{"id":58187,"date":"2021-03-28T12:56:11","date_gmt":"2021-03-28T16:56:11","guid":{"rendered":"http:\/\/stateofthenation.co\/?p=58187"},"modified":"2021-03-28T12:57:42","modified_gmt":"2021-03-28T16:57:42","slug":"nearly-4000-dead-in-europe-more-than-162000-after-dangerous-covid-injections","status":"publish","type":"post","link":"https:\/\/stateofthenation.co\/?p=58187","title":{"rendered":"Nearly 4,000 Dead In Europe & More Than 162,000 After Dangerous Covid Injections"},"content":{"rendered":"
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Total Media Blackout: Nearly 4,000 Dead In Europe & More Than 162,000 Injuries Following Experimental COVID-19 Injections<\/h1>\n

WRITTEN BY: TIM BROWN<\/p>\n

The complete media blackout of adverse effects and deaths following experimental COVID-19 injections is absolutely outrageous. Yet, they continue to peddle the fraudulent, unproved claim they are safe and effective. Nothing could be further from the truth. According to the European Database of Adverse Drug Reactions for COVID-19 \u201cVaccines,\u201d 3,964 people have died and 162,610 have been injured, and these are only the ones reported which are a very small percentage of the total.<\/p>\n

EudraVigilance<\/a>, the European database of suspected drug reaction reports, stated this about their database:<\/p>\n

This website was launched by the\u00a0European Medicines Agency<\/a>\u00a0in 2012\u00a0to provide public access to reports of suspected side effects\u00a0<\/strong>(also known as suspected adverse drug reactions). These reports are submitted electronically to\u00a0EudraVigilance<\/a>\u00a0by national medicines regulatory authorities and by pharmaceutical companies that hold marketing authorisations (licences) for the medicines.<\/em><\/p>\n

EudraVigilance is a system designed for collecting reports of suspected side effects. These reports are used for evaluating the benefits and risks of medicines during their development and monitoring their safety following their authorisation in the European Economic Area (EEA). EudraVigilance has been in use since December 2001.<\/em><\/p>\n

This website was launched to comply with the\u00a0EudraVigilance Access Policy<\/a>, which was developed to improve public health by supporting the monitoring of the safety of medicines and to increase transparency for stakeholders, including the general public.<\/em><\/p>\n

The\u00a0Management Board of the European Medicines Agency<\/a>\u00a0first approved the EudraVigilance Access Policy in December 2010.\u00a0A revision was adopted by the Board in December 2015 based on the 2010 pharmacovigilance legislation.<\/span>\u00a0The policy aims to provide stakeholders such as national medicines regulatory authorities in the EEA, the European Commission, healthcare professionals, patients and consumers, as well as the pharmaceutical industry and research organisations, with access to reports on suspected side effects.<\/em><\/p>\n

Transparency is a key guiding principle of the Agency, and is pivotal to building trust and confidence in the regulatory process. By increasing transparency, the Agency is better able to address the growing need among stakeholders, including the general public, for access to information. (Source<\/a>.)<\/em><\/p>\n

Health Impact News<\/a>\u00a0reports:<\/p>\n

Their report through March 13, 2021 lists 3,964 deaths and 162,610 injuries following injections of three experimental COVID-19 shots:<\/em><\/p>\n

COVID-19 MRNA VACCINE MODERNA (CX-024414)<\/a>,\u00a0COVID-19 MRNA VACCINE PFIZER-BIONTECH (TOZINAMERAN)<\/a>, and\u00a0COVID-19 VACCINE ASTRAZENECA (CHADOX1 NCOV-19)<\/a>.<\/em><\/p>\n

There is also data for a fourth experimental COVID \u201cvaccine,\u201d\u00a0COVID-19 VACCINE JANSSEN (AD26.COV2.S<\/a>). We have not included data from the Johnson and Johnson COVID shot in this report, but will do so in future reports.<\/em><\/p>\n

A\u00a0Health Impact News\u00a0subscriber in Europe ran the reports for each of the three COVID-19 shots we are including here, and here is the summary data through March 13, 2021.<\/em><\/p>\n

Total reactions<\/strong>\u00a0for the experimental mRNA vaccine\u00a0Tozinameran<\/b>\u00a0(code\u00a0BNT162b2<\/b>,\u00a0Comirnaty<\/b>) from\u00a0BioNTech<\/u><\/b>\/\u00a0<\/u><\/b>Pfizer:\u00a0<\/b>2,540\u00a0deaths\u00a0<\/strong><\/b>and 102,100 injuries to 13\/03\/2021<\/em><\/p>\n