Simone Matthews

We will continually update this page with new articles, scientific studies, videos & information.  Please also see our Individual Country Pages for Adverse Events – United States Adverse Events, United Kingdom Adverse Events, and Australia Adverse Events. Before reading below, I highly recommend watching this Video of World renowned experts (physicians, scientists, lawyers, activists etc.) […]

We will continually update this page with new articles, scientific studies, videos & information.  Please also see our Individual Country Pages for Adverse Events – United States Adverse Events, United Kingdom Adverse Events, and Australia Adverse Events. Before reading below, I highly recommend watching this Video of World renowned experts (physicians, scientists, lawyers, activists etc.)

We will continually update this page with new articles, scientific studies, videos & information.   Before reading below, I highly recommend watching this Video of World renowned experts (physicians, scientists, lawyers, activists etc.) discussing the many unanswered questions regarding the safety and effectiveness of the COVID vaccine. And also consider reading this article on the censorship

This weeks Adverse Reactions to COVID19 Vaccines per the VAERS Website…

The United Kingdom Government has granted temporary authorisation for the use of the mRNA Pfizer Vaccine & AstraZeneca Vaccine.  This means that the Vaccines are approved for emergency use even though clinical trials have NOT been completed & the vaccine is not officially approved. Phase III Pfizer trials are due for completion in January 2023,

COVID-19 vaccines approved for use in Canada currently include: Pfizer-BioNTech, Moderna, AstraZeneca, COVISHIELD (a version of the AstraZeneca vaccine manufactured by the Serum Institute of India and sponsored in Canada by Verity Pharmaceuticals Inc.) and Janssen (Johnson and Johnson). While the Janssen vaccine has been approved for use in Canada, it has not yet been

EudraVigilance 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