Billions Of Copies Of Residual DNA In A Single Dose Of COVID-19 mRNA Vaccine: Preprint

A new preprint study up for peer review finds billions of residual DNA fragments in the COVID-19 mRNA vaccine vials.

The lead author of the study, molecular virologist David Speicher, who has a doctorate in virology, told The Epoch Times that their study is “the largest study” on residual DNA in COVID-19 vaccines to date.

In our study, we measured DNA copies of spike, ori (origin of replication), and SV40 enhancer genes,” he told The Epoch Times. “The loads of SV40 enhancer-promoter, ori, and virus spike in Pfizer are up to 186 billion copies per dose.”

The spike he refers to is the DNA sequence of the SARS-CoV-2 spike protein, which can be transcribed to spike mRNA to be used in the COVID-19 mRNA vaccines to be translated to spike protein. The other two DNAs—SV40 enhancer genes and ori—help facilitate the replication of spike DNA.

However, the final mRNA vaccines should only include RNA and not residual DNA instructions for spike production.

The researchers sequenced the gene material in 27 mRNA vaccine vials from 12 different lots. Nineteen vials were from Moderna, and eight were from Pfizer.

“Further work is needed to investigate if anything in these vaccines is actually integrating into the human genome and what effect that may have,” the lead author wrote.

Keep reading

White House: Economy ‘Exceptionally’ Good and People Like Their Finances, But Don’t Feel Confident Due to COVID, War

On Monday’s broadcast of CNBC’s “Squawk Box,” White House National Economic Council Director Lael Brainard reacted to negative poll numbers on the economy by stating that “the economy is performing exceptionally well” but “people have been through a very challenging few years between the pandemic, and then the oil price spikes associated with Russia’s war. It’s going to take a while for them to feel really confident,” and most people “feel like their personal finances are better now than they were before.”

Co-host Andrew Ross Sorkin said, “Speak to this, though, because I think there [are] a lot of folks who have been waking up to headlines of poll results over the weekend, as it relates to Bidenomics versus, frankly, Trumponomics and where he stands — the president that is — compared to where…the former president stands in terms of how people are thinking about the economy and how, frankly, unhappy they remain about the economy.”

Brainard responded, “Look, if I look around the world, I don’t think there’s a leader out there who wouldn’t rather have the economic record that President Biden has today. We have been growing, 3% over the past year. We’ve had unemployment down below 4% for 21 months in a row. Real incomes are growing. Wealth — this is remarkable — wealth is up 37% for the median household since before the pandemic. And we’re growing faster and have lower inflation than any other advanced economy in the world. So, the statistics, I think, are very strong. Now, people have been through a very challenging few years between the pandemic, and then the oil price spikes associated with Russia’s war. It’s going to take a while for them to feel really confident, but if you look at surveys, 70% of Americans feel like their personal finances are better now than they were before. We’ve still got to work on kitchen table economics, there are still a lot of Americans sitting around their kitchen tables with costs of medicine, pharmaceuticals that are still too high, and we’re working on that.”

Keep reading

Covid inquiry hears Matt Hancock wanted to decide who lived and died

Former health secretary Matt Hancock wanted to decide “who should live and die” if the NHS was overwhelmed, the Covid inquiry has heard.

The revelation came to light in evidence presented by Sir Simon Stevens, the former NHS England chief.

In his witness statement, he said Mr Hancock thought he, not doctors or the public, should decide who to prioritise if hospitals became overwhelmed.

Sir Simon said: “Fortunately this horrible dilemma never crystallised.”

He told the inquiry: “The secretary of state for health and social care took the position that in this situation he – rather than, say, the medical profession or the public – should ultimately decide who should live and who should die.”

He added: “I certainly wanted to discourage the idea that an individual secretary of state, other than in the most exceptional circumstances, should be deciding how care would be provided.

“I felt we were well-served by the medical profession, in consultation with patients to the greatest extent possible, in making those decisions.”

Keep reading

Masks required in certain settings again in California

Beginning on Wednesday, lots of people heading into doctor’s offices or hospitals across the Bay Area will be required to mask up.

In some parts of California, masks will be required in hospitals and skilled nursing facilities in an effort to limit the spread of RSV, the flu and COVID. The mandate will last until the end of flu season in March.

Marin County and Santa Clara counties require everyone who enters medical facilities to mask up.  Alameda, San Mateo, Contra Costa, and Sonoma counties will require health care workers to mask up in patient care areas. 

In California, COVID positivity rates were on the rise starting in July, and peaked in late August. According to the Mercury News, wastewater data shows medium levels of COVID in all of Santa Clara County’s sewer sheds at the end of October, down from high transmission range over the last two months.

Dr. Peter Chin-Hong told KTVU medical professional don’t know what is going to happen during this flu season, so they’re opting to take a precautious approach. 

Though, not everyone in the health care industry agrees. 

Keep reading

Fauci NIH lab infected bats with Wuhan coronavirus, obtained from zoo near Camp David, report

A15-minute drive from the Camp David presidential retreat, a low-rated zoo gave the National Institutes of Health several bats to infect with a coronavirus from the same Chinese lab that some federal agencies believe is responsible for the SARS-CoV-2 outbreak, according to a new investigation and published research.

The White Coat Waste Project, which fights taxpayer funding of “wasteful government animal experiments,” said Monday it’s using Freedom of Information Act requests to get more details about the taxpayer-funded experiments documented in a 2018 paper in the journal Viruses.

Former National Institutes of Allergy and Infectious Diseases Director Dr. Anthony Fauci oversaw the NIH’s Rocky Mountain Laboratories in Montana when it did the research with bats from Maryland’s Catoctin Wildlife Preserve, whose Director of Animal Health Laurie Hahn is a former NIH “lead veterinary technician” for animal research.

The Viruses paper, authored by Montana lab researchers and Wuhan Institute of Virology collaborator Ralph Baric, of the University of North Carolina, determined that the “SARS-like WIV1-coronavirus” first isolated from Chinese rufous horseshoe bats could not cause a “robust infection” in the 12 Egyptian fruit bats from the zoo. Four were euthanized and tested.

Keep reading

Getting flu and COVID shot together still reasonable amid safety review of potential stroke risk: Experts

Older adults who received last year’s COVID booster and a high-dose version of the flu vaccine in the same visit may have a potential increased risk of stroke, according to a new FDA-funded study.

Experts urged that the results were preliminary and may be explained by other factors such as the fact that older adults are already at a higher risk for stroke due to their age.

“There is no need for panic, and emphatically no need to stop giving COVID and flu shots at the same time to older adults,” said Dr. Peter Chin-Hong, an infectious diseases specialist at the University of California, San Francisco, while he reiterated that more research is needed.

Keep reading

How Pfizer Hid Nearly 80% of COVID Vaccine Trial Deaths From Regulators

Pfizer-BioNTech delayed reporting vaccine-associated deaths among BNT162b2 clinical trial participants until after the U.S. Food and Drug Administration (FDA) issued an Emergency Use Authorization (EUA) for the product.

The vaccine makers also failed to account for a large number of subjects who dropped out of the trial.

Together, these strategies kept regulators and the public ignorant of a 3.7-fold increase in cardiac deaths among subjects who received the vaccine, according to analysis in the International Journal of Vaccine Theory, Practice, and Research.

The authors of the paper described it as a “forensic analysis,” defined by the U.S. National Institute for Standards and Technology as “the use of scientific methods or expertise to investigate crimes or examine evidence that might be presented in a court of law.”

Keep reading

FDA finds potential ‘safety signal’ of seizures in 2-5 yr olds after getting Covid-19 shots

A new preprint study led by the U.S. Food and Drug Administration (FDA) has detected a potential “safety signal” for seizures and convulsions in young children after receiving the monovalent Pfizer or Moderna mRNA Covid-19 vaccines.

Researchers observed the condition in children ages 2-4 for the Pfizer vaccine, and ages 2-5 for the Moderna vaccine.

The total number of cases was 72, with over 50% meeting the definition for febrile seizures.

The median time between vaccination and seizures or convulsions was two days, with 32% occurring the day of or the day after vaccination. All seizures and convulsions took place within seven days of vaccination.

The signal emerged through near real-time surveillance of more than 4 million vaccinated children.

The researchers of the preprint study cautioned that the results “should be interpreted carefully given study limitations.”

The study also identified a myocarditis/pericarditis safety signal in mostly male children 12-17 years old.

However, since each of these conditions were a “known adverse outcome,” according to the researchers, they did not conduct any further follow-up.

Data for the study were collected through health claims records from CVS Health, Optum and Carelon Research, which participate in the FDA’s Center for Biologics Evaluation and Research, and supplemented with data from state and local immunization information systems databases.

The study covered reports through January, February or March of this year — as little as 6 months after the approval of vaccinations for younger children.

Keep reading

COVID-19 Vaccines ‘May Trigger’ Rheumatic Inflammatory Diseases: Study

A new review suggests that COVID vaccines “may trigger” rheumatic immune-mediated inflammatory diseases, including arthritis, vasculitis, lupus, and adult-onset Still’s disease.

On average, patients developed rheumatic diseases 11 days after vaccine administration, according to the study. Seventy-five (over 27 percent) of these patients experienced total disease remission, and about 50 percent improved following treatment. Eight were admitted to intensive care, and two died from their symptoms.

The short time span between COVID-19 vaccine administration and the onset of R-IMIDs suggests the potential possibility of a cause-and-effect relationship,” the authors wrote.

Rheumatic immune-mediated inflammatory diseases (R-IMIDs) involve inflammation that manifests in the joints, tendons, muscles, and bones due to an unknown cause.

The study, led by researchers from the National Health Service in the United Kingdom, examined 271 participants from 190 case studies published worldwide.

Over 80 percent of the patients developed symptoms after their first or second dose of the COVID-19 vaccine, and most were treated and improved with corticosteroids.

Almost 57 percent of the injured patients received the Pfizer vaccine, nearly a quarter received the AstraZeneca vaccine, and 12 percent of the rheumatic diseases manifested after the administration of the Moderna vaccine.

Keep reading

The COVID Bailout of State and Local Governments Was Unnecessary

Two years after Congress authorized a hugely expensive bailout of state and local governments as part of a COVID-era emergency spending bill, most of the money still hadn’t been spent.

Perhaps the bailout wasn’t even needed in the first place?

In a new report, the Government Accountability Office (GAO) found that states (including Washington, D.C.) had spent just 45 percent of the funding they had received through the Coronavirus State and Local Fiscal Recovery Funds program, a $350 billion line item within the $2 trillion American Rescue Plan Act (ARPA), which passed in March 2021. Local governments had reported spending just 38 percent of their funds received through the same program.

Those figures are based on mandatory reports filed quarterly with the Treasury and reflect spending through the end of March 2023, two years after the bailout was approved by Congress.

“The new GAO study confirms that the ARPA spending was not needed,” Chris Edwards, chair of fiscal studies at the Cato Institute, tells Reason. “By the fall of 2020, it was clear that the states were in good fiscal shape and not facing Armageddon as many policymakers were claiming. They did not need federal handouts.”

Keep reading