402 Deaths Following COVID Vaccines in UK

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Between December 9, 2020, when the first Pfizer COVID vaccine was administered in the UK, and February 14, 2021, 402 deaths have been reported to the UK government’s system for COVID-related medical and vaccine injuries. This number undoubtedly should be much larger due to problems within the reporting system. The Oxford-AstraZeneca vaccine, which also has been given in the UK, has a 77% higher rate of injury and 24% higher rate of death compared to the Pfizer vaccine. Oxford-AstraZeneca now is planning to conduct vaccine trials with children. -GEG

UK Data Show 402 Reports of Deaths Following COVID Vaccines

Children’s Health Defense, author John Stone

Between Dec. 9, 2020 (when the first COVID vaccine was administered in the UK) and Feb. 14, 2021, 402 deaths following COVID vaccines have been reported to YellowCard, the UK government’s system for reporting side effects to COVID-related medicines, vaccines, devices, and defective or falsified products.

Britain’s regulator, the Medicines and Healthcare Products Regulatory Agency (MHRA), runs YellowCard, which is the nearest British equivalent to the Vaccine Adverse Events Reporting System or VAERS in the U.S.

So far, only the Pfizer-BioNTech and Oxford-AstraZeneca vaccines have been administered in the UK. The Pfizer vaccine was deployed during the second week of December 2020, and Oxford-AstraZeneca at the beginning of January. (Moderna’s COVID vaccine is approved for emergency use in the UK, but the country has not as of yet obtained any vaccines from the company).

The MHRA has expressed no concern about the number of reports of adverse events connected with these new products, even failing to note how much worse the Oxford product has performed in comparison to the Pfizer vaccine.

Similarly, the accumulation of hundreds of deaths has failed to register a flicker of concern from them.

In January, the deaths of 23 frail elderly in Norway made international news — and raised questions about whether we should even be vaccinating people who are already near death. While it’s true that thousands of frail elderly people inevitably die every week, the lack of evidence of an active attempt to find out what is going on in individual cases is troubling.

The MHRA responded to the Norwegian report by saying “it did not currently anticipate any specific concerns,” a highly prejudicial statement. At the time The BMJ (formerly the British Medical Journal) permitted a short on-line response from me under the title “Is the MHRA up to it?”:

“But the MHRA also did not detect concerns with narcolepsy and the Pandemrix vaccine in 2009 and was unapologetic nine years on in these columns (while Clifford Miller going through the available data found as many as 178 potentially related reports in the first 67 days) … More recently they did not anticipate problems with PEG and anaphylaxis before the rollout of the Pfizer BioNTech vaccine, though these were already identified by others…”

However, it is even more worrying that even after 400 reported deaths the British Medical Journal will not publish my letter critiquing the MHRA data.

A major difficulty is that the MHRA system breaks down the data so that it is impossible to connect these deaths with preceding adverse events, although most reports are said to include multiple reactions.

Yet it is reasonable to assume that the preponderance of these reported deaths were preceded by a sequence of events — otherwise no one would have thought to make a report. However, the YellowCard format masks this information.

As with any passive reporting database we are met with the paradox that no single vaccine death is confirmed (and any doctor who confirmed one would likely say good-bye to their career in the UK). We also know vaccine-related injuries are generally  under-reported by many times.

Nevertheless, the very distinct event profiles of two products filtered through the same same system after 15 million vaccine administrations would suggest that there is something to be investigated and explained.

The BMJ has declined to publish my successive letters on the subject of investigating COVID vaccine injuries and deaths, but here’s my latest (unpublished) letter to the publication:

Dear Editor:

Paul Thacker raises important concerns over transparency and the Oxford-AstraZeneca vaccine, but I believe there are also questions about safety.

In January, eyebrows were raised because of 23 deaths in frail elderly Norwegian patients following the Pfizer vaccine. Since then we seem to have come a dangerous distance.

MHRA data so far lists a combined 402 fatal reactions to the Pfizer BioNTech (197) and Oxford AstraZeneca (205) products. According to the MHRA publication, the data was updated Feb. 14 when approximately 8.3 million Pfizer and 6.9 million Oxford AstraZeneca products had been administered.

It is also remarkable how unfavorably the Oxford-AstraZeneca data compare with the Pfizer data. MHRA data show 26,823 reports related to Pfizer vaccines, including 77,207 reactions, and 31,427 reports related to Oxford-AstraZeneca, including 114,625 reactions.

Thus the Pfizer reports run at ~3.2 per 1,000 while the Oxford-AstraZeneca reports run at ~4.6 per 1,000: which translates to 43% more reports associated with the Oxford-AstraZeneca vaccine compared with Pfizer.

However, the Pfizer reports have an average of 2.9 reactions per report compared with 3.6 for the Oxford-AstraZeneca (again Oxford 24% higher) — so the rate of reactions reported is actually 77% higher overall for the Oxford-AstraZeneca vaccine.

When it comes to fatalities, the Oxford-AstraZeneca product records a rate of 3 in 100,000 while Pfizer has 2.4 in 100,000 which is again 25% higher for Oxford-AstraZeneca.

Tabulated, as of 14 Feb:

Pfizer BioNTech: 26,823 reports, 77, 207 reactions and 197 deaths (per 8.3 million doses).

Oxford Astra Zeneca: 31,427 reports, 114,625 reactions and 205 deaths (per 6.9 million doses)

Pfizer BioNTech:

Reports 1 in 309.5 doses

Reactions 2.9 per report

Fatal reactions 1 in 42,131

Oxford AstraZeneca:

Reports  1 in 219.5 doses

Reactions 3.6 per report

Fatal reactions 1 in 33,659

It is important to recognize that these data are by no means random: The reports are filtered through the same system (even though it is passive and likely to represent only a fraction of cases) and these products have quite distinct profiles.

The Oxford-AstraZeneca safety profile should also be borne in mind considering that the company is planning to conduct trials with children.

Whether it is ethical to administer vaccines with such open safety issues is one thing, but it is another when the data from one product seems to be so markedly inferior to the other.

Note that the linked MHRA documents (here, here and here) have a rolling update and this data will only be correct for the week Feb. 26 – March 4, 2021.

Finally, I would be grateful to have any errors of transcription or mathematics pointed out to me.

“© 3/2/2021 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

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Harry Zinn
Harry Zinn
2 months ago

Nice! When are they going to get it right? Are we for experimenting?

Edwad
Edwad
2 months ago

Thanks, interesting stats and info. I was wondering how the vaccines compared. Is there any info how nutrition including vitamin D and zinc (ionophore in lieu of HCQ fare please?

Phillip Mezzapelle
Phillip Mezzapelle
2 months ago

Sorry to hear this.

terry shead
terry shead
2 months ago

This experiment they call a vaxx is poison to your body, for F sake wake up you stupid people?

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