Mark Taliano

3,964 Dead 162,610 Injuries: European Database of Adverse Drug Reactions for COVID-19 “Vaccines”

By Brian Shilhavy

Global Research, March 25, 2021

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The European database of suspected drug reaction reports, EudraVigilance, is now tracking reports of injuries and deaths following the experimental COVID-19 “vaccines.”

Here is what EudraVigilance states about their database:

This website was launched by the European Medicines Agency in 2012 to provide public access to reports of suspected side effects (also known as suspected adverse drug reactions). These reports are submitted electronically to EudraVigilance by national medicines regulatory authorities and by pharmaceutical companies that hold marketing authorisations (licences) for the medicines.

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.

This website was launched to comply with the EudraVigilance Access Policy, 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.

The Management Board of the European Medicines Agency first approved the EudraVigilance Access Policy in December 2010. A revision was adopted by the Board in December 2015 based on the 2010 pharmacovigilance legislation. The 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.

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.)

Their report through March 13, 2021 lists 3,964 deaths and 162,610 injuries following injections of three experimental COVID-19 shots:

COVID-19 MRNA VACCINE MODERNA (CX-024414)COVID-19 MRNA VACCINE PFIZER-BIONTECH (TOZINAMERAN), and COVID-19 VACCINE ASTRAZENECA (CHADOX1 NCOV-19).

There is also data for a fourth experimental COVID “vaccine,” COVID-19 VACCINE JANSSEN (AD26.COV2.S). We have not included data from the Johnson and Johnson COVID shot in this report, but will do so in future reports.460 Dead 243,612 Reported Injuries from COVID-19 Vaccines Reported in the U.K.

Health Impact News subscriber 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.

Total reactions for the experimental mRNA vaccine Tozinameran (code BNT162b2Comirnaty) from BioNTechPfizer: 2,540 deaths and 102,100 injuries to 13/03/2021

COVID-19 MRNA VACCINE PFIZER-BIONTECH (TOZINAMERAN)

Total reactions for the experimental mRNA vaccine mRNA-1273 (CX-024414) from Moderna: 973 deaths and 5,939 injuries to 13/03/2021

COVID-19 MRNA VACCINE MODERNA (CX-024414)

Total reactions for the experimental vaccine AZD1222(CHADOX1 NCOV-19) from Oxford/AstraZeneca451 deaths and 54,571 injuries to 13/03/2021

COVID-19 VACCINE ASTRAZENECA (CHADOX1 NCOV-19)

This is public information funded by the European Medicines Agency (EMA), but it is obviously being censored by the corporate media.

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Featured image is from Viacheslav Lopatin | Credit: scaliger – stock.adobe.com

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Copyright © Brian Shilhavy, Global Research, 2021