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Kdo rozhoduje o schválení vakcíny pro nejmladší děti?

17.12.2021

Subtitle "Afrikaans" was produced by machine.Subtitle "አማርኛ" was produced by machine.Subtitle "العربية " was produced by machine.Subtitle "Ārāmāyâ" was produced by machine.Subtitle "azərbaycan dili " was produced by machine.Subtitle "беларуская мова " was produced by machine.Подзаглавието "България" е създадено от машина.Subtitle "বাংলা " was produced by machine.Subtitle "བོད་ཡིག" was produced by machine.Subtitle "босански" was produced by machine.Subtitle "català" was produced by machine.Subtitle "Cebuano" was produced by machine.Subtitle "ગુજરાતી" was produced by machine.Subtitle "corsu" was produced by machine.Podtitul "Čeština" byl vytvořen automaticky.Subtitle "Cymraeg" was produced by machine.Subtitle "Dansk" was produced by machine.Untertitel "Deutsch" wurde maschinell erzeugt.Subtitle "Untertitel" was produced by machine.Subtitle "Ελληνικά" was produced by machine.Subtitle "English" was produced by machine.Subtitle "Esperanto" was produced by machine.El subtítulo "Español" se 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17.12.2021

Kdo rozhoduje o schválení vakcíny pro nejmladší děti?

Evropská agentura pro léčiva EMA v současné době přezkoumává schválení vakcín proti kovidu na bázi genů pro děti od 5 let! Čí zájmy jsou zde skutečně zastoupeny? Životopis ředitelky EMA Emery Cookeové hovoří jasným jazykem ... [Přečtěte si více]

Kdo rozhoduje o schválení vakcíny pro nejmladší děti?

17.12.2021 | www.kla.tv/21012

Evropská agentura pro léčivé přípravky (EMA) v současné době přezkoumává schválení vakcíny proti kovidu od výrobců BioNTech a Pfizer pro děti ve věku od pěti do jedenácti let! Oznámila to EMA 18. října v Amsterdamu. Již dříve byly ve spěchu schváleny kontroverzní vakcíny na bázi genů, a to nejprve pro dospělé a poté i pro mladistvé od dvanácti let. Jako odborný orgán je prezentována EMA, která je zodpovědná za povolování léčivých přípravků a dohled nad nimi v EU. Nakolik je však agentura důvěryhodná a především nezávislá, a to i s ohledem na skutečnost, že "vakcína" má být brzy podána těm nejmenším? Emer Cookeová byl jmenována ředitelkou EMA dne 16. listopadu 2020. Má rozhodující vliv na schválení farmaceutického výrobku. Odkud pochází? - V letech 1985 až 1991 pracovala Cookeová na různých pozicích v irském farmaceutickém průmyslu. - V roce 1991 se stala členkou představenstva Evropské federace farmaceutického průmyslu a asociací (EFPIA). EFPIA je nejvýznamnější lobbistickou organizací evropského farmaceutického průmyslu s nejvyššími výdaji na lobbing, největším počtem kontaktů na EU a několika zapojenými lobbistickými agenturami. Zastupuje některé z největších světových farmaceutických společností, včetně společností AstraZeneca, Johnson & Johnson a Pfizer. Cookeová oficiálně zastupovala zájmy těchto farmaceutických společností v oblasti regulace až do roku 1998. - Emer Cookeová pak v letech 1998 až 2002 vedla farmaceutické oddělení Komise EU. Odtud přešla do agentury EMA, kde do roku 2016 působila jako vedoucí inspekce a vedoucí mezinárodních záležitostí. - Od listopadu 2016 do listopadu 2020 zastávala Cookeová funkci výkonné ředitelky EMA a byla tedy zodpovědná za veškeré regulační činnosti týkající se léčivých přípravků. Poté, co Cookeová převzala funkci v EMA, byly vakcíny proti kovidu ve velmi krátké době schváleny pro EU dalšími farmaceutickými společnostmi: - dne 21. prosince 2020 společností Pfizer a BioNTech, - dne 29. ledna 2021 společností AstraZeneca. - dne 12. března 2021 společností Johnson & Johnson. Když byly v souvislosti s očkováním od společnosti AstraZeneca hlášeny četné případy trombózy mozkových žil, z nichž některé skončily smrtí, zasadila se Emer Cookeová zejména o to, aby bylo povolení EU zachováno. Mimochodem, celkový rozpočet EMA na rok 2021 činí neuvěřitelných 386 milionů eur. Z toho 330 milionů eur pochází pouze z poplatků za schválení, které platí farmaceutické společnosti, tj. asi 86 procent. Rakouský poslanec Gerald Hauser si klade otázku, zda osoba s tak silným farmaceutickým vzděláním, jako je Cookeová, může o licenci rozhodovat nestranně: "Doktorka Emer Cookeová, která byla v polovině listopadu 2020 jmenována do rady EMA, tedy celý život pracovala pro farmaceutický průmysl. Lobbovala pro farmaceutický průmysl ve výkonné funkci a nyní je zodpovědná za schvalování, kontrolu a účinnost vakcín – jako i pro společnost AstraZeneca. Vážení kolegové. Co by na takový případ řekl člověk, který ani není vystudovaný parlamentář? Co by člověk řekl? Otevřené obchodování s důvěrnými informacemi, jasné zvýhodňování, úplatkářství, všechno možné. Tak to prostě je. Myslete na to, prosím, až zde v budoucnu budete agenturu EMA prezentovat jako důkaz správnosti testování léčivých přípravků." To vše samozřejmě vyvolává otázku důvěryhodnosti agentury EMA: Očkování, které již nyní způsobuje více úmrtí a vedlejších účinků než všechny ostatní "vakcíny" dohromady, má chránit malé děti před nemocemi? Injekce, která vydělává miliardy farmaceutickým společnostem, má být "výhodná" pro děti?! Zisky podniků v roce 2020 a 1. čtvrtletí 2021: Pfizer: 14,5 miliardy dolarů Johnson & Johnson: 21 600 milionů dolarů BioNTech: 1 100 milionů eur

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