Pfizer agrees to pay $2.3 billion for fraud settlement

Pharmaceutical giant Pfizer agrees to pay $2.3 billion for fraudulent marketing with the intent to defraud or mislead.   This is the largest health care fraud settlement in the US Justice Department’s history. [1, 2, 3, 4] In 2009 Pfizer’s total revenue was around $50 billion, with a declining trend from 2011 to 2020. [5].   Vaccine revenue in 2021 are responsible for 60% of Pfizer’s sales, with an expected $36 billion from vaccines alone! Will this Big Pharma company be a repeat offender in 2020?

WHO changes the definition of a ‘pandemic’

By May 6, 2009 the World Health Organisation (WHO) had lowered the standards for defining a pandemic, not taking into account the number of infections and death (page 9, point 25), allowing for a ‘pandemic’ to be declared when a new virus is NOT causing serious harm to most of the population. [2]  This definition change occured between the first lab confirmed cases of a novel Influenza A virus 0n April 29, 2009 in 9 countries and then on June 11, 2009 when cases were reported in a total of 74 countries and territories the WHO Director General Dr Margaret Chan declared a global pandemic for the 2009 H1N1 virus. [3, 4, 5] The declaration of a ‘pandemic’ after May 6, 2009 can be made simply if “a disease epidemic occurs when there are more cases of that [new] disease than normal.”  On May 3, 2009 there was the additional criteria of an “enormous number of deaths and illness” , this was removed. On May 4, 2009 "deaths and illness" were removed. [6 , 7] By changing the definition of “pandemic” in May 2009 the WHO can declare a PHEIC for the seasonal flu across the globe, excessive mortality and relative..> READ MORE

GAVI is launched

The Global Alliance for Vaccines and Immunisation (GAVI) "movement" was officially launched January 31, 2000  at the World Economic Forum (WEF) in Davos, Switzerland.  GAVI headquarters are based in Geneva, Switzerland. The board of GAVI held their first meeting held on October 28, 1999 in New York. The World Health Organization is a founding partner of GAVI with its Director-General, Dr Brundtland chairing the GAVI Board for the first two years. [1, 5] "Nearly three million children worldwide still die needlessly each year of vaccine-preventable illnesses," ... "For only US $17 per child, we can provide lifetime protection against the six historical scourges - polio, diphtheria, tuberculosis, pertussis, measles and tetanus. And for not much more, we can extend the protection to include hepatitis B, yellow fever and Haemophilus influenzae type b (Hib), the leading cause of pneumonia and meningitis." said Dr. Gro Harlem Brundtland , Director-General of the WHO and the chair of GAVI, and author of "Sustainable Development" "The Global Alliance for Vaccines and Immunization is a partnership dedicated to ensuring that all children, however poor, have equal access to these vaccines. The Alliance also works to spur the development of new vaccines against major killers that primarily..> READ MORE

Inventor of PCR test wins Nobel Prize in Chemistry

In 1983, Kary Mullis figured out the steps to amplify DNA sequences called process called  polymerase chain reaction (PCR).  On October 13, 1993 he was awarded the Nobel Prize in Chemistry for developing this procedure. [watch] [1] His prizes and patents can be found here. Kary Mullis said PCR test is used to “make a whole lotta somethin’ out of somethin’, and the “PCR test, if you do it well, you can find almost anything.” PCR tests are being used to “diagnose” COVID-19 disease, in both symptomatic and asymptomatic (healthy) people to determine if they are infectious.  The PCR test kits are not standardised, each one uses a different, tiny fragment of the SARS-CoV-2 virus genome, it doesn’t test for the whole virus and it cannot determine if the fragment is part of a viable infectious pathogen. [2]  Greater than 20 cycles are problematic, 45 cycles was recommended for SARS-CoV-2 testing protocol. The PCR technique can produce a billion copies of the target sequence in just a few hours. [3]

US VAERS established

The US Vaccine Adverse Event Reporting System (VAERS) was established in 1990 by the FDA and CDC an early warning system to detect possible safety problems for US-licensed vaccines. It "is a passive reporting system, meaning success depends on medical personnel, patients, and families taking the initiative to file reports". [1] In 1986 vaccine manufacture liability was removed, so this system became the main means of post-marketing surveillance of short and long-term vaccine safety.  The data collected is used to make claims about vaccine safety, which is only as good as the adverse event reports entered.  VAERS went online in 2002. The Harvard study commissioned by the CDC in 2007, concluded that “fewer than 1% of vaccine adverse events are reported” to VAERS. With this passive reporting system, that many US healthcare providers are not even aware they are require by law to report to, makes the robustness of the under-reported data poor, and thus affects the system’s ability to effectively identify “warning signals” or support the common claim that there is a “1 in a million” risk. A controlled study looking at anaphylaxis reactions following mRNA COVID-19 vaccines showed 2.47 events per 10,000 jabs (0.027%), yet VAERS data reports..> READ MORE

1986 Act: US government makes vaccine makers 100% Liability Free

Following a 1977 Immunization Conference which called for a "no-fault" compensation system, on the back of manufactures facing increasing lawsuits, California's Democrat Representative Henry Waxman introduced (for the second time) a bill to congress, which on October 14, 1986 was passed, and the National Childhood Vaccine Injury Act (NCVIA), HR5546, was then signed into law "with mixed feelings", [6] by President Ronald Reagan, "as part of a larger health bill on November 14, 1986" [1, 4, 5] Vaccine manufacture Wyeth (now Pfizer) allegedly told President Reagan that vaccines are "unavoidably unsafe" and that phrase is written in the preamble of the VICP statute, this phrase was reiterated in 2011 Supreme Court ruling. [9, 10] The National Childhood Vaccine Injury Act of 1986 (PL 99-660) established the [13]: National Vaccine Program (NVP) Office in 1986 - to coordinate R&D Vaccine Injury Compensation Program (VICP) - est 1988. The law established a Vaccine Injury Table [12] Noteworthy, in 1988 the Center for Biologics Evaluation and Research (CBER) was created within the FDA to regulate vaccines National Vaccine Advisory Committee (NVAC) Vaccine Adverse Events Reporting System (VAERS) Mandated a 6-month supply of vaccines The Department of Health and Human Services (HHS) then established the..> READ MORE

Swine Flu mass-vax program suspended after high numbers of Guillain-Barré Syndrome and 53 dead

On February 3, 1976, the New Jersey State Health Department sent the Center for Disease Control (CDC) in Atlanta isolates of virus from recruits at Fort Dix military base, New Jersey, who had influenza-like illnesses.  Some of the isolates were similar to 1918 pandemic, thus it was labelled "swine flu" but "surveillance activities at Fort Dix gave no indication that recruits had contact with pigs" [contrary to this report]. [1, 2]  One soldier died. On March 10, 1976 the ACIP committee determined at person-to-person transmission had occurred, they recommended that an immunization program be launched to prevent the effects of a possible pandemic. The vaccination program was established to "vaccinate 140 million Americans against the swine flu" in the "hopes to immunize "every man, woman, and child"".  45 million people were vaccinated in 10 weeks with what became known as the “swine flu vaccine”. The program was halted in many states due to unexpected high cases (1/100,000) of debilitating Guillain-Barré Syndrome (GBS) reported following vaccination "resulting in 53 deaths". [3, 4, 5, 6] The WHO claimed "the risk of GBS from the vaccine is slight" and it's cause is "unknown". On December 16, 1976, Dr. Theodore Cooper, Assistant Secretary of..> READ MORE

International Ban on Biological Warfare – Biological Weapons Convention

At a United Nations Biological Weapons Convention, which was signed in 1972, went into force on March 26, 1975.  Governments from around the world agreed to ban biological warfare, prohibiting their development, production, acquisition, transfer, stockpiling and use. [1]  This follows the 1925 Geneva Protocol which first banned the use of biological weapons, but countries were still able to develop and stockpile them. [2] By definition: “Biological weapons disseminate disease-causing organisms or toxins to harm or kill humans, animals or plants.  They generally consist of two parts – a weaponised agent [spike protein] and a delivery mechanism [virus or vaccine].” Curious: “Anyone who suggested bio-weapon in the beginning [of COVID-19 pandemic] were censored”…yet it is the perfect binary weapon" Dr Lee Merrit discusses. Is the spike protein a bio-weapon? By 2023 the UN's WHO are trying to use a Pandemic Treaty to get nations to ignore the BWC.

“Peer Review” officially becomes a term

In the 18th century, French and British societies developed practices for evaluating scientific research collectively to limit the “potential damage from any one individual’s incompetence, bias or prejudice.” “It was only in the late 20th century that refereeing was rebranded as “peer review”” and The Oxford English Dictionary (OED) determined that the term “peer review’ was first used in 1967.  The Royal Society have been “scrutinising” finding since 1830s. [1] Professionals acknowledge that “most readers read only the title and the abstract of a research paper and very few will go on to read the full paper.” This very fact provides a means for which journals can hide potentially life saving cheap therapies or counter-narrative information from time-poor trusting professionals, just to keep their highly influential, pharmaceutical sponsors happy. [2, 3] In addition, it has been reported that fake studies, written by ghostwriters, signed off by “credible authors”, and funded by pharma, get published in “peer review” journals! You will find also that journals are not interested in publishing conflicting data, and as such present a “biased sample of the true picture of all of the studies that have been conducted”, unbeknownst to the audience that trusts the perceived credibility..> READ MORE

Coronavirus is discovered in humans

“In 1965, scientists identified the first human coronavirus; it was associated with the common cold. The Coronavirus family, named for their crown-like appearance, currently includes 36 viruses.  Within that group, there are 4 common viruses that have been causing infection in humans for more than sixty years.”  [1 ] It quickly became an infectious replicatable viral experimentation model. [4] "Coronaviruses are relatively large enveloped viruses with a single-stranded positive-sense RNA genome of 26–32 kilobases that form their own taxonomic family within the Nidovirales order of viruses."  Zoonotic events (animal - human transmission) is said to be "the most likely source of the ... outbreaks in human" of the post 2002 SARS like viruses. [2] Since this time it is known that the coronavirus family of viruses mutate rapidly, especially in the spike protein area, have short-lived antibody response, which all makes creating a vaccine for this pathogen problematic. Coronavirus vaccines have never been "successful" prior to 2020. Fast forward to March 2020: Big Pharma, with tax-payer funding, created a COVID-19 “vaccine” in record time using brand new technology, never before trialed in humans until March 2020, to "protect" against a stated "novel" coronavirus.  A “vaccine” unlike any other, with no..> READ MORE