With “Adverse Reactions” figures coming through thick and fast, we present some updates from various Alternative News Sources.

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

by Brian Shilhavy
Editor, Health Impact News

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.

READ MORE

From the 3/19/2021 release of VAERS data:

Found 2,050 cases where Vaccine targets COVID-19 (COVID19) and Patient Died

Read the list at the link below:

Search Results from the VAERS Database (medalerts.org)

3 More EU Countries Hit Pause on AstraZeneca After Reports of Illness and Deaths

By Megan Redshaw

Denmark, Norway and Iceland today joined other EU countries in suspending use of the AstraZeneca-Oxford vaccine following reports of blood clots and the death of a 60-year-old woman in Denmark.Denmark, Norway and Iceland today announced they are joining other European countries in temporarily suspending use of the AstraZeneca-Oxford COVID vaccine following reports of blood clots in people who got the vaccine.

Denmark suspended the shots until further notice after a 60-year-old woman died from a blood clot which formed after she was vaccinated, reported Reuters.

The Danish decision came days after Austrian authorities announced they were suspending a batch of AstraZeneca’s COVID vaccine while investigating the death of one person and the illness of another after receiving the shots. The same batch used in Austria was used in Denmark, according to Reuters.

In Austria, a  49-year-old woman died of severe coagulation disorders, and a 35-year-old woman developed a pulmonary embolism –– an acute lung disease caused by a dislodged blood clot –– and is recovering, said The Federal Office for Safety in Health Care (BASG) in Austria.

Austrian newspaper Niederoesterreichische Nachrichten, broadcaster ORF and the APA news agency reported that both women were nurses at the same clinic where the vaccine batch was used.

In a statement provided to Reuters, AstraZeneca said the safety of its vaccine had been extensively studied in human trials and that peer-reviewed data had confirmed the vaccine was generally well tolerated.

Earlier this week, AstraZeneca reported “no confirmed serious adverse events associated with the vaccine” during trials and said it was working with Austria in its investigation.

Estonia, Latvia, Lithuania and Luxembourg have suspended all or part of their AstraZeneca vaccine roll-out as a precaution while they investigate concerns related to blood clots, reported France 24.

According to Reuters, Italy announced it banned a batch of the AstraZeneca COVID vaccine following the deaths of two men who had recently been vaccinated. One man was a 43-year-old naval officer who died after a suspected heart attack the day after his shot. The second man, a 50-year-old policeman, fell ill within 24 hours of his injection, never recovered and died 12 days after being vaccinated. Both men had received shots from AstraZeneca’s ABV2856 batch.

As of March 10, 30 cases of thromboembolic events had been reported to  EudraVigilance, the system for managing and analyzing information on suspected adverse reactions to medicines which have been authorized or are being studied in clinical trials in the European Economic Area.

As The Defender reported today, 12 prominent doctors and scientists are demanding that EU regulators address seven critical safety issues relating to the AstraZeneca, Pfizer and Moderna COVID vaccines, or withdraw approval of the vaccines for use in the EU.

The UK government is meanwhile urging people to “still go and get their COVID-19 vaccine,” stressing the suspension in multiple countries “is a precautionary measure,” reported EuroNews….READ MORE

20+ Countries Suspend Use of AstraZeneca Vaccine, But Regulators Insist ‘Benefits Outweigh Risks’

WHO and the EMA are investigating reports of blood clot-related injuries and deaths after the AstraZeneca COVID vaccine, but both say there’s no reason to stop using the vaccines…20+ Countries Suspend Use of AstraZeneca Vaccine, But Regulators Insist ‘Benefits Outweigh Risks’ • Children’s Health Defense

Martin comments: This is but a sample of the flood of reports of adverse reactions, injuries and deaths related to the rushed and experimental vaccines currently extant. Meanwhile a radio talkback host I heard yesterday quoted propaganda claiming the vaccine-hesitants and questioners to be ranked with “flat earthers” (now a common smear for anyone who questions the mainstream view on any controversial subject). As always, were recommend objective research and questioning rather than unthinkingly accepting that something is “safe” because “they said so on TV”. Think for Yourself.