healthimpactnews--2020-12-07--$218 MILLION Paid Out for Vaccine Injuries and Deaths in 2020 for FDA Approved Vaccines (NOT Fast-tr

$218 MILLION Paid Out for Vaccine Injuries and Deaths in 2020 for FDA Approved Vaccines (NOT Fast-tracked)

The federal government Advisory Commission on Childhood Vaccines ( ACCV ) under the U.S. Department of Health and Human Services met on December 3 , 2020 , and the Department of Justice reported that during a 3-month period from August 16th through November 15th this year , 166 cases of vaccine injuries were compensated through the National Vaccine Injury Compensation Program ( NVICP ) .
You can read the full report here .
The NVICP was started as a result of a law passed in 1986 that gave pharmaceutical companies legal immunity from being sued due to injuries and deaths @ @ @ @ @ @ @ suffering from a vaccine injury or death must sue the U.S. Government and go up against their top attorneys .
In the fiscal year 2020 the NVICP has paid out $ 218 MILLION in damages due to vaccine injuries and deaths .
( Source . )
Health Impact News is the only media source I am aware of that covers these quarterly meetings , and if we were to try and share articles like this one publishing these government reports , we would be accused of publishing “ fake news.
” ( Previous @ @ @ @ @ @ @ as you can clearly see by clicking on these links , all of these reports were submitted during their quarterly meeting on December 3 , 2020 , and are stored on the Health Resources & Services Administration government website .
So clearly the various “ fact checkers ” and Big Tech social media companies define “ real news ” as only what appears on the Big Pharma and government-endorsed corporate media outlets .
Anything outside of that is “ fake news ” to them if it disagrees with what they want you to @ @ @ @ @ @ @ do with the truth at all .
The $ 218 MILLION paid out for vaccine injuries and deaths this year was NOT paid by the pharmaceutical manufacturers .
It is funded from taxes paid on each vaccine , and as of September 30 , 2020 , that fund had a balance of over $ 4 BILLION .
( Source – p. 10 ) The other thing to understand is that these funds are paid on vaccines that have gone through the FDA full approval process , not fast-tracked vaccines approved for emergency use @ @ @ @ @ @ @ years to bring a new vaccine to market .
So none of these funds will be available to anyone who suffers injuries or dies due to the FDA fast-tracked for emergency use authorization ( EUA ) experimental COVID19 mRNA vaccine .
Injuries and deaths due to those vaccines fall under a different program , the CounterMeasures Injury Compensation Program ( CICP ) .
There are several differences between the NVICP and CICP : The CICP is designed to handle pandemic or other health emergency countermeasures as declared by the Secretary of HHS , @ @ @ @ @ @ @ spot initially for any injuries or deaths alleged as a result of receiving a COVID-19 vaccine .
First , the CICP does not allow the petitioner to seek reimbursement of attorney fees nor medical expert costs .
In the NVICP , these costs are reimbursable even when the petitioner loses as long as the initial claim was shown to have a reasonable basis .
These costs can run on average of $ 35,000 to $ 75,000 and as high as $ 300,000 .
I doubt if many petitioners can afford this cost out @ @ @ @ @ @ @ are basically on your own : just you and the Secretary of HHS .
A second reason is that when you submit your petition , copies of your medical records need to be included .
And that is all .
In the NVICP , generally your attorney will also submit research studies , expert reports to support your claim , but not so in the CICP .
A third reason is that if you are one of the very few who have been compensated in the CICP ( 8 % ) , there @ @ @ @ @ @ @ , and no award for loss of future wages .
There is in the NVICP , up to $ 250,000 for pain & suffering .
Currently , nearly 74 % of all claims are compensated in the NVICP , granted the vast majority are influenza vaccines administered to adults claiming shoulder injury or Guillain-Barre syndrome ( GBS ) .
A forth reason is that there is no judicial appeal process ; no higher court to appeal .
In the CICP , the appeal process is limited to appealing to the Secretary of HHS @ @ @ @ @ @ @ in the first place .
Renee Gentry , a Washington DC based attorney who practices in the NVICP , was quoted on my podcast Right on Point , with the following : “ In the CICP , you have the right to file a petition and lose.
” In short , your government is lying to you .
They have been telling the public for years that all vaccines are “ safe and effective , ” and that the “ science is settled.
” This lie is then proclaimed through the Pharma-funded corporate @ @ @ @ @ @ @ vigorously censored .
And this has always been for vaccines that went through the full , lengthy FDA approval process .
Why would you start believing them now when they are fully admitting that the new COVID vaccines are being fast-tracked , and that the mRNA vaccines are an entirely new class of vaccine never before distributed to the public ?
Comment on this article at VaccineImpact.com .
Having problems receiving our newsletters ?
See : How to Beat Internet Censorship and Create Your Own Newsfeed We Are Now on Parler and MeWe @ @ @ @ @ @ @ shut down , find us on Parler and MeWe for further instructions about where to find us .
Leaving a lucrative career as a nephrologist ( kidney doctor ) , Dr. Suzanne Humphries is now free to actually help cure people .
In this autobiography she explains why good doctors are constrained within the current corrupt medical system from practicing real , ethical medicine .
One of the sane voices when it comes to examining the science behind modern-day vaccines , no pro-vaccine extremist doctors have ever dared to debate her in public @ @ @ @ @ @ @ Big Pharma and government health authorities are trying to pass laws mandating vaccines for all children , and even adults .
Show your opposition to forced vaccinations and support the cause of Vaccine Impact , part of the Health Impact News network .

by Brian Shilhavy
Editor, Health Impact News
The federal government Advisory Commission on Childhood Vaccines (ACCV) under the U.S. Department of Health and Human Services met on December 3, 2020, and the Department of Justice reported that during a 3-month period from August 16th through November 15th this year, 166 cases of vaccine injuries were compensated through the National Vaccine Injury Compensation Program (NVICP).
You can read the full report here.
The NVICP was started as a result of a law passed in 1986 that gave pharmaceutical companies legal immunity from being sued due to injuries and deaths resulting from vaccines.
Today, anyone suffering from a vaccine injury or death must sue the U.S. Government and go up against their top attorneys.
In the fiscal year 2020 the NVICP has paid out $218 MILLION in damages due to vaccine injuries and deaths. (Source.)
Health Impact News is the only media source I am aware of that covers these quarterly meetings, and if we were to try and share articles like this one publishing these government reports, we would be accused of publishing “fake news.” (Previous reports are listed here.)
But as you can clearly see by clicking on these links, all of these reports were submitted during their quarterly meeting on December 3, 2020, and are stored on the Health Resources & Services Administration government website.
So clearly the various “fact checkers” and Big Tech social media companies define “real news” as only what appears on the Big Pharma and government-endorsed corporate media outlets. Anything outside of that is “fake news” to them if it disagrees with what they want you to know, and has absolutely nothing to do with the truth at all.
The $218 MILLION paid out for vaccine injuries and deaths this year was NOT paid by the pharmaceutical manufacturers. It is funded from taxes paid on each vaccine, and as of September 30, 2020, that fund had a balance of over $4 BILLION. (Source – p. 10)
The other thing to understand is that these funds are paid on vaccines that have gone through the FDA full approval process, not fast-tracked vaccines approved for emergency use. It typically takes 5 to 7 years to bring a new vaccine to market.
So none of these funds will be available to anyone who suffers injuries or dies due to the FDA fast-tracked for emergency use authorization (EUA) experimental COVID19 mRNA vaccine.
Injuries and deaths due to those vaccines fall under a different program, the CounterMeasures Injury Compensation Program (CICP).
There are several differences between the NVICP and CICP:
The CICP is designed to handle pandemic or other health emergency countermeasures as declared by the Secretary of HHS, and this will be the likely landing spot initially for any injuries or deaths alleged as a result of receiving a COVID-19 vaccine. First, the CICP does not allow the petitioner to seek reimbursement of attorney fees nor medical expert costs. In the NVICP, these costs are reimbursable even when the petitioner loses as long as the initial claim was shown to have a reasonable basis. These costs can run on average of $35,000 to $75,000 and as high as $300,000. I doubt if many petitioners can afford this cost out of their own pocket. So you are basically on your own: just you and the Secretary of HHS. A second reason is that when you submit your petition, copies of your medical records need to be included. And that is all. In the NVICP, generally your attorney will also submit research studies, expert reports to support your claim, but not so in the CICP. A third reason is that if you are one of the very few who have been compensated in the CICP (8%), there is no award for pain & suffering, and no award for loss of future wages. There is in the NVICP, up to $250,000 for pain & suffering. Currently, nearly 74% of all claims are compensated in the NVICP, granted the vast majority are influenza vaccines administered to adults claiming shoulder injury or Guillain-Barre syndrome (GBS). A forth reason is that there is no judicial appeal process; no higher court to appeal. In the CICP, the appeal process is limited to appealing to the Secretary of HHS who determined the fate of your petition in the first place. Renee Gentry, a Washington DC based attorney who practices in the NVICP, was quoted on my podcast Right on Point, with the following: “In the CICP, you have the right to file a petition and lose.” Think about that.
Read the full article here.
In short, your government is lying to you. They have been telling the public for years that all vaccines are “safe and effective,” and that the “science is settled.”
This lie is then proclaimed through the Pharma-funded corporate media, and any dissenting voices are vigorously censored.
And this has always been for vaccines that went through the full, lengthy FDA approval process.
Why would you start believing them now when they are fully admitting that the new COVID vaccines are being fast-tracked, and that the mRNA vaccines are an entirely new class of vaccine never before distributed to the public?
Comment on this article at VaccineImpact.com.
Book – The Vaccine Court “The Dark Truth of America’s Vaccine Injury Compensation Program” ORDER HERE!
See Also:
Understand the Times We are Currently Living Through
Leaving a lucrative career as a nephrologist (kidney doctor), Dr. Suzanne Humphries is now free to actually help cure people.
In this autobiography she explains why good doctors are constrained within the current corrupt medical system from practicing real, ethical medicine.
One of the sane voices when it comes to examining the science behind modern-day vaccines, no pro-vaccine extremist doctors have ever dared to debate her in public.
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100% Pre-shrunk Cotton
Order here!
Make a Statement for Health Freedom!
Big Pharma and government health authorities are trying to pass laws mandating vaccines for all children, and even adults.
Show your opposition to forced vaccinations and support the cause of Vaccine Impact, part of the Health Impact News network.
Order here!


healthimpactnews--2020-12-08--ER Medical Worker Treats Man Who Tried to Commit Suicide by Blowing His Brains Out – Appeals to Publ

ER Medical Worker Treats Man Who Tried to Commit Suicide by Blowing His Brains Out – Appeals to Public to Stop Complying with COVID Orders Like Masks Because Vaccines Are Next

A video going viral on Twitter earlier today featured a man who had just finished his shift in the hospital Emergency Room .
He is not identified in the video , but judging from the comments and someone who apparently knows him , he appears to be in Southern California somewhere .
They had just dealt with a patient who tried to kill himself by blowing his brains out , and is now brain dead .
He complains about how the mental abuse from COVID restrictions is harming way more people than any physical effects of COVID , and they @ @ @ @ @ @ @ kind of mental abuse than actual COVID cases .
He encourages everyone to stop watching the corporate news media on TV , which is brainwashing people right now to believe things that are not true about COVID .
He encourages everyone to stop complying with wearing a mask , because he believes that once they achieve full compliance on mask requirements to move around and participate in society , then they will pull a “ bait and switch ” on the public , and then start requiring that everyone be vaccinated with a @ @ @ @ @ @ @ in order to participate in society .
If this video becomes too popular , Twitter will probably remove it , so we put a copy on our Bitchute Channel .
To understand more fully how the corporate media on TV is brainwashing everyone , please watch the documentary “ Out of Shadows.
” It had tens of MILLIONS of views on YouTube before they removed it .

by Brian Shilhavy
Editor, Health Impact News
A video going viral on Twitter earlier today featured a man who had just finished his shift in the hospital Emergency Room. He is not identified in the video, but judging from the comments and someone who apparently knows him, he appears to be in Southern California somewhere.
They had just dealt with a patient who tried to kill himself by blowing his brains out, and is now brain dead.
He complains about how the mental abuse from COVID restrictions is harming way more people than any physical effects of COVID, and they are apparently seeing more cases from this kind of mental abuse than actual COVID cases.
He encourages everyone to stop watching the corporate news media on TV, which is brainwashing people right now to believe things that are not true about COVID.
He encourages everyone to stop complying with wearing a mask, because he believes that once they achieve full compliance on mask requirements to move around and participate in society, then they will pull a “bait and switch” on the public, and then start requiring that everyone be vaccinated with a dangerous vaccine that nobody actually needs, in order to participate in society.
If this video becomes too popular, Twitter will probably remove it, so we put a copy on our Bitchute Channel.
To understand more fully how the corporate media on TV is brainwashing everyone, please watch the documentary “Out of Shadows.” It had tens of MILLIONS of views on YouTube before they removed it.


healthimpactnews--2020-12-07--Former Medic Whistleblower Exposes How the Military is Testing Experimental Vaccines on Soldiers Usi

Former Medic Whistleblower Exposes How the Military is Testing Experimental Vaccines on Soldiers Using them as “Lab Rats”

With the new experimental fast-tracked COVID mRNA vaccines , a type of vaccine never before introduced to the general public , vaccine awareness and hesitancy is at an all-time high , and rightfully so .
However , for those of you just starting to investigate the issue of vaccines for the first time , you need to be aware that this is not a new issue , and many of us having been exposing the evil agendas behind vaccines for years .
I myself have covered this issue for a decade , while others have gone before me and have @ @ @ @ @ @ @ .
The U.S. military has been at the forefront of vaccine development for use in warfare , not “ public health , ” and they have a long history of testing experimental vaccines on our own troops .
When things go wrong and people are killed or harmed by these experimental vaccines , it is covered up , and often blamed on something else .
One of the first records of this happening was in 1918 , at Fort Riley , in Kansas , during WWI .
The soldiers were injected with an @ @ @ @ @ @ @ went horribly wrong , and a strain of bacterial pneumonia created a pandemic that ended up killing 50-100 million people .
You never heard about this ?
That ’ s because it was covered up and renamed “ the Spanish Flu.
” Kevin Barry has done a lot of research on this event , as he had family members die during this time , and you can read his research here : Did a Military Experimental Vaccine in 1918 Kill 50-100 Million People Blamed as “ Spanish Flu ” ?
In more recent @ @ @ @ @ @ @ backing up the fact that the military tested an experimental anthrax vaccine on our military members due to the alleged threat that Iraqi leader Saddam Hussein had “ weapons of mass destruction ” that were a threat to the U.S. Military , which were supposed to include anthrax .
We may never know how many of our military members died , or were permanently disabled due to this vaccine , but for years the military tried to cover it up as a “ mystery disease ” known as “ Gulf War Syndrome.
” @ @ @ @ @ @ @ testimony presented to the U.S. Congress , see : Gulf War Syndrome : Documents Prove UK and US Military Personnel were Injected with Untested Vaccines One medic who served in the military during this time has become a whistleblower , explaining the tragic story of how she found out that she was actually killing her fellow military members unknowingly with the anthrax vaccine .
After she determined that the anthrax vaccine was actually harming our troops , she took it up her chain of command .
But “ black suits ” were sent @ @ @ @ @ @ @ her and keep her quiet .
She is quiet no more .
While this was filmed in 2016 , it is actually FAR more relevant today as the world is on the precipice of starting a new , worldwide vaccine experiment with the COVID vaccines , and this can only be accomplished with the help of the military .
Therefore , military defectors may be our nation ’ s last hope to stop the COVID vaccine from destroying the lives of many people .
I am going to warn you right now , @ @ @ @ @ @ @ , and probably make you weep .
I cry every single time I watch it , knowing how many innocent lives were destroyed by this vaccine , and how evil our government has now become to have such a low value for human life .
Spread this video far and wide !
It could save many lives… This is the original YouTube version from Polly Tomney ’ s VAXXED channel , but we have copies on other platforms should it disappear .
Having problems receiving our newsletters ?
See : How to Beat @ @ @ @ @ @ @ We Are Now on Parler and MeWe !
If our website is seized and shut down , find us on Parler and MeWe for further instructions about where to find us .

by Brian Shilhavy
Editor, Health Impact News
With the new experimental fast-tracked COVID mRNA vaccines, a type of vaccine never before introduced to the general public, vaccine awareness and hesitancy is at an all-time high, and rightfully so.
However, for those of you just starting to investigate the issue of vaccines for the first time, you need to be aware that this is not a new issue, and many of us having been exposing the evil agendas behind vaccines for years.
I myself have covered this issue for a decade, while others have gone before me and have been covering this issue for many decades.
The U.S. military has been at the forefront of vaccine development for use in warfare, not “public health,” and they have a long history of testing experimental vaccines on our own troops.
When things go wrong and people are killed or harmed by these experimental vaccines, it is covered up, and often blamed on something else.
One of the first records of this happening was in 1918, at Fort Riley, in Kansas, during WWI. The soldiers were injected with an experimental bacterial meningitis vaccine.
The vaccine went horribly wrong, and a strain of bacterial pneumonia created a pandemic that ended up killing 50-100 million people.
You never heard about this? That’s because it was covered up and renamed “the Spanish Flu.”
Kevin Barry has done a lot of research on this event, as he had family members die during this time, and you can read his research here:
“Gulf War Syndrome”
In more recent times, there is now solid documentation backing up the fact that the military tested an experimental anthrax vaccine on our military members due to the alleged threat that Iraqi leader Saddam Hussein had “weapons of mass destruction” that were a threat to the U.S. Military, which were supposed to include anthrax.
We may never know how many of our military members died, or were permanently disabled due to this vaccine, but for years the military tried to cover it up as a “mystery disease” known as “Gulf War Syndrome.”
To learn more about this, including testimony presented to the U.S. Congress, see:
One medic who served in the military during this time has become a whistleblower, explaining the tragic story of how she found out that she was actually killing her fellow military members unknowingly with the anthrax vaccine.
After she determined that the anthrax vaccine was actually harming our troops, she took it up her chain of command. But “black suits” were sent from Washington D.C. to “re-educate” her and keep her quiet.
She is quiet no more. While this was filmed in 2016, it is actually FAR more relevant today as the world is on the precipice of starting a new, worldwide vaccine experiment with the COVID vaccines, and this can only be accomplished with the help of the military. Therefore, military defectors may be our nation’s last hope to stop the COVID vaccine from destroying the lives of many people.
I am going to warn you right now, that this video will deeply disturb you, and probably make you weep. I cry every single time I watch it, knowing how many innocent lives were destroyed by this vaccine, and how evil our government has now become to have such a low value for human life.
Spread this video far and wide! It could save many lives…
This is the original YouTube version from Polly Tomney’s VAXXED channel, but we have copies on other platforms should it disappear. (It has now been scrubbed from YouTube, so here is our Bitchute copy.)
See Also:
See Also:


healthimpactnews--2020-12-09--FDA Announces Deaths of Two Pfizer Vaccine Trial Participants as it Prepares to Issue Fast-track Aut

FDA Announces Deaths of Two Pfizer Vaccine Trial Participants as it Prepares to Issue Fast-track Authorization

The FDA released a 53-page “ briefing document ” for the experimental Pfizer COVID vaccine today in preparation for its December 10 , 2020 meeting to discuss giving emergency use authorization ( EUA ) for the vaccine to Pfizer , the world ’ s largest pharmaceutical criminal organization .
As is to be expected , the U.S. Pharma-controlled corporate media sang praises for Pfizer in the report in all of their press releases today , giving us a strong indication that the FDA is going to issue an EUA to Pfizer on Thursday .
When we look outside the U.S. @ @ @ @ @ @ @ see that other countries noticed the fact that people died during the Pfizer COVID vaccine trials , a detail completely left out of the U.S. press releases .
Of course , the FDA report claimed that the deaths had nothing to do with the vaccine , while offering no details or evidence to back up this claim .
You can read the report for yourself here .
An article published in The Jerusalem Post , for example , had this headline : FDA announces deaths of two Pfizer vaccine trial participants • Vaccines @ @ @ @ @ @ @ addition to the two deaths from the group receiving the COVID vaccine , four people in the “ placebo ” group also died during the trials .
Attempts by Health Impact News to find out what Pfizer used as a “ placebo ” have been unsuccessful .
This does not appear to be public knowledge .
If anyone knows , please contact us .
When conducting trials for new vaccines , an inert placebo , such as saline solution , is never used .
It is almost always another dangerous vaccine .
In @ @ @ @ @ @ @ trials , for example , when one of the participants from the “ placebo group ” died , it was revealed that the people in the placebo group were getting the meningitis vaccine , a vaccine that has had its own safety issues over the years with serious side effects .
Therefore , for the AstraZeneca COVID vaccine to appear “ safe ” it simply has to show that less people are injured or killed than the meningitis vaccine .
So what placebo did Pfizer use to try and make it look like @ @ @ @ @ @ @ Maybe the anthrax vaccine ?
?
The larger point here is that 6 people died in the vaccine trials , and you have to actually read the 53-page document to learn this , because the Pharma-funded corporate media will not report it .
Even with what they have reported here to the FDA to gain EUA authorization , why would anyone trust a drug company that is on record as having the largest FRAUD settlements in U.S. history with the DOJ ?
In 2009 they reached a fraud settlement with the U.S. Department @ @ @ @ @ @ @ the largest ever fraud settlement in the history of the DOJ at that time .
( Source . )
And they have continually been tried in court for FRAUD by the DOJ multiple times since 2009 !
As we have previously reported , all of these COVID vaccine trials are meaningless anyway , as they relied on the faulty PCR COVID test to determine results .
Doctors and scientists around the world have filed complaints and court documents demanding that these trials be halted and that these experimental vaccines not be approved because @ @ @ @ @ @ @ : “ Stay of Action ” Filed Against FDA to STOP Approval of COVID Vaccine for Using Faulty PCR Tests in Trials UK Government Warns Doctors About Infertility Possibility with Pfizer COVID Vaccine , But NO Warning to Patients !
DO NOT TRUST THE FDA !
The FDA will more than likely approve this dangerous experimental vaccine anyway , because they are simply an extension of the pharmaceutical industry , deriving most of their revenue from Big Pharma .
Scott Gottlieb now sits on the board of directors of Pfizer , and he @ @ @ @ @ @ @ .
No doubt current members of the FDA have also been promised lucrative careers in the pharmaceutical industry once they leave their government jobs , and therefore they are highly motivated to give Pfizer the green light to start mass vaccinating the public with their new COVID vaccine , which most certainly has not been proven either “ effective ” nor “ safe.
” The FDA ’ s own report issued today even admits that it can not guarantee the vaccine ’ s safety for immunocompromized groups , pregnant women and children .
@ @ @ @ @ @ @ guarantee that those receiving the vaccine will not be carriers of the virus , so social distancing , wearing masks , etc .
will still be enforced .
So who is going to line up and voluntarily receive this vaccine ?
The ignorant masses who only get their information from the pharma-funded corporate media .
Population reduction will soon be implemented at “ Warp Speed.
” Doctors Around the World Issue Dire WARNING : DO NOT GET THE COVID VACCINE !
!
Having problems receiving our newsletters ?
See : How to Beat @ @ @ @ @ @ @ We Are Now on Parler and MeWe !
If our website is seized and shut down , find us on Parler and MeWe for further instructions about where to find us .

by Brian Shilhavy
Editor, Health Impact News
The FDA released a 53-page “briefing document” for the experimental Pfizer COVID vaccine today in preparation for its December 10, 2020 meeting to discuss giving emergency use authorization (EUA) for the vaccine to Pfizer, the world’s largest pharmaceutical criminal organization.
As is to be expected, the U.S. Pharma-controlled corporate media sang praises for Pfizer in the report in all of their press releases today, giving us a strong indication that the FDA is going to issue an EUA to Pfizer on Thursday.
When we look outside the U.S. corporate media, however, we can see that other countries noticed the fact that people died during the Pfizer COVID vaccine trials, a detail completely left out of the U.S. press releases.
Of course, the FDA report claimed that the deaths had nothing to do with the vaccine, while offering no details or evidence to back up this claim. You can read the report for yourself here.
An article published in The Jerusalem Post, for example, had this headline:
In the UK, The Daily Mail is reporting that 4 of the people who received the Pfizer experimental COVID vaccine developed Bell’s Palsy, which paralyzes the face.
In addition to the two deaths from the group receiving the COVID vaccine, four people in the “placebo” group also died during the trials.
Attempts by Health Impact News to find out what Pfizer used as a “placebo” have been unsuccessful. This does not appear to be public knowledge. If anyone knows, please contact us.
When conducting trials for new vaccines, an inert placebo, such as saline solution, is never used. It is almost always another dangerous vaccine.
In the AstraZeneca and Oxford University COVID vaccine trials, for example, when one of the participants from the “placebo group” died, it was revealed that the people in the placebo group were getting the meningitis vaccine, a vaccine that has had its own safety issues over the years with serious side effects.
Therefore, for the AstraZeneca COVID vaccine to appear “safe” it simply has to show that less people are injured or killed than the meningitis vaccine.
So what placebo did Pfizer use to try and make it look like their vaccine was “safe?” Maybe the anthrax vaccine??
The larger point here is that 6 people died in the vaccine trials, and you have to actually read the 53-page document to learn this, because the Pharma-funded corporate media will not report it.
Even with what they have reported here to the FDA to gain EUA authorization, why would anyone trust a drug company that is on record as having the largest FRAUD settlements in U.S. history with the DOJ?
In 2009 they reached a fraud settlement with the U.S. Department of Justice for $2.3 BILLION, the largest ever fraud settlement in the history of the DOJ at that time. (Source.)
And they have continually been tried in court for FRAUD by the DOJ multiple times since 2009!
As we have previously reported, all of these COVID vaccine trials are meaningless anyway, as they relied on the faulty PCR COVID test to determine results. Doctors and scientists around the world have filed complaints and court documents demanding that these trials be halted and that these experimental vaccines not be approved because of these faulty COVID tests. See:
DO NOT TRUST THE FDA!
The FDA will more than likely approve this dangerous experimental vaccine anyway, because they are simply an extension of the pharmaceutical industry, deriving most of their revenue from Big Pharma.
Scott Gottlieb now sits on the board of directors of Pfizer, and he is the former director of the FDA. No doubt current members of the FDA have also been promised lucrative careers in the pharmaceutical industry once they leave their government jobs, and therefore they are highly motivated to give Pfizer the green light to start mass vaccinating the public with their new COVID vaccine, which most certainly has not been proven either “effective” nor “safe.”
The FDA’s own report issued today even admits that it cannot guarantee the vaccine’s safety for immunocompromized groups, pregnant women and children.
It also admits that it cannot guarantee that those receiving the vaccine will not be carriers of the virus, so social distancing, wearing masks, etc. will still be enforced.
So who is going to line up and voluntarily receive this vaccine?
The ignorant masses who only get their information from the pharma-funded corporate media. Population reduction will soon be implemented at “Warp Speed.”
See Also:
See Also:


healthimpactnews--2020-12-08--Doctors Around the World Issue Dire WARNING: DO NOT GET THE COVID VACCINE!!

In an effort to combat Big Pharma Corporate Media and Big Tech censorship , doctors around the world are frantically trying to warn the masses of the devastating effects of the experimental COVID vaccines about to be mass injected into the unsuspecting public assisted by military forces around the world .
What could possibly motivate these doctors , nurses , scientists , and other health professionals to make such an impassioned plea ?
What do they have to gain by taking the time to educate the public on the hidden dangers of a new class of vaccine about to be @ @ @ @ @ @ @ the world ?
They have NOTHING TO GAIN , and much to lose , including their careers , and possibly even their lives .
So why are they doing this ?
Why are these doctors and professionals being censored so much if the new COVID vaccines are in fact “ safe and effective ” ?
What is it that the media and the government are hiding that they don ’ t want the public to know ?
They are doing this because they are doctors and scientists who actually understand the REAL science @ @ @ @ @ @ @ potential consequences of those who choose to get this very toxic and dangerous vaccine , and they are trying to save as many people as possible from the carnage this vaccine is going to cause , which will include DEATH , brain injuries , life-long autoimmune disease , infertility , and more .
Please watch this video and their urgent pleas , and then share it with as many people as you can , because time is short !
Doctors for Truth : Tens of Thousands Medical Professionals Suing and Calling for End @ @ @ @ @ @ @ Weapons of Mass Destruction ” says Wyoming Medical Doctor and Manager for Wyoming ’ s State Public Health Department ( Trending ! )
Dr. Judy Mikovits and Dr. Sherri Tenpenny : A New COVID Vaccine Could Kill 50 Million People in the U.S. Censored Dr. Kaufman : “ They Want To Genetically Modify Us With COVID-19 Vaccine ” – Loses his Job and Willing to go to Jail to Resist Having problems receiving our newsletters ?
See : How to Beat Internet Censorship and Create Your Own Newsfeed We Are Now on Parler @ @ @ @ @ @ @ seized and shut down , find us on Parler and MeWe for further instructions about where to find us .

by Brian Shilhavy
Editor, Health Impact News
In an effort to combat Big Pharma Corporate Media and Big Tech censorship, doctors around the world are frantically trying to warn the masses of the devastating effects of the experimental COVID vaccines about to be mass injected into the unsuspecting public assisted by military forces around the world.
What could possibly motivate these doctors, nurses, scientists, and other health professionals to make such an impassioned plea? What do they have to gain by taking the time to educate the public on the hidden dangers of a new class of vaccine about to be inflicted upon the citizens of countries around the world?
They have NOTHING TO GAIN, and much to lose, including their careers, and possibly even their lives.
So why are they doing this? Why are these doctors and professionals being censored so much if the new COVID vaccines are in fact “safe and effective”? What is it that the media and the government are hiding that they don’t want the public to know?
They are doing this because they are doctors and scientists who actually understand the REAL science here, and who know the devastating potential consequences of those who choose to get this very toxic and dangerous vaccine, and they are trying to save as many people as possible from the carnage this vaccine is going to cause, which will include DEATH, brain injuries, life-long autoimmune disease, infertility, and more.
Please watch this video and their urgent pleas, and then share it with as many people as you can, because time is short!
From our Bitchute Channel and also on our Rumble Channel now.
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Over 11 MILLION Views!
COVID-19 “Vaccine” Casualties List
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healthimpactnews--2020-12-10--35,000 Soldiers Died from the Experimental Anthrax Vaccine – More Than Those Who Died in Combat in A

35,000 Soldiers Died from the Experimental Anthrax Vaccine – More Than Those Who Died in Combat in Afghanistan and Iraq Combined

Vaccine Syndrome is a film produced by Oscar nominated filmmaker Scott Miller , and provides exclusive interviews with military personnel who have had experience with the controversial anthrax vaccine .
The film claims that over 35,000 soldiers have died from the anthrax vaccine , according to a “ RAC-GWVI Government Report ” published in 2008 .
Compare that to how many soldiers have died in combat in both Iraq and Afghanistan , which is 6753 at the time of the filming .
The film starts out with a dramatized recreating of Lance Corporal Jared Schwartz , who refused to receive @ @ @ @ @ @ @ face a military tribunal without legal counsel , and read a prepared statement .
That statement can be found online , such as at the GulfWarVets.com website .
The film also mentions how pharmaceutical companies have legal immunity from any injuries or deaths resulting from vaccines , and that the civilian population only has recourse to sue the federal government in a special Vaccine Court .
However , military personnel are prohibited from suing in this court , which is part of the National Vaccine Compensation Program .
Watch the film here , @ @ @ @ @ @ @ Medic Whistleblower Exposes How the Military is Testing Experimental Vaccines on Soldiers Using them as “ Lab Rats ” Having problems receiving our newsletters ?
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Health Impact News
Vaccine Syndrome is a film produced by Oscar nominated filmmaker Scott Miller, and provides exclusive interviews with military personnel who have had experience with the controversial anthrax vaccine.
The film claims that over 35,000 soldiers have died from the anthrax vaccine, according to a “RAC-GWVI Government Report” published in 2008.
Compare that to how many soldiers have died in combat in both Iraq and Afghanistan, which is 6753 at the time of the filming.
The film starts out with a dramatized recreating of Lance Corporal Jared Schwartz, who refused to receive the anthrax vaccine.
He had to face a military tribunal without legal counsel, and read a prepared statement.
That statement can be found online, such as at the GulfWarVets.com website.
The film also mentions how pharmaceutical companies have legal immunity from any injuries or deaths resulting from vaccines, and that the civilian population only has recourse to sue the federal government in a special Vaccine Court.
However, military personnel are prohibited from suing in this court, which is part of the National Vaccine Compensation Program.
Watch the film here, or on our Bitchute Channel.
See Also:
See Also:


healthimpactnews--2020-12-09--“I Can’t Keep Watching Patients Die Needlessly!” Medical Professor Testifies to Congress that COVID

“I Can’t Keep Watching Patients Die Needlessly!” Medical Professor Testifies to Congress that COVID Cure Already Exists with Ivermectin

Dr. Pierre Kory M.D.
, a pulmonary and critical care specialist who is also an Associate Professor of Medicine at St. Luke ’ s Aurora Medical Center in Milwaukee , Wisconsin , pleaded with members of Congress to have the NIH , CDC , and FDA look at the “ mountains ” of data that he and his colleagues have gathered on the drug Ivermectin , which is already approved by the FDA as an anti-parasitic drug , and their success in treating COVID patients .
He states : “ If you take it , you will not get sick.
@ @ @ @ @ @ @ Frontline COVID-19 Critical Care Alliance ( FLCCC ) , and their success in treating patients with COVID has been so dramatic , that he referred to it as a “ miracle drug.
” Appearing as a witness Tuesday morning before the Senate Committee on Homeland Security and Governmental Affairs—which held a hearing on “ Early Outpatient Treatment : An Essential Part of a COVID-19 Solution ” — Dr. Pierre Kory , President of the Frontline COVID-19 Critical Care Alliance ( FLCCC ) , called for the government to swiftly review the already expansive @ @ @ @ @ @ @ Ivermectin .
The data shows the ability of the drug Ivermectin to prevent COVID-19 , to keep those with early symptoms from progressing to the hyper-inflammatory phase of the disease , and even to help critically ill patients recover .
Dr. Kory testified that Ivermectin is effectively a “ miracle drug ” against COVID-19 and called upon the government ’ s medical authorities—the NIH , CDC , and FDA—to urgently review the latest data and then issue guidelines for physicians , nurse-practitioners , and physician assistants to prescribe Ivermectin for COVID-19 .
The @ @ @ @ @ @ @ ) is comprised of some of the most highly published scientists in the world , with over 2000 peer-reviewed publications among them .
Dr. Kory states : I am severely troubled that the NIH , FDA , and CDC – I do not know of any task force that was assigned or compiled to review repurposed drugs in an attempt to treat this disease .
Everything has been about novel , and or expensive pharmaceutically engineered drugs ( like remdesivir and vaccines . )
We have a hundred years of medicine development .
@ @ @ @ @ @ @ medicines we use , and I do not know of a task force that has focused on repurposed drugs .
We have filled that void .
That is all we have done , focus on the things we know and the things we do .
We have a solution to this crisis .
There is a drug that is proving to be of miraculous impact .
And when I say “ miracle , ” I do not use that term lightly .
And I don ’ t want to be sensationalized when I @ @ @ @ @ @ @ recommendation based on MOUNTAINS of data that has emerged in the last 3 months .
Dr. Kory explains that the NIH recommendation NOT to use Ivermectin for COVID outside of clinical trials , was from August 27th , and that 3-4 months later , “ mountains ” of data have emerged from countries around the world showing the “ miraculous ” effectiveness of Ivermectin .
The most emotional part of Dr. Kory ’ s testimony was when he described what he was seeing in patients in the ICU .
I ’ ve cared @ @ @ @ @ @ @ can imagine .
They ’ re dying because they can not breathe .
I watch them every day .
They die .
By the time they get to me in the ICU , they are already dying .
They ’ re almost impossible to recover .
Early treatment is key .
We need to offload the hospitals .
We are tired .
I can ’ t keep doing this .
If you look at my manuscript , and if I have to go back to work next week , any further deaths are @ @ @ @ @ @ @ I can not be traumatized by that .
I can not keep caring for patients when I know that they could have been saved with earlier treatment .
And that drug that will treat them and prevent the hospitalization is Ivermectin .
Watch the full testimony .
This is on YouTube , but if it disappears , we have a copy on our Bitchute channel as well .
The U.S. Government and Big Pharma Are Guilty of Mass Murder !
This is now the second group of physicians who treat COVID patients that @ @ @ @ @ @ @ treating and healing COVID patients with a near 100 % success rate with older drugs that have already been approved by the FDA to the politicians sitting in Washington D.C .
The first group was the group called “ Frontline Doctors ” who presented their evidence for hydroxychloroquine , and their nearly 100 % success rate in treating patients and not having to send them to the hospitals .
Learn more about the Frontline Doctors and the hydroxychloroquine scandal here .
The U.S. Government is clearly guilty of mass murder !
The two @ @ @ @ @ @ @ of tens of thousands if not hundreds of thousands of American lives are FDA Director Stephen Hahn and NIAID Director Anthony Fauci .
These two men and others who serve with them have pushed to get new drugs to market instead , and now are poised to unleash a dangerous , fast-tracked COVID vaccine never before seen in the human population .
And the ONLY way they could approve these new drugs and vaccines , was to LIE about effective cures that already exist , which means all of these new drugs and @ @ @ @ @ @ @ Let ’ s not beat around the bush and let ’ s call this what it really is : Crimes Against Humanity !
Both of these men , and many others , need to be arrested for mass murder , tried in a court of law with a jury of their peers , and then executed by sentence of DEATH !
And for those of you still supporting President Donald Trump , who not only is allowing this to happen but encouraging it by rushing dangerous vaccines to market at “ Warp Speed @ @ @ @ @ @ @ how can you keep looking the other way when thousands of people are dying needlessly ?
?
Doctors Around the World Issue Dire WARNING : DO NOT GET THE COVID VACCINE !
!
Having problems receiving our newsletters ?
See : How to Beat Internet Censorship and Create Your Own Newsfeed We Are Now on Parler and MeWe !
If our website is seized and shut down , find us on Parler and MeWe for further instructions about where to find us .

by Brian Shilhavy
Editor, Health Impact News
Dr. Pierre Kory M.D., a pulmonary and critical care specialist who is also an Associate Professor of Medicine at St. Luke’s Aurora Medical Center in Milwaukee, Wisconsin, pleaded with members of Congress to have the NIH, CDC, and FDA look at the “mountains” of data that he and his colleagues have gathered on the drug Ivermectin, which is already approved by the FDA as an anti-parasitic drug, and their success in treating COVID patients.
He states: “If you take it, you will not get sick.”
Dr. Kory is president of the Frontline COVID-19 Critical Care Alliance (FLCCC), and their success in treating patients with COVID has been so dramatic, that he referred to it as a “miracle drug.”
From the organization’s website:
Appearing as a witness Tuesday morning before the Senate Committee on Homeland Security and Governmental Affairs—which held a hearing on “Early Outpatient Treatment: An Essential Part of a COVID-19 Solution”— Dr. Pierre Kory, President of the Frontline COVID-19 Critical Care Alliance (FLCCC), called for the government to swiftly review the already expansive and still rapidly emerging medical evidence on Ivermectin. The data shows the ability of the drug Ivermectin to prevent COVID-19, to keep those with early symptoms from progressing to the hyper-inflammatory phase of the disease, and even to help critically ill patients recover. Dr. Kory testified that Ivermectin is effectively a “miracle drug” against COVID-19 and called upon the government’s medical authorities—the NIH, CDC, and FDA—to urgently review the latest data and then issue guidelines for physicians, nurse-practitioners, and physician assistants to prescribe Ivermectin for COVID-19.
The Frontline COVID-19 Critical Care Alliance (FLCCC) is comprised of some of the most highly published scientists in the world, with over 2000 peer-reviewed publications among them. Dr. Kory states:
I am severely troubled that the NIH, FDA, and CDC – I do not know of any task force that was assigned or compiled to review repurposed drugs in an attempt to treat this disease. Everything has been about novel, and or expensive pharmaceutically engineered drugs (like remdesivir and vaccines.) We have a hundred years of medicine development. We are experts in all of the medicines we use, and I do not know of a task force that has focused on repurposed drugs. We have filled that void. That is all we have done, focus on the things we know and the things we do. We have a solution to this crisis. There is a drug that is proving to be of miraculous impact. And when I say “miracle,” I do not use that term lightly. And I don’t want to be sensationalized when I say that. That is a scientific recommendation based on MOUNTAINS of data that has emerged in the last 3 months.
Dr. Kory explains that the NIH recommendation NOT to use Ivermectin for COVID outside of clinical trials, was from August 27th, and that 3-4 months later, “mountains” of data have emerged from countries around the world showing the “miraculous” effectiveness of Ivermectin.
It basically obliterates transmission of this virus. If you take it, you will not get sick.
The most emotional part of Dr. Kory’s testimony was when he described what he was seeing in patients in the ICU.
I’m a lung specialist. I’m an ICU specialist. I’ve cared for more dying COVID patients than anyone can imagine. They’re dying because they cannot breathe. I watch them every day. They die. By the time they get to me in the ICU, they are already dying. They’re almost impossible to recover. Early treatment is key. We need to offload the hospitals. We are tired. I can’t keep doing this. If you look at my manuscript, and if I have to go back to work next week, any further deaths are going to be needless deaths. And I cannot be traumatized by that. I cannot keep caring for patients when I know that they could have been saved with earlier treatment. And that drug that will treat them and prevent the hospitalization is Ivermectin.
Watch the full testimony. We have a copy on our Bitchute channel as well.
The U.S. Government and Big Pharma Are Guilty of Mass Murder!
This is now the second group of physicians who treat COVID patients that have presented their evidence and experience in treating and healing COVID patients with a near 100% success rate with older drugs that have already been approved by the FDA to the politicians sitting in Washington D.C.
The first group was the group called “Frontline Doctors” who presented their evidence for hydroxychloroquine, and their nearly 100% success rate in treating patients and not having to send them to the hospitals.
Learn more about the Frontline Doctors and the hydroxychloroquine scandal here.
The U.S. Government is clearly guilty of mass murder! The two main bureaucrat doctors responsible for the deaths of tens of thousands if not hundreds of thousands of American lives are FDA Director Stephen Hahn and NIAID Director Anthony Fauci.
These two men and others who serve with them have pushed to get new drugs to market instead, and now are poised to unleash a dangerous, fast-tracked COVID vaccine never before seen in the human population.
And the ONLY way they could approve these new drugs and vaccines, was to LIE about effective cures that already exist, which means all of these new drugs and vaccines developed for COVID are ILLEGAL!
Let’s not beat around the bush and let’s call this what it really is: Crimes Against Humanity!
Both of these men, and many others, need to be arrested for mass murder, tried in a court of law with a jury of their peers, and then executed by sentence of DEATH!
And for those of you still supporting President Donald Trump, who not only is allowing this to happen but encouraging it by rushing dangerous vaccines to market at “Warp Speed” when nobody needs these vaccines, how can you keep looking the other way when thousands of people are dying needlessly??
See Also:
See Also:


healthimpactnews--2020-12-10--Life-Threatening Reactions to Pfizer COVID Experimental Vaccines Results in Warnings to People Who H

Life-Threatening Reactions to Pfizer COVID Experimental Vaccines Results in Warnings to People Who Have Allergies

Breaking : CHD Responds to News of Life-Threatening Reaction to Pfizer COVID Vaccine .
Will Regulators Take Action ?
In August , CHD asked regulators to investigate the use of polyethylene glycol ( PEG ) in COVID mRNA vaccines , which could have caused the severe allergic reactions reported this week by two of the first UK recipients of Pfizer ’ s vaccine .
Media outlets are reporting that two individuals who received the Pfizer-BioNTech COVID-19 mRNA vaccine developed severe anaphylactic reactions following the injection .
England ’ s National Health Service ( NHS ) warned Wednesday that people “ @ @ @ @ @ @ @ reaction to a vaccine , medicine or food ” should not be given the COVID-19 vaccine developed by U.S. pharmaceutical giant Pfizer and Germany ’ s BioNTech .
UK ’ s Medical and Health products Regulatory Agency , as reported by The Wall Street Journal , reminded health-care workers that vaccinations should only be carried out in facilities where resuscitation measures are available .
These warnings came after two National Health Service employees who were part of the first tranche to receive the vaccine on Tuesday suffered adverse reactions .
NHS England said @ @ @ @ @ @ @ medical workers who experienced anaphylactoid reactions to the Pfizer vaccine had a “ strong past history of allergic reactions.
” According to these news reports , documents published by the two companies showed that people with a history of severe allergic reactions were excluded from the clinical trials .
Therefore , this life-threatening adverse safety signal did not appear in their clinical trial safety data .
On Aug. 26 , Children ’ s Health Defense ( CHD ) sent a letter to Dr. Jerry Menikoff , director office for Human Research Protections Dept @ @ @ @ @ @ @ the Phase III Moderna mRNA-1273 vaccine .
The letter requested the Office for Human Research Protections investigate the use of polyethylene glycol ( PEG ) in Moderna ’ s COVID-19 mRNA vaccine .
Pfizer ’ s COVID vaccine , which also uses mRNA technology , also contains PEG .
Approximately 8 % of the U.S. population has highly elevated levels of anti-PEG antibodies .
The concerns we laid out in our letter about the Moderna vaccine were related to the fact that injecting a PEG-containing vaccine into individuals with pre-existing PEG antibodies could @ @ @ @ @ @ @ the case with a member of CHD , Harold Gielow , a retired military Lt. Col USMC who suffers with severe anaphylactic response to polyethylene glycol .
In fact , the last time Gielow was exposed to an injected drug that contained PEG , he went pulseless , requiring an injection of epinephrine .
His PEG allergy was diagnosed by Johns Hopkins .
Gielow has voiced outrage that PEG is classified by U.S. Food and Drug Administration ( FDA ) as biologically inert/inactive .
In fact , investigators who once assumed that the @ @ @ @ @ @ @ now questioning its biocompatibility and warning about PEGylated particles ’ promotion of tumor growth and adverse immune responses that include “ probably underdiagnosed ” life-threatening anaphylaxis .
These undesirable responses have , on occasion , halted clinical trials .
As a result , some scientists argue that it is time to develop alternatives to replace PEG .
American and Dutch researchers declared in 2013 : Dr. Menikoff recommended that our concerns be sent to Dr. Steven Hahn , director of the FDA and Dr. Marks , director of the FDA Center for Biologics @ @ @ @ @ @ @ 25 , the letter was sent and included with a cc to Dr. Anthony Fauci , director of the National Institute of Allergy and Infectious Diseases .
On Dec. 2 , we received a response from Dr. Hahn and Dr. Marks with a recommendation that we reach out directly to the mRNA vaccine manufacturers regarding our concerns with the use of PEG in their vaccines .
What is concerning about the response is the fact that in the letter we acknowledge that we had already reached out to Moderna ’ s scientists regarding @ @ @ @ @ @ @ informing vaccine trial recipients about the use of PEG in the vaccine , soliciting a history of PEG allergies and testing blood antibody levels to PEG .
Did the FDA officials actually read the letter ?
CHD ’ s concerns about PEG stem from the fact that PEG-specific immune responses can actually reduce the efficacy of vaccines and increase the occurrence of adverse events .
A 2016 study in Analytical Chemistry reported detectable and sometimes high levels of anti-PEG antibodies ( including first-line-of-defense IgM antibodies and later stage IgG antibodies ) in approximately @ @ @ @ @ @ @ about 56 % of historical specimens from the 1970s through the 1990s .
Of the 72 % with PEG IgG antibodies , 8 % had anti-PEG IgG antibodies > 500ng/ml.
, which is considered extremely elevated .
Extrapolated to the U.S. population of 330 million who may receive this vaccine , 16.6 million may have antibody levels associated with adverse effects .
The researchers confessed that the results were entirely unexpected .
The authors concluded that : On July 28 , Gielow wrote to CovPN citing the 2016 study ’ s conclusions and @ @ @ @ @ @ @ from CovPN was as follows : While the Moderna scientists allege that PEG antibody development is purely hypothetical , the scientific literature clearly documents that the immune system can and does form antibodies against PEG ( anti-PEG Abs ) in both animals and humans .
The existence of anti-PEG antibodies threatens patient safety through possible anaphylaxis reactions and re-exposure to PEG-containing drugs may greatly increase the chance for adverse effects due to B cell memory of anti-PEG Abs .
Thus , screening for and monitoring the levels of anti-PEG antibodies in blood before @ @ @ @ @ @ @ of particular importance to improve safety and maintain therapeutic efficacy .
The 2016 Analytical Chemistry findings and other studies indicate the widespread occurrence of anti-PEG Abs in the general population due to daily exposure to PEG-containing products .
The population ’ s increased exposure to PEG-containing products makes it “ natural to assume ” that anti-PEG antibodies will continue to be widespread.
” If high-titer anti-PEG Abs are present in blood , even people without known allergies may have severe hypersensitivity reactions when receiving PEG-containing therapeutics for the first time .
Moderna documents @ @ @ @ @ @ @ well aware of safety risks associated with PEG and other aspects of its mRNA technology .
In the corporate prospectus supporting Moderna ’ s stock market launch in late 2018 , the company was frank that its technical approach has numerous risks .
Specifically , Moderna acknowledged the potential for its proprietary lipid nanoparticles and PEG to produce “ systemic side effects , ” given the scientific literature ’ s documentation of these types of side effects for other LNPs .
In comments not generally seen by the public , Moderna stated ( @ @ @ @ @ @ @ concern over clinical trial participants ’ welfare , that section of the prospectus concluded that any one of these problems “ could materially harm [ the company ’ s ] business , financial conditions and prospects.
” As the excerpts from the Moderna prospectus illustrate , Moderna scientists are fully aware of PEG-related safety concerns .
In the prospectus , Moderna admits that “ unacceptable health risks or adverse side effects ” could make it difficult to recruit or retain clinical trial participants and also that an “ unfavorable benefit risk ratio could @ @ @ @ @ @ @ proceeds to market .
Addressing the efficacy side of the equation , a mid-2019 study by authors who “ are or have been employees of Moderna , Inc. and receive salary and stock options from Moderna , Inc. ” further admitted that anti-PEG antibodies “ present significant challenges to the clinical efficacy of PEGylated therapeutics and will require strategies to overcome [ their ] effects.
” In light of the recent acknowledgement of anaphylactic reactions to Pfizers ’ PEG-containing COVID-19 vaccine , CHD continues to have grave safety and efficacy concerns about the @ @ @ @ @ @ @ the high percentage of the population having preexisting antibodies to PEG .
While it ’ s unlikely that everyone with pre-existing PEG antibodies will have a severe reaction to a vaccine containing PEG , it is dangerous to assume that none will .
While vaccine manufacturers and federal agencies providing oversight on COVID vaccine development are quick to point out that the clinical trials did not identify safety concerns with the vaccine , they fail to mention the fact that the trial participants were excluded from the study if they had a history @ @ @ @ @ @ @ the trial were never screened for PEG antibodies .
Multiple previous studies regarding the prevalence of anti-PEG antibodies in the population have stated that pre-screening should be done prior to any administration of a PEG-containing medication .
Screening is likely to be even more important in the case of a vaccine intended for parenteral administration to as many people as possible that contains a substance to which the majority of the population unknowingly has antibodies .
Not characterizing trial participants ’ adverse reactions in relation to anti-PEG antibody presence and levels eliminates insights @ @ @ @ @ @ @ to prevent harmful adverse events .
Now we are left in a situation where life-threatening adverse events are occurring after widespread use of the vaccine has begun .
A finger needs to be pointed squarely at the vaccine manufacturers and regulatory agencies who buried their heads in the sand to legitimate safety concerns in their rush to approve a COVID vaccine .
Unfortunately , the public is now left to bear the burden of exposing these lapses in safety .
The views and opinions expressed in this article are those of the authors @ @ @ @ @ @ @ of Children ’ s Health Defense .
Lyn Redwood , RN , MSN – Lyn Redwood , R.N.
, M.S.N.
, is a Nurse Practitioner who became involved in autism research and advocacy when her son was diagnosed with autism .
In 1999 she calculated the level of mercury exposure received from multiple thimerosal ( mercury ) containing vaccines and found her son was exposed to levels 125 times EPA Federal Safety guidelines and suffered with mercury toxicity .
Since that time , Ms. Redwood has testified before the Government Reform Committee on @ @ @ @ @ @ @ taking unnecessary risks ?
” and before a subcommittee on Human Rights and Wellness , “ Truth revealed : New scientific discoveries regarding mercury in medicine and autism health in 2004.
” Having problems receiving our newsletters ?
See : How to Beat Internet Censorship and Create Your Own Newsfeed We Are Now on Parler and MeWe !
If our website is seized and shut down , find us on Parler and MeWe for further instructions about where to find us .
Unmasking Who is Behind the Plandemic and Rioting to Usher in @ @ @ @

Breaking: CHD Responds to News of Life-Threatening Reaction to Pfizer COVID Vaccine. Will Regulators Take Action?
In August, CHD asked regulators to investigate the use of polyethylene glycol (PEG) in COVID mRNA vaccines, which could have caused the severe allergic reactions reported this week by two of the first UK recipients of Pfizer’s vaccine.
by Lyn Redwood, RN, MSN
Children’s Health Defense
Media outlets are reporting that two individuals who received the Pfizer-BioNTech COVID-19 mRNA vaccine developed severe anaphylactic reactions following the injection.
England’s National Health Service (NHS) warned Wednesday that people “with a history of a significant allergic reaction to a vaccine, medicine or food” should not be given the COVID-19 vaccine developed by U.S. pharmaceutical giant Pfizer and Germany’s BioNTech.
UK’s Medical and Health products Regulatory Agency, as reported by The Wall Street Journal, reminded health-care workers that vaccinations should only be carried out in facilities where resuscitation measures are available.
These warnings came after two National Health Service employees who were part of the first tranche to receive the vaccine on Tuesday suffered adverse reactions.
NHS England said in a statement that both of the medical workers who experienced anaphylactoid reactions to the Pfizer vaccine had a “strong past history of allergic reactions.”
According to these news reports, documents published by the two companies showed that people with a history of severe allergic reactions were excluded from the clinical trials. Therefore, this life-threatening adverse safety signal did not appear in their clinical trial safety data.
On Aug. 26, Children’s Health Defense (CHD) sent a letter to Dr. Jerry Menikoff, director office for Human Research Protections Dept. of Health and Human Services regarding the Phase III Moderna mRNA-1273 vaccine. The letter requested the Office for Human Research Protections investigate the use of polyethylene glycol (PEG) in Moderna’s COVID-19 mRNA vaccine. Pfizer’s COVID vaccine, which also uses mRNA technology, also contains PEG.
Approximately 8% of the U.S. population has highly elevated levels of anti-PEG antibodies. The concerns we laid out in our letter about the Moderna vaccine were related to the fact that injecting a PEG-containing vaccine into individuals with pre-existing PEG antibodies could lead to life-threatening anaphylaxis.
Such was the case with a member of CHD, Harold Gielow, a retired military Lt. Col USMC who suffers with severe anaphylactic response to polyethylene glycol. In fact, the last time Gielow was exposed to an injected drug that contained PEG, he went pulseless, requiring an injection of epinephrine. His PEG allergy was diagnosed by Johns Hopkins.
Gielow has voiced outrage that PEG is classified by U.S. Food and Drug Administration (FDA) as biologically inert/inactive.
“It is anything but that,” Gielow said. “The incidences of hypersensitivity reactions to PEG are, understandably, increasing, although many with PEG hypersensitivity go undiagnosed, thus presenting an unreasonable hazard to administering these vaccines to a population, the vast majority of which is proven by science to have anti-PEG antibodies.”
In fact, investigators who once assumed that the polymer was largely “inert” are now questioning its biocompatibility and warning about PEGylated particles’ promotion of tumor growth and adverse immune responses that include “probably underdiagnosed” life-threatening anaphylaxis.
These undesirable responses have, on occasion, halted clinical trials. As a result, some scientists argue that it is time to develop alternatives to replace PEG. American and Dutch researchers declared in 2013:
“[T]he accumulating evidence documenting the detrimental effects of PEG on drug delivery make it imperative that scientists in this field break their dependence on PEGylation.”
Dr. Menikoff recommended that our concerns be sent to Dr. Steven Hahn, director of the FDA and Dr. Marks, director of the FDA Center for Biologics Evaluation and Research. On Sept, 25, the letter was sent and included with a cc to Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases.
On Dec. 2, we received a response from Dr. Hahn and Dr. Marks with a recommendation that we reach out directly to the mRNA vaccine manufacturers regarding our concerns with the use of PEG in their vaccines.
What is concerning about the response is the fact that in the letter we acknowledge that we had already reached out to Moderna’s scientists regarding the use of PEG and lack of informing vaccine trial recipients about the use of PEG in the vaccine, soliciting a history of PEG allergies and testing blood antibody levels to PEG.
Did the FDA officials actually read the letter?
CHD’s concerns about PEG stem from the fact that PEG-specific immune responses can actually reduce the efficacy of vaccines and increase the occurrence of adverse events.
A 2016 study in Analytical Chemistry reported detectable and sometimes high levels of anti-PEG antibodies (including first-line-of-defense IgM antibodies and later stage IgG antibodies) in approximately 72% of contemporary human samples and about 56% of historical specimens from the 1970s through the 1990s. Of the 72% with PEG IgG antibodies, 8% had anti-PEG IgG antibodies > 500ng/ml., which is considered extremely elevated. Extrapolated to the U.S. population of 330 million who may receive this vaccine, 16.6 million may have antibody levels associated with adverse effects.
The researchers confessed that the results were entirely unexpected. The authors concluded that:
“…sensitive detection and precise quantitation of anti-PEG Ab levels in a clinical setting will be essential to ensuring the safe use of PEGylated drugs in all target patient populations going forward.”
On July 28, Gielow wrote to CovPN citing the 2016 study’s conclusions and asked the following question:
“As Moderna’s mRNA-1273 candidate vaccine uses a PEGylated LNP vector, what procedures are included in the trial to mitigate this risk?”
The response from CovPN was as follows:
“Thank you so much for this scientific question. I consulted with several of the physician scientists working on the Moderna study, and they have provided me with this response to send on to you: “Pre-existing antibody levels, along with various genetic polymorphisms, may impact the safety profile of a biomedical intervention in a variety of populations. If there are significant safety signals from the CoVPN clinical trials, all efforts will be made to understand the mechanisms that may have contributed to these signals. Pre-screening populations based on hypothesized biomarkers, such as anti-PEG antibodies, is not a strategy currently employed in our clinical trials.”
While the Moderna scientists allege that PEG antibody development is purely hypothetical, the scientific literature clearly documents that the immune system can and does form antibodies against PEG (anti-PEG Abs) in both animals and humans.
The existence of anti-PEG antibodies threatens patient safety through possible anaphylaxis reactions and re-exposure to PEG-containing drugs may greatly increase the chance for adverse effects due to B cell memory of anti-PEG Abs.
Thus, screening for and monitoring the levels of anti-PEG antibodies in blood before and during treatment with PEG-containing drugs are of particular importance to improve safety and maintain therapeutic efficacy.
The 2016 Analytical Chemistry findings and other studies indicate the widespread occurrence of anti-PEG Abs in the general population due to daily exposure to PEG-containing products. The population’s increased exposure to PEG-containing products makes it “natural to assume” that anti-PEG antibodies will continue to be widespread.”
If high-titer anti-PEG Abs are present in blood, even people without known allergies may have severe hypersensitivity reactions when receiving PEG-containing therapeutics for the first time.
Moderna documents and publications indicate that the company is well aware of safety risks associated with PEG and other aspects of its mRNA technology. In the corporate prospectus supporting Moderna’s stock market launch in late 2018, the company was frank that its technical approach has numerous risks.
Specifically, Moderna acknowledged the potential for its proprietary lipid nanoparticles and PEG to produce “systemic side effects,” given the scientific literature’s documentation of these types of side effects for other LNPs. In comments not generally seen by the public, Moderna stated (p. 33):
[T]here can be no assurance that our LNPs will not have undesired effects. Our LNPs could contribute, in whole or in part, to one or more of the following: immune reactions, infusion reactions, complement reactions, opsonization reactions, [links added] antibody reactions . . . or reactions to the PEG from some lipids or PEG otherwise associated with the LNP. Certain aspects of our investigational medicines may induce immune reactions from either the mRNA or the lipid as well as adverse reactions within liver pathways or degradation of the mRNA or the LNP, any of which could lead to significant adverse events in one or more of our clinical trials.
Instead of expressing concern over clinical trial participants’ welfare, that section of the prospectus concluded that any one of these problems “could materially harm [the company’s] business, financial conditions and prospects.”
As the excerpts from the Moderna prospectus illustrate, Moderna scientists are fully aware of PEG-related safety concerns. In the prospectus, Moderna admits that “unacceptable health risks or adverse side effects” could make it difficult to recruit or retain clinical trial participants and also that an “unfavorable benefit risk ratio could inhibit market acceptance” if their product proceeds to market. Addressing the efficacy side of the equation, a mid-2019 study by authors who “are or have been employees of Moderna, Inc. and receive salary and stock options from Moderna, Inc.” further admitted that anti-PEG antibodies “present significant challenges to the clinical efficacy of PEGylated therapeutics and will require strategies to overcome [their] effects.” In light of the recent acknowledgement of anaphylactic reactions to Pfizers’ PEG-containing COVID-19 vaccine, CHD continues to have grave safety and efficacy concerns about the use of PEG in vaccines due to the high percentage of the population having preexisting antibodies to PEG. While it’s unlikely that everyone with pre-existing PEG antibodies will have a severe reaction to a vaccine containing PEG, it is dangerous to assume that none will. While vaccine manufacturers and federal agencies providing oversight on COVID vaccine development are quick to point out that the clinical trials did not identify safety concerns with the vaccine, they fail to mention the fact that the trial participants were excluded from the study if they had a history of severe allergic reactions and those in the trial were never screened for PEG antibodies. Multiple previous studies regarding the prevalence of anti-PEG antibodies in the population have stated that pre-screening should be done prior to any administration of a PEG-containing medication. Screening is likely to be even more important in the case of a vaccine intended for parenteral administration to as many people as possible that contains a substance to which the majority of the population unknowingly has antibodies. Not characterizing trial participants’ adverse reactions in relation to anti-PEG antibody presence and levels eliminates insights into these interactions is a missed opportunity to prevent harmful adverse events. Now we are left in a situation where life-threatening adverse events are occurring after widespread use of the vaccine has begun. A finger needs to be pointed squarely at the vaccine manufacturers and regulatory agencies who buried their heads in the sand to legitimate safety concerns in their rush to approve a COVID vaccine. Unfortunately, the public is now left to bear the burden of exposing these lapses in safety.
The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children’s Health Defense.
Lyn Redwood, RN, MSN – Lyn Redwood, R.N., M.S.N., is a Nurse Practitioner who became involved in autism research and advocacy when her son was diagnosed with autism. In 1999 she calculated the level of mercury exposure received from multiple thimerosal (mercury) containing vaccines and found her son was exposed to levels 125 times EPA Federal Safety guidelines and suffered with mercury toxicity. Since that time, Ms. Redwood has testified before the Government Reform Committee on “Mercury in medicine: Are we taking unnecessary risks?” and before a subcommittee on Human Rights and Wellness, “Truth revealed: New scientific discoveries regarding mercury in medicine and autism health in 2004.”
Read the full article at Children’s Health Defense.
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healthimpactnews--2020-12-10--New York State Assembly Introduces Bill Mandating COVID-19 Vaccine

New Yorkers will no longer get to decide if they will receive a COVID-19 vaccine if a bill calling for a mandatory vaccine gets approved .
New York State Assemblywoman Linda Rosenthal , a Democrat who represents New York ’ s 67th Assembly District , quietly introduced a bill on Dec. 4 that would require “ COVID-19 vaccine to be administered in accordance with the department of health ’ s COVID-19 vaccination administration program and mandates vaccination in certain situations.
” Every New Yorker , except those medically exempt , are required to receive the vaccine if the state ’ @ @ @ @ @ @ @ sufficient immunity from COVID-19.
” Barbara Loe Fisher , cofounder and president of the National Vaccine Information Center , described the legislation as inappropriate .
“ It is inappropriate for public health officials and state legislators to be introducing legislation that mandates use of an experimental vaccine being considered for release under an Emergency Use Authorization ( EUA ) , ” Fisher told The Epoch Times in an email .
“ Until a COVID-19 vaccine is formally licensed by the FDA and recommended for use by certain populations by the CDC , it @ @ @ @ @ @ @ said .
“ This kind of bill sends the wrong message to the public.
” The National Vaccine Information Center is a nonprofit organization that publishes “ information on diseases and vaccine science , policy , law and the ethical principle of informed consent.
” Read the full article at The Epoch Times .
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Unmasking Who is Behind the Plandemic and Rioting to Usher in the New World Order

by Meiling Lee
The Epoch Times
Excerpts:
New Yorkers will no longer get to decide if they will receive a COVID-19 vaccine if a bill calling for a mandatory vaccine gets approved.
New York State Assemblywoman Linda Rosenthal, a Democrat who represents New York’s 67th Assembly District, quietly introduced a bill on Dec. 4 that would require “COVID-19 vaccine to be administered in accordance with the department of health’s COVID-19 vaccination administration program and mandates vaccination in certain situations.”
Every New Yorker, except those medically exempt, are required to receive the vaccine if the state’s vaccination efforts do not achieve “sufficient immunity from COVID-19.”
Barbara Loe Fisher, cofounder and president of the National Vaccine Information Center, described the legislation as inappropriate.
“It is inappropriate for public health officials and state legislators to be introducing legislation that mandates use of an experimental vaccine being considered for release under an Emergency Use Authorization (EUA),” Fisher told The Epoch Times in an email. “Until a COVID-19 vaccine is formally licensed by the FDA and recommended for use by certain populations by the CDC, it remains an experimental vaccine,” she said. “This kind of bill sends the wrong message to the public.”
The National Vaccine Information Center is a nonprofit organization that publishes “information on diseases and vaccine science, policy, law and the ethical principle of informed consent.”
Read the full article at The Epoch Times.
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healthimpactnews--2020-12-10--CNN: ‘Don’t Be Alarmed’ if People Start Dying After Taking the COVID Vaccine

In an article on the COVID vaccine rollout , CNN says that Americans shouldn ’ t be alarmed if people start dying after taking the vaccine because “ deaths may occur that won ’ t necessarily have anything to do with the vaccine.
” The advisory appeared in an article titled ‘ Why vaccinate our most frail ?
Odd vote out shows the dilemma ’ in which Dr. Kelly Moore , associate director of the Immunization Action Coalition , cautions that vaccines don ’ t work as well on the frail and elderly compared to healthy people .
“ When @ @ @ @ @ @ @ residents , Moore said Americans need to understand that deaths may occur that won ’ t necessarily have anything to do with the vaccine , ” states the report .
“ We would not at all be surprised to see , coincidentally , vaccination happening and then having someone pass away a short time after they receive a vaccine , not because it has anything to do with the vaccination but just because that ’ s the place where people at the end of their lives reside , ” Moore said .
She @ @ @ @ @ @ @ alarmed to see people dying a day or two after receiving the COVID vaccination .
“ One of the things we want to make sure people understand is that they should not be unnecessarily alarmed if there are reports , once we start vaccinating , of someone or multiple people dying within a day or two of their vaccination who are residents of a long-term care facility .
That would be something we would expect , as a normal occurrence , because people die frequently in nursing homes.
” Having problems receiving our @ @ @ @ @ @ @ Internet Censorship and Create Your Own Newsfeed We Are Now on Parler and MeWe !
If our website is seized and shut down , find us on Parler and MeWe for further instructions about where to find us .
Unmasking Who is Behind the Plandemic and Rioting to Usher in the New World Order

by Paul Joseph Watson
Summit News
In an article on the COVID vaccine rollout, CNN says that Americans shouldn’t be alarmed if people start dying after taking the vaccine because “deaths may occur that won’t necessarily have anything to do with the vaccine.”
The advisory appeared in an article titled ‘Why vaccinate our most frail? Odd vote out shows the dilemma’ in which Dr. Kelly Moore, associate director of the Immunization Action Coalition, cautions that vaccines don’t work as well on the frail and elderly compared to healthy people.
“When shots begin to go into arms of residents, Moore said Americans need to understand that deaths may occur that won’t necessarily have anything to do with the vaccine,” states the report. “We would not at all be surprised to see, coincidentally, vaccination happening and then having someone pass away a short time after they receive a vaccine, not because it has anything to do with the vaccination but just because that’s the place where people at the end of their lives reside,” Moore said.
She then said Americans shouldn’t be alarmed to see people dying a day or two after receiving the COVID vaccination.
“One of the things we want to make sure people understand is that they should not be unnecessarily alarmed if there are reports, once we start vaccinating, of someone or multiple people dying within a day or two of their vaccination who are residents of a long-term care facility. That would be something we would expect, as a normal occurrence, because people die frequently in nursing homes.”
Read the full article at Summit News.
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healthimpactnews--2020-12-11--Health Impact News is on Gab!

Health Impact News is on Gab!

Twitter has already banned any articles from Health Impact News being shared on their platform , and Facebook has been removing our posts on the experimental COVID vaccine and is about to unpublish our main page , so we have now moved to Parler.com , MeWe.com and Gab.com for our Social Media posts .
In the event that our websites are seized , please go to our Parler account or our MeWe account until we get back up and running .
For the past month or so Parler and MeWe have been two of the most downloaded apps in the @ @ @ @ @ @ @ we chose to start with these two for now .
Both claim to provide free speech and no censorship .
Thank you for your continued support in trusting us for publishing the truth about Medical Tyranny and the rapid take-over of America and most of the world happening right now as the Eugenicist Gloablists make their move very rapidly now with the new COVID vaccines , and their stated goals in reducing the world ’ s population and installing a New One World Government .
This is no longer a conspiracy “ theory @ @ @ @ @ @ @ very eyes right now .
To the Jews who had believed him , Jesus said , “ If you hold to my teaching , you are really my disciples .
Then you will know the truth , and the truth will set you free.
” ( John 8:31-32 ) Having problems receiving our newsletters ?
See : How to Beat Internet Censorship and Create Your Own Newsfeed We Are Now on Parler , MeWe , and Gab !
If our website is seized and shut down , find us on Parler , MeWe @ @ @ @ @ @ @ to find us .
Unmasking Who is Behind the Plandemic and Rioting to Usher in the New World Order

by Brian Shilhavy
Editor, Health Impact News
Twitter has already banned any articles from Health Impact News being shared on their platform, and Facebook has been removing our posts on the experimental COVID vaccine and is about to unpublish our main page, so we have now moved to Parler.com, MeWe.com and Gab.com for our Social Media posts.
In the event that our websites are seized, please go to our Parler account or our MeWe account until we get back up and running.
For the past month or so Parler and MeWe have been two of the most downloaded apps in the various app stores, which is why we chose to start with these two for now. Both claim to provide free speech and no censorship.
Thank you for your continued support in trusting us for publishing the truth about Medical Tyranny and the rapid take-over of America and most of the world happening right now as the Eugenicist Gloablists make their move very rapidly now with the new COVID vaccines, and their stated goals in reducing the world’s population and installing a New One World Government.
This is no longer a conspiracy “theory,” but is unfolding before our very eyes right now.
To the Jews who had believed him, Jesus said, “If you hold to my teaching, you are really my disciples. Then you will know the truth, and the truth will set you free.” (John 8:31-32)
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healthimpactnews--2020-12-11--Australia Scraps Billion Dollar Coronavirus Vaccine After Participants Test HIV Positive

The Australian Government has scrapped a billion dollar coronavirus vaccine agreement with Australian biotech company CSL Limited to supply 51 million doses of a Covid-19 vaccine being developed by the University of Queensland after several trial participants returned false positive HIV test results .
The University of Queensland has abruptly ended its trials for coronavirus vaccine the Australian government had ordered in a $ 1 billion deal for 51 million doses .
The deal was terminated after participants returned false positive HIV test results over fears that vaccine mishap would damage the public ’ s confidence in the COVID-19 vaccination @ @ @ @ @ @ @ minister , Scott Morrison , said : Australian vaccine scientist Nikolai Petrovsky had warned the government about the risk of including HIV in a vaccine months before the $ 1billion deal was signed .
Mr Petrovsky told The Australian the problem with the use of HIV was clear in the ‘ hamster and mouse data ’ but his advice was ignored .
He said the early data suggested the vaccine itself was quite unstable .
Overall it just didn ’ t look like it was going to be a successful vaccine , that @ @ @ @ @ @ @ the government committed millions of dollars to it , it just seemed disproportionate .
The Covid-19 “ spike protein ” has been the focus of the University of Queensland vaccine , using molecular clamp technology to lock the protein into a shape which allows the immune system to be able to recognise and then neutralise the virus .
Covid ’ s spike proteins , like most surface viral proteins , are fairly unstable .
To ensure that the vaccine induced the right immune response , the clamp chosen comprises two fragments of a @ @ @ @ @ @ @ fragments provided the greatest stability to the vaccine .
Having problems receiving our newsletters ?
See : How to Beat Internet Censorship and Create Your Own Newsfeed We Are Now on Parler , MeWe , and Gab !
If our website is seized and shut down , find us on Parler , MeWe and Gab for further instructions about where to find us .
Unmasking Who is Behind the Plandemic and Rioting to Usher in the New World Order

by GreatGameIndia.com
The Australian Government has scrapped a billion dollar coronavirus vaccine agreement with Australian biotech company CSL Limited to supply 51 million doses of a Covid-19 vaccine being developed by the University of Queensland after several trial participants returned false positive HIV test results.
The University of Queensland has abruptly ended its trials for coronavirus vaccine the Australian government had ordered in a $1 billion deal for 51 million doses. The deal was terminated after participants returned false positive HIV test results over fears that vaccine mishap would damage the public’s confidence in the COVID-19 vaccination program.
On Friday the Australian prime minister, Scott Morrison, said:
University of Queensland vaccine will not be able to proceed based on the scientific advice, and that will no longer feature as part of Australia’s vaccine plan.
Australian vaccine scientist Nikolai Petrovsky had warned the government about the risk of including HIV in a vaccine months before the $1billion deal was signed.
Mr Petrovsky told The Australian the problem with the use of HIV was clear in the ‘hamster and mouse data’ but his advice was ignored. He said the early data suggested the vaccine itself was quite unstable.
Overall it just didn’t look like it was going to be a successful vaccine, that’s why we were surprised when the government committed millions of dollars to it, it just seemed disproportionate. The Covid-19 “spike protein” has been the focus of the University of Queensland vaccine, using molecular clamp technology to lock the protein into a shape which allows the immune system to be able to recognise and then neutralise the virus. Covid’s spike proteins, like most surface viral proteins, are fairly unstable. To ensure that the vaccine induced the right immune response, the clamp chosen comprises two fragments of a protein found in HIV, as those fragments provided the greatest stability to the vaccine. Read the full article at GreatGameIndia.com.
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