Tag Archives: BioNTech

Merck Partnered with Moderna in 2019 to Vaccinate America’s Farms Using mRNA Technology

From mercola.com. As previously noted Dr Mercola’s posts have a 48 hour limit then they are archived to subbed readers. The article is reproduced here in its entirety, with no source link. If you are interested in his articles you can sub for free and each has a link halfway down the article to download in pdf form. Finally, beware they are weaponizing your food. And have been doing so for some time. EWR

Story at-a-glance

  • For the last couple of years, I’ve recommended not eating pork due to its high linoleic acid (LA) content, but there’s an even bigger reason to avoid it now. Since 2018, pork producers have been using customizable mRNA-based “vaccines” on their herds
  • The very first RNA-based livestock vaccine, a swine influenza (H3N2) RNA shot licensed in 2012, was developed by Harrisvaccines. The company followed up with an avian influenza mRNA shot in 2015. Harrisvaccines was acquired by Merck Animal Health later that year
  • CureVac developed an mRNA-based rabies shot for pigs in 2016
  • The swine vaccine platform Sequivity, introduced in 2018, was developed by Merck in partnership with Moderna. Sequivity can produce endlessly customized “vaccines,” none of which undergo safety testing
  • Americans have been eating pork treated with gene therapy for nearly five years already, and even more of our meat supply is about to get the same treatment. mRNA-lipid nanoparticle shots for avian influenza are in the works, as are mRNA shots for cows. Lobbyists for the Cattlemen’s Association recently confirmed they intend to use mRNA “vaccines” in cattle, which might affect both dairy and beef
  • Missouri House bill 1169 would require labeling of products that can alter your genes. It would also require companies to share information about the potential transmissibility of gene-altering interventions, and asserts that fully informed consent must be given for all vaccines, gene therapies and medical interventions

For the last couple of years, I’ve recommended not eating pork due to its high linoleic acid (LA) content, but there’s an even bigger reason to avoid it now. Since 2018,1 pork producers have been using customizable mRNA-based “vaccines” on their herds, and this has slipped completely under the radar. I myself just found out about it. As described on Merck’s animal health website:2

“A revolutionary swine vaccine platform, SEQUIVITY harnesses RNA particle technology to create customized prescription vaccines against strains of influenza A virus in swine, porcine circovirus (PCV), rotavirus and beyond. It’s supported by a sophisticated dashboard filled with comprehensive data and insights …

Sequivity is a custom swine vaccine platform … Sequivity only targets swine pathogen gene sequences of interest. Doesn’t replicate or cause disease, delivering pathogen information to the immune system … There’s no need to transfer or handle live material like autogenous, killed or modified live vaccines …

Targets existing and evolving swine pathogens, including diseases not covered by conventional swine vaccines. Allows for the creation of multivalent formulations by blending RNA particles to target multiple swine pathogens in one shot.”

First RNA ‘Vaccine’ for Livestock Licensed in 2012

Merck was not alone in developing veterinary mRNA shots, however. They weren’t even first on the scene, although they later acquired the company that started it all.

The very first RNA-based livestock vaccine, a swine influenza (H3N2) RNA shot, was licensed over a decade ago in 2012, and was developed by Harrisvaccines.3,4 The company followed up with an avian influenza mRNA shot in 2015.5 Harrisvaccines was acquired by Merck Animal Health later that year.6,7

CureVac developed an mRNA-based rabies shot for pigs in 2016.8 (On a side note, they began conducting human rabies shot trials in 2020 in response to the World Health Organization’s goal to achieve “zero human rabies deaths by 2030.”9)

In 2016, Bayer also partnered with BioNTech to develop mRNA “vaccines” for both livestock and pets,10,11 but it doesn’t appear they ever launched anything. So, in retrospect, it appears Americans have been eating pork treated with gene therapy for the past five years, and even more of our meat supply is about to get contaminated with the same treatment.

In addition to the avian influenza RNA shot for chickens licensed in 2015, newer mRNA-lipid nanoparticle shots for avian influenza are also in the works.12 Iowa State University is also working on an mRNA shot for cows, and lobbyists for the Cattlemen’s Association recently confirmed they intend to use mRNA “vaccines” in cattle,13,14 which might affect both dairy and beef.

Merck and Moderna: Partners in mRNA Jab Race Since 2015

The same year Merck purchased Harrisvaccines (2015), it also entered into a partnership with Moderna to develop a number of undisclosed mRNA “vaccines.” It was slated to be a three-year collaboration, with a one-year optional extension, in which Merck would perform research and development and commercialization of five potential products using Moderna’s mRNA technology. As reported by Genetic Engineering & Biotechnology News at the time:15

“Moderna has agreed to design and synthesize the mRNA product candidates directed against selected targets through its mRNA Therapeutics™ platform.

The platform builds on the discovery that modified mRNA can direct the body’s cellular machinery to produce nearly any protein of interest — ranging from native proteins to antibodies and other entirely novel protein constructs with therapeutic activity inside and outside of cells.”

Endless Customization, Zero Safety Testing
Sequivity, introduced in 2018, was one of the products that came out of that partnership. As explained by Merck (both on its website and in the video above), Sequivity is not so much a single vaccine as it is a platform that can be endlessly customized — all without additional safety analyses over and beyond the initial ridiculously inadequate testing. As noted by Zoetis, the largest producer of veterinary drugs and vaccines:16
“Sequivity has safety and efficacy studies based on the platform with a historical initial isolate, not likely the isolate that customers would be requesting in their product.”
Sequivity is customized as follows:17
Pathogen is collected and sent to a diagnostic lab.
The gene of interest is sequenced and sent electronically to Sequivity analysts.
A synthetic version of the gene of interest is synthesized and inserted into the RNA production platform.
The RNA particles released from incubated production cells are harvested and formulated into a customized “vaccine.”
Using this platform, a customized “vaccine” can be created in as little as eight weeks. Now, what could go wrong by not testing every new shot for safety?
In my view, there are any number of safety hazards, as every pathogen has distinct effects, and tricking the animal’s body to produce that pathogen (or a pathogenic portion of that pathogen, as done with SARS-CoV-2) can have wildly unexpected side effects.
We’ve clearly seen this with the SARS-CoV-2 spike protein in humans. Pfizer’s own documentation lists 158,000 recorded side effects, and many of these diseases and conditions have never before been reported in response to a vaccine.
I reviewed this evidence in “Newly Released Pfizer Documents Reveal COVID Jab Dangers” and “CDC Aware of Hundreds of Safety Signals for COVID Jab.” Yet despite the obvious risks, the U.S. Food and Drug Administration has gone ahead and authorized updated COVID shots to be released on an annual basis without additional safety testing, and apparently safety testing of mRNA shots used in animals was foregone nearly five years ago!
The risk of dangerous side effects is one of the reasons why not all conventional vaccines work out. Some simply cause too many problems. Now we’re to believe that the possibility for dangerous side effects doesn’t exist just because we’re forcing the body to produce the antigen internally? If anything, the possibility for problems is higher than ever, as exposure to the antigen is continuous for a long period of time, possibly for the life of the animal.
Even Organic Pork Producers Can Use mRNA Shots
Unfortunately, due to search engines now only providing a short list of curated and heavily censored content, it’s been impossible to determine how many pork producers in the U.S. use Sequivity.
Without that data, I recommend erring on the safe side and avoiding pork altogether, including organic pork, as organic standards do not have any rules on the use of vaccines, mRNA-based or otherwise.18
Seeing how the Sequivity platform has been around for nearly five years already, it seems reasonable to assume nearly all large-scale swine producers have made this transition.
What Do the Cells in mRNA-Treated Meat Contain?
The question now is, how do mRNA shots affect the meat? For now, this is speculative, as we do not know whether veterinary mRNA shots are substituting uridine with pseudouridine, as was done in the COVID shots. But if they do, then one of the obvious concerns would be that the mRNA might end up in the final meat product that you eat because this substitution makes it extremely difficult to destroy. As explained by Dr. Peter McCullough:19
“Natural RNA is made of two purines adenine and guanine and two pyrimidines cytosine and uracil.
The replacement of uracil with its ribose ring (uridine) with N-1-methyl-pseudouridine, a synthetic product makes the genetic code for the Wuhan Spike protein better stabilized on lipid nanoparticles, long-lasting, and very efficient in terms of evading cellular destruction and able to undergo repeat reading by ribosomes for continued protein synthesis.
Morais et al20 indicate that both Pfizer and Moderna chose development strategies replacing all uridine units with pseudouridine, making the entire strand completely ‘unnatural’ to the human body. Thus vaccine consultants, companies, and patients unfortunately gambled on how long mRNA would be active within the human body.
Fertig et al21 found lipid nanoparticles with mRNA were measurable in plasma for — 15 days. Recently, Castruita et al22 demonstrated mRNA in blood out to 28 days. Röltgen et al23 have found mRNA in lymph nodes 60 days after injection.
None of these studies demonstrated complete clearance of mRNA from a group of patients.
This is worrisome since injections are recommended in some populations just a few months apart implying there will be stacking of long-lasting mRNA in the body without adequate opportunity for clearance and elimination.
We will look back for many years and ask: how could so many people readily accept injections of heavily modified synthetic genetic code giving the body instructions to manufacture a disease promoting and lethal protein engineered in a biosecurity lab in Wuhan, China?
Repeated administrations of mRNA studded with apparently indestructible pseudouridine may have changed the course of lives forever.”
If mRNA shots can cause significant disease in humans, how has it affected our pork supply for the last five years? And how will it affect beef and chicken in the future? Can consuming genetically manipulated meat affect your health? These are questions that currently do not have answers and must be thoroughly and comprehensively investigated.
Big Ag Didn’t Tell Us What They Were Doing
One of the most frustrating aspects of this is that the industry didn’t tell us they were using novel gene therapy to spin up customized “vaccines” in weeks without any safety testing. The only reason many of us became aware of this issue in recent weeks was because attorney Tom Renz started warning about it.
Missouri House bill 1169 would require labeling of products that have the ability to alter your genetics. It would also require companies to share information about the potential transmissibility of gene altering interventions.
In an April 2, 2023, Substack article, he wrote:24
“I have been talking about gene therapy vaccines being introduced into the food supply without providing people informed consent on my Twitter account … as well as pushing Missouri HB1169 which is our best bet of stopping this happening.
This is a nightmare scenario whereby people’s genetics are potentially altered with ‘factory foods’ without them even knowing. Let me begin by putting to rest any questions as to whether this can happen. The idea of vaccines in food has been around for a long time …
Here is an article published in the NIH25 (you know — by our government) talking about foods ‘under application’ to be genetically modified to become edible vaccines — FROM 2013 … The fact that food can be altered to act as a vaccine is not disputable.
Which foods and in what ways is more of a question. It is claimed that beef, pork, etc. cannot transfer vaccination from the meat to the consumer of the meat. At initial glance that would make sense (cow DNA and people DNA is quite different and an mRNA designed for cows would probably not be able to transfer directly to people), but that is NOT the whole story.
You have to remember that the additives in the mRNA vaccines are by no means ‘proven safe’ and we don’t even actually know what all is in these shots … Ultimately the mRNA jabs still have not undergone long-term testing because long-term testing can take 10-20 years and they have not existed that long so any claims about the safety or efficacy of the stuff that’s in them are garbage at best.
What we do know about the mRNA vaccines is that they do not stop the spread of disease26 … and really do not help in any way with anything. We also do know that these jabs were demonstrated, in vitro, to alter the genetic makeup of some cells and I would say it is incredibly likely that they do the outside the Petri dish.
Given that we are now talking about a new level of genetic engineering with unknown effects and no long-term studies, do the potential genetic changes the mRNA injections facilitate pose a long-term risk to humans that ingest the altered food? Before you say no, wouldn’t you prefer it be tested rather than being the subject of the experiment?”
Support Missouri House Bill 1169
As noted by Renz, Missouri House Bill 116927 would require labeling of products that can alter your genes. It also asserts that fully informed consent must be given for all vaccines, gene therapies and medical interventions, and would require companies to share information about the potential transmissibility of gene-altering interventions.
The pushback by industry against this bill has been enormous, which should tell you something. It doesn’t ban anything; it only requires transparency. That, apparently, is a serious threat to industry, and the most obvious reason for that is because they’d have to admit that all sorts of foods can have gene altering effects.
Not only might this destroy Big Ag, but it would also decimate any surreptitious attempts by Big Pharma to use the food supply as a tool to distribute vaccines unbeknownst to consumers. As noted by Renz, “Big pharma DOES NOT WANT people to know they are going to use food to alter their genetics.” Farmers are also being set up as the fall guys, and they need to be made aware of this.
“The lobbyists opposing this bill … are pushing to shut this bill down because factory mega-farmers like Bill Gates,28 the CCP, and others want to put vaccines in your food,” Renz continues.29 “These guys are supporting the big money but this will come at the expense of the family farmers.
The problem is that the major factory-farmers like Gates have legal teams that can set up defense shields against the torts that may come if the food supply starts poisoning people … 
Meanwhile, the small farmers will be at risk of being sued if it turns out that the food they are selling is unsafe despite the fact that most of them will not necessarily know what is happening.
If the corn growers, soybean, cattle, and pork associations actually cared about the farmers they would be demanding the seed companies and vaccine manufacturers indemnify the small farmers for these products rather than opposing a bill that would force them to tell the farmers what they are doing.
The corruption regarding this bill is amazing. Ultimately the labeling requirement would likely serve to protect farmers from being sued because the makers of seed and vaccines would have to make sure the farmers knew if they were putting potential gene therapies into their products. The opposition from the ag lobby is not to help the farmers, it is to help their own pockets.”
As noted by Renz, if this bill is passed in Missouri, it could help protect the food supply of the entire United States. In the meantime, I recommend avoiding all pork products, including organic ones, as they not only have high levels of the omega-6 fat, linoleic acid, because of the grains they are fed, but virtually all have been contaminated with the mRNA vaccines for the past five years.

Think Globally, Act Locally
National vaccine policy recommendations in the U.S. are made at the federal level but vaccine laws are made at the state level. It is at the state level where your action to protect your vaccine choice rights can have the greatest impact.
It is critical for EVERYONE to get involved now in standing up for the legal right to make voluntary vaccine choices in America because those choices are being seriously threatened.
Not only are lobbyists representing drug companies, medical trade associations and public health officials trying to persuade legislators to strip all vaccine exemptions from public health laws, but global political operatives lobbying the United Nations and World Health Organization are determined to take away the human right to autonomy and protection of bodily integrity.
We must take action to defend our constitutional republic and civil liberties, including the right to autonomy, in America. That includes reforming oppressive mandatory vaccination laws and stopping the digital health ID that will make vaccine passports a reality for us, our children and grandchildren if we don’t take action today.
Signing up to use the free online Advocacy Portal sponsored by the National Vaccine Information Center at www.NVICAdvocacy.org gives you immediate, easy access to your own state and federal legislators on your smartphone or computer so you can make your voice heard.
NVIC will keep you up to date on the latest bills threatening to eliminate — or expand — your legal right to make vaccine choices and give you guidance about what you can do to support or oppose those bills. So, please, as your first step, sign up for the NVIC Advocacy Portal.
CLICK HERE TO JOIN!
Share Your Story With Your Legislators and People You Know
If you or a family member has suffered a serious vaccine reaction, injury or death, please talk about it. If we don’t share information and experiences with one another, everybody feels alone and afraid to speak up.
If you want to protect your legal right to say “no” to vaccines you do not believe are safe or effective, make an appointment to personally talk with someone you have elected to office at the local, state and federal level or write a letter in your own words stating your concerns.
Attend school board and city council and town hall meetings in your community that will impact your right to know and freedom to make decisions about how you or your children will live and stay healthy. If you have a different perspective on a story about vaccination that appears in your local newspaper, write a letter to the editor.
I must be frank with you: You have to be brave because there is a lot of censorship of conversations that challenge “official” narratives about vaccination. You likely will be strongly criticized for daring to talk about the “other side” of the vaccine story and for defending your informed consent rights. Be prepared for it and have the courage to stand your ground.
Only by sharing our perspective and what we know to be true will the public conversation about vaccination open up so people are not afraid to talk about it.
While our rights are being threatened, the vaccine injured are being swept under the carpet and treated like nothing more than statistically acceptable “collateral damage” of one-size-fits-all mandatory vaccination laws. Way too many people are being put at risk for injury and death and there is nothing scientific or moral about that. We should not be treating human beings like guinea pigs.

Internet Resources Where You Can Learn More
I encourage you to visit the four websites of the National Vaccine Information Center (NVIC), at www.NVIC.org, a nonprofit charity that has been educating the public about the need to prevent vaccine injuries and deaths since 1982. The information you get on their websites is fully referenced and will help you become an effective vaccine choice advocate in your community:
NVIC.org — This website was established in 1995 and is the oldest and largest consumer operated website publishing information on diseases and vaccines on the internet. Learn about vaccine reactions, injuries and deaths and the history and current status of vaccine science, policy, law and ethics in the U.S. on more than 2,000 web pages.
NVICAdvocacy.org — This communications and advocacy network, established in 2010, is your gateway to taking action to protect your right to make vaccine choices where you live.
TheVaccineReaction.org — This weekly journal newspaper published by NVIC since 2015 is dedicated to encouraging an “enlightened conversation about vaccination, health and autonomy.”
MedAlerts.org — This is a user-friendly search engine for the federal Vaccine Adverse Event Reporting System (VAERS) established under the 1986 National Childhood Vaccine Injury Act and sponsored by NVIC since 2006. Search for descriptions of vaccine injuries and deaths reported to VAERS on this popular website.
Find A Doctor Who Will Listen and Care
If your doctor or pediatrician refuses to provide medical care to you or your child unless you agree to get vaccines you don’t want, I strongly encourage you to have the courage to find another doctor. Harassment, coercion and refusal to provide medical care to someone declining one or more doses of government recommended vaccines is a violation of the informed consent ethic.
Unfortunately, it is becoming routine among members of the medical establishment to be reluctant to share vaccine decision-making power with patients and parents of minor children, especially during the aggressive push for all Americans to get COVID shots.
There are doctors out there who respect the precautionary and informed consent principles, so take the time to locate a doctor who treats you with compassion and is willing to listen and respect the health care choices you make for yourself or your child.

Sources and References

Photo: EWR

Ex-Pfizer Head of Research Says COVID Vaccine Could Sterilize Women

A former head of respiratory research at Pfizer and a former public health department head have filed a joint petition to the European Medicine Agency, asking for the immediate suspension of all SARS-CoV-2 vaccine studies.

Dr. Michael Yeadon and Dr. Wolfgang Wodarg said certain safety concerns with the vaccines have not been addressed. One problem is that the PCR test is notoriously inaccurate. But another, more pressing issue is that the spike proteins in the vaccines contain synctytin-homologous proteins, which can cause infertility.

Also concerning is that the mRNA vaccines from BioNTech/Pfizer contain polyethylene glycol, which can cause potentially life-threatening reactions to the vaccine. The duo said they filed the lawsuit in December because the vaccines’ studies have not been long enough to know what the long-term side effects might be.

SOURCE: Principia Scientific International December 10, 2020

VIA: https://blogs.mercola.com/sites/vitalvotes/archive/2021/01/19/expfizer-head-of-research-says-covid-vaccine-could-sterilize-women.aspx

Image by Ria Sopala from Pixabay

10 Dead In Germany Within 4 Days Of Covid-19 Vaccine Inoculation; Probe Ordered

German specialists probe as 10 people died soon after getting inoculated against the novel Coronavirus disease, the deceased were aged between 79 to 93 years.

After the deaths of 10 people who passed away soon after having been inoculated against the novel coronavirus disease, Specialists from Germany’s Paul Ehrlich Institute are looking into it. Brigitte Keller-Stanislawski, the head of the institute’s department of the safety of medicinal products and medical devices, said on Thursday.

READ | COVID-19: Two WHO Team Members To Wuhan Test Positive, Being Retested In Singapore

The deceased were aged between 79 to 93, all with antecedent diseases. The time between vaccination and death ranged from several hours to four days, according to the medical expert.

“Until yesterday we had nine cases; we have to wait for the data from Lower Saxony [about another alleged case], then there will be 10. We are talking about patients in extremely grave condition, with multiple diseases, who were receiving palliative treatment. I have already said that we are studying these cases … Based on our current data we assume they died from their main diseases, coinciding in time with the vaccination,” Keller-Stanislawski said at a press conference.

READ | COVID-19: UK Travel Ban On South America, Portugal Over New Variant Fears

Germany’s Vaccination Campaign 

Using the vaccine developed by the companies Pfizer and BioNTech, Germany launched a vaccination campaign against COVID-19 in late December. Till this date, 842,000 people have received the vaccine. Those over 80 are the first ones to get vaccinated followed by the residents and staff at nursing homes as well as medical personnel.

The institute also reported six anaphylaxis (severe, potentially life-threatening allergic reaction) cases. So far, including 51 severe ones, there have been 325 cases of side-effects allegedly related to the vaccine. Those results are within expectations and correspond to the US vaccination statistics, Keller-Stanislawski stated.

SOURCE

LINK: https://www.republicworld.com/world-news/europe/10-dead-in-germany-within-4-days-of-covid-19-vaccine-inoculation-probe-ordered.html?fbclid=IwAR0P-fGve4-8u0OykRRhQfW17oaV4VXnZPybDqXqZ4vZG2QgBVfZRUUx8sY

Image by hakan german from Pixabay

12,400+ Israelis test POSITIVE for Covid-19 despite receiving Pfizer/BioNTech jab

More than 12,400 people in Israel have tested positive for coronavirus after being vaccinated with the Pfizer/BioNTech jab, including 69 who had received their second dose, the country’s Health Ministry said.

Some 189,000 people were tested for Covid-19 after being vaccinated, with 6.6 percent getting a positive result, according to ministry data reported by Israeli outlets. The majority were apparently infected shortly after receiving the first jab of the two-part vaccine – a period when the inoculation isn’t expected to have kicked in yet.

READ MORE

LINK: https://virutron.com/12400-israelis-test-positive-for-covid-19-despite-receiving-pfizer-biontech-jab/?fbclid=IwAR0vDhedE5CMQ3iBXondKYyJOwDtMV9C_6eL0I4HYkPfLQX8SZSOr3ZIMV0

Image by Gerd Altmann from Pixabay

13 deaths linked to Pfizer vaccine jabs – ‘We see nothing alarming,’ says Norwegian drugs regulator

We were warned not to be surprized at the elderly dying … and here they are proving that with this normalizing of deaths from the vaccine. (We were told the elderly were a priority for care?) EWR
______________________________________________________________________

At least 13 people have died in Norway due to side effects of the Pfizer/BioNTech Covid-19 vaccine, the national medicines regulator has revealed. All were frail and elderly people who had unusually strong reactions to the jabs.

Norway launched its Covid-19 immunization program on December 27, including residents of nursing homes on the priority list.

Since then, 23 people have died shortly after receiving the injections. Norwegian medics are evaluating all such cases and have linked 13 of them to the side effects of the vaccine, according to local media.

“We do not see anything alarming with these figures. All deaths are in elderly and frail people with underlying diseases,” Dr. Steinar Madsen, the medical director of the national drug regulator, the Norwegian Medicines Agency, explained.

For context, Norway has a population of over five million. Madsen previously said that between 350 and 400 people die at the country’s nursing homes each week as he predicted that some elderly people may not react well to the vaccine.

In addition to those who died, there were also 29 vaccine recipients who had developed significant side effects, including nine serious cases and seven mild ones, the official reported. All Covid-19 vaccines can sometimes cause adverse reactions like fever and nausea.

The Norwegian Public Health Institute updated its Covid-19 vaccination guidelines earlier this week to reflect the new data. The document now instructs medics to thoroughly evaluate nursing home residents before giving them the vaccine.

For very ill people who are not expected to live long, the benefit of the jab “may be marginal or negligible,” the guidelines say. – RT.com

For the most definitive protection of the entire family from the potential adverse effects of vaccinations, eliminate the risks and high costs of hospitalization, and help the body decisively cure itself from cancer, or any other conditions caused by any known and unknown type of viruses or bioweapons, try the electronic Virutron® PRO Full Spectrum Antiviral + CES System and worry no more…

SOURCE: https://virutron.com/we-see-nothing-alarming-says-norwegian-drugs-regulator-after-13-deaths-linked-to-pfizer-vaccine-jabs/

Norway investigating death of two people who received Pfizer’s coronavirus vaccine

Norway is investigating the death of two nursing home residents who died after receiving doses of the Pfizer and BioNTech coronavirus vaccine.

It comes after a paediatric surgery assistant in Porto was found dead two days after receiving jabs of Pfizer’s vaccine.

READ MORE

https://www.wionews.com/world/norway-investigating-death-of-two-people-who-received-pfizers-coronavirus-vaccine-354716?fbclid=IwAR0swAZHgN8BWJcPIs-P4jg-n6HESYrBHB5swQwe6Z-mz555-ZlRzvfdUzE

What Vaccine Trials?

COVID 19 vaccine trials appear to have caused some confusion. Hopefully, this article might help clear things up a bit. People genuinely appear to believe that the COVID 19 vaccines have undergone clinical trials and have been proven to be both safe and effective. That belief is simply wrong.

The main point is this. If you decide to have Pfizer and BioNTech’s experimental mRNA-based BNT162b2 (BNT) vaccine, or any other claimed COVID 19 vaccine for that matter, you are a test subject in a drug trial.

The mRNA in the BNT vaccine was sequenced from the 3rd iteration of the original WUHAN published Genome SARS-CoV-2 (MN908947.3). However, the WHO protocols Pfizer used to produce the mRNA do not appear to identify any nucleotide sequences that are unique to the SARS-CoV-2 virus. When investigator Fran Leader questioned Pfizer they confirmed:

The DNA template does not come directly from an isolated virus from an infected person.

Nor are there any completed clinical trials for these vaccines. Trials are ongoing. If you are jabbed with one, you are the guinea pig. This may be fine with you but it’s not a leap of faith I or my loved ones wish to take. However, everyone is different.

On December the 8th the BBC reported a study in the Lancet and categorically stated:

The Oxford/AstraZeneca Covid vaccine is safe and effective, giving good protection, researchers have confirmed

The BBC had no justification to make this claim.

READ MORE

LINK: https://off-guardian.org/2021/01/03/what-vaccine-trials/

Photo: Pixabay.com

Every New Zealander will be able to be vaccinated says PM as Govt secures another two Covid-19 vaccines (video)

Do ask to see the full inserts to check possible side effects if you intend to take up this offer. Since it’s been sparsely tested, you really should be privy to any possible adverse effects, given they are not generally offered to the recipients.

RELATED: https://envirowatchrangitikei.wordpress.com/2020/12/26/fyi-pfizers-fact-sheet-for-their-new-cv-vaccine-note-there-is-no-fda-approved-vaccine-to-prevent-covid-19/

EWR
____________________________________________________________________________

The government has secured another two vaccines, enough for every New Zealander and its Pacific partners, Prime Minister Jacinda Ardern says.

The additional vaccines being pre-purchased are from pharmaceutical companies AstraZeneca and Novavax.

A total of 7.6 million doses will come from AstraZeneca – enough for 3.8 million people, and 10.72 million doses from Novavax – enough for 5.36 million people. Both vaccines require two doses to be administered.

The government already has to pre-purchase agreements for 750,000 courses from Pfizer/BioNTech and 5 million from Janssen.

The cost of the new pre-purchase agreements was not disclosed, but the vaccines will be free to New Zealanders, the government said.

READ MORE

https://www.rnz.co.nz/news/national/433029/govt-secures-another-two-covid-19-vaccines-pm-says-every-new-zealander-will-be-able-to-be-vaccinated

MHRA urgently seeks software tool to process the expected high volume of Covid-19 vaccine Adverse Drug Reactions – Tenders Electronic Daily

Thanks to the FlyingCuttlefish blog for this link. At 9 minutes in the video hear immunologist and toxicologist Prof. Stefan Hockertz give evidence about the untested Pfizer vaccine for covid to the German Corona Committee, which includes lawyer Reiner Fuellmich.

TRANSCRIPT: It is about “vaccines that could eventually be compulsory or forced on us by social pressure and those from BioNTech and Pfizer which have received an authorisation for use in the UK. Interestingly, in a country which 3 or 4 weeks ago made us aware about a public tender showing new computer and server capacity must be provided in order to handle the sheer number of side effect reports that are expected through using such an mRNA vaccine.


We have neither a phase 1 or a phase 2 reasonably carried out so my accusation is much more serious. Safety, efficacy & quality checks in the pre-clinical areas haven’t been done at all. And this is the real crime. This work MUST be done and it has totally NOT BEEN DONE. This whole system must be tested in animals which are suitable, and this must first be determined … by examining the liver, the kidneys etc., the complete histology has to be looked into, a very elaborate aspect, and naturally the function, especially of the immune system must be proven. None of this has been done. Definitively there is no toxicological data available. I know this for two reasons, firstly I have asked BioNTech several times with no reply. If there was any data they could at least have told me that the experiments were done. They wrote to inform me quite clearly that they have “no data available yet”. This came from a Senior Medical Director who is responsible for the total phase of the trial. This for me is a kind of proof on the one hand of silence … meaning … “we don’t have anything”, and on the other hand they are indeed admitting that they have nothing. This means we are making experiments on people without knowing the safety of the product.”

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