AstraZeneca Covid-19 Vaccine Suspended across Europe. “Possible Autoimmune Reactions, Blood Clotting, Stroke and Internal bleeding”

By Prof Michel Chossudovsky (via Global Research)

Several European countries have now suspended the mRNA AstraZeneka Vaccine including Denmark, Norway, Iceland, Austria, Bulgaria. And more recently: Germany, Netherlands, Ireland, France, Italy, Estonia, Lithuania, Luxembourg and Romania. Thailand and the Democratic Republic of the Congo (DRC) have also suspended the AstraZeneka vaccine. 

On March 10, 2021, an open letter was submitted by a Collective of prominent medical doctors and scientists to the European Medicines Agency (EME):

Urgent Open Letter from Doctors and Scientists to the European Medicines Agency regarding COVID-19 Vaccine Safety Concerns By Doctors for COVID Ethics, March 10, 2021

The letter (posted on Global Research) describes:

“serious potential consequences of COVID-19 vaccine technology, warning of possible autoimmune reactions, blood clotting abnormalities, stroke and internal bleeding, “including in the brain, spinal cord and heart”.

See also the Press Release issued by the Doctors for COVID Ethics

In recent developments (March 15, 2021), Germany’s Ministry of Health has confirmed the “temporary suspension” of the AstraZeneca COVID-19 vaccine: ,

“The European Medicines Agency is to  decide “whether and how the new information will affect the authorization of the vaccine” pending an investigation.  (Deutsche Welle).

The mRNA Vaccine in the US. Pfizer-BioNTech and Moderna Inc.

Sofar the suspensions apply only to AstraZeneca which is being marketed in Europe and several other countries. 

Two other major pharmaceutical conglomerates, namely Pfizer-BioNTech and Moderna Inc. are involved in marketing the mRNA vaccine technology, which is categorized in the US as an “experimental” drug.

In the US, the “Green Light” to market the experimental Pfizer-BioNTech mRNA vaccine was granted back in December 2020, despite the fact that according to the FDA, the vaccine is an “unapproved product”.

The FDA in an ambiguous statement  (see below) has provided a so-called Emergency Use Authorization (EUA) to the Pfizer-BioNTech vaccine, namely “to permit the emergency use of theunapproved product, … for active immunization…” (see below)

Injuries and Deaths Attributed to Pfizer and Moderna mRNA Vaccine

CDC data on “adverse reactions” to the two major Covid mRNA vaccines marketed in the US (Pfizer and Moderna), confirm the incidence of “pulmonary embolism, which is an “acute lung disease caused by a dislodged blood clot.” (Brian Shilhalvy, Vaccine Impact News).

“The CDC is reporting 120 cases of pulmonary embolisms, including 12 DEATHS following injections of the two experimental COVID mRNA injections currently in the U.S.

Seven of the deaths followed the Moderna mRNA COVID shot, while five deaths followed the Pfizer mRNA COVID shot. (Ibid)

Based on the CDC data on deaths and the”adverse reactions”, the suspension of the Pfizer-Moderna mRNA vaccine should be implemented in the United States without delay.

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