Showing posts with label FDA. Show all posts
Showing posts with label FDA. Show all posts

Sign Petition FDA To Investigate Pfizer's Clinical Trial Fraud

Sign Petition FDA Needs To Investigate Pfizer's Clinical Trial Fraud Allegations

Should the FDA investigate Pfizer's clinical trial fraud allegations? Or look the other way?

The Correct Way to Handle the Pandemic

https://www.vacsafety.org/

Vaccines

  1. Stop the vaccines now. The current COVID vaccines kill more people than they can possibly save from COVID, even if they were 100% effective so should be taken off the market immediately. For example, the vaccine may kill 117 kids for every kid that is saved from COVID.

  2. The liability exemption is now lifted retroactively. Patients who have been harmed by the COVID vaccines can now sue the drug company for damages up to $100M per case of fatality or disability.

  3. Every post-vaccination ailment, affliction and death appearing within 4 weeks of vaccination that appears at a rate of 10X or more vs. baseline should be attributed to the vaccine unless and until proven otherwise, by irrefutable evidence, with costs of all diagnostic procedures to be born by the pharmaceutical manufacturer.

  4. For future approved vaccines, informed consent provide shall include any and all symptoms that are elevated in VAERS by 10X or more over “baseline” reporting rates.

  5. For future approved vaccines, require autopsies for anyone who dies within 2 weeks of getting the vaccine. The autopsy reports should be posted in a public database with Names and other PHI related data redacted

  6. Failure to file a VAERS report for anyone who dies within 30 days of COVID vaccination shall be liable to a fine of $100,000 per incident.

Pfizer, FDA Hid Failed Clinical Trials Data, Says BlackRock Advisor

Article copied from Childrenshealthdefense.com

In an interview with Naomi Wolf, former BlackRock investment advisor Edward Dowd explained why Wall Street lost faith in Pfizer and Moderna stocks when Pfizer and the U.S. Food and Drug Administration tried to hide clinical trial data.

In an interview with Naomi Wolf, of the Daily Clout, investment advisor Edward Dowd discussed why investors are dumping COVID-19 vaccine makers’ stocks.

Dowd, a former managing director with BlackRock from 2002 to 2012, grew BlackRock’s growth strategy from $2 billion-$14 billion over 10 years.

Wolf introduced Dowd:

“He’s the extraordinarily kind of courageous, well-informed whistleblower who has come forward to explain to audiences why in his view, Pfizer has committed a fraud.”

Dowd described how his initial caution about taking the experimental COVID vaccine led him to research data related to Pfizer’s clinical trials.

Dowd told Wolf:

“I learned from a friend in the biotech industry that Pfizer had failed its all-cause mortality endpoint in the initial trial … All-cause mortality is the gold standard in any drug trial at the FDA. When you fail that endpoint, the drug is not approved.”

When Big Pharma and the U.S. Food and Drug Administration (FDA) were unwilling to release vaccine safety data, Dowd grew even more skeptical about the vaccines, he said, and was compelled to speak out privately and publicly about what he believed was a major deception:

“I got more loud about fraud when the FDA decided to hide the clinical data for 75 years. I’m an investor, so let me just say how I think about the world. I don’t wait for people to tell me what just happened. My job was to come up with an analysis, mosaic and investment thesis, and then over time I’d be proven right.

“So I don’t wait for The New York Times, The Wall Street Journal or The Washington Post to tell me anything. Because by the time that happens, the opportunity to make money is lost. So I started screaming fraud as soon as I saw that — because it’s unprecedented to hide data from the public.”

It was a report from the CEO of a major life insurance company that confirmed Dowd’s doubts:

“If this vaccine was as deadly and injurious as we thought, we’d see the insurance companies and the funeral home results. These are databases that aren’t being hidden from us by the government. So, unfortunately, in early January, a signal was launched by One America.

“The CEO didn’t really know what he was saying or the implications of it — because he didn’t think it was the vaccine, but he got on a Chamber of Commerce call in Indiana, and he said that in the second half of 2021, he was seeing a 40% increase in all-cause mortality —  non-COVID. And to put some meat on those bones, a 10% increase he said would be a three-standard deviation [increase], which in math in my world is a big deal.”

Dowd described the impact on the financial world and on his current work:

“Wall Street is listening to me now because they’re nervous and a lot of them are jabbed as well. And if you look at the stocks of Moderna and Pfizer, Moderna is down 70% and Pfizer is down 20 plus percent.

“So my goal has been to raise consciousness across the country and the globe, by pointing out that even though the mainstream media is not going to save us — and it doesn’t seem like the politicians or the regulators are, because they’re in on it — we have to spread the word.”

Wolf asked Dowd about the repercussions of his public position:

“One of the things you’ve said, unequivocally, not mincing words — this is fraud. So if you are not right, that’s actionable, I believe, and Pfizer and Moderna could come at you with a libel suit or a slander suit. But I believe that has not happened yet. Will you speak to that?”

Dowd replied:

“I don’t have a medical license to take away. I don’t have a bar license to take away. I’m an investor. And throughout the history of Wall Street, investors have what we call a thesis. So I present this as a thesis — I’m a hundred percent convinced it’s fraud. I’ve laid out my case and it’s starting to appear, it’s coming to light that it is, but I can say this is freedom of speech. They can sue me if they want. I don’t suspect they will.”

Dowd said he’s been waiting for a “hit piece on me,” but there haven’t been any yet. He said because what he’s presenting is an investment thesis, he’s protected under free speech laws.

“Here’s the problem, Dowd said. “The proof of the fraud is showing up in real-life results. And that is becoming undeniable and impossible to hide.”

Read these related articles:

FDA officials resigned

FDA Advisory Panel Votes 16-2 For No Booster Shots.

Dr. Steve Kirsch Bombshell Testimony at FDA Vaccine Hearing

Naomi Wolf, former BlackRock investment advisor Edward Dowd

List of COVID Disinformation Spreaders That Need To Be Investigated

US Surgeon General Vivek Murthy

Steve Kirsch believe that all of these people are involved in “The proliferation of false or misleading narratives, which sow discord or undermine public trust in U.S. government institutions” and have collectively led to the tragic death of over 1M Americans.

Ivermectin Adoption By Country Wordwide Map

confirmed death rate by country chart

Strictly regular use of ivermectin as prophylaxis for COVID-19 leads to a 90% reduction in COVID-19 mortality rate, in a dose-response manner: definitive results of a prospective observational study of a strictly controlled 223,128 population from a city-wide program in Southern Brazil

Is the Mexican or US Government More Corrupt From Drug Money?

El Chapo vs Big Pharma Corruption

Dr. Robert Malone explains how Big Pharma influences public health policies implemented by the CDC and FDA on Candace Owens show. 


Stockholm Syndrome, Human Psychology, and COVID Lockdowns


Bill Gates has systematically monopolized the global response to infectious disease through non-profits. 

Judge Orders FDA To Show Pfizer Data Hidden From Public

room full of paper

On behalf of a client, my firm requested that the FDA produce all the data submitted by Pfizer to license its Covid-19 vaccine.  The FDA asked the Court for permission to only be required to produce at a rate of 500 pages per month, which would have taken over 75 years to produce all the documents. 

I am pleased to report that a federal judge soundly rejected the FDA’s request and ordered the FDA to produce all the data at a clip of 55,000 pages per month!

This is a great win for transparency and removes one of the strangleholds federal “health” authorities have had on the data needed for independent scientists to offer solutions and address serious issues with the current vaccine program – issues which include waning immunity, variants evading vaccine immunity, and, as the CDC has confirmed, that the vaccines do not prevent transmission.

1. The FDA shall produce the “more than 12,000 pages” articulated in its own proposal, see ECF No. 29 at 24, on or before January 31, 2022.

2. The FDA shall produce the remaining documents at a rate of 55,000 pages every 30 days, with the first production being due on or before March 1, 2022, until production is complete.

3. To the extent the FDA asserts any privilege, exemption, or exclusion as to any responsive record or portion thereof, FDA shall, concurrent with each production required by this Order, produce a redacted version of the record, redacting only those portions as to which privilege, exemption, or exclusion is asserted.

4. The Parties shall submit a Joint Status Report detailing the progress of the rolling production by April 1, 2022, and every 90 days thereafter.[6]

SO ORDERED on this 6th day of January, 2022.

Robert Malone on the Joe Rogan Experience Podcast


Dr. Robert Malone is the inventor of the nine original mRNA vaccine patents, which were originally filed in 1989 (including both the idea of mRNA vaccines and the original proof of principle experiments) and RNA transfection. Dr. Malone, has close to 100 peer-reviewed publications which have been cited over 12,000 times. Since January 2020, Dr. Malone has been leading a large team focused on clinical research design, drug development, computer modeling and mechanisms of action of repurposed drugs for the treatment of COVID-19. Dr. Malone is the Medical Director of The Unity Project, a group of 300 organizations across the US standing against mandated COVID vaccines for children. He is also the President of the Global Covid Summit, an organization of over 16,000 doctors and scientists committed to speaking truth to power about COVID pandemic research and treatment.

Joe Rogan and Robert Malone


Massive Private Equity Companies Like Black Rock & Vanguard Control Our World

Watch 51 minutes into this video where Robert Malone discusses this massive investment capital that is driving destructive Government decision-making and big pharma corruption.  

Consolidation of capital is no longer constrained by a nation-state.  These massive private equity companies now control the World and all they care about is the return on investment.  They control all decisions in Government and the Federal Reserve.  They have war game tools to train politicians. 


Racing to $20 Trillion
BlackRock capital pie chart
BlackRock $4.3 Trillion
This was 2013 over 8 years ago!

Few people are as qualified to comment on the course of the COVID pandemic and the mass vaccination campaign as Dr. Malone. In this important interview, he shares his unique and deep insights on matters of critical national and international importance 

In an exclusive and explosive one-hour interview with Veronika Kyrylenko of The New American, pioneering mRNA scientist Dr. Robert Malone explains the intensely corrupt workings of the government regulatory bodies that have mismanaged the pandemic, discusses the problems with the vaccine program and delves into potentially explosive and game-changing revelations about the shady origins of the Covid-19 pandemic in Wuhan, China.

Who is Dr. Robert Malone? While working at the Salk Institute in 1988, Dr. Malone discovered important findings about in-vivo and in-vitro RNA transfection. He continued his work on the technology a year later at the biopharma start-up Vical where he conducted additional experiments. According to his bio, “The mRNA, constructs, reagents were developed at the Salk institute and Vical by Dr. Malone.” His research has also included important work on DNA vaccines. In addition to his fundamental work developing mRNA and DNA vaccine technology, Malone is also a medical doctor. According to his bio, Dr. Malone “received his medical training at Northwestern University (MD) and Harvard University (Clinical Research Post Graduate) medical school, and in Pathology at UC Davis."

Few people are as qualified to comment on the course of the COVID pandemic and the mass vaccination campaign as Dr. Malone. In this important interview, he shares his unique and deep insights on matters of critical national and international importance. 

https://www.rwmalonemd.com/

Pfizer Clinical Trail Data Won't Be Released Until 2096. What Are They Hiding?

As attorney Siri writes “this is “Not a typo.” They are demanding 75 years of data secrecy. Yes, the FDA is agreeing to share about 12,000 pages in the first couple of months but thereafter they would release, at a snail’s...

Outrageous Lack of Transparency—Pfizer Now Asks Court for 75 Years to Hide Details of COVID-19 Vaccine Trial Results.

TrialSite has tracked attorney Aaron Siri and his client’s Freedom of Information Act (FOIA) case against Pfizer for full disclosure of clinical trials documentation. Siri shared in a previous post that the Food and Drug Administration (FDA) asked a federal judge to delay the full disclosure of all relevant documentation till 2076—55 years from now! 

Siri, who is a partner with the law firm Siri Glimstad representing the Public Health and Medical Professionals for Transparency (PHMPT) countered to the court that Pfizer should disclose the entire batch of documentation within 108 days which just happens to be the amount of time it took for the Gold Standard regulatory agency to review and approve Pfizer’s vaccine. After the court-ordered both parties to submit updated briefs, now in what can only be considered an insult to injury, Pfizer “doubles down.” Meaning the pharmaceutical company now wants to hide the extent of all of the material information till 2096.

Here are some Tweets showing what they are hiding . . .

Still Loaded With Antibodies 1 Year Later After Covid 19 Infection

Labcorp Antibodies Test Results Positive
SEE OTHER TEST RESULTS BELOW
Why Is Natural Immunity Still Being Ignored By The Corrupt Government & Corporate Media?

Blood test results from Labcorp show an unvaccinated family of four people still have antibodies 1 year later after infection.  Family of people with ages ranging from 12-48 still are loaded with antibodies.  

Can this family get a vaccine mandate exemption?


Here is the language used by the criminals running the CDC.  All eligible people should be vaccinated, including unvaccinated people who have previously been infected and have detectable antibodies.

Numerous immunologic studies (NO STUDIES LINKED?) have consistently shown that vaccination of individuals who were previously infected enhances their immune response, and growing epidemiologic evidence indicates that vaccination following infection further reduces the risk of subsequent infection, including in the setting of increased circulation of more infectious variants.


Risk of an MIS-like illness or the known risks of COVID-19 vaccination such as the rare risk of myocarditis following COVID-19 vaccination for people who meet the following criteria:

  1. Clinical recovery has been achieved, including return to normal cardiac function;
  2. It has been ≥90 days since their diagnosis of MIS-C;
  3. They are in an area of high or substantial community transmission of SARS-CoV-2, or otherwise have an increased risk for SARS-CoV-2 exposure and transmission; and
  4. Onset of MIS-C occurred before any COVID-19 vaccination.
People diagnosed with MIS-C or MIS-A after COVID-19 vaccination

In the rare instance of a person developing MIS-C, MIS-A, or a similar clinical illness after receipt of a COVID-19 vaccine, referral to a specialist in infectious diseases, rheumatology, or cardiology should be considered. Because MIS-C and MIS-A are conditions known to occur with SARS-CoV-2 infection, these individuals should be assessed for laboratory evidence of current or prior SARS-CoV-2 infection. Healthcare and public health professionals should also consider requesting a consultation from the Clinical Immunization Safety Assessment COVIDvax project. In addition, all illnesses consistent with MIS-C or MIS-A occurring in persons who received any COVID-19 vaccine should be reported to VAERS.

FDA today: 42% of children 5-11 have natural immunity

42% of children 5-11 have natural immunity

Labcorp Antibodies Test Results Positive

Labcorp Antibodies Test Results Positive

Labcorp Antibodies Test Results Positive

Court Orders FDA To Comply With FOIA Docs Request

FDA FOIA

The Food and Drug Administration (FDA) released the first batch of documents related to Pfizer’s Covid-19 vaccine after a federal judge ordered that they must comply with a massive Freedom of Information Act (FOIA) request that was filed by a government accountability group called Public Health and Medical Professionals for Transparency.

The esteemed group of more than 30 professors and scientists asked the federal government to share any and all data that factored into the agency’s hasty decision to grant Pfizer’s experimental mRNA vaccine an emergency use authorization (EUA) – which amounts to a trove of over 329,000 documents.

In a shameless effort to bury the information, the FDA challenged the FOIA request in court. After the agency was told that it must turn over the documents, Justice Department lawyers representing the FDA asked a federal judge to allow them an unthinkable 55 years to process the request, saying that they would be able to release just 500 pages a month.

A motion that was also filed by the same group of doctors and scientists is currently pending in federal court that would force the FDA to expedite processing and releasing these documents.

Meanwhile, the FDA still has to comply with the original order to begin turning over documents. Lo and behold, the first release is a bombshell.

According to an official Pfizer document that is titled Cumulative Analysis of Post-Authorization Adverse Event Records Reports, in just the first 90 days of the vaccine’s roll out under the FDA’s EUA – from December 1st. 2020 – February 28th, 2021 – there were TENS OF THOUSANDS of reported adverse reactions, including OVER 1200 DEATHS. 

https://twitter.com/iGNORANTCHiMP/status/1465992238689923081

The report only included adverse events to the vaccine that researchers considered “serious cases,” there were thousands more submissions that were left out of this data.

Any cases deemed “non-serious” would be processed within 90 days, but this report was released before 90 days of Pfizer’s vaccine being available had even passed.

“Due to the large numbers of spontaneous adverse event reports received for the product, the MAH has prioritised the processing of serious cases, in order to meet expedited regulatory reporting timelines and ensure these reports are available for signal detection and evaluation activity.

Non-serious cases are processed as soon as possible and no later than 90 days from receipt. Pfizer has also taken a multiple actions to help alleviate the large increase of adverse event reports.”

In all, the report states that there were a total of 42,086 case reports of individuals who had an adverse reaction to Pfizer’s vaccine worldwide, with the largest number (13,739) coming from the United States and from the UK (13,404).

According to the documents women (29,914) were over 3x more likely to experience a reaction than men (9182). A total of 1223 individuals had a fatal reaction to the experimental Pfizer vaccine. 

https://twitter.com/iGNORANTCHiMP/status/1465999494177345537

How did the FDA not immediately pull the experimental jab out of circulation? Let alone grant multiple extensions of the EUA to Pfizer while working with the fraudulent Biden regime to push a needle into the arm of every single American.

The document also makes it clear that the data only includes “recorded adverse events,” which even the author admits is likely just a portion of the true number of adverse reactions that took place. 

Again, keep in mind, this is within the first 90 days of the Pfizer jab’s availability. 

From the Pfizer document:

“Reports are submitted voluntarily, and the magnitude of underreporting is unknown.

Some of the factors that may influence whether an event is reported include: length of time since marketing, market share of the drug, publicity about a drug or an AE, seriousness of the reaction, regulatory actions, awareness by health professionals and consumers of adverse drug event reporting, and litigation.”

Pfizer’s “confidential” Covid-19 vaccine adverse reaction review ends with thousands of conditions that are of “special interest” and could possibly develop after taking their experimental jab. The single-space typed list continues for an astonishing 9 pages.

Yet somehow the paper concludes that the “review of available data” was good enough and demonstrated a “favorable benefit-risk balance” for the rushed vaccine.

What’s the benefit-risk balance on a virus that has a 99.9% recovery rate? The benefit – at least for Pfizer – is clear; It doesn’t matter how many otherwise healthy lives are lost – they are CASHING IN to the tune of $1,000 PER SECOND with a projected $36 BILLION in profit this year from the vaccine alone – it’s criminal. 

Smoking gun confidential Pfizer document exposes FDA criminal cover-up of VACCINE DEATHS… they knew the jab was killing people in early 2021… three times more WOMEN than MEN

The full document can be found here.

The FDA clearly agreed with Pfizer, extending the EUA despite the high number of deaths and serious reactions in the short amount of time Pfizer’s jab had been available.

What else are they hiding?

Fact Checking The Fact Checker Lies & Fake News

fact checker lies

Full article comments

One of the downsides of telling the truth in this environment is that it seems everyone and their brother wants to tear all your arguments to shreds.

I could spend full time just refuting all the hit pieces written about the content I’ve produced. Here’s my fact check of the fact-checkers as a repurposed graphic:

Rather than address every point of every fact check, here is a checklist for things that a thorough fact checker should be able to answer, but can’t or won’t.

Note that this is a quick list I put together in about 30 minutes. There are more, but you get the idea:

  1. What is my motivation for suddenly, at age 65, becoming a spreader of misinformation and conspiracy theories? And why did it only happen right after hearing about my friends who had died or been disabled by the COVID vaccines? Do you even know me or have we ever met?

  2. Dr. Toby Rogers computed 117 deaths per kid saved in ages 5 to 11? Do you agree with his analysis? 20,000 people read that article and couldn’t find a hole. So where did he go wrong and how can be sure you got it right and he got it wrong?

  3. If this is all done out of Kirsch's ego, then how is it that 30 other scientists, statisticians, and doctors all agree with him? Why did all of these people suddenly become conspiracy theorists? What’s their motivation for the fraud and deception?

  4. If the vaccines are safe, how come Alex Berenson also thinks the vaccines are unsafe? Is he also a crackpot? Isn’t it unfair just to attack Kirsch? Berenson and Kirsch hardly ever talk, yet came to the same conclusion. What about Del Bigtree? He found the same thing. In fact, Bigtree’s attorney calculated a VAERS URF of 50 well before Kirsch did. So why pick on Kirsch?

  5. If the fact checker uses a pseudonym, why can’t you tell us what your name is?  Are you going to tell us who funded you to do the hit piece?

  6. Will you debate us in a recorded Zoom call where you can answer all our questions? We are eager to find out how we were fooled by all this data.

  7. If the vax is so safe, why are there so many death entries in VAERS this year?

  8. If you think there is simply “over-reporting” in VAERS this year, what is your actual evidence of that? All the people we talked to are reporting more events because there are more events happening. In fact, most people report that there are at least 100X more events this year than in previous years. So it seems like VAERS is actually under-reported this year, and not over-reported, don’t you think?

  9. There are 5,288 symptoms that haven’t been reported for ANY vaccine in the last 5 years that are being reported for the first time in these vaccines. Why?

  10. Why are there more adverse event reports this year than for every vaccine in the last 30 years combined?

  11. If the URF isn't 41, what is the true URF and did you calculate it using the CDC-approved methodology like we did? (see The reporting sensitivity of the Vaccine Adverse Event Reporting System (VAERS) for anaphylaxis and for Guillain-Barré syndrome).

  12. If we got it wrong, then tell us: How many people do you estimate have been killed by the COVID vaccines and how do you know?

  13. One of the ways we computed the number of deaths from the vaccine was using an independent polling company. How was that gamed?

  14. Why are athletes dropping by a 60X rate after the vax rollout?

  15. How did Ernest Ramirez's son die?

  16. How do you explain the causes of death of the 14 cases the CDC examined? 5 of them died from cardiac arrest!

  17. How does he explain the results of Peter Schirmacher?

  18. Why did Taiwan report more deaths from the vaccine than from COVID?

  19. Why is the line slope going the wrong way in the Harvard study?

  20. How do you explain that the biodistribution showing accumulation in the ovaries correlate with the high numbers of VAERS symptoms for menstrual problems many with huge elevations compared to baseline (previous vaccines).

  21. Why are cardiologists reporting highly elevated # of cases of heart disease in kids after the vax rolled out?

  22. Why is the cardio testing lab at UCSF now filled with kids 7 to 10 only AFTER the vaccines rolled out for that age range?

  23. Why is a top California neurologist needing to report 2,000 VAERS events this year when in the last 11 years she's never need to report a single adverse event?

  24. How do we explain the families where 3 relatives, all previously healthy, die within days after the COVID shot?

  25. How do we explain Gavin Newsom being diagnosed with GBS within days after his booster? Isn’t it perfectly safe?

  26. How did 2 cricket players recently vaccinated drop on the field within 10 minutes of each other? Bad luck?

  27. Why does the CDC *REFUSE* to calculate and use the proper URF for VAERS when interpreting the safety data? Pfizer PROVED that VAERS is 5X underreported for myocarditis, and the CDC will not even acknowledge that? John Su is using a URF of 1. That is clearly false and misleading. Why are you not going after him? That is truly evil and corrupt. I’m not the bad guy here. This was in plain sight of the public (Pfizer slide with the Optum data (see my article about this).

  28. How come undertakers report a huge increase in business right after the vaccines rolled out?

  29. Why aren't the nursing homes disputing Abrien Aguirre's account that there were 10 times as many deaths from the vaccines than from COVID?

  30. How come the CDC hasn't ascribed even a single death from the vaccines in light of Schirmacher's study? That’s inexplicable isn’t it?

  31. Why are there so many vaccine-injured people that Facebook had to remove groups of 250,000 and more (multiple times).

  32. Why aren't the vaccine injured getting any press?

  33. Why did YouTube censor Dr. Peter Doshi's testimony? UCSF Professor Aditi Bhargava spoke as well and was censored. Why? Are you speaking out about that?

  34. How come Jessica Rose’s myocarditis paper was pulled by the publisher? Are you making a stink about the corruption of science here? Or are you just trying to discredit me?

  35. What about Maddie de Garay? Why didn't the FDA, CDC, or Pfizer ever investigate? Why did Janet Woodcock assure me they would and then did nothing? Why didn't they report the truth and stop the trial on the permanent paralysis. Her result aligns PERFECTLY with the mechanism of action of the drug? How can they have eliminated the vax as the cause without ever talking to her? They are supposed to assume it is the vax until they can show otherwise.

  36. What about the 5X exclusions (vs placebo group) in the Pfizer trial? That can't be by chance can it?

  37. How come there were so few all-cause deaths in the Pfizer study? It was supposed to be a representative group! There should be been around 110 deaths in each group, right?

  38. How come Pfizer 6 months study shows more all cause deaths in the treatment group in than in the placebo group? Where is the PROOF that the vaccines are saving lives? Whoops!!!! No proof at all of a single life saved. As a fact checker, why aren’t you calling that out? Instead you are targetting me. Hmmmm.

  39. Why were there 4X as many cardiac arrests in the vax group vs. placebo in the Pfizer Phase 3 study (6 month)? Seems pretty high. It wasn’t just bad luck since we see all these athletes in plain sight dropping. So isn’t it more likely than not this is real?

  40. Aren’t you concerned that the trials going forward are too underpowered to resolve any of these questions?

  41. Wasn’t there gaming in the Pfizer Phase 3 trials on adverse event reporting where people found it difficult/impossible to report AEs.

  42. Despite the gaming of the AE reports, aren’t you alarmed at the statistically significant large increase in overall morbidity in all of the COVID vaccine trials (the paper US COVID-19 Vaccines Proven to Cause More Harm than Good… by J. Bart Classen, MD).

  43. How come the NIH and WHO did absolutely nothing when the fluvoxamine Phase 3 trial was published in Lancet? They didn't even note it in the guidelines. Did you protest that? Why not? It’s December 2, 2021 and the fluvoxamine recommendation was Last Updated: April 23, 2021. The Lancet article was widely covered by all major media, but the NIH did nothing. How do you explain that? Why aren’t you spending your valuable time focusing on that?

  44. How come nobody can cite a SINGLE RCT that shows that masks work against COVID?

  45. How come Professor Jeffrey Morris changed the topic whenever we tried to show him that the symptoms in VAERS were dose dependent? (Note: dose dependency is one of the most impressive indicators of causality, but we use all Bradford-Hill criteria to assess causality).

  46. Dr. Steven A. Anderson of the FDA is supposed to be monitoring the VAERS data like a hawk. We have people highly qualified to who have spent months analyzing the VAERS data. Why does Dr. Anderson refuse to meet with us?

  47. How come the FDA and CDC outside committee members all turned down a $1M research grant just to talk to us for a few hours and answer questions? What are they afraid of?

  48. If the CDC and FDA members are independent, why did one of them admit in a private conversation that if they didn’t vote the way the FDA /CDC wanted they would be kicked off the committee like Martin Kulldorff.

  49. If the vaccines are so safe, then why did CDC insiders tip off a friend of mine in January not to get the vaccines?

  50. If the excess deaths in VAERS was not caused by the vaccine, then what is causing it and why isn’t the CDC investigating? These causes of death were not normal.

  51. While it is amusing for people to refer to the Mclachlan VAERS study and argue that all the deaths were normal, that’s simply not what the study said. Shall we go through all 250 cases one by one? The paper said “Despite this, there were only 14% of the cases for which a vaccine reaction could be ruled out as a contributing factor in their death.” So it is interesting that some people can definitively state that the vaccine didn’t cause their death. Are these fact checkers willing to go through the cases one by one with Scott and our team and show us all how we got it wrong?

When you find a “fact check” that addresses those 51 questions, that would be great because I have another 130 questions just like those which I’d love to hear them explain as well.

Debunking Steve Kirsch’s latest claims about covid vaccine deaths

Here is the Medium article. Whoever wrote this “fact check” clearly spent a lot of time putting together his case. Basically, this nameless, faceless person claims that Crawford cherry picked data and that the excess death data doesn’t line up with a deadly vaccine. I just learned about this on Dec 1 at 11pm.

The author says my motivation is ego and fame. Wow. This shows you the quality of his work. Is the author willing to challenge my team in a recorded debate? I seriously doubt it. But I’ve got an open invitation to do just that! Let’s find the truth. We are not afraid of a challenge. Is he? If you are “The Gift of Fire,” then please respond in the comments.

He asks in his title: “What motivates a tech millionaire to fight against covid vaccines?” I’d have a lot more respect for him if was able to get that simple question right. But he can’t even get that one right. Everyone who knows me and works with me will tell you the answer: “Mr. Kirsch just wants to save lives.” I would argue if he can’t get something simple like that out, that we should have a lot less confidence in anything else he says.

So rather than spend our time debunking his debunk, I want to issue a challenge to our anonymous “do gooder.” We’ll address all of your points in your article, if you address all the points above all in a LIVE RECORDED zoom call where we can set the record straight.

How about it?

Healthfeedback fact check

Today, for example, someone sent me this link from the “experts” at healthfeedback.org that fact checked two statements that they claim that I made:

  1. "the ovaries get the highest concentration of [lipid nanoparticles from RNA vaccines]. This turns the ovaries into a very large manufacturing plant to turn out toxic spike protein"

  2. "FDA experts reveal the Covid-19 Vaccines are killing at least 2 people for every 1 life they save"

The short story is the first statement was taken completely out of context and was referring to a chart that was limited to showing the body parts where we did not expect to see any lipid nanoparticle (LNP) delivered. The second was a quote from The Expose that I never claimed. It was their mistake, not mine.

If we address the “context problem” of the first one and they mistake by The Expose in the second one, we are left with:

  1. When we look at areas of the body where we didn’t expect to see the LNPs, the ovaries has the highest accumulation.

  2. The VAERS data shows that the vaccines are killing at least 2 people for every life that they might save. It’s not just me that says that. The Walach and Kostoff papers, published in peer reviewed medical journals, say the same thing.

The facts supporting both of these statements are pretty straightforward.

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