Growing list of expert scientists and doctors endorsing urgent letter regarding vaccine safety

Emer Cooke, Executive Director, European Medicines Agency, Amsterdam, The Netherlands

28 February 2021

Dear Sirs/Mesdames,

FOR THE URGENT PERSONAL ATTENTION OF: EMER COOKE, EXECUTIVE DIRECTOR OF THE EUROPEAN MEDICINES AGENCY

As physicians and scientists, we are supportive in principle of the use of new medical interventions which are appropriately developed and deployed, having obtained informed consent from the patient. This stance encompasses vaccines in the same way as therapeutics.

We note that a wide range of side effects is being reported following vaccination of previously healthy younger individuals with the gene-based COVID-19 vaccines. Moreover, there have been numerous media reports from around the world of care homes being struck by COVID-19 within days of vaccination of residents. While we recognise that these occurrences might, every one of them, have been unfortunate coincidences, we are concerned that there has been and there continues to be inadequate scrutiny of the possible causes of illness or death under these circumstances, and especially so in the absence of post-mortems examinations.

In particular, we question whether cardinal issues regarding the safety of the vaccines were adequately addressed prior to their approval by the European Medicines Agency (EMA).

As a matter of great urgency, we herewith request that the EMA provide us with responses to the following issues:

1. Following intramuscular injection, it must be expected that the gene-based vaccines will reach the bloodstream and disseminate throughout the body [1]. We request evidence that this possibility was excluded in pre-clinical animal models with all three vaccines prior to their approval for use in humans by the EMA.

2. If such evidence is not available, it must be expected that the vaccines will remain entrapped in the circulation and be taken up by endothelial cells. There is reason to assume that this will happen particularly at sites of slow blood flow, i.e. in small vessels and capillaries [2]. We request evidence that this probability was excluded in pre-clinical animal models with all three vaccines prior to their approval for use in humans by the EMA.

3. If such evidence is not available, it must be expected that during expression of the vaccines’ nucleic acids, peptides derived from the spike protein will be presented via the MHC I — pathway at the luminal surface of the cells. Many healthy individuals have CD8-lymphocytes that recognize such peptides, which may be due to prior COVID infection, but also to cross-reactions with other types of Coronavirus [3; 4] [5]. We must assume that these lymphocytes will mount an attack on the respective cells. We request evidence that this probability was excluded in pre-clinical animal models with all three vaccines prior to their approval for use in humans by the EMA.

4. If such evidence is not available, it must be expected that endothelial damage with subsequent triggering of blood coagulation via platelet activation will ensue at countless sites throughout the body. We request evidence that this probability was excluded in pre-clinical animal models with all three vaccines prior to their approval for use in humans by the EMA.

5. If such evidence is not available, it must be expected that this will lead to a drop in platelet counts, appearance of D-dimers in the blood, and to myriad ischaemic lesions throughout the body including in the brain, spinal cord and heart. Bleeding disorders might occur in the wake of this novel type of DIC-syndrome including, amongst other possibilities, profuse bleedings and haemorrhagic stroke. We request evidence that all these possibilities were excluded in pre-clinical animal models with all three vaccines prior to their approval for use in humans by the EMA.

6. The SARS-CoV-2 spike protein binds to the ACE2 receptor on platelets, which results in their activation [6]. Thrombocytopenia has been reported in severe cases of SARS-CoV-2 infection [7]. Thrombocytopenia has also been reported in vaccinated individuals [8]. We request evidence that the potential danger of platelet activation that would also lead to disseminated intravascular coagulation (DIC) was excluded with all three vaccines prior to their approval for use in humans by the EMA.

7. The sweeping across the globe of SARS-CoV-2 created a pandemic of illness associated with many deaths. However, by the time of consideration for approval of the vaccines, the health systems of most countries were no longer under imminent threat of being overwhelmed because a growing proportion of the world had already been infected and the worst of the pandemic had already abated. Consequently, we demand conclusive evidence that an actual emergency existed at the time of the EMA granting Conditional Marketing Authorisation to the manufacturers of all three vaccines, to justify their approval for use in humans by the EMA, purportedly because of such an emergency.

Should all such evidence not be available, we demand that approval for use of the gene-based vaccines be withdrawn until all the above issues have been properly addressed by the exercise of due diligence by the EMA.

There are serious concerns, including but not confined to those outlined above, that the approval of the COVID-19 vaccines by the EMA was premature and reckless, and that the administration of the vaccines constituted and still does constitute “human experimentation”, which was and still is in violation of the Nuremberg Code.

In view of the urgency of the situation, we request that you reply to this email within seven days and address all our concerns substantively. Should you choose not to comply with this reasonable request, we will make this letter public.

This email is copied to:

Charles Michel, President of the Council of Europe

Ursula von der Leyen, President of the European Commission.

Doctors and scientists can sign the open letter by emailing their name, qualifications, areas of expertise, country and any affiliations they would like to cite, to Doctors4CovidEthics@protonmail.com

References and endorsing signatories

at https://doctors4covidethics.medium.com/urgent-open-letter-from-doctors-and-scientists-to-the-european-medicines-agency-regarding-covid-19-f6e17c311595

New Research Points to Link Between AstraZeneca Vaccine and Blood Clots

Thanks Judy, another perfectly timed link.

Researchers in Norway and Germany say they’ve identified antibodies that provoke immune reactions leading to the type of cerebral blood clots experienced by some people who received AstraZeneca’s COVID vaccine. https://childrenshealthdefense.org/defender/link-astrazeneca-vaccine-blood-clots

Vaccine: twenty countries suspend injections; does that make you “hesitant?”

The reason for the “pause?” A “small” number of people have developed blood clots. If you believe just a few people with blood clots caused 20 countries to stop giving the jabs, I have condos on Mars for sale. https://blog.nomorefakenews.com/2021/03/22/vaccine-twenty-countries-suspend-injections-does-that-make-you-hesitant/

Researchers fast-track coronavirus vaccine by skipping key animal testing first

The covid gene therapy trials did animal testing with one flaw, they did them out of order. In other words, they failed to complete animal testing first. Instead, they did animal testing alongside human trials, which did not follow historic and important safety protocols recommended by authorities. https://www.livescience.com/coronavirus-vaccine-trial-no-animal-testing.html

Researchers rush to test coronavirus vaccine in people without knowing how well it works in animals

Regulators require that a manufacturer show a product is safe before it goes into people, and while it isn’t enshrined in law, researchers almost always check that a new concoction is effective in lab animals before putting human volunteers at potential risk. https://www.statnews.com/2020/03/11/researchers-rush-to-start-moderna-coronavirus-vaccine-trial-without-usual-animal-testing/

Death of an African Freedom Fighter, Confronted Big Pharma and the Corrupt Covid Cabal

Everybody in the Covid trenches felt the shock death to be connected to John Magufuli’s provocation to the global Covid industrial complex last May, when he covertly had non-human samples—from fruits, goats, sheep, and car oil—tested for Covid on the PCR test, returning positive results from a paw-paw, a quail, and a goat.

You’d never have a clue Magufuli was loved in his country at all if you only looked at Western media headlines, consistent in their icy Covid-Imperial tone—projecting that Magufuli was rightfully swept away by the very “virus” he “denied” while alive. https://www.thelibertybeacon.com/john-magufuli-death-of-an-african-freedom-fighter-confronted-big-pharma-and-the-corrupt-covid-cabal/

May the spirit/soul of John Magufuli rest in peace.

Western media propaganda is sustained by the devotion, attention, and money [consent] of unaware people. Perhaps sharing the above letter will spark curiosity to help people become more aware. Thank you.

Without Prejudice and Without Recourse
Doreen A Agostino
http://freetobewealthy.net
Via ethernet to safeguard life

fluproof

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