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France & Merkel beg citizens to take Oxford jab after millions of doses remain unused
https://youtu.be/anXByp82G5s
EU lawmaker likens AstraZeneca to ‘unreliable second-hand car salesman’ as low European jab confidence hampers vaccine uptake
Doses of the Oxford-AstraZeneca Covid-19 vaccine are going unused across the EU amid low confidence in the jab after the company was repeatedly criticized by Brussels for not sharing sufficient data and supply problems.
Speaking on Thursday, EU lawmaker Esther de Lange, a vice president of the European People’s party, reiterated the challenge of getting “reliable data” from AstraZeneca.
Quote:AstraZeneca is behaving like an unreliable second-hand car salesman. Getting reliable data from this company is still a challenge.
Such criticism of the jab by public figures in Europe has been commonplace in recent months. French President Emmanuel Macron suggested the vaccine was “quasi-ineffective,” and it wasn’t given approval for the over 65s, the most-at-risk demographic, in France and Germany despite a WHO (World Health Organization) recommendation.
Read more: EU lawmaker likens AstraZeneca to ‘unreliable second-hand car salesman’ as low European jab confidence hampers vaccine uptake
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02-27-2021, 12:37 PM
(This post was last modified: 03-06-2021, 09:29 PM by Steve.)
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Hitchens caves: ‘I’ve had the Covid jab – and all it cost me was my freedom’. He says he had it for selfish reasons, but it’s not selfish, it’s self-destructive on so many levels, and all his credibility as a defender of freedom went with it
So sorry, Your Majesty, but I have had my first Covid vaccination for wholly selfish reasons. I did not do it for the good of others but for my own convenience. And I will have my second for the same purpose.
A very important part of my family now lives abroad and I am deeply tired of not being able to see them.
I get the strong sense that any sort of travel, and plenty of other things, will be impossible if I don’t have the necessary vaccine certificate.
I hope it becomes known as the Blair Passport – as it is largely the warmongering Creature’s idea and people will come to hate it, as they have come to hate so many of his actions.
So I have been more or less forced to have an immunisation I would not normally have bothered with.
Don’t, if you are wise, dare call me an ‘anti-vaxxer’. I have, in a long life, been injected against tetanus, smallpox, TB, polio, diphtheria and yellow fever. I’m a fiend for preventive medicine and the precautions I take when I’m in malarial areas are so elaborate my companions laugh at them – from swallowing horrible protective medicines to blasting my hotel room with ultra-strength death sprays to exterminate any possible mosquitoes. These are all terrible diseases and I think it’s wise to do this.
PETER HITCHENS: I've had the Covid jab – and all it cost me was my freedom https://t.co/z5J3zyIV5N
— Peter Hitchens (@ClarkeMicah) February 27, 2021
Read more: Hitchens caves: ‘I’ve had the Covid jab – and all it cost me was my freedom’. He says he had it for selfish reasons, but it’s not selfish, it’s self-destructive on so many levels, and all his credibility as a defender of freedom went with it
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Bait & Switch: NHS ‘COVID’ Tracking App to be Used for New Vaccine Passport
Despite repeated denials and obfuscations by various UK government ministers, it’s now become clear that Boris Johnson’s government has been planning for vaccine passports all along. In fact, it appears to be the end goal and fulcrum of all the supposed ‘mitigation’ policies which have been pushed on the public over the last 12 months.
Back in December of 2020, when Michael Gove was asked directly about whether there were any plans to introduce a new “vaccine passport” in order to restrict unvaccinated peoples’ access to places such as shops, supermarkets, pubs, venues, restaurants and for travel, the Cabinet Office minister flatly told the BBC, “That’s not the plan.”
Not quite a straight answer, but but most people took it on faith at the time. He was then asked a subsequent time, and again denied it, saying “no.”
In early February, after The Times reported that the government would be implementing COVID vaccine passports in time for summer, Vaccines Minister Nadhim Zahawi responded by categorically denying it.
Speaking to Sky News, he stated, “One, we don’t know the impact of the vaccines on transmission.
“Two, it would be discriminatory and I think the right thing to do is to make sure that people come forward to be vaccinated because they want to rather than it be made in some way mandatory through a passport.”
Despite these and other public denials by politicians, today it has been revealed that the government’s NHS COVID Track & Trace App will be transitioned into the “digital certificate” which allows people to use their smart phone to prove they have received the experimental COVID vaccine, or have tested negative for coronavirus.
According to a new report in The Times, Downing Street is considering allowing businesses to demand to see a person’s vaccine passport before allowing them entry to a premises. This is allegedly “to ensure that staff or customers are at much lower risk of being infectious,” but one cannot ignore what a authoritarian tool of social and behavioural control this is.
https://21stcenturywire.com/2021/02/24/b...-passport/
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03-09-2021, 08:40 AM
(This post was last modified: 03-11-2021, 05:06 PM by Steve.)
Study shows extreme long term risk exists with RNA based Vaccines -
https://sarahwestall.com/study-shows-ext...-vaccines/
One nurse dead and another one injured as Austria suspends AstraZeneca vaccine -
https://nexusnewsfeed.com/article/human-...ca-vaccine
Covid-19: Several European countries suspend AstraZeneca vaccinations over blood clot fears -
https://www.france24.com/en/europe/20210...clot-fears
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Flu-like illness to ‘protect’ you from what they say is a ‘flu-like’ illness: Flu-like symptoms an expected side-effect of ‘Covid vaccines’, says Cult-owned WHO laughing at you and taking the piss
An influenza-like illness is a likely side effect of being inoculated against Covid-19, the World Health Organization’s global advisory committee on vaccine safety said in a statement on Monday.
The committee said that the benefit-risk balance of Covid-19 vaccines “remains favorable” after it reviewed the data for influenza-like illness among health-care workers who had received the jab. Its review, conducted virtually on February 25, found that the vaccines may induce flu-like symptoms, including headache, fatigue, muscle aches, feverishness and chills.
The side-effects were reported during the first few days after inoculation in clinical trials in several countries
“Most symptoms were mild to moderate and resolved within a few days,” the statement said, adding that side effects were more common among the under-55s.
The committee concluded that its safety advice for the vaccines could remain unchanged, because the side-effect reports are consistent with what would be expected. It advised that people who suffer headache, fever or muscle aches after their first dose should still get their follow-up booster jab as planned, and that people should be made aware of the potential side effects prior to vaccination.
Read More: Flu-like illness an expected side-effect of Covid vaccines, says WHO, with symptoms including fever and headache
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03-11-2021, 07:54 AM
(This post was last modified: 03-11-2021, 08:03 AM by Steve.)
FB GROUP POST ...
LONDON, England, March 5, 2021 (LifeSiteNews) — Among people in the U.K., 35 cases of deafness and 25 cases of blindness have been reported by people who have taken the experimental mRNA COVID-19 vaccines. The numbers are derived from the U.K. Yellow Card vaccine reporting scheme, which is the British equivalent to the American Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS).
Both the Pfizer/BioNTech and Oxford/AstraZeneca mRNA COVID vaccines were given temporary authorization in the U.K. by the Medicines and Healthcare products Regulatory Agency (MHRA), the former in mid-December 2020, and the latter at the beginning of January 2021. Since then, the Yellow Card scheme has flagged a combined 191,832 individual adverse events, or side effects, of varying degrees of injury. Of the injuries recorded, AstraZeneca’s vaccine consistently performed the worst, accounting for 60% of all adverse events, and 58% of deaf and blind reports. Additionally, of the 402 fatalities, 197 were reported following use of the Pfizer formula, and 205 after taking AstraZeneca’s vaccine.
The latest data, which runs up to February 19 and was published on February 22, reveals a plethora of debilitating side-effects, but this has not alarmed officials at the MHRA who maintain that “no other new safety concerns have been identified from reports received to date.” They conclude from this that the “overall safety experience with both vaccines is so far as expected from the clinical trials.”
The regulator doubled down on supporting the jabs, stating that the “expected benefits of the vaccines in preventing COVID-19 and serious complications associated with COVID-19 far outweigh any currently known side effects,” including deafness, blindness, and death.
The MHRA justified this position by citing the passively analytical nature of recordings on the Yellow Card scheme: It is a self-reporting system. This means that none of the serious injuries, or even the deaths, are confirmed by a licensed doctor, giving the MHRA some leeway to declare that “the available evidence does not currently suggest that the vaccine caused the event.” Rather, the MHRA favors use of the term “temporally-related” to describe the succession of adverse events from injection with the vaccine, which they describe as “events occurring following vaccination but may or may not be caused by the vaccine.”
A pattern of adverse results has been established regarding use of the Pfizer vaccine, which can be seen by examining its use in the U.S., following the award of “Emergency Use Authorization” by the Food and Drug Administration (FDA) in December. In both the U.K. and the U.S., use of the Pfizer vaccine has brought about similar results, accounting for the majority of post-vaccination injuries in America. VAERS has recorded 19,907 cases of adverse events arising after taking a COVID-19 vaccine, 64% of which are linked to Pfizer’s mRNA vaccine, and 36% attributable to Moderna’s equivalent jab.
In the U.S., VAERS reported 23 cases of complete deafness and 27 of unilateral deafness, with Pfizer’s jab making up 76% of complaints. Additionally there have been 29 cases of partial or complete blindness, over half of which followed the Pfizer vaccine.
https://www.lifesitenews.com/news/uk-35-...cine-shots
https://www.who.int/news-room/q-a-detail...evelopment
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Five countries halt use of one batch of AstraZeneca jab after fatal blood clot
Austria’s national medicines regulator has suspended use of a batch of the AstraZeneca vaccine after four patients were diagnosed with dangerous blood clotting conditions after receiving their jab.
One person died of multiple thrombosis – formation of blood clots within blood vessels – 10 days after their vaccine, the European Medicines Agency (EMA) said.
A second patient was diagnosed with pulmonary embolism – where blockages form in the arteries in the lungs – but is now recovering.
As of Tuesday this week, two other clotting conditions had been identified in patients that had received a dose from the same batch.
The EMA said there is currently no evidence that the vaccine caused the conditions, and that thrombosis is not listed as a potential side effect of the vaccine.
Read more: Five countries halt use of one batch of AstraZeneca jab after fatal blood clot
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03-12-2021, 09:21 AM
(This post was last modified: 03-12-2021, 08:41 PM by Steve.)
Urgent Open Letter from Doctors and Scientists to the European Medicines Agency regarding COVID-19 Vaccine Safety Concerns ...
https://doctors4covidethics.medium.com/u...e17c311595
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.
2947 Americans die in 7 days from the Pfizer jab -
https://www.brighteon.com/a89e5d43-529a-...8ecd30fcc8
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12 Prominent Scientists and Doctors to EU Regulators: Address ‘Urgent’ Safety Concerns or Halt ‘Covid Vaccines’
A group of prominent scientists and doctors want the European Medicines Agency (EMA) to answer “urgent” safety questions about the three COVID-19 vaccines authorised for use in the EU, or withdraw the vaccines’ authorisation.
In an open letter published this week, the group questioned “whether cardinal issues regarding the safety of the vaccines were adequately addressed prior to their approval” by the EMA.
The EMA, which is the EU equivalent of the U.S. Food and Drug Administration, approved three vaccines for emergency use in the EU: the Pfizer-BioNtech, Moderna and Oxford-AstraZenecavaccines.
In their letter, 12 scientists and doctors noted a “wide range of side effects” is reported following vaccination of previously healthy younger individuals with the gene-based COVID-19 vaccines.
They wrote:
“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 their original letter, sent Feb. 28 via email to the EMA, the group asked the EMA to provide responses to seven safety-related issues 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.”
Read more: 12 Prominent Scientists and Doctors to EU Regulators: Address ‘Urgent’ Safety Concerns or Halt ‘Covid Vaccines’
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