Each day we’re learning more about how the COVID-19 spike protein triggers damage to systems. Data obtained through FOIA show Moderna’s Spikevax has significant safety concerns.
Story at a Glance
- A systematic review of post-jab autopsies concluded that mRNA COVID shots are causally linked to lethal myocarditis. Considering these findings, the authors are calling for “risk stratification and mitigation in order to reduce the population occurrence of fatal COVID-19 vaccine-induced myocarditis.”
- Data obtained through Freedom of Information Act (FOIA) litigation against the U.S. Food and Drug Administration (FDA) by the public interest group Defending the Republic (DTR) show Moderna’s Spikevax has significant safety concerns.
- In one of Moderna’s studies, 16 participants in the COVID jab group died suddenly, yet only two were autopsied. Despite this lack of investigation, Moderna concluded that none of the deaths was associated with the jab.
- Moderna’s studies also recorded a number of serious adverse events in the jabbed groups, including Bell’s palsy, shingles, heart attacks, pulmonary embolisms, transient ischemic attacks, lymphoma, and miscarriages. However, even when life-threatening injuries occurred within days of injection, Moderna arbitrarily concluded that none was associated with its jab.
- Pfizer made its COVID booster appear more effective than it actually is by giving the real booster to people who were far healthier than the controls.
Dr. McCullough and his team systematically reviewed all autopsy reports involving COVID-19 jab-related myocarditis published through July 3, 2023. Fourteen papers detailing 28 autopsies fit the inclusion criteria.
mRNA Jabs Causally Linked to Lethal Myocarditis
As reported by the authors:3“The cardiovascular system was the only organ system affected in 26 cases. In two cases, myocarditis was characterized as a consequence from multisystem inflammatory syndrome (MIS).
“The mean and median number of days from last COVID-19 vaccination until death was 6.2 and 3 days, respectively. Most of the deaths occurred within a week from the last injection. We established that all 28 deaths were causally linked to COVID-19 vaccination by independent adjudication.
“The temporal relationship, internal and external consistency seen among cases in this review with known COVID-19 vaccine-induced myocarditis, its pathobiological mechanisms and related excess death, complemented with autopsy confirmation, independent adjudication, and application of the Bradford Hill criteria to the overall epidemiology of vaccine myocarditis, suggests there is a high likelihood of a causal link between COVID-19 vaccines and death from suspected myocarditis in cases where sudden, unexpected death has occurred in a vaccinated person.”Considering these disturbing findings, Dr. McCullough and his team call for “urgent investigation ... for the purpose of risk stratification and mitigation in order to reduce the population occurrence of fatal COVID-19 vaccine-induced myocarditis.”
Moderna Trial Data Reveal Safety Problems
The infuriating reality is that this risk—as well as many others—was evident in the original trials, despite their short duration, but the vaccine makers used all sorts of tricks to hide these effects.“The records ... include important information related to the safety profile of Spikevax, which was first authorized for emergency use in the United States in December 2020 and in January 2022 received full approval for adults.
“‘The public can be assured that Spikevax meets the FDA’s high standards for safety, effectiveness and manufacturing quality required of any vaccine approved for use in the United States,’ Acting FDA Commissioner Dr. Janet Woodcock said in a statement earlier this year.
“But the new data call this view into question. The advocacy group says that the tens of thousands of pages of clinical trial data released by the FDA supports the conclusion that there is ‘serious doubt’ about both the safety of Spikevax and the FDA’s standards for approval.”For the record, as with Pfizer’s trial data, the FDA had to be forced by a court order to release Moderna’s data. The agency initially rejected DTR’s FOIA request claiming there was “no compelling need” for the public to review that information. As it turns out, Moderna’s clinical trial data reveal shocking safety issues that neither the company nor the FDA has admitted publicly.
Side Effects Shrugged Off Without Investigation
For example, in one of Moderna’s studies, 16 participants in the COVID jab group died suddenly, yet only two were autopsied. Despite this lack of investigation, Moderna concluded that none of the deaths was associated with the jab. “It seems they purposely decided not to investigate suspicious deaths in case the Moderna vaccine might be the cause,” DTR said in a press release.6The studies also recorded a number of serious adverse events in the jabbed groups, including Bell’s palsy, shingles, heart attacks, pulmonary embolisms, transient ischemic attacks, lymphoma, and miscarriages. However, even when life-threatening injuries occurred within days of injection, Moderna arbitrarily concluded that none was associated with its jab.
Pfizer Booster Trial Trickery Discovered
In related news, Drs. Vinay Prasad, Tracy Høeg, and Ram Duriseti recently highlighted evidence showing Pfizer also employed “healthy vaccine bias” in its booster trial to make the COVID booster appear more effective than it is. How? Pfizer simply gave the real booster to people who were far healthier than the controls.“Using observational methods, Arbel et al. (Dec. 23, 2021, issue) calculated an adjusted 90% lower mortality due to COVID-19 among participants who received a first BNT162b2 vaccine (Pfizer-BioNTech) booster than among those who did not receive a booster.
“They found 65 COVID-19–associated deaths (reported as 0.16 per 100,000 persons per day) among participants in the booster group and 137 (reported as 2.98 per 100,000 persons per day) among those in the nonbooster group—a 94.6% difference.
“In a subsequent letter (March 10, 2022, issue), Arbel et al. reported 441 deaths not related to COVID-19 in the booster group and 963 deaths not related to COVID-19 in the nonbooster group ...
“Using the person-days of exposure included in the 2021 article by Arbel et al. and the deaths not related to COVID-19 reported in the subsequent letter, we estimated the mortality not related to COVID-19, according to vaccination status, with the following formula: the ratios of total deaths not related to COVID-19 to COVID-19-related deaths, according to vaccination group, multiplied by mortality due to COVID-19, according to vaccination group, which accounts for person-days of exposure.
“The mortality not related to COVID-19 was calculated as (441/65) × 0.16 = 1.09 per 100,000 persons per day in the booster group as compared with (963/137) × 2.98 = 20.95 per 100,000 persons per day in the nonbooster group.
“This corresponds to a 94.8% lower mortality not related to COVID-19 among participants in the booster group and indicates a markedly lower incidence of adverse health outcomes in the booster group.
“Underlying health plays a substantial role in COVID-19-related mortality. The unadjusted differences in mortality related to COVID-19 and mortality not related to COVID-19, according to vaccination status, were essentially the same in the 2021 study by Arbel and colleagues.
“These findings arouse strong concern regarding unadjusted confounding. The adjusted 90% lower mortality due to COVID-19 reported among the participants who received a booster cannot, with certainty, be attributed to boosting.
“‘Healthy vaccinee bias in this population may have also led to overestimates of vaccine effectiveness in similar studies from Clalit Health Services. Inclusion of mortality not related to COVID-19 in all observational COVID-19 vaccine studies would provide important context.”In a July 20, 2023, Twitter post, Dr. Prasad commented:8
“This week in NEJM, Tracy Beth Hoeg, RD & I prove that Israeli studies, which FDA relied upon, are CONFOUNDED. Boosters reduce non-COVID deaths far too much to be true. Israeli authors concede this in reply. Wow! Millions got unproven boosters. FDA failed.”
Why CDC Changed the Definition of Breakthrough Infection
While we’re on the topic of trickery and bias, a recent investigation by The Epoch Times reveals the U.S. Centers for Disease Control and Prevention (CDC) changed its definition of “breakthrough infection” to avoid having to admit the shots didn’t work. Zachary Stieber with The Epoch Times writes:9“The CDC altered its definition of COVID-19 cases among the vaccinated, leading to a lower number of cases classified as a breakthrough, according to documents obtained by The Epoch Times.
“In early 2021, the CDC defined post-vaccination cases as people who tested positive seven or more days after receipt of a primary vaccination series, according to one of the documents.10 The definition was changed on Feb. 2, 2021, to include only cases detected at least 14 days after a primary series, another document11 shows.
“‘We have revised the case definition,’ Dr. Marc Fischer, head of the CDC’s Vaccine Breakthrough Case Investigation Team, wrote to colleagues at the time. The rationale for the change was redacted ...
“The breakthrough case definition was revised after multiple CDC officials emailed about the vaccines failing to prevent infection. Dr. Fischer said in one email on Dec. 21, 2020, that he was directed by a superior ‘to start working on a protocol to evaluate COVID vaccine failures or breakthrough cases.’
“Then-CDC Director Dr. Rochelle Walensky highlighted an editorial on Jan. 30, 2021, that described variants as a ‘growing threat’ of escaping the protection from vaccines ...
“At about the same time, CDC officials circulated a one-page document about investigating post-vaccination cases ... The version of the document that The Epoch Times received was fully redacted ... the CDC declined to provide any other versions of the document.”Why was the rationale for this decision redacted? And why was the document announcing an investigation into post-jab cases redacted? CDC spokesman Scott Pauley defended the change in definition, saying “many cases of COVID-19 were incubating for up to two weeks before becoming symptomatic,” but didn’t clarify why this explanation—if true—was deemed necessary.
Dr. Harvey Risch, professor emeritus of epidemiology at the Yale School of Public Health, told Mr. Stieber, “There was ‘no cogent rationale’ for excluding early cases and other events among the vaccinated, whether they occurred within seven days or 14 days.”
Mr. Stieber also contacted Dr. Jay Bhattacharya, professor of health policy at Stanford University, who said that “rather than playing games with the definition of breakthrough cases,” the CDC should have informed the recently jabbed that they had little or no protection for the first two weeks.
Got the Jab? Take Action to Safeguard Your Health
If you already got one or more jabs and now have concerns about your health, what can you do? Well, first and foremost, never take another COVID booster, or another mRNA gene therapy shot. You need to end the assault on your system.Other Helpful Treatments and Remedies
Other treatments and remedies that may be helpful for COVID jab injuries include:- Hyperbaric oxygen therapy, especially in cases involving stroke, heart attack, autoimmune diseases, and/or neurodegenerative disorders. To learn more, see “Hyperbaric Therapy—A Vastly Underused Treatment Modality.”
- Lower your omega-6 intake. Linoleic acid is consumed in amounts 10 times higher than the ideal by well over 95 percent of the population and contributes to massive oxidative stress that impairs your immune response. Seed oils and processed foods need to be diligently avoided. See “Linoleic Acid—The Most Destructive Ingredient in Your Diet” for more information.
- Pharmaceutical-grade methylene blue, which improves mitochondrial respiration and assists in mitochondrial repair. A dose of 15 to 80 milligrams a day could go a long way toward resolving some of the fatigue many suffer post-jab. It may also be helpful in acute strokes. The primary contraindication is if you have a G6PD deficiency (a hereditary genetic condition), in which case you should not use methylene blue at all. To learn more, see “The Surprising Health Benefits of Methylene Blue.”
- Near-infrared light, as it triggers the production of melatonin in your mitochondria14 where you need it most. Mopping up reactive oxygen species, it also helps improve mitochondrial function and repair. Natural sunlight is 54.3 percent infrared radiation,15 so this treatment is available for free. For more information, see “What You Need to Know About Melatonin.”
- Lumbrokinase and serrapeptidase are both fibrinolytic enzymes that, when taken on an empty stomach one hour before a meal, or two hours after, will help reduce your risk of blood clots.
◇ References
- 1, 2, 3 Preprints.org July 18, 2023
- 4, 6 Defending the Republic Moderna FOIA
- 5 Epoch Times July 21, 2023
- 7 A Single Dose Intramuscular Injection Tissue Distribution Study of mRNA-1647 in Male Sprague-Dawley Rats
- 8 Twitter Vinay Prasad July 20, 2023
- 9 The Epoch Times July 22, 2023
- 10 Earlier CDC Breakthrough Definition Document
- 11 Revised Breakthrough Definition Document
- 12 Covid19criticalcare.com
- 13 DrMichellePerro.com
- 14 Physiology February 5, 2020 DOI: 10.1152/physiol.00034.2019
- 15 Journal of Photochemistry and Photobiology February 2016; 155: 78-85