Africa’s Amazing Covid Numbers (and More Heart Issues)

Two articles I want to get onto my site… and the first one about Africa I have used in the past… actually, Tokyo’s Medical Association Chairman (Haruo Ozaki) uses this information in his recommending to Japan to use Ivermectin. Here is my response from a conversation posted a while back:

AFRICA

  • Z.L., Ross T. has no idea what they are talking about. Nor does he actually step outside the boobtube to find out. Some African countries have handed out Hydroxychloroquine (HCQ) as well as Ivermectin yearly to it population. You can see these countries doing very well. This is part of the reason Tokyo’s Medical Association Chairman (Haruo Ozaki) recommends Ivermectin has again recommended it. He first recommended it in February, but just recently said Japan has not heeded his warning. (RPT: More Straight Talk About Covid-19 Prophylactics)

More on Africa:

…..Last year, health officials predicted millions would die in Africa from COVID, but instead, the continent has a death rate (161.26 per million population) lower than the world average (653.52 per million population), and Africa is described by the World Health as being “one of the least affected regions in the world” in its weekly pandemic reports.

According to a recent report from the Associated Press, COVID-19 seems to have become a thing of the past. In Zimbabwe, for example, only 33 new cases and zero deaths were recorded last week.

[….]

A study published in April 2020 in the American Journal of Tropical Medicine and Hygiene warned that, “there is currently no evidence that CQ or HCQ, two low-cost drugs for which we have extensive experience for treatment of malaria and rheumatic disorders, has beneficial effects on the clinical course of COVID-19 patients,” and then warned that, “the off-label use of CQ and HCQ to prevent or treat COVID-19 in Africa and elsewhere must be viewed with greatest caution, considering potential serious toxicities and benefit versus risk. If the effectiveness of these and other drugs is established in global trials, therapeutics for COVID-19 will require further operational evaluation in Africa.”

Because of the high rates of malaria in Africa, CQ and HCQ are widely available there and have been used to treat malaria for decades. It’s a cheap, off-patent drug, that was unfortunately highly politicized in the early weeks of the pandemic because President Trump cited a study showing it was potentially a gamechanger in the fight against COVID.

Unfortunately, Democrats cared more about defeating Trump in the election than saving lives, and fueled hysteria against the drugs. Anyone touting the drug’s potential was silenced, including doctors. Many peer-reviewed studies have shown that HCQ contributes to less severe symptoms and lower mortality when administered early. Unfortunately, those studies were ignored while studies that claimed HCQ caused higher mortality were given wide coverage in the media… and some turned out to be bogus.

Imagine how many lives might have been saved had we really been “in this together” instead of so many being “in this to get Trump.”

(PJ-MEDIA)

And this same story via Doctors for COVID Ethics

According to a recent news story, “scientists are mystified” about the low numbers of COVID-19 cases and deaths in African countries: “Africa doesn’t have the vaccines and the resources to fight COVID-19 that they have in Europe and the U.S., but somehow they seem to be doing better.”

Interestingly, aside from confirming yet again that the vaccines don’t work, the African data also provide evidence supporting the efficacy of hydroxychloroquine. A new study by economists Hideki Toya and Mark Skidmore, which carefully controlled for other plausible contributing factors such as age distribution, healthcare capacity, and sunlight (exposure to which increases vitamin D levels), shows a convincing protective effect of hydroxychloroquine. While this is primarily an antimalarial drug, its antiviral properties have long been recognized. The same is true of ivermectin, which shows compelling activity against SARS-CoV-2 in vitro and also in vivo.

Note that the morbidity and mortality data analyzed by Toya and Skidmore are unaffected by vaccination rates, since they are from early 2020. You can read their study here: LIGHTHOUSE ECONOMICS

See also my:

“India’s “Crushing” of the Curve In States Using IVER and HCQ”

WHAT IS A MAN’S LIFE WORTH?

A Chicago-area judge saved a grandfather’s life with the single question that exposes hospitals blocking doctors from using a safe, FDA-approved drug: Why? (RESCUE with Michael Capuzzo)

Sun Ng, a retired contractor from Hong Kong, traveled to Illinois to celebrate his only granddaughter’s first birthday. He got covid and was near death in a Chicago-area hospital. All other options were exhausted, but the hospital refused to give Mr. Ng a generic, FDA-approved drug with an extraordinary safety record that a doctor believed could safe his life.

Finally, a judge asked the right question about ivermectin.

“What’s the downside?”

Put another way: If a man is dying of covid in an ICU and all else has been tried, why not order a hospital to give a safe, last-ditch drug?

Edward Hospital, located near Chicago, offered three arguments as to why Sun Ng, seventy-one, should not be given ivermectin:

  • There could be side effects.
  • Ordering ivermectin would violate its policies.
  • Forcing the issue would be “extraordinary” judicial overreach.

On each argument, DuPage County Circuit Court Judge Paul Fullerton firmly disagreed.

“I can’t think of a more extraordinary situation than when we are talking about a man’s life,” he said in a November 5 decision that is a model of rational decision-making in an irrational era.

“I am not forcing this hospital to do anything other than to step aside,” he continued in a Zoom hearing. “I am just asking—or not asking—I am ordering through the Court’s power to allow Dr. Bain to have the emergency privileges and administer this medicine.”

The hospital ultimately stepped aside. Dr. Alan Bain, an internist, administered a five-day course of 24 milligrams of ivermectin, from November 8 through November 12.

Ng, who with his wife, Ying, had come from Hong Kong to celebrate their granddaughter’s birthday, was able to breathe without a ventilator within five days—he, in fact, removed the endotracheal himself. He left the ICU Tuesday, November 16, and, although confused and weak, was breathing Sunday without supplemental oxygen on a regular hospital floor.

“Every day after ivermectin, there was accelerated and stable improvement,” said Dr. Bain, who administered the drug in two previous court cases after hospitals refused. “Three times we’ve shown something,” he told me. “There’s a signal of benefit for ventilator patients.”

Ng’s remarkable progress stands in sharp relief to the repeated attempts by Edward-Elmhurst Health, the hospital’s managing system, to thwart the use of ivermectin. It succeeded in having the court’s initial November 1 order dismissed by claiming Ng was in better health than his lawsuit contended (he wasn’t). It then defied the November 5 order, saying Dr. Bain was not vaccinated (a negative test resolved the issue).

Moreover, after Ng’s treatment was complete, the hospital system filed notice that it would appeal the order that had already been carried out. It did this even though Sun Ng seemed to have benefited greatly.

The patient’s improvement, or condition generally, did not seem to matter…..

(READ IT ALL…. A WONDERFUL STORY)

Dr. Marik received his medical degree from the University of the Witwatersrand, Johannesburg, South Africa. Dr. Marik did Critical Care Fellowship in London, and Ontario, Canada. Dr. Marik has worked in various teaching hospitals in the USA, since 1992. He is a board certified in Internal Medicine, Critical Care Medicine, Neurocritical Care and Nutrition Science. Dr. Marik is currently Professor of Medicine and Chief of Pulmonary and Critical Care Medicine, Eastern Virginia Medical School in Norfolk, Virginia. Dr. Marik has written over 500 peer-reviewed papers and books, 43,000 scholarly citations of his work, and a research “H” rating higher than many Nobel Prize winners, 80 book chapters and authored four critical care books. He has been cited over 25,000 times in peer reviewed publications.

MRNA ISSUES CONTINUE

More heart issues confirmed with the mRNA vaccines:

Bad news about the dangers that mRNA vaccines may pose to the heart and blood vessels keeps coming.

A new study of 566 patients who received either the Pfizer or Moderna vaccines shows that signs of cardiovascular damage soared following the shots. The risk of heart attacks or other severe coronary problems more than doubled months after the vaccines were administered, based on changes in markers of inflammation and other cell damage.

Patients had a 1 in 4 risk for severe problems after the vaccines, compared to 1 in 9 before.

Dr. Steven Gundry, a Nebraska physician and retired cardiac surgeon, presented the findings at the Scientific Sessions of the American Heart Association’s annual conference in Boston last week. An abstract is available in Circulation, the AHA’s scientific journal……..

(ALEX BERENSEN | Steven R Gundry: Originally published in the AMERICAN HEART ASSOCIATION journal, Circulation)

Steve Kirsch INTERVIEW

In this interview, Steve Kirsch, executive director of the COVID-19 Early Treatment Fund, reviews some of the COVID jab data he’s presented to the U.S. Food and Drug Administration and the Centers for Disease Control and Prevention during various meetings.

  • Data suggest 1 in 317 boys aged 16 to 17 will get myocarditis from the COVID shots, and after a third booster, that number may be even higher
  • VAERS reporting is likely underreported by a factor of 41. Since there are over 8,000 domestic deaths reported to VAERS, and 98% of those deaths are “excess deaths,” this suggests that as many as 300,000 Americans may have died from the COVID shots thus far
  • Calculations based on government data from 35% of the world’s population suggest we’re killing approximately 411 people per million doses on average. Moderna and Pfizer are both two-dose regimens, which pushes this to 822 deaths per million fully vaccinated. And that’s just the short-term mortality. We still have no concept of how these shots might impact mortality and morbidity in the longer term
  • An Italian investigation found that if the COVID mortality definition were changed to only include those cases where there were no preexisting comorbidities, the mortality from COVID comes out to just 2.9% of the overall reported number. This suggests that if a COVID death was redefined to being a death actually “from” COVID rather than “with” COVID, the death count could be substantially smaller than 760,000 deaths and may be smaller than the number killed by the vaccines
  • The deadliest vaccine ever made is the smallpox vaccine, which killed 1 in 1 million vaccinated people. The COVID shots kills 822 per million fully vaccinated, making it more than 800 times deadlier than the deadliest vaccine in human history

CDC Admits Tainted Statistics (Plus: Vaccine Updates)

NATURAL IMMUNITY BETTER

This is a truncated version of Epoch Times fuller video entitled:

  • “CDC Admits Having No Records of ‘Naturally Immune People’ Transmitting Virus | Facts Matter” (YouTube)

(Facts Matter’s RUMBLE Channel is here)

Natural Immunity Versus Vaccine Immunity (DENNIS PRAGER)

On August 25, 2021, medRxiv published a “preprint” study by ten Israeli scientists, all associated with an Israeli research institute, Maccabitech, in Tel Aviv. Among the 10 are three MDs, three professors of epidemiology, two professors at the Tel Aviv University School of Public Health and an adjunct researcher at the Division of Cancer Epidemiology and Genetics at the National Institutes of Health in the United States. The study’s conclusion: “This study demonstrated that natural immunity confers longer lasting and stronger protection against infection, symptomatic disease and hospitalization caused by the Delta variant of SARS-CoV-2, compared to the BNT162b2 two-dose vaccine-induced immunity

On August 26, 2021, Science, one of the world’s most widely cited science magazines, published by the American Association for the Advancement of Science, published an article on the Israeli study. Its opening sentence reads: “The natural immune protection that develops after a SARS-CoV-2 infection offers considerably more of a shield against the Delta variant of the pandemic coronavirus than two doses of the Pfizer-BioNTech vaccine, according to a large Israeli study

Martin Kulldorff, a professor of medicine at Harvard Medical School, confirmed the Israel study: “In Israel, vaccinated individuals had 27 times higher risk of symptomatic COVID infection compared to those with natural immunity from prior COVID disease

A Cleveland clinic study came to the same conclusion. Published on June 5, 2021, also on medRxiv, it concluded that “Individuals who have had SARS-CoV-2 infection are unlikely to benefit from COVID-19 vaccination

Even before the Israeli and Cleveland Clinic studies, a New York University study comparing vaccine immunity to natural immunity concluded that people who had had COVID-19 were better protected against the virus: “In COVID-19 patients, immune responses were characterized by a highly augmented interferon response which was largely absent in vaccine recipients.”

A Rockefeller University study published on August 24, 2021, concluded, as the Israel study did, that “a natural infection may induce maturation of antibodies with broader activity than a vaccine does.” The study immediately added that getting natural immunity entails contracting COVID-19, and “a natural infection can also kill you.” But that valid warning does not negate its conclusion in favor of natural immunity. Nor does the study warn that getting the vaccine may also induce harmful consequences. To its everlasting shame, that is a taboo subject in America’s medical community despite the fact that the Vaccine Adverse Event Reporting System (VAERS) website of the Centers for Disease Control and Prevention lists over 700,000 cases of suspected injury and more than 17,000 otherwise unexpected deaths temporally associated with COVID-19 vaccines….

SEE MORE:

  • 128 Research Studies Affirm Naturally Acquired Immunity to Covid-19: Documented, Linked, and Quoted (BROWNSTONE INSTITUTE)
  • Top Doctor Says New CDC Study on Natural Immunity Is ‘Highly Flawed’ (TOWNHALL)

New Harvard HCW Study Shows Recovered Immunity Is Far Stronger Than Vaccine Protection

A new study from Harvard (Continued Effectiveness of COVID-19 Vaccination among Urban Healthcare Workers during Delta Variant Predominance) tracked vaccinated and unvaccinated Massachusetts healthcare workers and showed 0 infections in 74,557 person-days for previously infected patients compared to 49 infections out of 830,084 person-days for fully vaccinated patients.

In short, if you’ve recovered from COVID, it is completely nonsensical for you to be vaccinated. You have virtually no chance of being re-infected.

Summing it up:

  1. Recovered patients much more protected from re-infection than vaccinated patients
  2. Recovered patients, even if they get COVID, cannot pass it on to anyone else as far as we know (as the CDC was forced to reveal under FOIA from Aaron Siri)
  3. We don’t know if subsequently getting vaccinated after recovering will improve or degrade points 1 or 2

In short, vaccine mandates that don’t exempt those who have recovered are unethical and a danger to the health of society. They are preventing us from getting to “herd immunity” which we can achieve through allowing natural infection and treating with effective early treatment protocols.

The study also concluded that the vaccine efficacy was 76.5% (95% CI: 40.9–90.6%) against Delta. Yet other data shows the vaccines do nothing or make things worse. I didn’t see an obvious flaw in this study regarding that determination. I don’t know if they used different Ct values for vaccinated or unvaccinated. If anyone sees a flaw, please comment below.

Summary

This study adds more evidence that recovered immunity >> vaccine immunity. Even if the vaccines were perfectly save, forcing everyone to get vaccinated is both unnecessary and jeopardizes public health.

Even if I ignore all the other data sources and only believe this one small study, it doesn’t change my opinion on the safety of these vaccines. DO NOT GET VACCINATED.

You are always better off getting COVID, getting early treatment as soon as you have symptoms (safer and more effective than any vaccine), and then you are done.

This is what Aaron Rodgers did. He maximized benefits for himself, his teammates, and society. Win-win-win.

But according to people like Jonathan Sarfati, these must all be “one-offs.” (As he responded to me posting the Israeli study in conversation a while back.)

LONG COVID FOLLIES

The quote from Doc Sowell is related directly to the article that follows it.

The difference between survey results and demonstrable realities was also pointed out by the author of Hillbilly Elegy: “In a recent Gallup poll, Southerners and Midwesterners reported the highest rates of church attendance in the country. Yet actual church attendance is much lower in the South.”

Thomas Sowell, Discrimination and Disparities (New York, NY: Basic Books, 2018), 23-25

Long Covid Doesn’t Exist, Volume One Zillion

A huge French study shows BELIEVING you had Covid is associated with many later symptoms. But ACTUALLY having had Covid isn’t associated with any (except loss of sense of smell).

…..The researchers also found that almost 60 percent of the people with antibodies HAD NO IDEA THEY HAD EVEN HAD COVID AT ALL. Meanwhile, while more than half the people who said they had had Covid had no antibodies. (Welcome to the plague so severe most halfway healthy adults don’t even know they’ve had it.)

The study strongly suggests that many people are using previous Covid diagnoses – either real or imagined – to help explain away common physical symptoms such as joint pain or cough. It also suggests that actually being infected Covid is far less risky than thinking you have been infected with Covid for many people.

The researchers concluded by explaining that people who claim they have long Covid may need help “to identify cognitive and behavioral mechanisms that may be targeted to relieve the symptoms.” Which is a very polite way of putting the truth.

This study should slow, if not stop, the rush to medicalize long Covid. It is yet more proof that the illness is a group of squishy (if painful and difficult) symptoms looking for a name – and more importantly a billing code.

But so many patients and physicians and public health experts are now invested (in some cases literally) in making long Covid real that the gravy train will likely roll on.

DANGERS from VACCINES

Recent anecdotal examples:

  • (Told to me) Friday (or Thursday… I forget), one of our regular vendors dropped off some material and during our normal conversating he mentioned his nephew (a 40-year old healthy dude) died within days of getting his booster. He got his booster, almost immediately after starting feeling funny. After 2-days he went to the hospital, ended up in coma, and died. Just thought I would share. The entire family blames the booster…. I bet Pfizer won’t.
  • (In comment section below the above) An exercise instructor friend of mine got the booster and within a day experienced respiratory and circulatory distress — and has been in the hospital most of a month and isn’t really improving. Perhaps coincidental. Perhaps something else?
  • (Private Message) My father in law had a stroke about 15 days after his booster. I’m positive that was the cause
  • My grandma (vaccinated) got covid from the vaccinated and is fighting for her life.

When do the anecdotes become enough?

Taiwan Blocks Second Pfizer Doses For Teens

And they aren’t even CONSIDERING allowing kids 5-11 to get Covid vaccinated at this point

Because of myocarditis.

Rare, mild myocarditis.

Except it’s neither of those things.

Imma say it again: if you let your healthy teen – much less your healthy child – get this vaccine, you are insane.

The public health frenzy to vaccinate kids is the ultimate example of process at all costs, the flywheel spinning ever faster, unmoored from reality.

I believe the children are our future Because, you know, they are the future.

So why are we subjecting them to even the tiniest smidgen of risk over this illness, which essentially can’t touch them?

[…..]

Or maybe the Taiwanese just hate their kids.

Yeah, if it makes you feel better, you’re welcome to believe that.

Another Major Red Flag About Covid Vaccines And Death (This one coming from data on more than 4 million vaccinated Swedes)

People appear to die at rates 20 percent or more above normal for weeks after receiving their second Covid vaccine dose, according to data from a huge Swedish study.

The figures are buried in a preprint paper on vaccine effectiveness released last month. The headline finding of the paper was that protection against Covid, including severe cases, plunged after six months.

The researchers did not explicitly examine deaths from all causes – which have risen since the summer in many countries that have highly vaccinated populations.

But on page 32 of the 34-page report, a chart shows that 3,939 of 4.03 million Swedes who received the second dose died less than two weeks later.

[….]

Over a one-year period, that rate of death would translate into an annual mortality rate of about 2.5 percent a year – 1 person in 40 – almost three times the overall Swedish average. In a typical year, about 1 in 115 Swedes dies.

Of course, that huge gap does not account for an important confounding factor: younger people, who have a much lower risk of death, were less likely to be vaccinated.

But Sweden also provides detailed data on overall deaths nationally, making a crude baseline comparison possible…..

We Are Killing Our Kids. Does Anyone Care? (Kids that would have never died from COVID are now dying after getting the vaccine. Will it ever end?)

Recently, Dr. Toby Rogers did a risk-benefit analysis showing we’ll kill 117 kids for every kid we save from COVID with the vaccines aged 5 to 11.

The ratio doesn’t really change if they change the dose, e.g., to a third of the adult dose. It means fewer kids saved and fewer kids killed, but Toby estimates the ratio would be about the same. Whether it is 117 or 10, it doesn’t matter. We will kill a lot more kids than we will ever save with these vaccines.

What Toby predicted is now coming true.

We can’t show it is 117 to 1, but we can show for sure we are killing more kids than we are saving because kids that would have never died before are now dying with COVID, only children with pretty severe health problems would die: we don’t know of a single kid, 5 to 11, who died from COVID who didn’t have some pretty serious health issues before they got COVID.

Those days are now gone. We’re now killing the healthy kids.

The vaccines rolled out for kids 5 to 11 starting on November 7. It is now just 12 days later and we are now killing perfectly healthy kids.

I just got this text: (to the right)

That’s hardly an isolated incident.

These deaths simply are never ever going to reported in the NY Times or on CNN. So you’re never going to hear about them except from alternate media sources like this substack article. So only around 20,000 people will ever see these deaths.

Here’s another example. Another canary in the coal mine.

First time in her 14-year career: seeing an 8 year old with myocarditis

I saw this Tweet from one of my followers. First time in her 14 year career she has ever seen an 8 year old child with myocarditis. Welcome to the “new normal.”

It’s happening for older kids too, not just the youngest. Here’s a video of Ernest Ramirez who lost his only child, his 16-year old son. I’ve talked to Ernest. His son had zero health issues. He got the first dose of Pfizer and just 5 days later his heart had doubled in size and he died of cardiac arrest while in the park. Dr. Peter McCullough, one of the nation’s most respected cardiologists reviewed the autopsy report and determined the vaccine killed the child. But the CDC simply ignores that because the medical examiner who did the autopsy (after a huge amount of pleading by the father) just said his son died of heart failure, not the vaccine.

Please click the image to watch the video, it’s only 2 minutes long:

WEAKENING mRNA VACCINES

More Proof The mRNA Covid Vaccines Don’t Produce Long-Lasting Immunity (If you like a functional T-cell response from your vaccines, Moderna and Pfizer may not be for you. The DNA vaccines might be better. [They could hardly be worse.])

Researchers from Harvard have more bad news for people who received the mRNA Covid vaccines from Pfizer and Moderna.

The vaccines produce a markedly weaker T-cell coronavirus response than AstraZeneca’s DNA vaccine, according to a letter the researchers published yesterday in the New England Journal of Medicine.

The antibodies from the mRNA vaccines also fade far more quickly, though they initially peak at a higher level than those the DNA vaccines cause our bodies to make in response to the spike proteins they produce.

Combined with the disappearing antibodies, the lack of T-cell response helps explain why the mRNA vaccines begin to fail against coronavirus infection just months after the second dose.

T-cells play a crucial part in our response to infection, helping produce a long-term immune response that will last after initial antibodies wane.

The vaccine-generated antibodies were already known to fade quickly. The researchers confirmed that finding. But they also examined T-cells and found that the mRNA vaccines produced only about 1/7 as strong a CD8+ T-cell response as the AstraZeneca vaccine.

CD8+ T-cells are part of what scientists called the “adaptive” immune system. They attack and kill cells that have been infected with the virus, keeping the virus from multiplying as quickly. They are a crucial part of immunity against reinfection because although they take a while to gain strength when a pathogen first appears, they can spool up more quickly if it reappears months or years later.

The research hints that the DNA vaccines from AstraZeneca and Johnson & Johnson may remain protective for longer than the mRNA vaccines…..

Pfizer Whistleblowers

Nick Karl, Pfizer Scientist:

  • “When somebody is naturally immune — like they got COVID — they probably have more antibodies against the virusWhen you actually get the virus, you’re going to start producing antibodies against multiple pieces of the virus… So, your antibodies are probably better at that point than the [COVID] vaccination.”

Chris Croce, Pfizer Senior Associate Scientist:

  • “You’re protected for longer” if you have natural COVID antibodies compared to the COVID vaccine. “I work for an evil corporation Our organization is run on COVID money.”

(PROJECT VERITAS)

(I assume this is a whistleblower Democrats don’t like.) BMJ listens to evidence from whistleblower over the Pfizer vaccine trial.

Revelations of poor practices at a contract research company helping to carry out Pfizer’s pivotal covid-19 vaccine trial raise questions about data integrity and regulatory oversight. (British Medical Journal)

In autumn 2020 Pfizer’s chairman and chief executive, Albert Bourla, released an open letter to the billions of people around the world who were investing their hopes in a safe and effective covid-19 vaccine to end the pandemic. “As I’ve said before, we are operating at the speed of science,” Bourla wrote, explaining to the public when they could expect a Pfizer vaccine to be authorised in the United States.

But, for researchers who were testing Pfizer’s vaccine at several sites in Texas during that autumn, speed may have come at the cost of data integrity and patient safety. A regional director who was employed at the research organisation Ventavia Research Group has told The BMJ that the company falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial. Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding. After repeatedly notifying Ventavia of these problems, the regional director, Brook Jackson, emailed a complaint to the US Food and Drug Administration (FDA). Ventavia fired her later the same day. Jackson has provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails.

[…..]

Concerns Raised

In her 25 September email to the FDA Jackson wrote that Ventavia had enrolled more than 1000 participants at three sites. The full trial (registered under NCT04368728) enrolled around 44 000 participants across 153 sites that included numerous commercial companies and academic centres. She then listed a dozen concerns she had witnessed, including:

  • Participants placed in a hallway after injection and not being monitored by clinical staff

  • Lack of timely follow-up of patients who experienced adverse events

  • Protocol deviations not being reported

  • Vaccines not being stored at proper temperatures

  • Mislabelled laboratory specimens, and

  • Targeting of Ventavia staff for reporting these types of problems.

Within hours Jackson received an email from the FDA thanking her for her concerns and notifying her that the FDA could not comment on any investigation that might result. A few days later Jackson received a call from an FDA inspector to discuss her report but was told that no further information could be provided. She heard nothing further in relation to her report.

In Pfizer’s briefing document submitted to an FDA advisory committee meeting held on 10 December 2020 to discuss Pfizer’s application for emergency use authorisation of its covid-19 vaccine, the company made no mention of problems at the Ventavia site. The next day the FDA issued the authorisation of the vaccine.8

In August this year, after the full approval of Pfizer’s vaccine, the FDA published a summary of its inspections of the company’s pivotal trial. Nine of the trial’s 153 sites were inspected. Ventavia’s sites were not listed among the nine, and no inspections of sites where adults were recruited took place in the eight months after the December 2020 emergency authorisation. The FDA’s inspection officer noted: “The data integrity and verification portion of the BIMO [bioresearch monitoring] inspections were limited because the study was ongoing, and the data required for verification and comparison were not yet available to the IND [investigational new drug].”

Other Employees’ Accounts

In recent months Jackson has reconnected with several former Ventavia employees who all left or were fired from the company. One of them was one of the officials who had taken part in the late September meeting. In a text message sent in June the former official apologised, saying that “everything that you complained about was spot on.”

Two former Ventavia employees spoke to The BMJ anonymously for fear of reprisal and loss of job prospects in the tightly knit research community. Both confirmed broad aspects of Jackson’s complaint. One said that she had worked on over four dozen clinical trials in her career, including many large trials, but had never experienced such a “helter skelter” work environment as with Ventavia on Pfizer’s trial.

“I’ve never had to do what they were asking me to do, ever,” she told The BMJ. “It just seemed like something a little different from normal—the things that were allowed and expected.”

She added that during her time at Ventavia the company expected a federal audit but that this never came.

After Jackson left the company problems persisted at Ventavia, this employee said. In several cases Ventavia lacked enough employees to swab all trial participants who reported covid-like symptoms, to test for infection. Laboratory confirmed symptomatic covid-19 was the trial’s primary endpoint, the employee noted. (An FDA review memorandum released in August this year states that across the full trial swabs were not taken from 477 people with suspected cases of symptomatic covid-19.)

“I don’t think it was good clean data,” the employee said of the data Ventavia generated for the Pfizer trial. “It’s a crazy mess.”

A second employee also described an environment at Ventavia unlike any she had experienced in her 20 years doing research. She told The BMJ that, shortly after Ventavia fired Jackson, Pfizer was notified of problems at Ventavia with the vaccine trial and that an audit took place.

Since Jackson reported problems with Ventavia to the FDA in September 2020, Pfizer has hired Ventavia as a research subcontractor on four other vaccine clinical trials (covid-19 vaccine in children and young adults, pregnant women, and a booster dose, as well an RSV vaccine trial; NCT04816643NCT04754594NCT04955626NCT05035212). The advisory committee for the Centers for Disease Control and Prevention is set to discuss the covid-19 paediatric vaccine trial on 2 November.

Double Vaxxed Updates and Vaccine Prohibitions Growing

DOUBLE VAXED:

As previously posted in my “First Wave and Current Wave Covid Comparisons | Singapore” — I note Singapore’s outbreak, but here is more:

Singapore’s Ministry of Health reported a major increase in breakthrough infections of COVID-19 for four straight days despite being ranked Number 5 in the world in vaccination rate.  Over 80 percent of the country is vaccinated for COVID-19.

As of 7 October 2021, 83% of the population has received two doses of COVID-19 vaccines, and 85% has received at least one dose, according to the latest report.

(GATEWAY PUNDIT)

My grab from REUTERS COVID TRACKER:

NORDIC COUNTRIES and the VACCINES:

  • (CBS) Stockholm — Sweden’s Public Health Agency on Wednesday recommended a temporary halt to the use of the Moderna COVID-19 vaccine among young adults, citing concerns over rare side effects to the heart. It said the pause should initially be in force until December 1, explaining that it had received evidence of an increased risk of side effects such as inflammation of the heart muscle (myocarditis) and inflammation of the pericardium (pericarditis).

This is in addition to Finland, Sweden, Norway, and Denmark saying young men should not get the vaccine.

The STEPHEN LENDMAN BLOG adds some additional clarity:

….At this time, Sweden, Denmark, Norway, Finland and Iceland halted use of toxic Moderna jabs for young people.

It’s because they risk contraction of myocarditis — inflammation of the heart muscle that causes arrhythmias.

It also risks blood clots in the heart, a stroke or heart attack that can cause death.

Finnish Institute for Health and Welfare’s chief physician Hanna Nohynek MD said Moderna jabs will not be administered to males under age-30.

Sweden banned the drug for everyone in the country under age-30.

Denmark followed suit for all Danes under age-18.

On Friday, Iceland halted use of the drug altogether, a statement by its chief epidemiologist saying the following:

Moderna jabs “will not be used in Iceland while further information is obtained on (its) safety” — that doesn’t exist and won’t be found if honest evaluation is undertaken.

The European Medicines Agency is examining Sweden’s report.

Canada’s public health agency said it’s monitoring cases of myocarditis and pericarditis.

The latter is inflammation of tissue surrounding the heart….

Also, a recent story of a whistleblower is thus (via LIFE SITE NEWS):

Whistleblower says nearly 50,000 Medicare patients have died from covid vaccination

A whistleblower has provided government data documenting 48,465 deaths within 14 days of COVID-19 vaccination among Medicare patients alone, according to medical freedom rights attorney Thomas Renz.

The announcement Saturday was made by the Ohio-based attorney, who remains involved in several major cases brought against federal agencies relating to fraud and violations of medical freedom rights….