Biden’s Evil Circus on Promotion of Dangerous mRNA Covid Vaccines reopens Worldwide
Introduction by Fabio Giuseppe Carlo Carisio
All Italian articles linked in the one can be read in English with simultaneous machine translation available
A panel of independent advisers to the Centers for Disease Control and Prevention (CDC) will meet next month to make recommendations on updated COVID-19 vaccines ahead of the fall season, according to a U.S. government website on Friday.
New Vaccine Campaign launched in US and UE without CDC and EMA Final Approval
The CDC’s immunization panel is scheduled to vote on the vaccines at a Sept. 12 meeting, a notice posted on the federal register website showed.
«Vaccine makers such as Pfizer (PFE.N) and its German partner BioNTech SE (22UAy.DE), Moderna (MRNA.O) and Novavax (NVAX.O) have created versions of their shots aimed at the XBB.1.5 subvariant of the virus» reported The Defender (Children’s Health Defense website led by the lawyer Robert F. Kennedy jr)
The subvariant, which has been renamed the “Kraken” (like the legendary sea monster and a Rothschild fund…) is estimated to have originated between November and December 2022 in or around New York state in the US.
Meanwhile CDC (US Centers fo Disease Control and Prevention) has detected a new SARS-CoV-2 variant labeled BA.2.86 (renamed Eris). CDC is continually monitoring for new variants and studying their potential impact on public health.
https://www.gospanews.net/2023/01/14/covid-incubo-kraken-con-propaganda-per-bezos-gates-rothschild-biologo-canadese-fa-paura-marketing-coi-nomi-delle-varianti-omicron/
«Based on what CDC knows now, existing tests used to detect and medications used to treat COVID-19 appear to be effective with this variant. BA.2.86 may be more capable of causing infection in people who have previously had COVID-19 or who have received COVID-19 vaccines. Scientists are evaluating the effectiveness of the forthcoming, updated COVID-19 vaccine. CDC’s current assessment is that this updated vaccine will be effective at reducing severe disease and hospitalization. At this point, there is no evidence that this variant is causing more severe illness. That assessment may change as additional scientific data are developed. CDC will share more as we know more» wrote CDC in its official website (more details below).
On the basis of these alarms, US President Joseph Biden has already asked the Congress for new funding for the next vaccination campaign which will be implemented on mRNA (or recombinant protein) gene serums which have not yet obtained the definitive OK from the CDC but only from the institution American drug regulator or Food and Drug Administration.
Like monkeys trained by Washington, some European Union nations, including Italy, have already announced the start of the new autumn vaccination campaign with the new monovalent anti-Covid for the XBB 1.5 variant although the pharmacological products have not yet obtained the approval neither by the European Medicines Agency nor by the Italian Medicines Agency.
However, in the meantime it has been discovered that the Italian Minister of Health of Giorgia Meloni’s government, Professor Orazio Schillaci, former rector of the University of Rome Tor Vergata partner in mRNA projects with the main Big Pharma, has invested in American biotech companies such as Inovio which, thanks to WHO and Bill Gates’ NGOs, are experimenting with a new type of mRNA gene serum in the world.
https://www.gospanews.net/2023/08/19/ministro-schillaci-specula-su-big-pharma-finanziata-da-gates-e700mila-investiti-in-biomediche-usa-che-testano-anche-vaccini-dna-covid/
In short. The director of the evil circus of dangerous mRNA vaccines, i.e. Joseph Biden, cracked the whip and all the protagonists of the show of the pandemic created in the laboratory with SARS-Cov-2 manmade in a China-US-EU affair immediately began to play their part.
To facilitate the acceptance of the new mRNA genetic sera among the population, the CDC has decided to discontinue its its V-APP for VAERS pharmacovigilance program which has monitored millions of adverse reaction reports including tens of thousands with a fatal outcome.
This occurs more than a year after the same database managed by the CDC stopped monitoring the so-called Covid-breakthrough phenomenon, i.e. the symptomatic and serious infections from SARS-Cov-2 that caused hospitalization or death in people vaccinated for a very short time, confirming the suspicions of a tragic and chilling correlation.
Read all details in articles below.
Fabio Giuseppe Carlo Carisio
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Biden to ask US Congress to fund new Covid vaccine
US President Joe Biden has announced that he plans to request additional funding from Congress to develop a new Covid-19 vaccine, adding that it is likely everybody will be encouraged to take the new shot.
Speaking to reporters on Friday, the president was asked if the White House was planning a response to a reported uptick in Covid cases. The US Center for Disease Control and Prevention (CDC) had previously announced a 21.6% increase in Covid-related hospitalizations and a 21.4% increase in Covid-related deaths in recent weeks. The numbers are, however, still far below the levels seen during the pandemic.
Biden responded by stating that he has already signed off on a proposal to have Congress fund a new vaccine “that is needed, that’s necessary, that works.”
“It will likely be recommended everybody get it no matter whether they’ve gotten it before or not,” he added.
The president’s announcement comes after CNN suggested last week that people should mask up again as the US Center for Disease Control (CDC) and the World Health Organization (WHO) warned of a surge in coronavirus cases and new variants.
“If you’re at high risk of serious illness or death from Covid-19, it’s time to dust off those N95 masks and place them snugly over your nose and mouth to protect yourself from a recent uptick of the virus,” CNN wrote, citing “a growing number of experts.”
On August 17, the CDC announced on X, formerly Twitter, that it was tracking a new “highly mutated lineage of the virus that causes Covid-19” called BA.2.86. The agency said it had detected the virus in the US, Denmark, the UK, and Israel.
The WHO confirmed on the same day that the BA.2.86 variant was “under monitoring” due to the large number of mutations it carries, but noted that only a handful of sequences of the variant had been reported so far.
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The organization reiterated its calls for better surveillance, sequencing, and reporting of Covid cases, but did not call for any mask mandates or lockdowns.
Nevertheless, some institutions in the US – such as the Morris Brown College in Atlanta, Georgia, several hospitals in New York, and the Lionsgate film studios – have already begun to reinstate mask requirements for anyone on their premises.
Originally published by Russia Today
All links to previous Gospa News articles have been added aftermath
CDC Says New COVID-19 Variant Could Cause Infections in Vaccinated People
by Jack Philips – Originally published by The Epoch Times
All links to previous Gospa News articles have been added aftermath
The U.S. Centers for Disease Control and Prevention (CDC) stated on Aug. 23 that the new BA.2.86 COVID-19 lineage may cause infection in people who received vaccines or previously had the virus.
The CDC stated that it’s too soon to know whether this might cause more severe illness than previous variants. But because of the high number of mutations detected in this lineage, there are concerns about the effectiveness of immunity from vaccines and previous infections, according to the agency.
“The large number of mutations in this variant raises concerns of greater escape from existing immunity from vaccines and previous infections compared with other recent variants,” the CDC stated in its assessment. “For example, one analysis of mutations suggests the difference may be as large as or greater than that between BA.2 and XBB.1.5, which circulated nearly a year apart.”
But it also stated that “virus samples are not yet broadly available for more reliable laboratory testing of antibodies, and it is too soon to know the real-world impacts on immunity.”
The agency noted that it detected at least two cases with the BA.2.86 variant in the United States, although few other details were provided. It was also found in Israel, the UK, South Africa, and Denmark.
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One of the BA.2.86 cases was found in a person detected via the CDC’s traveler surveillance system, while it noted that cases being found in several countries is evidence of international transmission.
“Notably, the amount of genomic sequencing of SARS-CoV-2 globally has declined substantially from previous years, meaning more variants may emerge and spread undetected for longer periods of time,” the assessment reads.
“It is also important to note that the current increase in hospitalizations in the United States is not likely driven by the BA.2.86 variant. This assessment may change as additional data become available.”
The CDC noted that most of the U.S. population has COVID-19 antibodies from a previous infection, vaccination, or both and stated that it’s likely that the antibodies will provide some protection against the variant.
The agency stated on Aug. 23 that the slight recent increase in hospitalizations in the United States isn’t likely driven by the BA.2.86 lineage.
extract by Jack Philips – Originally published by The Epoch Times where article continues
CDC Shuts Down V-safe App for Reporting COVID Vaccine Injuries
Former U.S. Food and Drug Administration adviser David Gortler, doctor of pharmacy, said ending the safety monitoring of a new vaccine still promoted for universal use is “unprecedented.”
by David Gortler – originally published on The Defender and Brownstone Institute
All links to previous Gospa News articles have been added aftermath
If you go there today, V-safe directs users to the U.S. Food and Drug Administration’s (FDA) Vaccine Adverse Event Reporting System (VAERS) website for adverse event reporting, even though officials continually derided VAERS as “passive” and “unverified.”
VAERS and V-safe are mutually exclusive safety collection databases operated by the FDA and CDC, respectively. VAERS is an older way of collecting safety data where one can fill out a form online, manually, or by calling a toll-free number, whereas V-safe is a device “app” that requires online registration.
Both VAERS and V-safe collect personal information, lot numbers, dates and associated information, but V-safe was an active collection system geared towards a younger app-using demographic.
Here is the last report before deletion:
Does this mean that the CDC believes that the mRNA COVID-19 injections are so safe, that there is no need to monitor adverse event reports any longer?
What is the argument against continued monitoring, especially since the V-safe website was already up and paid for?
While the CDC’s V-safe was stealthily and abruptly turned off, refusing to accept new safety reports, to this very day the CDC continues to urge everyone ages 6 months and older to stay up to date with COVID-19 vaccines and boosters.
As a drug safety expert, I personally can’t cite another example of any agency or manufacturer halting the collection of safety data. It seems even worse because mRNA technology is relatively new with long-term manifestations unknown.
On top of this, both manufacturers and the FDA refuse to share the list of ingredients, such as lipid nanoparticles, which could affect individuals differently and take a long time to manifest clinically.
Safety data collection should never stop
Now, contrast that with the fact that the National Highway Traffic and Safety Administration (NHTSA) will still accept a safety report for a 30-year-old Ford Bronco II.
Indeed, this is an oddly specific example, but only because I drove this exact vehicle as a family hand-me-down as a student, through my residency, fellowship, for my tenure as a Yale professoron the mean streets of New Haven and even during my years at the FDA as a medical officer /senior medical analyst.
Like mRNA shots, Bronco IIs are still available on the market and people are still using them up to this very day.
My Bronco became an intermittent topic of conversation with friends and FDA colleagues. One day, I was informed by a patrolling security guard at the FDA that it was the oldest car on campus.
https://www.gospanews.net/en/2023/08/26/covid-vaccines-killer-pathologies-in-a-name-only-spikeopathy-huge-chilling-study-on-mrna-genic-serums-serious-adverse-reactions/
I didn’t know much about cars (or mRNA technology) back then, but when a fellow FDA-er informed me that my Bronco II had noteworthy safety problems and that the NHTSA still had their eye on this vehicle (rollover accidents were more common and more fatal) I addressed the problem: I got rid of the reliable relic, even though I really liked it.
NHTSA is still accepting safety reports on things like my 30-year-old Ford Bronco II, but the CDC isn’t accepting new safety reports on 2-year-old novel mRNA vaccines.
Unlike my old Bronco, mRNA injections have only been on the market for about two years, and according to the FDA VAERS database, mRNA “vaccines” have been named the primary suspect in over 1.5 million adverse event reports, of which there are >20,000 heart attacks and >27,000 cases of myocarditis and pericarditis just in the U.S. alone.
Worldwide numbers would be greater. According to many references, including an FDA-funded study out of Harvard, VAERS reports represent fewer than 1% of vaccine adverse events that actually occur.
Extract by David Gortler article – originally published on The Defender and Brownstone Institute where article continues
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