EU Vaccine Injury Reporting System Shows More Than 330,000 Adverse Events Following COVID Jabs – May 7, 2021

Officially, as of April 17 — 7,766 reports of deaths and 330,218 reports of injuries following injections of the four COVID vaccines approved for emergency use in the EUModernaPfizer,AstraZeneca and Johnson & Johnson, marketed under the Janssen brand.

According to the report, injury and death report totals for each vaccine were:

  • Pfizer-BioNTech: 4,293 deaths and 144,607 injuries
  • Moderna: 2,094 deaths and 15,979 injuries
  • AstraZeneca: 1,360 deaths and 169,386 injuries
  • Johnson & Johnson (Janssen): 19 deaths and 246 injuries

(This is only in Europe. You can roughly calculate the numbers for world wide injuries and deaths. Plus, remember that only about 1% of injuries and deaths get reported. So a more accurate number for Europe would be to add two zeros – 33,021,800 injuries, and 776,600 deaths just in Europe.)

The European database of drug reaction EudraVigilance tracks reports of injuries and deaths following the experimental COVID-19 “vaccines.” Health Impact News compiled the latest data on reports of COVID vaccine injuries and deaths in EU countries following vaccination with all four COVID vaccines approved in the EU for emergency use.

Cardiac and blood/lymphatic disorders were among the most commonly reported injuries.

You can see the break down of the data by vaccine, type of injury and country on Health Impact News website.

According to its website, EudraVigilance was launched by the European Medicines Agency in 2012. Reports of suspected adverse events are submitted electronically to EudraVigilance by national medicines regulatory authorities and by pharmaceutical companies that hold marketing authorizations (licenses) for the medicines. This is public information funded by the European Medicines Agency (EMA), and anyone can use the EudraVigilance system and verify this data. 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.)

Denmark and Norway have completely suspended use of the AstraZeneca experimental COVID-19 shots. So why would any sane person opt for this deadly shot – especially when the shot is more dangerous than the disease it claims to guard against?  A statement issued by the Norwegian Institute of Public Health stated that the AstraZeneca COVID “vaccine” is more dangerous than COVID itself, especially for young people.

The EMA, CDC, WHO, politicians, and news media continue to recommend it.


This entry was posted in Articles. Bookmark the permalink.