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COVID Vaccine Manufacturers Given Legal Immunity for Injuries or Deaths Caused by Fast-tracked Vaccines

In light of the COVID-19 pandemic, the United States and other countries around the globe have opened the door for accelerated development, testing and fast track licensure of experimental COVID-19 vaccines. The question many people have is: who will assume product liability when COVID-19 vaccines cause harm to an individual who has been vaccinated? AstraZeneca plc, a multinational pharmaceutical and biopharmaceutical company headquartered in Cambridge, England, has been granted product liability protection for the COVID-19 vaccine the company is developing by most countries with which it has made vaccine supply agreements. Liability questions have been a central issue in negotiations between AstraZeneca and countries seeking COVID-19 vaccine supply contracts. In the U.S., vaccine manufacturers are shielded from liability under the 2005 Public Readiness and Emergency Preparedness (PREP) Act if a vaccine or drug developed in response to a health emergency like a pandemic causes the death or permanent injury of an individual who receives it during pre-licensure clinical trials or after it is released for public use. The PREP Act was part of a series of “Bioshield” laws created in response to national security fears after 9/11 and subsequent reported weaponized microbe threats, which prompted Congress to encourage pharmaceutical companies to develop anti-bioterrorism vaccines by, in part, eliminating liability for injuries and deaths caused by those vaccines.

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Bill Gates Outspends U.S. Government and Provides $18 BILLION to WHO for COVID Vaccines

The World Health Organization (WHO) announced today their plan to vaccinate every person on the planet with a COVID-19 vaccine. In order to do this, they have received $18 BILLION from two organizations funded by Bill Gates: GAVI and the Vaccine Alliance and the Coalition for Epidemic Preparedness Innovations (CEPI). It is hard to keep track how much money the U.S. Government has given Big Pharma companies to develop a COVID vaccine, but I believe it is still less than $5 BILLION. That means Bill Gates has just outspent the U.S. Government for COVID vaccine development by about 3 to 1.

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FDA could Approve “at least one” COVID-19 Vaccine Before November Election

The pharmaceutical industry's marketing trade publication, FiercePharma, published an article this week where analysts predicted that the U.S. Food and Drug Administration could approve "at least one" new COVID 19 vaccine before the November elections. FDA chief Stephen Hahn, however, testified before the House Energy and Commerce Committee yesterday (June 23, 2020), and stated that the FDA was breaking from the White House's "Warp Speed" timeline for vaccine development, stating that "data and science" would drive the agency's decision making. Hahn was responding to a Congressional inquiry, with a letter being sent to him by three chairs from the House Committee on Oversight and Reform who were concerned about the safety of a "fast-tracked" vaccine. This begs the question, considering that more than $1 TRILLION has already been spent by the U.S. Government to develop COVID vaccines, who is calling the shots here on the COVID vaccine? President Trump has publicly endorsed the "Operation Warp Speed" COVID vaccine project, which is run by a military general and medical authorities all with ties to Bill Gates. Stephen Hahn is President Trump's hand-picked man to run the FDA, coming out of a career in cancer research in Texas. So as America and the world look to the future and a possible COVID vaccine that some doctors claim will be a new kind of DNA vaccine never before used on humans that could have devastating results with many lives lost or destroyed, will the FDA really be transparent with test results and only rely on "data and science?" Because if so, such a vaccine would probably be years away, and certainly not within this year. And if the FDA does, in fact, take this position, will President Trump, as the commentary in FiercePharma states, "push the FDA behind the scenes to issue an approval or emergency authorization"? I guess it depends on who is calling the shots. Will the President and the FDA, or Bill Gates and his collaborators in the U.S. Government such as Dr. Fauci, Dr. Deborah Birx, CDC Director Robert Redfield, and now Operation Warp Speed Director Dr. Moncef Slaoui, be the ones to make the decision to further advance their goals of reducing the world's population? In fact, I think it is appropriate to ask the question: Is the decision to approve this COVID vaccine a requirement for someone to be elected as President of the United States in November?

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COVID Vaccine Will Only be Good for a Short Time – Multiple Shots Will be Needed

Pharmaceutical companies racing to fast-track a COVID vaccine are already warning the public that any vaccine that comes into the market will probably only offer temporary "protection," laying the ground work for a COVID vaccine that will probably be similar to the annual flu vaccine, where a new shot is needed every year. The flu vaccine is already the most dangerous vaccine in the market, comprising the bulk of settlements for injuries and deaths in the U.S. Vaccine Court. FiercePharma, the marketing trade publication for the vaccine industry, quoted AstraZeneca CEO Pascal Soriot from an interview he gave on a Belgian radio station: “We think that it will protect for about a year.” FiercePharma also reports that AstraZeneca expects to have their vaccine ready by October this year. Soriot said that “if all goes well, we will have the results of the clinical trials in August/September,” as quoted by Reuters. “We are manufacturing in parallel,” he added. “We will be ready to deliver from October if all goes well.” Soriot is not the only one saying that multiple shots will be needed for COVID treatment. Dr. Fauci has said the same thing, as Marco Cáceres reports in this article from The Vaccine Reaction.

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As COVID Vaccines Head into Phase 3 Trials Big Pharma Prepares for Increase in Flu Vaccines for Fall

An article published in FiercePharma, a pharmaceutical marketing trade publication, is reporting that the National Institute of Health is preparing to test experimental COVID vaccines entering into phase 3 of development on over 90,000 people this summer. The three drug companies entering phase 3 trials are Moderna, AstraZeneca and Johnson & Johnson. Given the recent bad publicity Moderna received from the small sample size tested so far, one has to wonder if the drug companies will be transparent in releasing the results of these trials, both negative and any positive outcomes. Given the fact that the U.S. taxpayers are picking up the tab on these trials, the companies have a legal and moral obligation to be transparent in the results of these trials. Meanwhile, flu vaccine manufacturers are already preparing for this fall's flu season and planning on manufacturing more flu vaccines than they did last year. According to FiercePharma, the manufacturers are looking at "creative ways" of injecting more people, by setting up mobile clinics in parking lots, parks or community centers. I would not be surprised to see them giving them out in churches and other religious institutions as well. In another article published this week by Beth Snyder Bulik in FiercePharma, it is revealed that Big Pharma invests heavily in tracking social media conversations about COVID treatments and other drugs, and also in advertising and using "influencers" to get their message out. There can be no doubt now that Big Tech social media companies work with Big Pharma while suppressing any other natural treatments that would compete with them.

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Editors of The Lancet and the New England Journal of Medicine: Pharmaceutical Companies are so Financially Powerful They Pressure us to Accept Papers

Philippe Douste-Blazy, MD, is a cardiologist and former French Health Minister who served as Under-Secretary General of the United Nations. He was a candidate in 2017 for Director of the World Health Organization. In a videotaped interview on May 24, 2020, Dr. Douste-Blazy provided insight into how a series of negative hydroxychloroquine studies got published in prestigious medical journals. He revealed that at a recent Chatham House top secret, closed door meeting attended by experts only, the editors of both, The Lancet and the New England Journal of Medicine expressed their exasperation citing the pressures put on them by pharmaceutical companies. He states that each of the editors used the word “criminal” to describe the erosion of science. He quotes Dr. Richard Horton who bemoaned the current state of science: “If this continues, we are not going to be able to publish any more clinical research data because pharmaceutical companies are so financially powerful; they are able to pressure us to accept papers that are apparently methodologically perfect, but their conclusion is what pharmaceutical companies want.”

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Pfizer, Merck, AZ, J&J and Moderna selected as ‘Warp Speed’ finalists for COVID Vaccine

As millions of Americans remain out of work, and small businesses continue to face insurmountable odds to reopen as many are being damaged and looted in cities all across the U.S., the government continues to pour BILLIONS of dollars into the pharmaceutical industry in what is probably the largest transfer of wealth seen in the U.S. since World War II. We previously reported on the government's "Warp Speed" project to fast-track a Coronavirus vaccine with unlimited resources of federal funding. Operation Warp Speed is headed by General Gustave Perna, and Dr. Moncef Slaoui, the former chairman of GlaxoSmithKline’s vaccines division. Dr. Slaoui has strong ties to Dr. Anthony Fauci, Bill Gates, and Big Tech, particularly Google. President Trump has previously stated that the U.S. Military would help deploy over 300 million doses of a Coronavirus vaccine later this year. FiercePharma has reported that the Trump Administration narrowed down the finalists among the pharmaceutical companies competing to develop the Coronavirus vaccine to: AstraZeneca, Merck, Pfizer, Johnson & Johnson and Moderna. British drugmaker AstraZeneca, in addition to securing $1.2 billion from the U.S. Government for their Coronavirus vaccine, just also received $750 million from the Bill Gates funded Coalition for Epidemic Preparedness Innovations (CEPI) and Gavi, the Vaccine Alliance, which work together with the World Health Organization to distribute vaccines worldwide, particularly the poorer countries. So it looks pretty clear at this point, that Phase 3 of the Plandemic is to inoculate the entire world's population with a COVID-19 vaccine. If this ends up being a new mRNA-based vaccine never before seen in the market, Dr. Sherri Tenpenny and Dr. Judy Mikovits are predicting 50 million deaths and untold injuries just within the United States.

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COVID Experimental Vaccine Victim Claims “Sickest in His Life” after Being Injected with Experimental Vaccine

You know Ian Haydon from many appearances on CNN and other networks celebrating his heroic act of volunteering to test Moderna’s experimental COVID vaccine. The sun has now set on Haydon’s television career. He is no longer useful to the Pharmedia narratives that all vaccines are always safe for all people, that Moderna’s business partners, Tony Fauci and Bill Gates, were justified in skipping animal studies and that Moderna’s vaccine will soon rescue us from the Pandemic. Ian Haydon is now an embarrassment to Fauci, Gates, and their CNN cheerleaders. He will therefore vanish into the censorship twilight. Moderna chose Haydon for the study because of his robust good health. He was among the 15 volunteers in the high dose group. Within 45 days, three of these—a shocking 20%—experienced “serious” adverse events according to Moderna’s press release meaning they required hospitalization or medical intervention.

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Not Wanting to Get Left Behind, Merck Nabs $38 MILLION from U.S. Government to Develop COVID Vaccine

Despite the fact that they are currently embattled in two federal lawsuits for fraud regarding the development of their MMR and Gardasil vaccines, Merck jumped into the COVID-19 race and nabbed $38 MILLION of American taxpayer funds to develop COVID products, including vaccines, it was announced today. The transfer of American wealth to the criminal pharmaceutical industry continues as millions are out of work and non-pharmaceutical businesses go bankrupt.

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Moderna COVID Vaccine Trial Sees 20% “Serious” Injury Rate as U.S. Invests BILLIONS More on Experimental COVID Vaccines

On Monday this week (May 18, 2020) Moderna put out a press release stating that they had seen positive results to the first phase of their COVID-19 vaccine trial. The news sent their stock prices surging, as the pharmaceutical company is working with Dr. Anthony Fauci and the National Institute for Allergy and Infectious Diseases which Fauci heads. However, that all changed on Tuesday, May 19, 2020, when Stat News published an article stating that Moderna did not produce any data to back their claims. Robert F. Kennedy, Jr. also published his own observation on the little bit of data that was disclosed via his Instagram Account: CATASTROPHE! Moderna Vaccine has 20% "Serious" Injury Rate in High Dose Group! The U.S. Government has invested about half a million dollars in the Moderna experimental COVID vaccine so far. Now today, Thursday May 21st, while record numbers of Americans in the millions and climbing are without jobs, UK drug company AstraZeneca has announced that it has received $1.2 BILLION from the U.S. Government to receive 300 million vaccine doses starting this fall of a COVID-19 vaccine that is still in development and not even approved yet. While the future of a COVID-19 vaccine is still uncertain, one thing is very clear: a vast majority of the wealth of the United States is being transferred to Big Pharma as thousands of businesses are now closing down due to the COVID-19 scare while the U.S. Government gives hundreds of BILLIONS of dollars to Big Pharma.

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