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COVID-19 mRNA Vaccines Lessons Learned Fact Check!

COVID-19 mRNA Vaccines Lessons Learned Fact Check!

Let’s take a look at the recent “peer-reviewed” study on the lessons learned about COVID-19 mRNA vaccines, and find out what the facts really are!

 

COVID-19 mRNA Vaccines: Lessons Learned??

Some people are excitedly sharing a “peer-reviewed” study on the lessons learned about COVID-19 mRNA vaccines, while calling for the mRNA COVID-19 vaccines to be removed.

Mary Talley Bowden MD : Peer-reviewed article published in @CureusInc : COVID shots must be pulled off the market. If you are a physician or politician, now is the time to be on the right side of history.

Recommended : Are Residual DNA In mRNA Vaccines Dangerous?!

 

COVID-19 mRNA Vaccines Lessons Learned : My Fact Check

Let’s go through the “peer-reviewed” study on the lessons learned about COVID-19 mRNA vaccines, and see what the facts really are!

Fact #1 : Cureus Relies On Post-Publication Peer Review

Let me start by pointing out that the journal Cureus relies on “post-publication peer review”.  Even though this paper was marked as “peer-reviewed”, it was an “unusually fast” peer review.

Cureus uses “an unusually fast” peer-review process of just “a few days”, and relies heavily on “post-publication peer review”, as its Editor in Chief John R. Adler explained to Retraction Watch in 2015:

Yes, Cureus has an unusually fast review process, which is an important part of the journal’s philosophy. We believe that post publication peer review, a focus of our journal through commenting and our unique SIQ process, is potentially a more powerful way to discern truth.

In other words – the pre-publication peer review appears to be superficial, and Cureus relies on the scientific community to peer-review the papers after publication.

Fact #2 : It Regurgitates Long-Debunked Claims

The paper in question is called “COVID-19 mRNA Vaccines: Lessons Learned from the Registrational Trials and Global Vaccination Campaign” by Mead et. al. which includes anti-vaccine activists like Jessica Rose, Steve Kirsch, and Peter McCullough.

While it is being heralded as something new, the paper appears to be nothing more than a regurgitation of long-debunked claims about mRNA COVID-19 vaccines. Let’s just take a look at a few:

COVID-19 Vaccine Clinical Trials Were Too Short?!

The paper claimed that no vaccine was permitted for market release without a testing period of at least four years, using the mumps vaccine by Merck as example. That’s not true.

The Mumpsvax (Jeryl Lynn strain) vaccine was developed and approved in a record four years, but its testing did not last four years. The mumps vaccine clinical trial in 1966 (abstract) only lasted 6 months.

This paper gives the results of a large field trial of the vaccine conducted among schoolchildren in North Carolina.

Vaccination was carried out in November 1966, every tenth child receiving a placebo preparation. Serum specimens were obtained at the time of vaccination and 4 weeks later from 556 children representing a cross-section of the total group of participants.

During the 180 days of post-vaccination surveillance, 56 cases of mumps were reported among the study population and 69 cases among non-participants.

There is no requirement by health authorities that testing or assessing any vaccine should last 10 years. The typical vaccine development time of 10-15 years is not a reflection of how much time a clinical trial needs to run, but rather the time it “generally” takes to create a vaccine, gather resources, get approvals, run clinical trials, process the data, file for approval, etc.

COVID-19 vaccines were so quickly developed because scientists all over the world collaborated on the effort, while governments funded their development, and fast-tracked their clinical trials and manufacturing preparations.

The speedy development of COVID-19 vaccines was also enabled by new vaccine platforms using mRNA or DNA technologies, in which genetic information from the new virus only needed to be “plugged in” to produce a new vaccine.

More importantly – the paper provided no evidence that the accelerated development of COVID-19 vaccines has actually resulted in unsafe vaccines.

Recommended : Did COVID-19 Vaccines Cause 17 Million Deaths?!

mRNA COVID-19 Vaccines Were Not Proven Safe / Effective?

The Mead et. al. paper claimed or suggested that the clinical trials did not show that the mRNA COVID-19 vaccines were safe or effective because too few people in the unvaccinated (placebo) group died from COVID-19.

Well, not only is that a “misunderstanding” of the clinical trial results (see the next section), many studies have been conducted into the safety and efficacy of the mRNA vaccines for COVID-19 since they were deployed.

Those real world studies (example, example, example) consistently showed that the mRNA vaccines for COVID-19 are safe and effective.

Low Absolute Risk Shows No Need To Vaccinate?!

The Mead et. al. paper repeats the old trope that the low absolute risk (AR) seen in the mRNA vaccine clinical trials mean there is no need for anyone to get vaccinated. That’s simply not true, and is a (deliberate?) misunderstanding of statistical calculations.

The Absolute Risk Reduction (ARR) will “always appear low” because it depends very much on the “event rate”. As the Meedan Health Desk explained:

Let’s say a study enrolled 20,000 patients into the control group and 20,000 in the vaccine group. In that study, 200 people in the control group got sick and 0 people in the vaccine group got sick.

Even though the vaccine efficacy would be a whopping 100%, the ARR would show that vaccines reduce the absolute risk by just 1% (200/20,000= 1%).

For the ARR to increase to 20% in our example study with a vaccine with 100% efficacy, 4,000 of the 20,000 people in the control group would have to get sick (4,000/20,000= 20%).

Hence, the Relative Risk Reduction (RRR) is used instead to determine a vaccine’s efficacy, because it tells us how much risk is reduced in the vaccinated group, compared to the unvaccinated control group.

To be clear – the clinical trials and post-vaccination monitoring and studies have clearly shown that mRNA COVID-19 vaccines are effective in preventing severe disease and deaths from COVID-19.

Recommended : Hybrid Immunity Better Than Natural / Vaccine Immunity!

mRNA Vaccines Do Not Prevent Transmission?!

The Mead et. al. paper claimed that the CDC said that “COVID-19 products would stop transmission”, but in the end “COVID-19 mRNA products do not prevent transmission or infection”. Well, that’s not really true.

For one thing – the CDC never said that COVID-19 vaccines would stop transmission. In fact, the CDC article the paper linked to only said that the vaccines appear to reduce (not stop) transmission:

… a growing body of evidence suggests that COVID-19 vaccines also reduce asymptomatic infection and transmission.

To be clear – the COVID-19 vaccines were primarily designed to reduce or prevent severe disease and death, which is why transmission for not an endpoint for their clinical trials. It would have been a nice bonus to block transmission completely, but partially reducing transmission is not too bad.

mRNA Vaccines Have A Lot Of AESIs?!

The Mead et. al. paper warns us about the many Adverse Events of Special Interest (AESI) reported after COVID-19 vaccinations. The problem is – those AESI are not actual vaccine side effects!

The AESI list for the Pfizer-BioNTech COVID-19 vaccine for example has 9 pages of 1,291 adverse events, but that is not a list of the mRNA vaccine side effects. It is a list of “adverse events” that Pfizer must look for during the post-vaccination monitoring period. Not only are these “adverse events” not specific to the Pfizer mRNA vaccine, they include:

Needless to say – those adverse events are not vaccine side effects, or are any indication of vaccine performance or safety in any way.

Recommended : COVID-19 Vaccine Causes Turbo Skin Cancer – Melanoma?!

Lots Of Deaths + Hospitalisation Were Reported?!

The Mead et. al. paper also claimed that two large drug safety reporting systems in the US and Europe have over 7.8 million reports of adverse events, with “death, hospitalisations, and life-threatening reactions”. It is probably referring to VAERS and EudraVigilance.

The thing is – VAERS / Yellow Card / EudraVigilance data are all unverified, and may contain duplicated information. That’s why they are all prefaced with warnings like:

In addition, open systems like VAERS, or the UK Yellow Card system, are very susceptible to abuse because they allow anyone from anywhere to post anything they want, without evidence or verification.

Anti-vaccination activists can, for example, key in unlimited numbers of adverse reaction reports, even if they never received a single dose of the COVID-19 vaccine!

Autopsy Reports Show Deaths Caused By Vaccines?!

The Mead et. al. paper claimed that “autopsy studies” showed that 74% of deaths were “judged to have been caused by the COVID-19 mRNA products”.

The problem is – the study it referred to was a preprint by one of its own authors – Peter McCullough, that was removed by The Lancet for violating its “screening criteria”.

This preprint has been removed by Preprints with The Lancet because the study’s conclusions are not supported by the study methodology. Preprints with The Lancet reserves the right to remove a paper that has been posted if we determine that it has violated our screening criteria.

Not only was that study just a “review” of autopsy reports, many of the cases had other far more likely causes of death.

Recommended : Did CDC Alter Death Certificates To Remove Vaccine Deaths?!

mRNA Vaccines Are Contaminated By DNA?!

The paper suggested that the mRNA vaccines are contaminated with DNA “orders of magnitude higher than the EMA’s limit”.

The truth is – residual DNA is found in all biological products manufactured using cells, and has not shown any health risk after being studied for many decades.

In any case, the amount of residual DNA in mRNA vaccines were found to be far below regulatory limits.

Pfizer Vaccine Has DNA From SV40 Virus That Causes Cancer?!

The paper also warned about the Simian Virus 40 (SV40) promoter found in samples of the Pfizer mRNA vaccine. Why? Because it warns – the SV40 virus “induces lymphomas, brain tumors, and other malignancies in laboratory animals”.

First of all – after decades of studies, there is still no conclusive evidence that the SV40 virus can cause cancers in humans. However, out of an abundance of caution, the SV40 virus is considered to potentially cause cancer in humans.

In any case, the SV40 promoter is a DNA sequence that is often used to manufacture mRNA, and is not dangerous. It certainly poses no cancer risk, because the part of the SV40 that can potentially cause cancer – the T-antigen, is not present in the SV40 promoter, or the Pfizer mRNA vaccine.

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Dr. Adrian Wong has been writing about tech and science since 1997, even publishing a book with Prentice Hall called Breaking Through The BIOS Barrier (ISBN 978-0131455368) while in medical school.

He continues to devote countless hours every day writing about tech, medicine and science, in his pursuit of facts in a post-truth world.

 

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