- In recent months, two Pfizer officials have bragged about moving vaccine science forward at a speed that disallows proper scientific protocols from being followed, and the release of reformulated mRNA COVID boosters without testing is now the norm
- In November 2022, recently retired head of vaccine R&D at Pfizer, Kathrin Jansen, said “we flew the aeroplane while we were still building it. We couldn’t wait for data, we had to do so much at risk.” Pfizer compressed its vaccine development timeline from 10 years to a mere nine months by simultaneously developing and testing the product in human trials
- Pfizer and other COVID jab makers hid side effects by eliminating the control groups long before the studies were over
- Vaccine makers are readying to release other mRNA shots, many of which are being fast-tracked and predicted to receive authorization in months rather than years. Moderna is working on a three-in-one shot for COVID, flu and RSV (respiratory syncytial virus), and they seem to expect releasing it before clinical trials are finished
- Pfizer quoted and relied on data from Israel when it sought approval from the FDA, and as it turns out, the Israeli government hid information about side effects. It didn’t even implement its surveillance system until a year after the shots rolled out, and when the data were analyzed, researchers concluded there were causative links between certain side effects and the jabs
In the video above, Del Bigtree with The Highwire reviews how the precautionary principle and long-standing safety guidelines in medicine have been eliminated with the COVID shots, and how data showing harms are being ignored, suppressed and manipulated to hide the truth.
In recent months, no less than two Pfizer officials have bragged about moving vaccine science forward at a speed that virtually guarantees that proper scientific protocols will be abandoned.
As noted in that interview, Pfizer compressed its vaccine development timeline from 10 years to a mere nine months. Well, you cannot do that unless you cut certain corners and develop and test the product more or less simultaneously. In this case, human trials began even though the preliminary testing was extremely minimal.
They Did Everything at Your Risk
“We got creative — we couldn’t wait for data, we had to do so much ‘at risk,’” Jansen said. There are those words again — doing everything “at risk.” In other words, the risks were not part of the equation, and let’s be clear, the risk they’re referring to is the risk a person takes when they take the shot.
Pfizer’s primary focus was to create a shot that minimized the symptoms of infection, but aside from that, there was no time to assess side effects or long-term drawbacks of the technology, such as antibody-dependent enhancement, myocarditis, or spontaneous abortions.
This is probably why Pfizer and the other COVID jab makers all decided to eliminate the control groups long before the studies were even over. This way, side effects could be hidden, and we see the effects of that decision now.
Myocarditis, blood clots, lethal heart attacks, strokes, cancer and sudden death are all skyrocketing, but since there’s no official control group to compare with, those trends are written off as either normal or coincidental. You’ve probably seen that heart attacks are now blamed on everything from hot weather and cold showers to soil microbes in your garden, climate change and loud noises.
Other mRNA Approvals Expected With Little or No Data
For example, Moderna is working on a three-in-one shot for COVID, flu and RSV (respiratory syncytial virus), and they seem to fully expect releasing it before clinical trials are finished. As reported by CBC News:4
In addition to fast-tracking mRNA injections for a variety of respiratory viruses, vaccine makers are also loading their pipelines with mRNA shots for diseases such as cancer, multiple sclerosis (MS), birth defects and rarer diseases.
Curiously, while mRNA shots are being hailed as the new and improved answer for every ill, Moderna president Stephen Hoge and chief technical officer Juan Andres cashed out hundreds of millions of their stock options earlier this year,5 which seems odd if everything is going well and no future trouble is expected.
Government and Corporate Interests Have Become One
Aiding and abetting the circumvention of the precautionary principle are contract research firms that run medical research trials for drug companies and federal agencies alike, thereby giving the drug companies the inside track on drug approvals.6,7
As noted by investigative journalist Paul Thacker, the COVID pandemic has erased the boundaries between corporate interests and those of our government, and with that, there are few left to trust.work with the National Institutes of Health to determine how companies run some drug trials; Pfizer hired a CRO to run their COVID-19 vaccine trial; a CRO calmed fears about the safety of AstraZeneca’s COVID-19 vaccine after the FDA and NIH
Making an already dangerous situation worse, vaccine companies and governments are working overtime to hide and suppress data showing the COVID jabs are a medical disaster, and have hidden unfavorable data from the very beginning. The basic data gathering has also been shockingly lax across the world, considering the stakes.
As noted by MIT professor Retsef Levi in The Epoch Times interview above,9,10 Pfizer quoted and relied on data from Israel when it sought approval from the FDA, and as it turns out, the Israeli government hid information about side effects.
Even more surprising, Levi claims the Israeli government lied when it said it had a robust system for monitoring and tracking side effects from the start. That surveillance system wasn’t launched until a year after the rollout of the shots, Levi says. A research team was eventually hired to analyze the data, and their findings were disconcerting.
Unlike what was told to the public, many of the side effects were both common and long-lasting. The Ministry of Health was advised to think in terms of “medical-legal” when communicating this to the public, as the Ministry might be held liable for telling the public side effects were rare and of short duration.
In other words, they were informed they’d grossly misinformed the public and could be held accountable for injuries. The Ministry’s solution? Fire the research team and alter the report’s data and conclusions.
In the interview, Levi explains how some of the data manipulation was done. For example, they massively lowered the number of post-jab menstrual irregularities by counting both women and men. You don’t need to be a scientist to realize that by counting men, who cannot menstruate, you end up with a wild misrepresentation of the incidence of menstrual irregularities.
Most egregious of all, the Ministry hid the fact that the research team found clear evidence of causality, as patients, when rechallenged with another dose, would experience a resurgence of symptoms and/or a worsening of symptoms. Adding insult to injury, even though the Ministry knows exactly who these patients are, they have not reached out to help them medically or compensate them for injuries that have been clearly linked to the shots.
New Zealand Booster Campaign Linked to Excess Deaths
Similarly, an earlier study13,14,15 published June 28, 2022, found that, in New Zealand, the age groups that were most likely to have received a COVID booster in the winter of 2021 had 7% to 10% more excess deaths than age groups that were ineligible for boosters.