Operation Disclosure | By David Lifschultz, Contributing Writer
Submitted on May 13, 2021
300,000 VACCINE ADVERSE EVENTS
Compliments of the Lifschultz Organization founded in 1899
In reviewing this data it is important to note that reporting rarely picked 1/10 to 1/100 of the actual adverse events or deaths.
EU Vaccine Injury Reporting System Shows More Than 330,000 Adverse Events Following COVID Vaccines
on May 7, 2021
The European database of suspected 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.
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 EU: Moderna, Pfizer,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
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.
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 continues to recommend it. They did, however, add a safety warning to the J&J shots, due to fatal blood clots. (Source)
David Lifschultz
THE LIFSCHULTZ ORGANIZATION
DAVID@LIFSCHULTZORGANIZATION.COM
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