Professor Murakami of Tokyo University of Science Pfizer's mRNA vaccine had plasmid DNA, so when I checked it, I was surprised to find the SV40 sequence.
SV40 is a promoter of cancer viruses, and the presence of this sequence facilitates the translocation of DNA to the human nucleus. easier to enter the genome. Even though it's a sequence that is completely unnecessary to make an mRNA vaccine. Why SV40?
The plasmid DNA map submitted by Pfizer to the EMA (European Medicines Agency) does not appear to include SV40. Why did you hide it?
Dr. Aseem Malhotra tells Joe Rogan that a reanalysis of Pfizer and Moderna's original clinical trial data shows that their COVID mRNA vaccines *INCREASE* your risks of serious adverse events, hospitalization, and death:
"In my whole career, looking at all of the drugs and knowing about many different prescribed medications, I've never seen something that when you look at the data has such poor effectiveness and unprecedented harms. In the summer of last year, in the journal Vaccine, the highest-impact medical journal for vaccines, they published a reanalysis of Pfizer and Moderna's original double-blinded randomized controlled trial.
This is the highest quality of scientific evidence. Joseph Fraiman is an ER doctor and clinical data scientist from Louisiana. Associate editor of the BMJ, Dr. Peter Doshi. Dr. Robert Kaplan from Stanford. Some real eminence of integrity published this reanalysis, and what they found was this. In the trials that led to the approval of regulators worldwide, you were more likely to suffer a severe adverse event from taking the vaccine, hospitalization, disability, or life-changing event than you were to be hospitalized with COVID.
This mRNA vaccine should likely have never been approved for a single human in the first place, and that rate of serious adverse events is at least 1 in 800... 1 in 800 is a very, very high figure. We've pulled other vaccines for much less. The 1976 Swine Flu vaccine was pulled because it was found to cause a debilitating neurological condition called Guillan-Barre syndrome in about 1 in 100,000 people. The Rotavirus vaccine was suspended in 1999 because it was found to cause a form of bowel obstruction in kids in 1 of 10,000. This is at least 1 in 800. It's a no-brainer. So the question is, why have we not paused it?"
Everything we were told about Covid-CCP injection was lie. The drug companies knew it was a lie. The governments of USA and Britain knew it was a lie. They even agreed to li
QUOTE: In the days leading up to the U.S. Food and Drug Administration's approval of Pfizer's COVID-19 vaccine, U.S. and U.K. health officials entered into a "mutual confidentiality agreement" to keep vaccine adverse events under wraps.
• U.S. and U.K. health officials discussed "anaphylactoid reactions" due to COVID-19 shots and emphasized their "mutual confidentiality agreement" regarding the topic. • The news was revealed in 57 pages of heavily redacted U.S. Department of Health and Human Services (HHS) records via a Freedom of Information Act (FOIA) lawsuit. • A government email exchange from May 14, 2021, also discusses concerns about administering COVID-19 shots along with other vaccines during pregnancy • Regulatory filings show Pfizer knew of its shots' waning effectiveness in April 2021 but didn't publicly acknowledge it until late July 2021. • Preclinical studies for Pfizer's COVID-19 shots also warned of rhabdomyolysis, which is the breakdown of skeletal muscles, but the trial reported it was "completed with no safety concerns."
In the days leading up to the U.S. Food and Drug Administration's (FDA) approval of Pfizer-BioNTech's COVID-19 shot, an agreement was made to keep serious adverse reactions under wraps.
U.S. and U.K. health officials discussed "anaphylactoid reactions" due to COVID-19 shots and emphasized their "mutual confidentiality agreement" regarding the topic.
The news was revealed by Judicial Watch, which obtained 57 pages of heavily redacted HHS records via a FOIA lawsuit.
Initially, Judicial Watch submitted a FOIA request in August 2021 that specifically asked for:
"All emails sent to and from members of the Vaccines and Related Biological Products Advisory Committee regarding adverse events, deaths and/or injuries caused by investigatory vaccines for the prevention or treatment of SARS-CoV-2 and/or COVID-19 currently produced by Pfizer/BioNTech, Moderna and/or Johnson & Johnson."
The request was ignored, prompting the lawsuit that ultimately revealed the confidentiality agreement between U.S. and U.K. regulators.
"Why are we engaged in a secret deal to keep secret information about adverse events related to the vaccines?" Judicial Watch president Tom Fitton asked. "I just think it's troubling. The documents speak for themselves."
Attorney General Paxton launched an investigation into the pharmaceutical companies Pfizer, Moderna, and Johnson & Johnson concerning whether they engaged in gain-of-function research and misled the public about doing so.
Paxton is also investigating whether the companies misrepresented the efficacy of their Covid-19 vaccines and the likelihood of transmitting Covid-19 after taking the vaccines in violation of the Texas Deceptive Trade Practices Act. The investigation will also look into the potential manipulation of vaccine trial data. This investigation concerns potentially fraudulent activity that falls outside the scope of legal immunity granted to manufacturers of the Covid-19 vaccine. It will also review the companies' controversial practice of reporting the metric of "relative risk reduction" instead of "absolute risk reduction" when publicly discussing the efficacy of their vaccines. In recent years, certain pharmaceutical companies have had record-breaking financial success, driven in part by sales made from products related to the Covid-19 pandemic. This vested interest in the success of these Covid-19 products, combined with reports about the alarming side effects of vaccines, demands aggressive investigation. Texas's investigation will force these companies to turn over documents the public otherwise could not access. Attorney General Paxton is committed to discovering the full scope of decision-making behind pandemic interventions forced on the public, especially when a profit motive or political pressure may have compromised Americans' health and safety. Efforts by the federal government to coerce compliance with unjust and illegal pandemic interventions, even at the cost of citizens' employment, means this investigation into the scientific and ethical basis on which public health decisions were made is of major significance. Given the unprecedented political power and influence over public health policies that pharmaceutical companies now wield, it is more important than ever that they are held accountable if they take dangerous, illegal actions to boost their revenues.
On May 1, 2023, the Biden Administration announced its plans to end certain Federal COVID-19 vaccination requirements, including those for Federal employees and Federal contractors, at the end of the day on May 11. In the coming days, President Biden will be issuing an Executive Order rescinding the vaccination requirement for Federal employees and COVID-19 safety protocols for Federal contractors, effective at 12:01 am on May 12, 2023.
Despite expectations that the Covid vaccine mandate for travelers entering the US would be dropped when the federal government ends the nation’s public health emergency on May 11, the Centers for Disease Control and Prevention (CDC) announced on Thursday that the policy will be updated rather than dropped.
The updated policy will allow travelers who have received at least one vaccine dose on or after August 16 to enter the country, as the CDC believes that many who have received a one dose since this date may have received the more-protective bivalent shot.
In its update, the CDC said: “Noncitizens who are nonimmigrants and seeking to enter the United States by air are required to show proof of being fully vaccinated against COVID-19 before boarding a flight to the United States from a foreign country.”
“If you are not fully vaccinated against COVID-19, you will NOT be allowed to board a flight to the United States, unless you meet the criteria for an exception under the Proclamation and CDC’s Amended Order,” the CDC added. A booster dose is not needed to meet this requirement.”
This decision makes the US an outlier internationally, as few countries still require visitors to have received a Covid vaccine for entry, including Angola and Indonesia.
Dr. Doug Badger, a senior research fellow at the Heritage Foundation, told the Daily Mail: “Neither the European Union nor Canada imposes such a requirement.”
The move puts the US at odds with most countries, including the UK, France, and the European Union, which have already dropped their vaccination requirements for visitors amid mounting evidence that they do not slow the spread of the virus. China, in line with most of the rest of the world, also does not require travelers to have a Covid vaccine, but they do require a negative Covid test result at least 48 hours before travel.
Tetanus vaccine may be laced with anti-fertility drug. International / developing countries
PIP: A priest, president of Human Life International (HLI) based in Maryland, has asked Congress to investigate reports of women in some developing countries unknowingly receiving a tetanus vaccine laced with the anti-fertility drug human chorionic gonadotropin (hCG). If it is true, he wants Congress to publicly condemn the mass vaccinations and to cut off funding to UN agencies and other involved organizations. The natural hormone hCG is needed to maintain pregnancy. The hormone would produce antibodies against hCG to prevent pregnancy. In the fall of 1994, the Pro Life Committee of Mexico was suspicious of the protocols for the tetanus toxoid campaign because they excluded all males and children and called for multiple injections of the vaccine in only women of reproductive age. Yet, one injection provides protection for at least 10 years. The Committee had vials of the tetanus vaccine analyzed for hCG. It informed HLI about the tetanus toxoid vaccine. HLI then told its World Council members and HLI affiliates in more than 60 countries. Similar tetanus vaccines laced with hCG have been uncovered in the Philippines and in Nicaragua. In addition to the World Health Organization (WHO), other organizations involved in the development of an anti-fertility vaccine using hCG include the UN Population Fund, the UN Development Programme, the World Bank, the Population Council, the Rockefeller Foundation, the US National Institute of Child Health and Human Development, the All India Institute of Medical Sciences, and Uppsala, Helsinki, and Ohio State universities. The priest objects that, if indeed the purpose of the mass vaccinations is to prevent pregnancies, women are uninformed, unsuspecting, and unconsenting victims.
States Consider Legislation to Restrict Use of mRNA Technology in Livestock
At least five states are considering legislation to restrict the use of mRNA technology or gene therapies in livestock, or demand full disclosure to consumers on product packaging. The states considering such bills include North Dakota, Tennessee, Arizona, Idaho, and Missouri.
North Dakota – SB2384
Seeks to ban the use of mRNA vaccines in humans
Introduces a penalty for anyone breaking the prohibition
Tennessee – House Bill 0099
Amends existing law to prohibit the manufacture or sale of livestock or meat that contains mRNA “vaccine of vaccines materials” without a conspicuous label that there are such ingredients in the product
Arizona – House Bill 2762
Requires conspicuous labeling of all aquatic, livestock, or poultry products that received mRNA vaccines
Prohibits these products from being labeled as organic
Idaho – House Bill 154
Makes it a misdemeanor offense for anyone who provides or administers a vaccine using mRNA technology “for use in an individual or any other mammal in this state”
Missouri – HB1169
Requires product labeling of all livestock meat containing “potential gene therapy products”
Requires informed consent from consumers for the use of mRNA technology in livestock
Holly Jones, a Republican in Missouri’s House of Representatives, states that lobbyists accused her of creating fear among consumers and affecting the “bottom line.” She introduced the bill in Missouri requiring the labeling of all livestock meat containing “potential gene therapy products.”.
“Everyone has a right to choose what they put in their bodies,” she said.
Elon tweeted this: