; Johnsona"},"content":{"rendered":"\n<p><strong>Iz Hrvatskog zavoda za javno zdravstvo priop\u0107eno je kako je Europska agencija za lijekove zatra\u017eila hitan sastanak s predstavnicima farmaceutske tvrtke Johnson &amp; Johnson, te \u0107e sastanak biti odr\u017ean tijekom dana\u0161njeg dana.&nbsp;<\/strong><\/p>\n\n\n\n<p>Ameri\u010dke zdravstvene agencije preporu\u010dile su privremeno zaustavljanje cijepljenja cjepivom&nbsp;<strong>Johnson &amp; Johnsona<\/strong>&nbsp;nakon \u0161to se kod \u0161est osoba pojavio rijetki poreme\u0107aj, koji uklju\u010duje krvne ugru\u0161ke, a tvrtka Johnson &amp; Johnson objavila je kako \u0107e odgoditi uvo\u0111enje svog cjepiva protiv COVID-a u Europi. Prema najavama, prve doze toga cjepiva u Hrvatsku su trebale sti\u0107i sutra.<\/p>\n\n\n\n<p>Savjetni\u010dki odbor&nbsp;<strong>Centra za kontrolu i prevenciju bolesti<\/strong>&nbsp;(CDC) sastat \u0107e se u srijedu kako bi pregledao slu\u010dajeve povezane s cjepivom&nbsp;<strong>Johnson &amp; Johnsona<\/strong>, dok \u0107e&nbsp;<strong>Agencija za hranu i lijekove<\/strong>&nbsp;(FDA) pregledati analizu, poru\u010dile su te dvije agencije u zajedni\u010dkom priop\u0107enju.&nbsp;<br><br><strong>Johnson &amp; Johnson<\/strong>&nbsp;u me\u0111uvremenu \u0107e odgoditi uvo\u0111enje svog cjepiva u Europi.<br><br>&#8211; Sigurnost i dobrobit ljudi koji upotrebljavaju na\u0161e proizvode na\u0161 su glavni prioritet, priop\u0107ili su iz tvrtke Johnson &amp; Johnson, podsjetiv\u0161i da je u Sjedinjenim Dr\u017eavama ve\u0107 primijenjeno vi\u0161e od 6,8 milijuna doza njihova cjepiva protiv COVID-a otkako je odobreno potkraj velja\u010de.<br><br>Iz&nbsp;<strong>Europske komisije<\/strong>&nbsp;su poru\u010dili da su u kontaktu s tom tvrtkom kako bi dobili obja\u0161njenje za to odluku.<\/p>\n\n\n\n<p><strong>Svjetska zdravstvena organizacija<\/strong>&nbsp;(WHO) na upit o slu\u010dajevima zgru\u0161avanja krvi kod pacijenata koji su primili cjepivo tvrtke Johnson &amp; Johnson odgovorila je kako \u010deka izvje\u0161\u0107a Europske agencije za lijekove (EMA) i Ameri\u010dke agencije za hranu i lijekove (FDA) te prati globalnu bazu podataka ne\u017eeljenih pojava.<\/p>\n\n\n\n<p>Svih \u0161est cijepljenih kod kojih su zabilje\u017eene nuspojave \u017eene su u dobi izme\u0111u 18 i 48 godina, a simptomi su se pojavili \u0161est do 13 dana nakon cijepljenja. U svim slu\u010dajevima nastale su cerebralna venska sinusna tromboza (CVST) i trombocitopenija (manjak krvnih plo\u010dica &#8211; trombocita). CDC i FDA navode da je takav ishod nakon cijepljenja ekstremno rijedak.<\/p>\n\n\n\n<p><br>Jedna je \u017eena umrla, a druga je u te\u0161kom stanju hospitalizirana u Nebraski, objavio je New York Times.<br><br>Cijena dionice tvrtke Johnson &amp; Johnson pala je za 3%.&nbsp;<br><br>Potez ameri\u010dkih regulatora slijedio je manje od tjedan dana nakon \u0161to je europski regulator za lijekove rekao da pregledava slu\u010dajeve pojave krvnih ugru\u0161aka kod \u010detiriju osoba u SAD-u koje su primile to cjepivo.<br><br>Farmaceutska tvrtka Johnson &amp; Johnson po\u010dela je u ponedjeljak s isporukom cjepiva Europskoj uniji i do kraja lipnja trebala je isporu\u010diti 55 milijuna doza, a u tre\u0107em tromjese\u010dju dodatnih 120 milijuna doza. Hrvatska je rezervirala 900.000 doza tog cjepiva.<br><br>Australija trenuta\u010dno ne planira dodati J&amp;J-ovo cjepivo protiv koronavirusa u svoj imunizacijski program, priop\u0107ile su vlasti u utorak. Ta zemlja odustaje od nabave cjepiva koja su potencijalno povezana sa slu\u010dajevima pojave krvnih ugru\u0161aka.<\/p>\n\n\n\n<p>Izvor:hrt.hr<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Iz Hrvatskog zavoda za javno zdravstvo priop\u0107eno je kako je Europska agencija za lijekove zatra\u017eila hitan sastanak s predstavnicima farmaceutske tvrtke Johnson &amp; Johnson, te \u0107e sastanak biti odr\u017ean tijekom dana\u0161njeg dana.&nbsp; Ameri\u010dke zdravstvene agencije preporu\u010dile su privremeno zaustavljanje cijepljenja cjepivom&nbsp;Johnson &amp; Johnsona&nbsp;nakon \u0161to se kod \u0161est osoba pojavio rijetki poreme\u0107aj, koji uklju\u010duje krvne ugru\u0161ke, [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":11317,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"h5ap_radio_sources":[],"footnotes":""},"categories":[1],"tags":[],"class_list":["post-12612","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-bihiregija"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>EMA zatra\u017eila hitan sastanak s predstavnicima Johnson &amp; 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