Last week, Pascal Soriot, the French-born Australian and Chief Executive Officer of the British-Swiss pharmaceutical company, AstraZeneca plc., whose vaccine for COVID-19 has produced reports of 875,000 adverse drug reactions in the U.K. public, including 1,334 deaths, was knighted “for services to U.K. sciences and leadership in the global response to the COVID-19 pandemic”.
Other British nationals made knights or dames for their part in the U.K. vaccination programme include Sir Andrew Pollard, Director of the Oxford Vaccine Group that in April 2020 entered into a partnership with AstraZeneca to develop its viral-vector vaccine; Dame Sarah Gilbert, the Oxford Project Leader; Sir Adrian Hill, Sir Peter Horby and Sir Martin Landray, who were also responsible for conducting the development and trials of the Oxford vaccine; and Sir Aziz Sheikh, who was responsible for demonstrating the effectiveness of both the Oxford/AstraZeneca and BioNTech/Pfizer injections.
In addition to those directly involved in the AstraZeneca vaccine, other senior figures in the U.K. vaccination programme rewarded with knighthoods include Sir Chris Whitty, Chief Medical Office of England; Sir Jonathan Van-Tam, Deputy CMO; Sir Gregor Smith, CMO of Scotland; Sir Frank Atherton, CMO of Wales; and Sir Patrick Vallance, Chief Government Scientific Adviser. These were all senior members of the Scientific Advisory Group for Emergencies (SAGE), and therefore arguably responsible for the tens of thousands of deaths caused by removing medical diagnosis, care and treatment for 68.8 million Britons under two years of lockdown, which has contributed to excess deaths in the U.K. not attributed to COVID-19 far above average in 2022. They also personally authorised the injection of the unlicensed, experimental and dangerous vaccines into the British public — another, but still unacknowledged, contributing factor.
Senior female figures in the U.K. vaccination programme to receive damehoods include Dame Emily Lawson, Chief Commercial Officer at NHS England who oversaw their injection of the AstraZeneca, Pfizer and Moderna vaccines into millions of Britons; Dame Jenny Harries, the Chief Executive Officer of the sinisterly-named U.K. Health Security Agency, the merger of Public Health England, NHS Track and Trace and the Joint Biosecurity Centre, responsible for policing and enforcing censorship and restrictions in the UK Biosecurity State; and, finally, Dame June Raine, Chief Executive Officer of the Medicines and Healthcare products Regulatory Agency (MHRA), who on December 30th 2020 granted temporary authorisation to the AstraZeneca/Oxford viral vector vaccine for COVID-19, even though the clinical trials are not due to be completed until February 2023.
By March 2021, less than three months since it began to be injected into a terrorised public not only in the U.K. but across Europe and the world, the incidents of blood clots with low blood platelets and deaths following injection with the Oxford/AstraZeneca vaccine were so numerous that its use was suspended or banned in Austria, Bulgaria, Canada, the Congo, Cyprus, Denmark, France, Germany, Iceland, Indonesia, Ireland, Italy, Latvia, Luxembourg, Malaysia, the Netherlands, Norway, Portugal, Romania, Slovenia, South Africa, Spain, Sweden and Thailand. In the U.K., however, it continued to be injected into people whose informed consent about the risks, dangers and consequences of doing so had been censored by the Government, media and National Health Service.
Three months before it was authorised, in September 2020, the Oxford trials for the AstraZeneca vaccine was paused after a U.K. participant suffered spinal cord inflammation; yet it took a month to send the vaccine trial safety data to the U.S. Food and Drug Administration (FDA). In November 2020, it was revealed that AstraZeneca’s claim that its vaccine has an efficacy of 90% was based on a trial only administered to individuals up to 55 years of age, a demographic with a far lower chance of developing the symptoms of COVID-19. In April 2021, the Lancet, one of the oldest medical journals in the world, estimated that, although the AstraZeneca vaccine has a relative risk reduction of 67%, the absolute risk reduction is only 1.9%. neither of which come near the claims of 90% efficacy made by AstraZeneca or the NHS medical professionals administering it to the British public. The following month, May 2021, Transparency International Global Health accused AstraZeneca of a lack of transparency over its vaccine trials, secret contracts with governments, and conducting “science by press release”.
Far from resulting from the pressures of producing a vaccine in record time, these questions over the probity of AstraZeneca were consistent with the company’s record of malpractice and bribery. In 2010, AstraZeneca paid $520 million in fines to settle charges by the U.S. Federal Government for illegally marketing the anti-psychotic drug Seroquel to children and elderly patients for uses not approved by the Food and Drug Administration (FDA). In 2013 it was revealed that pharmaceutical companies were paying U.K. doctors £40 million every year to promote their drugs, with the U.K. office of AstraZeneca paying £671,400 in fees to 903 doctors plus £30,200 for their travel and hotel bills. In 2016, AstraZeneca agreed to pay $5.5 million to settle charges of violating the Foreign Corrupt Practices Act by bribing doctors in China and Russia in order to boost sales of their pharmaceutical products. And in April 2018, it was revealed that AstraZeneca had paid €17.9 million in secret payments to ‘independent’ healthcare professionals to endorse their products, including the use of vaccines. There is nothing to indicate this systemic bribery has stopped. Indeed, since 2000, AstraZeneca has paid $1.381 billion in fines: $594 million for healthcare-related offences; $556.2 million in government-related offences under the False Claims Act; $198 million for safety-related offences; $21 million under the Foreign Corrupt Practices Act; and $5.52 million for ‘kickbacks and bribery’.
By mid 2021, however, when the peoples of the world had begun to wake up to the dangers of injecting its product into their bodies, AstraZeneca had reaped the profits from its secret contracts with the governments of those people, having agreed deals to sell 100 million doses of its vaccine to the U.K., 400 million doses to Europe, 700 million doses to the U.S. and the GAVI Vaccine Alliance, and 1 billion doses to India. As a result of these contracts, AstraZeneca’s net profit in the second quarter of 2020 rose to £581.18 million, compared to just £99.94 million in the same quarter the previous year. But the game of cash for lives was up. In November 2021, AstraZeneca, which sold £1.64 billion of its vaccine in the first nine months of 2021, announced it was reneging on its promise to sell at cost “for the duration of the pandemic”, which it now declared was in the “endemic phase”. A year later, AstraZeneca dropped its submission for approval for its vaccine by U.S. regulators.
In the U.K., however, the adverse drug reactions (ADRs) to the Oxford/AstraZeneca vaccine were so numerous that even the DHSC, SAGE, the MHRA and the NHS couldn’t completely deny them, and only 59,700 doses have been administered as part of the U.K. vaccination programme’s third and ‘booster’ campaigns. But the injuries and deaths following injection continued to rise. According to the ‘Yellow Card’ reports of adverse drug reactions and deaths sent to the Medicines and Healthcare products Regulatory Agency, between July 28th 2021 and November 23rd 2022, the 259,700 doses of the AstraZeneca vaccine injection into the U.K. public caused an additional 54,000 adverse drug reactions and 270 deaths.
And yet, with the exception of a handful of the 81 deaths from thrombo-embolic events (blood clotting), the MHRA responsible for authorising the use and guaranteeing the safety of the experimental biotechnology injected into the U.K. public as COVID-19 vaccines continues to insist that all these injuries and deaths are ‘natural’, ‘coincidental’ and ‘expected’. What the Regulatory Agency doesn’t explain is how, if there is no causal connection to the injections, there is such a huge disparity in the proportion of injuries and deaths to doses between the different brands of vaccines, which after 169 million doses injected we would expect to even out. Based on the reports received by the MHRA, the AstraZeneca injection has a far higher number of ADRs per report (3.54) than Pfizer’s (2.88). The chances of having at least one ADR per dose also varying hugely, with those injected with the AstraZeneca vaccine having a 0.5% chance of an ADR per dose, compared with 0.2% from Pfizer’s vaccine and 0.19% per cent from Moderna’s.
Moreover, as of November 23rd 2022, the age of the deceased whose deaths within seven days of injection have been reported to the MHRA are as follows:
- Under 18 years of age: 9 dead;
- 18-29: 49 dead;
- 30-39: 90 dead;
- 40-49: 138 dead;
- 50-59: 218 dead;
- 60-69: 305 dead;
- 70-79: 471 dead;
- 80+: 713 dead;
- unknown age: 369 dead.
With the average life expectancy in the U.K. being 82 years of age, these figures do not support the MHRA’s claim that these deaths were ‘natural’, ‘coincidental’ and ‘expected’. On the contrary, what they strongly indicate is causality of different degrees between these experimental viral-vector and mRNA injections and the recorded 1.5 million injuries and 2,362 deaths they have caused, and, respectively, the thousands and millions of others that haven’t been officially recorded.
On October 16th 2020, The Human Medicines (Coronavirus and Influenza) (Amendment) Regulations 2020 modified The Human Medicines Regulations 2012 to allow temporary authorisation of the unlicensed COVID-19 vaccines. But it also extended complete immunity from civil liability to the scientists, pharmaceutical companies and medical professionals responsible for their manufacture, distribution and administering to the U.K. public. So Pascal Soriot, KBE, and his fellow knights and dames have nothing to fear from the British courts.
As a measure of the contempt in which he regards his victims, not only in this country but across the world, after he was knighted by King Charles III at Windsor Castle last week, Pascal Soriot, KBE, declared that the concerns around the AstraZeneca injection had been “overblown by the media” and that the incidents of injury and death were “extremely rare”. “Extremely rare”, however, the term also used by the MHRA and the British Heart Foundation to dismiss the deaths and injuries caused by the COVID-19 vaccines, is medically inaccurate for injuries of this frequency.
In May 2019, the Medicines and Healthcare products Regulatory Agency estimated that only 10% of serious Adverse Drug Reactions and between 2% and 4% of non-serious ADRs are reported to them. According to definitions used by the National Institute for Health and Care Excellence, an executive non-departmental public body of the Department of Health and Social Care in England, Adverse Drug Reactions to the AstraZeneca injections are a long way from ‘extremely rare’ or even ‘very rare’ (affecting less than 1 in 10,000 people, or a risk of 0.01%). On the contrary, they are ‘uncommon’ (between 1 in 1,000 and 100 people, or a risk of 0.1 to 1%) if 100% of ADRs are reported; ‘common’ (between 1 in 100 and 1 in 10 people, or a risk of 1% to 10%) if 10% of ADRs are reported; and ‘very common’ (affecting more than 1 in 10 people, or a risk of 10% or higher) if only 2% of ADRs are reported.
Notwithstanding the denials of the MHRA and NHS and the legal immunity conferred by changes to U.K. legislation, and taking reported adverse events as a lower bound, Pascal Soriot, KBE, is morally responsible for injuring at least a quarter of a million Britons and killing 1,334 with his company’s viral-vector ‘vaccine’. This is the man the U.K. Monarch has chosen to honour and to protect with a knighthood.
Simon Elmer is the author of The Road to Fascism: For a Critique of the Global Biosecurity State, which is available in hardback, paperback and e-book.
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