Wait until everyone discovers that clinical trials are in principle not possible for "countermeasures". I am waiting for an MD or a PhD "expert" to announce this to the world. 3,2,1...
PS. I did explain this to Dr. Drew several months ago, but he still looks freshly confused when Josh explains it to him again...
A true drug trial? Hardly. It is more common than you think that many drugs have such manipulated trails as to be virtually non-relevant. Otherwise, 3/4 of big pharma drugs would never get approval. They shouldn't anyway, but the FDA is a bought and paid for source of providing the road to drugs being marketed without any top line trials. Use all big pharma products at your own risk...even OTC garbage.
It absolutely was a bait and switch. And the FDA knew and was a full participant. It's not even arguable. It's right their in their own records.
On Aug 23, 2021, the FDA - to much fanfare - announced it had LICENSED a VACCINE against Covid-19!!! COMIRNATY®, made by the German company BioNTech.
That product's marketing start date for marketing in the United States was Aug. 23, 2021 - it's marketing END date was ALSO Aug 23, 2021. Yes, the same exact day it was licensed for use in the US, it was also pulled from the market and would never be produced.
INSTEAD, the FDA (in its own regulatory letters rto Pfizer and BioNTech) in a now infamous footnote, simply declared that BNT162b2 - the Pfizer product that had ONLY an Emergency Use Authorization - was close enough to be "interchangeable" with the licensed product.
"Interchangeability" is a defined term under the PHSA 42 USC 262(k) and has a whole series of requirements before any two biologics can be declared "interchangeable." The FDA "waived" its "enforcement discretion" and allowed military folks to be forced to take the unlicensed, EUA product - and the entire country fell for it.
My colleagues and I have been screaming about this for 2 straight years now and no one has been listening. For those with a PACER account, I welcome anyone to check these filings.
See Wilson v. Austin, 4:22-cv-00438-ALM, ECF 41.
Or Botello v. US, 1:23-cv-00174-TMD, ECF 13.
The receipts are publicly available and have been. No court will touch this and the DoD, with help from FDA had one of its own officials - Asst SecDef for Health Affairs Terry Adirim - completely unqualified and with no legal authority to do so - simply declared that BNT162b2 were "interchangeable" and therefore that soldiers could be forced to take an EUA product without their consent.
Why do we always think lawsuits and fines? This is a criminal government scheme. If there is no recourse for justice, what do we have? Despotism. Despots are deposed.
EGM: Not to take away from this very important post but regarding the issue of whether or not the bait and switch has been done before ["oh, we can just switch to a radically new production process for a biologic drug without testing” is, as far as i know, unprecedented in FDA history."], the same thing was done in the1976 Influenza A H1N1 Swine flu scam. That was the year they had 45 million Americans get a vaccine that wasn't tested before they stopped it. That vaccine was also a disaster. Three men died of heart attacks after getting the vaccine from the same Pittsburgh clinic and , all for a Swine Flu "pandemic" where not a single confirmed case was confirmed anywhere in the world in the 9 months leading up to the rollout.
From my book, "Heroes and Villains: The COVID-19 Book of Lists": "In February, CDC Director Dr. David Sencer distributed a memo calling for mass immunization for the swine flu. A month after that, President Ford was officially notified of the outbreak and endorsed the idea of mass immunization.
The vaccine manufacturers made two demands: 1) that there must be a guaranteed profit for them, and, 2) that the government provide the manufacturers with indemnity from liability for any adverse effects arising out of the, as yet to be manufactured, vaccine. Both demands were met and the vaccination was manufactured and run through a testing protocol.
But something odd happened. The vaccines that got administered were not the ones tested. They used a different vaccine that was developed later but never tested in the kind of trials we have come to expect when new injections are introduced to the public.
The administration of the untested vaccine began on October 1, 1976. A year later, when asked if the vaccines were tested before being administered to the general public, Dr. Sencer said, "I…can't say. I would have to… I don't know. I would have to check the records. I haven't looked at this for some time."
What!? He was the Director of the CDC. He formulated the plan and was in charge of the vaccine rollout. It was his "baby". How could he not know they hadn't tested the vaccine?
But there was an even bigger problem. It turns out, over the nine months that elapsed between the Fort Dix outbreak- at this point looking very questionable- and the date of the first injection, there was never a single additional case of swine flu confirmed anywhere in the world. "There had been several cases reported by the news media, but none confirmed", admitted Dr. Sencer.
Nine months is a very long time for not a single case of the disease popping up somewhere. Dr. Sabin, the inventor of one of the polio vaccines, wrote an editorial in the New York Times entitled "Washington and the Flu" in which he argued for a "wait-and-see" strategy by stockpiling the vaccines until it was clear they were needed. His advice was ignored.
In just the first month, three recipients died from heart attacks shortly after being vaccinated at the same Pittsburg clinic. That batch was recalled but vaccination continued. More and more recipients contracted Guillain-Barre Syndrome (GBS), a nervous system disorder that can cause paralysis and death.
The vaccine rollout continued through the Fall and early Winter months. During all this time, not a single additional case of Swine Flu was found. The GBS cases, however, were accumulating rapidly. The vaccines were finally discontinued on December 15, 1976, after 45 million people received the injection. More than 362 recipients across America contracted Guillain-Barre Syndrome and 300 died. Many of the remainder were left paralyzed. The survivors (or the families of the deceased) applied for compensation from the U.S. Government since the manufacturers were granted indemnity from liability.
The case of the Swine Flu "outbreak" and vaccine launch of 1976 is not the same as the COVID-19 pandemic and vaccine launch of 2020, but there are some similarities and a few important lessons to take home. Similarities include, 1) the lack of informed consent provided to the recipients, 2) pharmaceutical industry shenanigans such as switching to a formulation that was not tested properly, 3) the incompetence, fraud, and prevarication that came out of the CDC and the attempts of the Director to cover up what was done, 4) the U.S. government's aggressive advertising campaign to get people to take the vaccines and 5) the President's participation at the time, urging people to get vaccinated without any justification for it.
There was no justification for pressuring the public to get these vaccines. In the case of the Swine Flu in 1976, nobody had the disease and in the case of COVID-19, we knew that the vaccine did not perform as promised. The real-world vaccine data never came close to meeting safety and efficacy standards given that the original disease had an infection fatality rate of .1% for all ages and much lower than that in those under 60. The risk was tiny in young adults and negligible in children, reaching a risk of death of only one in a million in small children. Nevertheless, the vaccines were approved and continue to be pushed to this day by government doctors such as Ashish Jha and CDC Director Rochelle Walensky for children as young as six months of age. The trials did not justify approval in this age group, let alone a campaign to promote them to new mothers.
The 1976 consent form everyone was asked to sign did not disclose the risk of potential side effects such as Guillain-Barre Syndrome. The forms only mentioned sore arm, fever, muscle aches, etc. This is exactly what happened with the Covid-19 vaccines. Parents were not warned about complications such as myocarditis, by the people administering the jabs even after the CDC knew about the increased risk.
In 1977, Dr. Sencer claimed he was not told GBS and other neurological complications were part of the risk profile. A younger member of the team, however, stated that he absolutely had informed Dr. Sencer and others regarding potential neurological complications including GBS, before the rollout commenced. How did he know? He performed a literature search.
The take-home lesson from all of this is that because we never punished the perpetrators for their egregious acts in 1976 and several similar examples of the same thing since then, we had to live through it again this time.
I believe that if we had prosecuted the people who committed the criminal acts of 1976, and sent them to prison if found guilty, almost fifty years of public abuse at the hands of Big Pharma would have been averted or greatly reduced."
This reminds me of Aug-Sep 2021 when FDA fully approved the pfizer product... there was some talk about the legal sleight of hand where the approval was actually for a different product/formulation that was not actually available. And IIRC, there was even a successful court case where members of the US military challenged the mandate based on the above.
This is good to know but not surprising. I am beyond outrage. My only question is how long before I can support myself selling my uncontaminated blood and plasma?
I knew it was a lie from the beginning. Confirmation came with "it just stays in the arm". You are ONE body. What goes in the arm goes everywhere else in the body. What B. S. that it just stays in the arm.
And that isn't the only issue, as bad as it is. There is also the question as to the ability of the bacterial plasmids to enter the human cell nucleus and incorporate into human DNA, One of the contaminants is an agent KNOWN to facilitate this process. That's yet another queastion : WTF was THAT doing in there, which in turn raises another key question of this "possibly" being by design. The E.Coli plasmids also incorporate code for resistance to several antibiotics - yet another concern. If human DNA is "contaminated" as seems most likely, then the issue of longer-term AEs is now even more unceratin than ever and it might be the case that what we are seeing already is just the start of what is to come.
We now know why Pfizer tried so hard to prevent vials of its prodiuct falling into the "wrong hands". These new revelations are truly shocking have opened up a Pandors'a Box of important new questions, some of which as outlined above.
This is a VERY serious and important development which needs to be closely monitored because the consequences of new facts could be explosive.
When we live in a world where food trucks have more regulation that vaccines, probably time to appreciate that sketchy chimicanga you ate at 3 AM last Saturday night, just a little more, and just keep telling yourself, "it could have been so much worse".
What everyone needs to understand is that there will be no consequences. Anything and everything that could get in the way was neutralized years ago. This didn’t start in the last five years, it’s been in the works for a long time. If you’re waiting for the “good guys” to say ENOUGH and put a stop to it, you’re going to be left waiting. Protect you and yours the best you can. These takeovers last years before they implode. I’m sorry, but that’s reality
My son worked for a company that manufactured pipe for the oil and gas industry. Dangerous business. People were hurt and people died. But it was cheaper to pay the OSHA fines than fix their process, so that’s what they did. When they tried to promote him he quit. He wasn’t going to be a front man for that
If you look at the research done by Sasha Latypova and Dr David Martin. These shots were created by the pharmaceutical companies under DOD contracts. The DOD did not require them to be safety tested or efficacy tested. The reality is our government ( DARPA, DOD ) created these bio weapons and used the pharmaceutical companies to manufacture them to kill the American people. It’s all documented in the presentation that Dr David Martin gave before the European Parliament.
I have a horrible suspicion that ALL the NPI's and injections were mandated and synchronised globally because every country is a signatory to the 2005 International Health Regulations.
In other words, the WHO issued instructions on all measures, from face masks to mRNA injections.
There is no bus big enough to throw the WHO under. It also has a liability shield - it is simply immune from any and all prosecution by anyone. All care and no responsibility - welcome to One World government.
Notice how there is no enquiry into the crass actions and advice of the WHO for the last four years?
And now? Al the breaches of Nuremburg, all the sins of omission and commission by all players acting on WHO instructions will be further strengthened under IHR amendments and a new pandemic treaty to include monitoring, surveillance and control - via digital passports and censorship. ALl governments will become even more subordinate.
We only have a month for the last lot of amendments agreed in May 2022 have to be passed as enabling legislation in every country in the world.
Silence = Consent and our leaders helped draft the amendments and are SILENY on now opposing them.
Not ethe chain of command in the US. From the WHO to DOD and the Secretary of HHS - just a few people. The US obeys WHO PHEIC terms and every medic in the US has no liability of they follow HHS/FDA/CDC instructions. So it progresses in every country.
As soon as they step out of that HHS Overton Window - fired and disbarred and censored.
Sounds like they just put random shit in a vial.
Wait until everyone discovers that clinical trials are in principle not possible for "countermeasures". I am waiting for an MD or a PhD "expert" to announce this to the world. 3,2,1...
PS. I did explain this to Dr. Drew several months ago, but he still looks freshly confused when Josh explains it to him again...
A true drug trial? Hardly. It is more common than you think that many drugs have such manipulated trails as to be virtually non-relevant. Otherwise, 3/4 of big pharma drugs would never get approval. They shouldn't anyway, but the FDA is a bought and paid for source of providing the road to drugs being marketed without any top line trials. Use all big pharma products at your own risk...even OTC garbage.
It absolutely was a bait and switch. And the FDA knew and was a full participant. It's not even arguable. It's right their in their own records.
On Aug 23, 2021, the FDA - to much fanfare - announced it had LICENSED a VACCINE against Covid-19!!! COMIRNATY®, made by the German company BioNTech.
That product's marketing start date for marketing in the United States was Aug. 23, 2021 - it's marketing END date was ALSO Aug 23, 2021. Yes, the same exact day it was licensed for use in the US, it was also pulled from the market and would never be produced.
INSTEAD, the FDA (in its own regulatory letters rto Pfizer and BioNTech) in a now infamous footnote, simply declared that BNT162b2 - the Pfizer product that had ONLY an Emergency Use Authorization - was close enough to be "interchangeable" with the licensed product.
"Interchangeability" is a defined term under the PHSA 42 USC 262(k) and has a whole series of requirements before any two biologics can be declared "interchangeable." The FDA "waived" its "enforcement discretion" and allowed military folks to be forced to take the unlicensed, EUA product - and the entire country fell for it.
My colleagues and I have been screaming about this for 2 straight years now and no one has been listening. For those with a PACER account, I welcome anyone to check these filings.
See Wilson v. Austin, 4:22-cv-00438-ALM, ECF 41.
Or Botello v. US, 1:23-cv-00174-TMD, ECF 13.
The receipts are publicly available and have been. No court will touch this and the DoD, with help from FDA had one of its own officials - Asst SecDef for Health Affairs Terry Adirim - completely unqualified and with no legal authority to do so - simply declared that BNT162b2 were "interchangeable" and therefore that soldiers could be forced to take an EUA product without their consent.
Why do we always think lawsuits and fines? This is a criminal government scheme. If there is no recourse for justice, what do we have? Despotism. Despots are deposed.
EGM: Not to take away from this very important post but regarding the issue of whether or not the bait and switch has been done before ["oh, we can just switch to a radically new production process for a biologic drug without testing” is, as far as i know, unprecedented in FDA history."], the same thing was done in the1976 Influenza A H1N1 Swine flu scam. That was the year they had 45 million Americans get a vaccine that wasn't tested before they stopped it. That vaccine was also a disaster. Three men died of heart attacks after getting the vaccine from the same Pittsburgh clinic and , all for a Swine Flu "pandemic" where not a single confirmed case was confirmed anywhere in the world in the 9 months leading up to the rollout.
From my book, "Heroes and Villains: The COVID-19 Book of Lists": "In February, CDC Director Dr. David Sencer distributed a memo calling for mass immunization for the swine flu. A month after that, President Ford was officially notified of the outbreak and endorsed the idea of mass immunization.
The vaccine manufacturers made two demands: 1) that there must be a guaranteed profit for them, and, 2) that the government provide the manufacturers with indemnity from liability for any adverse effects arising out of the, as yet to be manufactured, vaccine. Both demands were met and the vaccination was manufactured and run through a testing protocol.
But something odd happened. The vaccines that got administered were not the ones tested. They used a different vaccine that was developed later but never tested in the kind of trials we have come to expect when new injections are introduced to the public.
The administration of the untested vaccine began on October 1, 1976. A year later, when asked if the vaccines were tested before being administered to the general public, Dr. Sencer said, "I…can't say. I would have to… I don't know. I would have to check the records. I haven't looked at this for some time."
What!? He was the Director of the CDC. He formulated the plan and was in charge of the vaccine rollout. It was his "baby". How could he not know they hadn't tested the vaccine?
But there was an even bigger problem. It turns out, over the nine months that elapsed between the Fort Dix outbreak- at this point looking very questionable- and the date of the first injection, there was never a single additional case of swine flu confirmed anywhere in the world. "There had been several cases reported by the news media, but none confirmed", admitted Dr. Sencer.
Nine months is a very long time for not a single case of the disease popping up somewhere. Dr. Sabin, the inventor of one of the polio vaccines, wrote an editorial in the New York Times entitled "Washington and the Flu" in which he argued for a "wait-and-see" strategy by stockpiling the vaccines until it was clear they were needed. His advice was ignored.
In just the first month, three recipients died from heart attacks shortly after being vaccinated at the same Pittsburg clinic. That batch was recalled but vaccination continued. More and more recipients contracted Guillain-Barre Syndrome (GBS), a nervous system disorder that can cause paralysis and death.
The vaccine rollout continued through the Fall and early Winter months. During all this time, not a single additional case of Swine Flu was found. The GBS cases, however, were accumulating rapidly. The vaccines were finally discontinued on December 15, 1976, after 45 million people received the injection. More than 362 recipients across America contracted Guillain-Barre Syndrome and 300 died. Many of the remainder were left paralyzed. The survivors (or the families of the deceased) applied for compensation from the U.S. Government since the manufacturers were granted indemnity from liability.
The case of the Swine Flu "outbreak" and vaccine launch of 1976 is not the same as the COVID-19 pandemic and vaccine launch of 2020, but there are some similarities and a few important lessons to take home. Similarities include, 1) the lack of informed consent provided to the recipients, 2) pharmaceutical industry shenanigans such as switching to a formulation that was not tested properly, 3) the incompetence, fraud, and prevarication that came out of the CDC and the attempts of the Director to cover up what was done, 4) the U.S. government's aggressive advertising campaign to get people to take the vaccines and 5) the President's participation at the time, urging people to get vaccinated without any justification for it.
There was no justification for pressuring the public to get these vaccines. In the case of the Swine Flu in 1976, nobody had the disease and in the case of COVID-19, we knew that the vaccine did not perform as promised. The real-world vaccine data never came close to meeting safety and efficacy standards given that the original disease had an infection fatality rate of .1% for all ages and much lower than that in those under 60. The risk was tiny in young adults and negligible in children, reaching a risk of death of only one in a million in small children. Nevertheless, the vaccines were approved and continue to be pushed to this day by government doctors such as Ashish Jha and CDC Director Rochelle Walensky for children as young as six months of age. The trials did not justify approval in this age group, let alone a campaign to promote them to new mothers.
The 1976 consent form everyone was asked to sign did not disclose the risk of potential side effects such as Guillain-Barre Syndrome. The forms only mentioned sore arm, fever, muscle aches, etc. This is exactly what happened with the Covid-19 vaccines. Parents were not warned about complications such as myocarditis, by the people administering the jabs even after the CDC knew about the increased risk.
In 1977, Dr. Sencer claimed he was not told GBS and other neurological complications were part of the risk profile. A younger member of the team, however, stated that he absolutely had informed Dr. Sencer and others regarding potential neurological complications including GBS, before the rollout commenced. How did he know? He performed a literature search.
The take-home lesson from all of this is that because we never punished the perpetrators for their egregious acts in 1976 and several similar examples of the same thing since then, we had to live through it again this time.
I believe that if we had prosecuted the people who committed the criminal acts of 1976, and sent them to prison if found guilty, almost fifty years of public abuse at the hands of Big Pharma would have been averted or greatly reduced."
Sorry for such a long post.
This reminds me of Aug-Sep 2021 when FDA fully approved the pfizer product... there was some talk about the legal sleight of hand where the approval was actually for a different product/formulation that was not actually available. And IIRC, there was even a successful court case where members of the US military challenged the mandate based on the above.
This is good to know but not surprising. I am beyond outrage. My only question is how long before I can support myself selling my uncontaminated blood and plasma?
I knew it was a lie from the beginning. Confirmation came with "it just stays in the arm". You are ONE body. What goes in the arm goes everywhere else in the body. What B. S. that it just stays in the arm.
And that isn't the only issue, as bad as it is. There is also the question as to the ability of the bacterial plasmids to enter the human cell nucleus and incorporate into human DNA, One of the contaminants is an agent KNOWN to facilitate this process. That's yet another queastion : WTF was THAT doing in there, which in turn raises another key question of this "possibly" being by design. The E.Coli plasmids also incorporate code for resistance to several antibiotics - yet another concern. If human DNA is "contaminated" as seems most likely, then the issue of longer-term AEs is now even more unceratin than ever and it might be the case that what we are seeing already is just the start of what is to come.
We now know why Pfizer tried so hard to prevent vials of its prodiuct falling into the "wrong hands". These new revelations are truly shocking have opened up a Pandors'a Box of important new questions, some of which as outlined above.
This is a VERY serious and important development which needs to be closely monitored because the consequences of new facts could be explosive.
When we live in a world where food trucks have more regulation that vaccines, probably time to appreciate that sketchy chimicanga you ate at 3 AM last Saturday night, just a little more, and just keep telling yourself, "it could have been so much worse".
Sasha Latypova and Katherine Watt explain all this quite clearly.
What everyone needs to understand is that there will be no consequences. Anything and everything that could get in the way was neutralized years ago. This didn’t start in the last five years, it’s been in the works for a long time. If you’re waiting for the “good guys” to say ENOUGH and put a stop to it, you’re going to be left waiting. Protect you and yours the best you can. These takeovers last years before they implode. I’m sorry, but that’s reality
My son worked for a company that manufactured pipe for the oil and gas industry. Dangerous business. People were hurt and people died. But it was cheaper to pay the OSHA fines than fix their process, so that’s what they did. When they tried to promote him he quit. He wasn’t going to be a front man for that
If you look at the research done by Sasha Latypova and Dr David Martin. These shots were created by the pharmaceutical companies under DOD contracts. The DOD did not require them to be safety tested or efficacy tested. The reality is our government ( DARPA, DOD ) created these bio weapons and used the pharmaceutical companies to manufacture them to kill the American people. It’s all documented in the presentation that Dr David Martin gave before the European Parliament.
I have a horrible suspicion that ALL the NPI's and injections were mandated and synchronised globally because every country is a signatory to the 2005 International Health Regulations.
In other words, the WHO issued instructions on all measures, from face masks to mRNA injections.
There is no bus big enough to throw the WHO under. It also has a liability shield - it is simply immune from any and all prosecution by anyone. All care and no responsibility - welcome to One World government.
Notice how there is no enquiry into the crass actions and advice of the WHO for the last four years?
And now? Al the breaches of Nuremburg, all the sins of omission and commission by all players acting on WHO instructions will be further strengthened under IHR amendments and a new pandemic treaty to include monitoring, surveillance and control - via digital passports and censorship. ALl governments will become even more subordinate.
We only have a month for the last lot of amendments agreed in May 2022 have to be passed as enabling legislation in every country in the world.
Silence = Consent and our leaders helped draft the amendments and are SILENY on now opposing them.
Not ethe chain of command in the US. From the WHO to DOD and the Secretary of HHS - just a few people. The US obeys WHO PHEIC terms and every medic in the US has no liability of they follow HHS/FDA/CDC instructions. So it progresses in every country.
As soon as they step out of that HHS Overton Window - fired and disbarred and censored.