World Council for Health Calls for an Immediate Stop to All COVID Shots. 'Experimental Vax is Unsafe Due to a High No. of Injuries/Deaths Reported. Promotion of Vax Violates Basic Principles of Law'

Globally renowned experts, including Dr. Paul Alexander, Dr. Byram Bridle, Dr. Geert Vanden Bossche, Prof. Dolores Cahill, and Drs. Sucharit Bhakdi, Ryan Cole, Richard Fleming, Robert W. Malone, Peter McCullough, Mark Trozzi, Michael Yeadon, Wolfgang Wodarg, and Vladimir Zelenko, among many others, consistently warn the world about the adverse effects resulting from Covid-19 experimental injections; they also warn about their longterm effects, which cannot be known at this time since most clinical trials will be not completed until 2023, and some as late as 2025.

In June 2021, Dr. Tess Lawrie, co-founder of the World Council for Health and member of the Council’s Steering Committee, courageously described the global crisis and called for urgent action: “There is now more than enough evidence on the [UK] Yellow Card system to declare the COVID-19 vaccines unsafe for use in humans. Preparation should be made to scale up humanitarian efforts to assist those harmed by the COVID-19 vaccines and to anticipate and ameliorate medium to longer term effects.”

From [HERE] A new report prepared by the World Council for Health (WCH) has confirmed that data on adverse drug reactions from the experimental Covid-19 vaccines exist in an amount sufficient for the recall of similar products in the past.

The organization called “for an Immediate Stop to the Covid-19 Experimental “Vaccines”” [MORE]

The report was prepared to determine whether sufficient pharmacovigilance data exist on official and public databases (WHO VigiAccess, CDC VAERS, EudraVigilance, and UK Yellow Card Scheme) to establish a safety signal on the novel Covid-19 injections.

On all databases, it was found that adverse drug reaction (ADR) reports linked to Covid-19 injections are more numerous than other similar products by a factor of between 10 and 169 (see graph below). Many of the ADR reports are serious in nature and there exists sufficient evidence of associated harm on these databases to indicate a product recall.

Total Adverse Events per Pharamacovigilance Database

In total, more than 40,000 deaths are linked to the novel Covid-19 vaccines in the official databases analysed.

In addition, the WCH pharmacovigilance report found that several thousand adverse drug reactions on official databases are related to the use of the experimental Covid-19 vaccines among young boys and girls for whom the vaccine had not been approved at the time.

The purpose of pharmacovigilance databases is to provide a signal of safety, and not to prove causality. To ensure that harms are detected in time, suspicion that an event is linked to the administration of the medicine is enough to register an event. “There is no need to prove that the medicine caused the adverse reaction, just the suspicion is good enough,” Dr. June Raine, head of the UK’s Medicines and Healthcare products Regulatory Agency, said in 2006. When sufficient pharmacovigilance data show a signal of harm, administration of the product should be ceased, the product recalled, and the safety signal investigated.

It should also be noted that such systems of passive surveillance result in significantly fewer ADR reports than active surveillance reporting. As a result, the actual number of adverse events that occurred in temporal relation to Covid-19 injections is likely to be much higher than revealed by the available official data.

In December 2021, World Council for Health called on regulators and governments around the world to immediately cease use of all experimental Covid-19 injections. 

Dr. Tess Lawrie, co-founder of the World Council for Health, calls for people to come together to raise awareness of vaccine injury so that those harmed can get the help they deserve. “It is concerning that a grassroots organisation has had to do this work and point out that none of these experimental vaccines are safe according to publicly available official data. Why have the regulators not done their job and protected us?“