The people responsible for the deaths of nearly a million Americans
Introducing the members of the NIH COVID-19 Treatment Guidelines committee.
The members of COVID-19 Treatment Guidelines Panel of the NIH apparently doesn’t seem to place any value on human life. In this article, I will show several examples of this.
At no time is there ever a risk-benefit analysis where a dollar amount is placed on the value of a human life. For example, if there are 100 trials and 90% of the trials were positive and 10% were neutral, should the NIH recommend the drug?
Unfortunately, they aren’t accountable to anyone, so they will never have to defend their recommendations.
Nearly a million people have died in the US due to their failure to correctly assess what the data says and recommend interventions that are more likely to be beneficial than detrimental.
What do they do instead? They recommend you take a vaccine that is more likely to kill you than save you.
I’ve invited any of them to discuss this in a recorded meeting with me and a few of my colleagues, but even with a “name your price” incentive, none of them will accept because they know their decisions are not defensible.
In an email to a professor of medicine at a top university, I noted that no matter what the evidence says, they won’t change their recommendations. The professor wrote back, “Suspect you may be correct.” I won’t reveal his name so he doesn’t get fired. That means that fact checkers can’t attack this article with ad hominem attacks on my credentials. And they can’t attack this article on the data either.
If you are fact checking my article, please let’s have a recorded conversation about it before you write your fact check. If you don’t do that, you are being disingenuous.
Hydroxychloroquine (HCQ)
I was one of the funders of Dr. Boulware’s study on HCQ.
The study showed it was effective for COVID when given early, but the effect wasn’t statistically significant because the trial didn’t enroll enough patients.
However, David Wiseman subsequently discovered that the effect was statistically significant if one factors in the delivery time of the drug. When the mainstream journals refused to publish his analysis, he published it on a preprint server.
Here’s the summary of all the studies:
In particular, there were:
- 338 studies from 5,372 scientists show a statistically significant improvement in mortality.
- The 15 studies that looked at mortality found an average of 72 percent reduction in mortality.
- The drug has been officially adopted for early treatment in all or part of at least 35 countries
- In one US study (Tyson), the drug, in combination with other drugs, reduced the risk of death by ↓99.8 percent with a p-value of <0.0001 (which means it’s unlikely this happened by pure chance)
Suppose you just got COVID. Your doctor offers you the drug as part of your treatment. Do you say:
- Yes
- I can’t tell if it will help or hurt
- No
Given this data, I’d guess everyone who understands the data would choose #1. That’s what I would choose.
The NIH Guidelines committee however says the correct answer is #3: do not use.
They said this because in the 2 trials they chose to look at, the drug didn’t reduce the time you were sick.
In other words, by the NIH reasoning, who cares if the drug reduces your risk of death by 72 percent! If it didn’t reduce the time you were sick, it should not be used.
The logic here is inexplicable. We ignore the significant death benefit in 15 studies, and instead choose 2 studies where it did change the time you remained sick for?!?!?
In short, lives don’t matter to the NIH panel. They will simply focus on studies and on metrics that make the drug look like it does nothing.
Fluvoxamine
The highest level of proof in evidence-based medicine is a meta-analysis and systematic review that is published in a peer-reviewed medical journal.
For fluvoxamine, we now have that as of April 6, 2022: Fluvoxamine for Outpatient Management of COVID-19 to Prevent Hospitalization: A Systematic Review and Meta-analysis.
What did the NIH do with that new information? They ignored it. Their rating of NEUTRAL for fluvoxamine won’t change even though the drug passed the highest bar in evidence-based medicine.
Evidence doesn’t matter. Fluvoxamine had a 12X mortality benefit (if you start taking it early as shown in the TOGETHER trial). That’s way better than any vaccine. But who cares?
The committee ignores all the data and says it can’t figure out if the drug will help or not.
They will not be held accountable to anyone. No public challenges allowed!!!
Ivermectin
It’s the same deal with ivermectin. Lots of studies. But with ivermectin there are multiple peer-reviewed meta-analysis and systematic reviews saying the drug works.
Same reaction from the committee.
They aren’t sure if the drug works or not.
Take a look at the data:
The NIH says that there is insufficient evidence to make a recommendation. Yup. Only 82 studies from 815 scientists with 129,808 patients in 27 countries.
Do you think we need more evidence?
Other drugs
There are lots of other supplements and drugs that have convincing data.
Most all these drugs have a very low side effect profile and so anything where the green line is solely to the left of the vertical bar is highly likely to be helpful.
However, NIH doesn’t recommend any of them being used except for Molnupiravir, Paxlovid, and Remdesivir.
Now, I challenge you to cover the drug labels on the left and pick out those three drugs from the line up below. It’s impossible, isn’t it?
Do you see a pattern here? The only drugs getting approval from the NIH are proprietary drugs from big drug companies. That’s the common factor.
Here is the irony
Every one of the repurposed drugs or supplements listed in the table above has a better risk-benefit profile than the vaccine. We don’t recommend the drugs/supplement. We do recommend the vaccine. It makes no sense.
Why I say the committee members are responsible for nearly 1M deaths
The Fareed-Tyson early treatment protocol has been available since March 2020. It has a 99.8 percent mortality reduction. They told the NIH about the protocol in July 2020.
There have been around 850,000 COVID deaths since then. Had the NIH recommended the Fareed-Tyson protocol when they were notified, nearly 850,000 lives could have been saved. At the time, there were no better alternatives. Why ignore it?
Conflicts of interest
Panel members had conflicts of interest that were disclosed and not disclosed.
These would normally be a problem, but here it just doesn’t matter because nobody is holding them accountable.
My challenge
I invite the members of the NIH committee who voted to recommend against any repurposed drugs and/or supplements to an open debate to discuss this with me and a few of my colleagues. I’ll even throw in a financial incentive to make it worth your time. Name your price.
See more here: substack.com
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Alcheminister
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All of the policy makers, “virus believers”, pharma peddlers, corrupt “doctors”, EM promoters, tech companies, mask manufacturers, etc.
It’s not merely a couple of NIH asshats. Huge amounts of collusion, conspiring and numerous factors.
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Russ D
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“Covid deaths” are …
Deaths from flu
Deaths from pneumonia
Deaths from depression
and most of all .. deaths caused by the “covid vaccines”
In fact most declared unvaccinated deaths from COVID are actually Hospital murders, paid for by our Government. Hospitals denying treatment, denying food and water to those who reject remdesivir and ventilators, who deny repurposed drugs, following CDC protocols–they are guilty of murder. There is no excuse, there is no claiming ignorance. The Hospital Administrators and these doctors who participate in this are guilty.
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Brian James
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04/18/2022 /TOO MUCH TO IGNORE: COVID vaccines cause 16,633% more miscarriages compared to flu vaccines
There had been an increase in the number of women who have lost their unborn or newly born children in the United States following their Wuhan coronavirus (COVID-19) vaccination. The number has now surpassed 4,000, just 16 months after the first COVID vaccine was given emergency use authorization.
https://www.bigpharmanews.com/2022-04-18-covid-vaccines-cause-16633-percent-more-miscarriages.html
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Brian James
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Feb 7, 2022 Yes, a life insurance company can deny an applicant coverage based on COVID-related answers
Insurance experts say while some companies may deny an applicant for a new policy coverage, some will not.
https://youtu.be/a027eEITjpY
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Andy
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The flu “vaccines” are mRNA DNA Experiments too, and they contain the same type of nanotech as the Covid injections ref. Dr. Sam Bailey recent videos ft. her Husband Dr. Mark Bailey and a man who has analysed the vials in depth. I forget his name, sorry. No disrespect to anyone intended.
So the figures would likely be even more damning if ‘All’ mRNA injections were taken into account no doubt
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Doug Harrison
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“In short, lives don’t matter to the NIH panel. They will simply focus on studies and on metrics that make the drug look like it does nothing.”
This is exactly the reasoning that arose from the Rockefeller study of medical science in the early 20th century. I cannot remember the name of the study’s leader but he was a school teacher and he recommended that medical science be conducted with the advancement of that science having precedence over the welfare of those upon whom experiments sere conducted. In effect following the German principle of the conduct of science.
Always remember that Rockefeller was a eugenicist who did not want to share his world with the great unwashed.
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Mark Tapley
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Hello Doug:
To understand the massive allopathic fraud that has been perpetrated on the whole world now for over 150 years we need to go back to the elite’s medical front man and Fauci of his time, Louis Pasteur that has always been held up as a medical hero and selfless icon to the world. In 40 years of unmitigated fraud and deception Pasteur painted the portrait of todays germ theory fake virus medical scam. Using not pathogenic transmission but only toxic poisoning (usually his favorites arsenic and mercury) he killed about a score of his “patients” and many livestock as he spread the germ theory lie. His medical diary has now been published exposing what really was being transmitted.
Rothschild associate Rockefeller with Simon and Abraham Flexner founded the Rockefeller foundation (founder of the criminal CDC) and with the use of a dozen deadly “para Typhoid” vaccines with the addition of massive overdosing of the new drug aspirin and control of the media, generated the 1918 flu as the beginning of the big Pharma allopathic gold mine for the brainwashed public. A little later would come the manmade Polio, and then the addition of the neuro toxin aluminum to accelerate disabilities, especially the almost never heard of but now epidemic of autism.
As you mention, the Rockefeller’s were at the forefront (with Harriman, Carnegie and Bush family) of the Eugenics mov. which started in Long Island N.Y. and was used by the various states in forced sterilization of 60,000 people, long before the Rockefeller’s funded the Kaiser Wilhelm Inst. in Germany. After the war this Eugenics mov. laid low for a while but then resurged under the auspices of “genetic research.”
Now that we are in the post industrialized world, the elite more than every are determined to reduce plantation herd size to a more manageable and cost efficient level. As literary elite and friend of the Royals, Bernard Shaw stated, most people are just useless eaters. The Georgia Guide Stones call for a plantation reduction to 500 million total. Thats all the WEF, CFR, Trilaterals and Club of Rome crowd need to keep things going in the Neo feudal world of Agenda 2030-21. Get ready goyim, to track you’re carbon credits.
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Tom
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You could argue that big pharma and their poison drugs, vaccines and mRNA injections have murdered 10 million people over the last 20 years.
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