Many experts have been warning people about the dangers of a vaccine designed to alter your body’s basic functions.
The dangers of the COVID ‘vaccine’ seem to be getting worse… all for a cold virus with a 99% recovery rate (better than the FLU), and now, records show that nearly 4,000 people are dead and over 162,000 have had “adverse” reactions to the supposed ‘miracle.’ In fact, the Former Pfizer VP has warned that the vaccine is possibly being “used for massive-scale depopulation.”
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:
Posted: Mar 29, 2021 / 11:31 PM EDT / Updated: Mar 29, 2021 / 11:31 PM EDT
WARNING: The following article and video contain graphic images
GOOCHLAND COUNTY, Va. (WRIC) — A Virginia man suffered a severe reaction after getting his COVID-19 vaccine and doctors believe it was a direct result of the shot.
Richard Terrell got the one-dose Johnson & Johnson vaccine earlier this month. He suffered a severe rash that spread over his entire body and turned his skin red. The 74-year-old was admitted to the hospital and spent five days at the VCU Medical Center.
Terrell was released from the hospital and is now sharing his vaccination story as he recovers from the comfort of his Goochland County home. He said that he’s still very weak and that it will take some time for him to fully recover, but he’s thankful to have received his dose.
“It all just happened so fast. My skin peeled off,” Terrell said as he looked down. “It’s still coming off on my hands now.”
On March 6, Terrell received the Johnson & Johnson vaccine in Ashland, Virginia. He said that everything went perfectly fine, however four days later he started experiencing symptoms.
“I began to feel a little discomfort in my armpit and then a few days later I began to get an itchy rash, and then after that I began to swell and my skin turned red,” Terrell explained.
