On the cover image the study of the German University Hospital of Wuerzburg and the first signatory Isabelle Wagenhäuser
by Fabio Giuseppe Carlo Carisio for VT Europe
Among the first to enthusiastically welcome the bivalent anti-Covid vaccines in Italy was the Piedmont Region, led by President Alberto Cirio and linked to Bill Gates, the world emperor of Big Pharma of experimental and dangerous gene serums, with multiple projects ranging from promotion of the International Alba White Truffle Fair even to the use of Artificial Intelligence in military technologies in a NATO project located in Turin, the epicenter of the Piedmont Aerospace District.
In fact, the Piedmontese governor together with the regional Health Councilor Luigi Icardi boasted of having “burned the time” for the start of the administration of the fifth dose to the most fragile, elderly and immunosuppressed patients, although the latest research has revealed that they are precisely those more at risk of lethal “breakthrough infections”, i.e. contagion from Covid-19 following inoculation for still undetermined causes that some studies attribute precisely to vaccines…
“TRIVACCINATI PIU’ A RISCHIO DI CONTRARRE COVID SINTOMATICO”. Nuovo Studio guidato da Medico CDC USA. Mentre il Piemonte parte con la Quinta Dose
Now the Wuerzburg University Hospital, in Germany, is sounding a very worrying alarm: the new bivalent boosters cause more and more serious adverse reactions than those not updated for the two Omicron variants.This is a very serious warning for two reasons.
Primarily because the real danger of primary doses of messenger RNA gene serums has not yet been ascertainedsince, as denounced by the British Medical Journal and previewed by Gospa News, the Food and Drug Administration has not published data on serious adverse reactions collected with active pharmacovigilance(follo-up controls of cases) while the EudraVigilance platform for passive pharmacovigilance (reports of undesirable effects) in the European Union, for mysterious reasons, has not been updated since September!
STRAGE DA COVID TRA VACCINATI. Ma AIFA ed EudraVigilance Celano i Morti da “Infezioni-Breccia”. Studi e Allarmi negli USA. Soprattutto per i Fragili
It is self-evident that if the seriousness of the consequences produced by the anti-Covid vaccines of the first two doses and by the monovalent boosters are not known, which cumulatively have already resulted in millions of reports of serious side effects including tens of thousands of lethal ones, the greatest danger detected for that of bivalents is much more worrying but of a totally unknown extent…
Secondly, this research by zealous German university doctors reveals a consequence that the most serious experts in virology and pharmacology, however, expected as the new vaccines for the fourth dose have only been tested on mice and approved without necessary and in-depth clinical studies. as secretly “solicited/imposed” by the American CDC, the Centers of Diseases Control and Prevention, to the Food and Drug Administration which must authorize the use of each new drug in the USA.
British Medical Journal’s BOMB: “US FDA Hides Data on Serious Adverse Events after Covid Vaccines”
And since the EMA, the European Medicines Agency, and the AIFA, the Italian Medicines Agency, i.e. the regulatory bodies that are supposed to monitor compliance with the safety standards of medicines, act by “copying and pasting” the FDA by virtue of global pressure, exerted by Gates’ NGOs also with munificent lobbying activity towards politicians and public officials of the various nations, every type of anti-Covid vaccine approved by the USA ends up in the protocols recommended by the European and Italian health authorities without the slightest in-depth counter-verification.
The most sensational case of this attitude occurred for the authorization to administer the first doses of the anti-Covid gene serum Comirnaty to children under the age of 5, produced by the American pharmaceutical company Pfizer together with the German Biontech.
EXCLUSIVE: Pfizer Paper confirms Genic Experiments on 5yo Kids. “Myocarditis Risks by Vaccines, Little Data… We”ll Study After FDA Authorization”
Thanks to an affirmative vote from a doctor in blatant conflicts of interest after receiving funding from Pfizer’s partner GSK of Big Pharma in London, the CDC’s Advisory Committee on Immunization Practices (ACIP) recommended him to the FDA , although the same manufacturer had warned the health authorities that there were no studies on the risks of myocarditis, one of the most terrible adverse reactions widespread among young people as also highlighted in the vaccine leaflets.
Scandal on Vaccines for Children: GSK (Pfizer Partner) Funded with $18thousand a Member of CDC who Approved the Jabs since 5yo
Well EMA and AIFA both approved emergency use on minors, concealing this dramatic gap and despite the fact that the number of serious cases of covid in children was very low.
In the previous investigation we saw how the University Hospital of Nimes revealed a significant increase among young people in cases of myocarditis, an inflammation of the heart that is often even lethal. Now let’s see why Comirnaty’s bivalent booster turns out to be much more dangerous than the monovalent booster produced by the same company.
A French University Hospital’s Shock Study: “Myocarditis in Young People and Embolism in Women Growing after Vaccination Campaign”. Alarms by an US Cardiologist Too
THE ALARMING STUDY OF THE WUERZBURG UNIVERSITY HOSPITAL
The outcome of the new German study therefore immediately appears disturbing, although detailed in a limited number of people, non-randomized (i.e. without double-blind counter-verification with individuals administered placebo) and not yet reviewed by third parties.
«In the light of emerging SARS-CoV-2 variants of concern (VOC), bivalent COVID-19 vaccines combining the wild-type spike mRNA with an Omicron VOC BA.1 or BA.4-5 spike mRNA became available. This non-randomized controlled study examined adverse reactions, PRN (pro re nata) medication intake and inability to work after a fourth COVID-19 vaccination among 76 healthcare workers. As fourth dose either the original, monovalent BNT162b2mRNA (48.7%) or the bivalent BNT162b2mRNA original/Omicron BA.4-5 vaccine (51.3%) was administered».
We read in the Summary of the research entitled “Bivalent BNT162b2mRNA original/Omicron BA.4-5 booster vaccination: adverse reactions and inability to work compared to the monovalent COVID-19 booster” and published on MedRxiv last November 8 in pre-print ( pending peer review). The pharmacological identification code reported is that of the Comirnaty vaccine produced by Pfizer and Biontech.
CDC Pushed for COVID-19 Boosters Without Clinical Trials: Disturbing Emails: “Pfizer Recommends It and I Trust in their Guidance”
It was conducted by academics Isabell Wagenhäuser (first signatory) and Manuel Krone (corresponding author), from the Infection Control and Antimicrobial Stewardship Unit, University Hospital Wuerzburg, Julia Reusch and Nils Petri, Department of Internal Medicine I, University Hospital Wuerzburg, Lukas B. Krone, Department of Physiology, Anatomy and Genetics, University of Oxford, UK, Oliver Kurzai, Institute for Hygiene and Microbiology, University of Wuerzburg,
«The rate of adverse reactions for the second booster dose was significantly higher among participants receiving the bivalent 84.6% (95% CI 70.3%-92.8%; 33/39) compared to the monovalent 51.4% (95% CI 35.9-66.6%; 19/37) vaccine (p=0.0028). Also, there was a trend towards an increased rate of inability to work and intake of PRN medication following bivalent vaccination».
«In view of preprints reporting inconclusive results in neutralizing antibody levels between the compared vaccines, our results and further studies on safety and reactogenicity of bivalent COVID-19 booster vaccines are highly important to aid clinical decision making in the choice between bivalent and monovalent vaccinations» can even be read in the Abstract.
This study was funded by the Federal Ministry for Education and Science (BMBF) through a grant provided to the University Hospital of Wuerzburg by the Network University Medicine on COVID-19 (B-FAST, grant-No 01KX2021) as well as by the Free State of Bavaria with COVID-research funds provided to the University of Wuerzburg, Germany. Nils Petri is supported by the German Research Foundation (DFG) funded scholarship UNION CVD.
This would be enough to immediately trigger an investigation by the EMA and AIFA, assuming that the doctors in charge of pharmacovigilance take the stomach ache of reading the new studies on vaccines as it does in its little Gospa News…
But one detail makes the research of the German public health structure even more significant: the corresponding author is Manuel Krone, deputy director of the Infection Control and Antimicrobial Management Unit of the German hospital, who had to declare a conflict of interest having received «honoraria from GSK and Pfizer outside the submitted work».
If a doctor on the payroll of the New York pharmaceutical manufacturer of Comirnaty and a university of German nationality such as Biontech, a partner of the American Big Pharma in the production of this vaccine, manage to make these data public, they can certainly be considered reliable even before the definitive review by the fellow scientists of the medical journal MedRxiv.
There is only one gap in this study: there is no distinction between mild and severe reactions which can also be guessed from the percentage of vaccinated health workers with incapacity for work. But even in this sense, a further element is missing: the length of the period of incapacity.
Criminal FDA and CDC Ignore Law and Approve New COVID Vaccine Boosters with ZERO Testing on Humans: On Mice Only
This research confirms all the concerns expressed by authoritative doctors such as the Milanese surgeon Andrea Stramezzi regarding the dangers of the new boosters…
The alarm bell has been sounded.
But we fear that the new Italian Minister of Health Orazio Schillaci, involved in a partnership with Pfizer through the University of Rome Tor Vergata of which he is rector, does not dare to flea a bivalent gene serum tested only on mice just as he does not seem to intend to launch a commission of inquiry into adverse reactions from vaccines and deaths caused by early home therapies ignored by the Italian health authorities.
Fabio Giuseppe Carlo Carisio
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MEDRXIV – Bivalent BNT162b2mRNA original/Omicron BA.4-5 booster vaccination: adverse reactions and inability to work compared to the monovalent COVID-19 booster
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Fabio is Director and Editor of Gospa News; a Christian Information Journal.
Fabio Giuseppe Carlo Carisio, born on 24/2/1967 in Borgosesia, started working as a reporter when he was only 19 years old in the alpine area of Valsesia, Piedmont, his birth region in Italy. After studying literature and history at the Catholic University of the Sacred Heart in Milan, he became director of the local newspaper Notizia Oggi Vercelli and specialized in judicial reporting.
For about 15 years he is a correspondent from Northern Italy for the Italian newspapers Libero and Il Giornale, also writing important revelations on the Ustica massacre, a report on Freemasonry and organized crime.
With independent investigations, he collaborates with Carabinieri and Guardia di Finanza in important investigations that conclude with the arrest of Camorra entrepreneurs or corrupt politicians.
In July 2018 he found the counter-information web media Gospa News focused on geopolitics, terrorism, Middle East, and military intelligence.
His articles were published on many international media and website as SouthFront, Reseau International, Sputnik Italia, United Nation Association Westminster, Global Research, Kolozeg and more…
His investigations was quoted also by The Gateway Pundit, Tasnim and others
He worked for many years for the magazine Art & Wine as an art critic and curator.
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Fabio always dances around the simple fact that COVID-19 was a US bioweapon. It was deployed first in China and finally in the USA. Trumpoid anti-vaxxers continually ignore what VT’s, John Hankey, reported in 2020, that Trump and his inner circle were vaccinated in November 2019, only days after the virus was deployed against China.
Fabio, what do you expect from a bioweapon? It kills people! Do you really think that the US Plains Indians were all upset about the medical care they received after smallpox-infected blankets were given to them by the US Army?
It is now widely demonstrated by multiple studies that genetically modified Spike-toxic vaccines kill much more than the original version of SARS-Cov-2 which, initially, was widespread not only in China but also in Italy, Iran and Russia. in different genotypes much more powerful than those scattered in South Korea (Obama’s partner in the Global Health Security Agenda).
As Montagnier well explained precisely because it was an “artificial” virus it would have lost its most harmful component over time. In fact they then created OImicron and now they are trying another one …
I have a lot of doubt that Trump got his vaccine in 2019 as the whole bacteriological weapon deal has been handled by the Democrats since 1999 with Bill Clinton.
In fact, Trump was hospitalized with severe symptoms and was treated with Regeneron. But everything can be when dealing with a covidiot and dazed elephant!
Fabio, why do you have such a hard time accepting the fact that COVID-19 was a US bioweapon? It was deployed in the USA, as Gordon claims, a “fund-raiser.” That would be the $6+ trillion bailout of the big banks and corporations that happened in the spring of 2020 with the collapse of the derivatives market. Whether Trump actually got the vaccine in November of 2019 is immaterial. We do know that according to Reuters… WASHINGTON (Reuters) – “The White House has ordered federal health officials to treat top-level coronavirus meetings as classified, an unusual step that has restricted information and hampered the U.S. government’s response to the contagion, according to four Trump administration officials.” Why would he do that, Fabio?
Do you really believe that Trump was “vaccinated”? That he would take anything internally from the drug dealers he knew were Jersey bullshit artists That he actually had the virus? Anything? We’re talking about the world’s greatest sociopathic liar.
Tommy I highlighted in 58 inquiries of the cycle WuhanGates and in my book that SARS-Cov-2 is a bio-weapon man-made not only by US but also by China, Eu, Canada, Australia, Ukraine and UK. Please read all those investigations then express your opinion. If you don’t want to read all, please read at least the one on Clinton-Zemin biological deal…
And the one on UK final research
Blind faith that the USA would NEVER attack another country with a bioweapon laced into a flu virus is not any help to rid planet of a continuing pandemic killing millions, as the pandemic itself was induced by a top secret bioweapon attack.
Nor is blind faith that government and oligarch funded scientists and labs “just trying to help” will rid planet of continuing pandemic as THEY DO NOT EVEN KNOW what they are making vaccines, treatments, or antidotes for!!!
If the bioweaponed virus Trump attacked Iran with in February 2020 was of open-sourced genetic structure, and not top secret, they couls easily be able to come up with safe vaccines, antidotes. or treatments that really work well. You would think at least…
But, being a top secret bioweapon attack on Iran, not one research labratory in the world has a chance to come up with something to stop the next “variant” (mutation) to whatever it was that was they poured into Iran (city of Qom) This done immediately after the Iranians attacked the two US airbases in Iraq with ICBM missles – and the missle attacks in retaliation for the assasination of Solemeini by Trump with help of Israel.
Its the bioweapon used on Iran causing the problems – its super top secret, both the attack and “viral code” itself.
I’m just so happy I live in a country with a healthy free press keeping us all informed on all the science we are convinced will save us.
You live in Outer Mongolia? LOL
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