Straight Dope on Medicine: mRNA Vaccine Death

Author

Scott Ganser
July 17, 2023

The Intercept[i]

People aren’t supposed to die from the mRNA Covid vaccines. They are supposed to be “safe and effective.”

They were neither.

And they are trying to cover it up.

You aren’t supposed to know.

But I’ll tell you.

In this case, the cure may be more deadly than the disease.

Naomi Wolf details how Pfizer artificially dropped 200 people from their definitive trial to get the 95% efficacy that the FDA wanted. That is never done. It is unethical, manipulative, and deceptive.

In two legal actions in LA and Ohio, her team is taking Pfizer to task with the DOJ. They concealed an 87% miscarriage and spontaneous abortion rate in one section of their documents.[ii]

Now it begins to make sense why Pfizer wanted to delay disclosure for 75 years.

If you go to her website, dailyclout.io, she has posted a fantastic interview with Dr. Peter McCullough. Dr Peter McCullough, Dr. Harvey Risch, and colleagues were censored by the formerly respected scientific journal The Lancet: their paper, removed within 24 hours, found that 74% of the deaths following mRNA vaccine injection were likely caused by the injection.[iii]

It was on the Lancet’s preprint server but was removed because the Lancet hierarchy took issue with their “methodology.” McCullough has printed papers for years using the same methodology. It wasn’t a problem then.

The real problem is their conclusion.

Which the corrupt medical establishment doesn’t want to hear and seeks to suppress.

The Lancet deemed this such a problem that they removed the article within 24 hours.

The Story

McCullough was contacted by a student from the Michigan University of Public Health who wanted to investigate deaths associated with Covid and the mRNA vaccine. They thought to investigate all the public deaths that occurred after vaccination.

They would have to tease out all the confounding conditions like kidney disease, liver disease and heart issues. This would have to be clean and provide a clear signal linking mRNA vaccination and death. They searched through hundreds and hundreds of papers and finally narrowed it down to 44 papers which had autopsies. In all, they had 325 cases.

These reviewers had an advantage in that they now had 2.5 years of history of the vaccine. The original authors did not. This helped because the vaccine is known to cause blot clots. Before the history had accumulated, that fact was not known.

The criterion used to attach the vaccine to deaths were that it would have to be either the direct cause or contribute greatly to it. Also, to count the death, the patient must have received a recent injection.

Most of these deaths caused by the vaccine had a single organ system involved. Unsurprisingly, the most prominent one was the cardiovascular system. A small percentage had multisystem inflammatory disorder, which arose in young children or adolescents.

Corruption reared its ugly head when the team sought to get the paper published. The New England Journal of Medicine rejected it after a few days. Then it went to the Journal of the American Medical Association, or JAMA as it is affectionately known, and they punted it after an hour.

Transparency International

There is some positive news to fetch out of this. While the manuscript was up on the Lancet preprint server, the downloads were hundreds per minute. People wanted to know, and they were getting the information.

McCullough had never seen anything like this.

One reason might be that they had 48 pages of evidence tables. It was a thorough job.

The average death, post-injection, was 14 days.

A Suspicious Death

Óscar Cabrera Adames suggested on social media posts that he developed the rare heart disease, myocarditis, after receiving two doses of a COVID vaccine.[iv]

The 28-year-old professional Dominican basketball player Óscar Cabrera Adames passed away this week after an apparent heart attack while he was possibly undergoing a stress test, according to reports.

Typically, defibrillators are right there, and this is therefore doubly shocking.

“I got a damn Myocarditis from taking a f—ing vaccine. (I got 2 doses of Pfizer) And I knew it! Many people warned me,” Cabrera Adames wrote on social media.

“But guess what? It was compulsory or I couldn’t work. I am an international professional athlete and I am playing in Spain. I have no health problem, nothing, not hereditary, no asthma, NOTHING! I suddenly collapsed to the ground in the middle of a match and almost died. I’m still recovering and I’ve had 11 different cardiology tests done and guess? They find nothing,” he added.

He died about 2 years after taking the vaccine.

What is the Mechanism of Death?

This is the $20,000 question, and the one everyone wants to know the answer to. We see the deaths, but we’d like to understand what is going on.

1. Myocarditis or heart inflammation

2. Progression of atherosclerotic cardiovascular disease

Myocarditis is damage to the heart muscle. When damaged, the electrical current does not conduct smoothly though that tissue, and an abnormal heart rhythm forms. This causes sudden cardiac death.

This explains the sudden deaths we have seen on European soccer fields, age under 35.

European soccer deaths B.C. (before covid vaccine): 29 cases per year.

European soccer deaths A.C. (after covid vaccine): 283 per year.

Pretty damning. Vaccine injections were mandatory, of course.

They are killing people with their safety measures.

In most cases, with these athletic deaths, there are no antecedent symptoms. About 1/3 are resuscitated, whereas 2/3 die on the field.

Lipid Nanoparticles

These are present in the vaccine formulations. They go everywhere in the body. This includes the heart muscle. They are notorious for causing syncytial formation, fusing of cells.[v]

The virus itself causes syncytial formation.

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus is highly contagious and causes lymphocytopenia, but the underlying mechanisms are poorly understood. We demonstrate here that heterotypic cell-in-cell structures with lymphocytes inside multinucleate syncytia are prevalent in the lung tissues of coronavirus disease 2019 (COVID-19) patients. These unique cellular structures are a direct result of SARS-CoV-2 infection, as the expression of the SARS-CoV-2 spike glycoprotein is sufficient to induce a rapid (~45.1 nm/s) membrane fusion to produce syncytium, which could readily internalize multiple lines of lymphocytes to form typical cell-in-cell structures, remarkably leading to the death of internalized cells.

What else produces the spike glycoprotein?

Answer: the mRNA vaccine.

In the March 14 issue of Circulation, we see a connection between spike and myocarditis.[vi]

Extensive antibody profiling and T-cell responses in the individuals who developed postvaccine myocarditis were essentially indistinguishable from those of vaccinated control subjects, despite a modest increase in cytokine production. A notable finding was that markedly elevated levels of full-length spike protein (33.9±22.4 pg/mL), unbound by antibodies, were detected in the plasma of individuals with postvaccine myocarditis, whereas no free spike was detected in asymptomatic vaccinated control subjects (unpaired t test; P<0.0001).

The heart may take up lipid nanoparticles preferentially because it is a source of fuel:80 percent lipids and 20% glucose.

Athletes are always exercising, so physical activity draws more of the lipid nanoparticles to the heart to support the elevated activity. A Brazilian paper cites two periods when athletes are especially prone to suffering death due to mRNA vaccine. The first is when they are exercising. Also, between 3 am and 6 am. Why? Because the body is producing surges of adrenaline.

What about Progression of Atherosclerotic Disease?

Here we have a “straw that breaks the camel’s back” scenario. Over time multiple subclinical cellular events result in the development of unstable, vulnerable atherosclerotic lesions, which leads to the rupture of atherosclerotic plaques, culminating in the often catastrophic clinical manifestation of myocardial infarction or ischemic stroke.[vii]

There was an American Heart Association abstract with first author Gutler which rose some suspicions, if not alarms. He measured a whole variety of blood factors before and after vaccination known to trigger atherosclerotic plaque rupture in arteries.

There were astronomical elevations afterwards.

These plaques were being “set up to fail.”

The conclusion was that these vaccines were going to provoke heart attacks. Cholesterol blockages would give way, fracture and fissure, and a blood clot forms on it. Heart attacks are a result.

Give me some good news

Are we just helpless in the face of this? Of course not.

The spike protein is the primary culprit. It is doing the most damage. We now have products that can degrade it.

Human enzymes cannot break it down. Nattokinase from soy can. It is Japanese. It can be taken orally, and there is preclinical evidence available now supporting its use.

Bromolain is also under review. It is from pineapple stem. It diminishes the expression of ACE-2 and TMPRSS2 in VeroE6 cells and dramatically lowers the expression of S-Ectodomain. Importantly, bromelain treatment reduced the interaction between S-Ectodomain and VeroE6 cells. Most importantly, bromelain treatment significantly diminished the SARS-CoV-2 infection in VeroE6 cells. Altogether, our results suggest that bromelain or bromelain rich pineapple stem may be used as an antiviral against COVID-19.[viii]

A new study published in the Nutrients Journal highlights the impact of curcumin supplementation on the immune response following the immunization of Coronavirus disease 2019 (COVID-19) survivors with a primary series of monovalent COVID-19 vaccines.

Curcumin is a polyphenol obtained from the rhizomes of the turmeric plant Curcuma longa, with supposed anti-inflammatory, antiviral, and antioxidant activity. It targets multiple pro-inflammatory pathways like the nuclear factor-kappa B (NF-kB), resulting in reduced levels of a host of inflammatory cytokines and chemokines such as interleukin (IL)-6, interferon (IFN) γ, monocyte chemoattractant protein (MCP)-1, and tumor necrosis factor (TNF)-α.

Curcumin is safe even at relatively high doses and is well tolerated by the body. However, it is poorly bioavailable and is rapidly broken down in the liver in humans. Therefore, better formulations should be used to test their immunomodulatory and anti-inflammatory activities.[ix]

The current study was carried out between June 2021 and May 2022. The novel curcumin formulation HydroCurc (CURC) was tested for its effects on circulating inflammatory biomarkers in adults who had recovered from COVID-19. This was compared with the effects of a placebo.

What did the study show?

The scientists found that the levels of certain inflammatory biomarkers dropped significantly in the CURC group relative to the placebo group. IL-6, and MCP-1 both showed a decline. Others did not show a significant difference.

These two biomarkers have been considered to point to increased odds for acute and persistent dysregulation of inflammation, whether in COVID-19 or chronic inflammatory conditions. This is the first time the benefits of curcumin have been explored in people with previous COVID-19, followed by vaccination.

The study comprised 31 participants, all of whom had received similar vaccine types. The mean interval from the COVID-19 diagnosis to their participation in the trial was ~280 days. Almost three-quarters of the participants were female, with a mean age of ~28 years.

All participants were given a 500 mg tablet, either of CURC or placebo, twice a day for four weeks.

How bad is it?

This is a difficult question to answer. The corporate press and the corrupt medical establishment are doing their best to keep people from questioning what is going on and from finding out what is going on.

Anyone who is doing the work gets vilified and smeared mercilessly. If you don’t think everything is perfect and that there might be a problem, then you are a crackpot, a nutjob and a conspiracy theorist.

Ad hominem attacking to the max.

However, that is a logical fallacy and not an argument.

It is an insult. That’s all.

No one should be swayed by it.

Edward Dowd, formerly from Blackrock, is doing the heavy lifting. There are others as well.[x]

At this point, we should insert the “alternative” corporate explanation. “Yes, there were excess deaths, but it was not the vaccine. Instead, it was drug overdose, suicide and missed cancer screenings.” Those are all up but pointing to those does not dismiss the contention that the vaccine is at work. Dowd points to “timing.” August of 2021 was when everyone was under the gun to get vaccinated. Either that or lose your job. That is correlated with a spike in deaths.

Conclusion

These vaccines are bad. And they aren’t really vaccines. They are gene editing technology. The mRNA vaccines had a 28-day trial and have been administered to about 5 billion people worldwide. Now we are starting to find out what we really did.
Pfizer and Moderna mRNA COVID-19 vaccines were associated with an excess risk of serious adverse events of special interest of 10.1 and 15.1 per 10,000 vaccinated over placebo baselines of 17.6 and 42.2 (95 % CI −0.4 to 20.6 and −3.6 to 33.8), respectively.

The Pfizer trial exhibited a 36 % higher risk of serious adverse events in the vaccine group; risk difference 18.0 per 10,000 vaccinated (95 % CI 1.2 to 34.9); risk ratio 1.36 (95 % CI 1.02 to 1.83). The Moderna trial exhibited a 6 % higher risk of serious adverse events in the vaccine group: risk difference 7.1 per 10,000 (95 % CI –23.2 to 37.4); risk ratio 1.06 (95 % CI 0.84 to 1.33).[xi] 

Don’t look at that. Avert your eyes.
What did Doshi et al conclude?

In the Moderna trial, the excess risk of serious AESIs (15.1 per 10,000 participants) was higher than the risk reduction for COVID-19 hospitalization relative to the placebo group (6.4 per 10,000 participants). [3] In the Pfizer trial, the excess risk of serious AESIs (10.1 per 10,000) was higher than the risk reduction for COVID-19 hospitalization relative to the placebo group (2.3 per 10,000 participants).

In other words, you would be better off not taking the vaccine.

Some people are beginning to get it.[xii]

Denmark was highly vaccinated and had a huge incidence of excess death.[xiii]

1 people die in its vaccine cohort and 17 people die in its placebo cohort.

Death isn’t the only negative outcome. Dowd goes on to say that 1.2 million people have been disabled from the 100 million that work in the United States, since February of 2021.

Vaccine Death Reporting

Bear in mind that this is more than likely a very low figure and not accurately reflecting the magnitude of the problem.[xiv]

Another disclosure from Western Australia. John Campbell reports on this. It is a graph of adverse reactions from the vaccine.[xv]

The blue arrow indicates when the shots were given. He describes this as “an outrageous amount of adverse reactions.”

These Covid mRNA vaccines should be banned.


[v] Zhang, Z., Zheng, Y., Niu, Z. et al. SARS-CoV-2 spike protein dictates syncytium-mediated lymphocyte elimination. Cell Death Differ 28, 2765–2777 (2021). https://doi.org/10.1038/s41418-021-00782-3

[viii] Sagar S, Rathinavel AK, Lutz WE, Struble LR, Khurana S, Schnaubelt AT, Mishra NK, Guda C, Broadhurst MJ, Reid SPM, Bayles KW, Borgstahl GEO, Radhakrishnan P. Bromelain Inhibits SARS-CoV-2 Infection in VeroE6 Cells. bioRxiv [Preprint]. 2020 Sep 16:2020.09.16.297366. doi: 10.1101/2020.09.16.297366. Update in: Clin Transl Med. 2021 Feb;11(2):e281. PMID: 32995771; PMCID: PMC7523097.

[xi] Fraiman J, Erviti J, Jones M, Greenland S, Whelan P, Kaplan RM, Doshi P. Serious adverse events of special interest following mRNA COVID-19 vaccination in randomized trials in adults. Vaccine. 2022 Sep 22;40(40):5798-5805. doi: 10.1016/j.vaccine.2022.08.036. Epub 2022 Aug 31. PMID: 36055877; PMCID: PMC9428332.