Exempting Big Pharma from COVID-19 Vaccines Liability

Tuesday, 4 August 2020

Exempting Big Pharma from COVID-19 Vaccines Liability

Global Research, August 03, 2020

House and Senate leaders are discussing whether to include this exemption for COVID-19 vaccines under development in new legislation likely to be passed and signed into law in the coming days.

Most likely, tort liability protection for Big Pharma will be approved.

All vaccines contain harmful to human health toxins — including mercury, aluminum, formaldehyde, and phenoxyethanol (antifreeze).

Vaccines can be more hazardous than diseases they’re designed to protect against, most people unaware of the risks, establishment media concealing them.

Toxins in vaccines weaken the human immune system, making vaxxed individuals vulnerable to potentially life-threatening illnesses — young children and the elderly most at risk.

In developing vaccines, most clinical trials fail. Years of development precede the production and marketing of new ones.

Despite years of research, no successful coronavirus vaccines were ever developed.

Yet a race is on by drug and biotech companies to develop, produce, and mass-vax millions of people in the coming months against COVID-19.

Last week, Thailand Medical News reported that to date,

“more than 13,782 scientific studies have been published with regards to the COVID-19 disease and the SAR-CoV-2” virus that causes it.
“There are more than 2,472 clinical trials either planned or in progress with regards to COVID-19 disease in terms of repurposed drugs, new pharmaceuticals, supplements, herbal and traditional medicine, antibodies, vaccines, medical devices etc.”
“There are about 126 completed clinical trials to date.”
“There are more than 372 existing drugs being studied for repurposing to treat various aspects of the COVID-19 disease along with 17 new pharmaceutical preparations, 64 phytochemicals from plants and herbs and 38 proteomes.”
“There are more than 148 vaccine candidates in development stages.”
“There are at least…127,000 scientific researchers from around the world from various specialties and fields working on various aspects to find solutions for the COVID-19 disease.”

Rushed development of vaccines amounts to playing Russian roulette with human health.

Instead of protecting the public from health hazards, US ruling authorities, in cahoots with Big Pharma, are promoting use of potentially dangerous vaccines ahead — in lieu of proved effective, widely available, inexpensive hydroxychloroquine (HCQ) when used with either azithromycin or doxycycline and zinc. More on this below.

In 2005, the US Public Readiness and Emergency Preparedness Act (PREPA) became the law of the land.

It “authorizes the Secretary of the Department of Health and Human Services to issue a declaration that provides immunity from liability (except for willful misconduct) for claims of loss caused, arising out of, relating to, or resulting from administration or use of countermeasures to diseases, threats and conditions determined by the Secretary to constitute a present, or credible risk of a future public health emergency to entities and individuals.”

It granted Big Pharma tort liability protection for avian influenza vaccines, including from vaccine safety laws enacted by states — at the discretion of HHS.

In 2011, the US Supreme Court in Bruesewitz v. Wyeth ruled in favor of protecting Big Pharma from state tort liability lawsuits that seek damages for injuries or death attributed to use of a vaccine.

Writing for the majority, Justice Anthony Scalia argued that the 1986 National Childhood Vaccine Injury Act preempts all vaccine design defect claims against vaccine manufacturers brought by plaintiffs seeking compensation for injury or death.The Great COVID-19 Vaccines to the Rescue Hoax. “Making A Billion Dollars” vs. “Harmful Side Effects”

The majority 6 – 2 ruling held that “a vaccine side effect could always have been avoidable by use of a different vaccine not containing the harmful element.”

Ignored was that ALL vaccines contain harmful to human health substances.

Perhaps one day vaccines will be largely or entirely safe to use as directed, clearly not so now, why Big Phama should be held liable for injury or death from use of their vaccines and other drugs that cause physical harm when used as directed.

The same goes for all products and services sold by companies to consumers or other firms.

COVID-19 vaccine developers want liability protection from products they’ll market in the months ahead.

Note: The highly touted Moderna COVID-19 vaccine induced adverse reactions in over half of clinical trial participants, some cases severe — what’s been unreported by major media.

Other COVID-19 vaccines in development may face similar issues, notably because they’re being rushed to market in the coming months. Consumers beware.

Last week, James Todaro MD quoted former New England Journal of Medicine editor-in-chief Marcia Angel, saying the following:

“Now primarily a marketing machine to sell drugs of dubious benefit, (the pharmaceutical) industry uses its wealth and power to co-opt every institution that might stand in its way, including the US Congress, the Food and Drug Administration, academic medical centers, and the medical profession itself.”

Dr. Todaro stressed the following:

“In the history of medicine, no single drug has been so singularly attacked by the media, World Health Organization, government officials and institutional health experts as hydroxychloroquine (HCQ),” adding:
“Approved as a ‘safe and cost-effective’ essential medicine by the WHO, CDC and regulatory authorities across Europe, hydroxychloroquine has been prescribed to millions of patients over the past 65 years.”
“Despite decades of known safety, hydroxychloroquine was labelled ‘dangerous’ and a ‘poisonous substance’ after showing promise as a therapeutic for COVID-19.”

Full-court press negative publicity by the NYT, WaPo, CNN, and other establishment media demeans HCQ, ignoring its effectiveness in treating COVID-19 when properly administered during the disease’s early stage.

Epidemiologist Harvey Risch MD stressed that HCQ was shown to be “highly effective (when) given (to patients) very early in the course of treating” COVID-19 — especially when given in combination with the antibiotics azithromycin or doxycycline and the nutritional supplement zinc.”

Why is this information being suppressed? Why isn’t the public fully informed?

It’s because of the hugely profitable market potential Big Pharma hopes to cash in on by convincing millions of people to be mass-vaxxed against COVID-19.

Most people are unaware of possible harmful to health side effects they could experience early or much later, including major illnesses.

Robert F. Kennedy Jr’s Children’s Health Defense.org website (CHD) explained that

“severe acute respiratory syndrome (SARS – 2003 was) was a dress rehearsal…for Covid-19 in 2020,” adding:

Research showed that Chloroquine (CQ) and HCQ are prophylactically and therapeutically effective in treating the coronavirus.

“In early April, a survey of US physicians found that two-thirds (65%) would prescribe CQ or HCQ ‘to treat or prevent COVID-19 in a family member,’ and roughly the same percentage (67%) would take it themselves.”
“In May, the White House doctor confirmed HCQ’s excellent benefit-to-risk ratio.”
“For the biopharma companies poised to profit from new drugs and Covid-19 vaccines…it is not an attractive option to keep older drugs that have outlived their patent” protection.”

Instead of advocating for HCQ’s widespread use, the Big Pharma controlled FDA revoked authorization for its use in treating COVID-19.

The nation’s top-ranked Mayo Clinic medical facility falsely claims no effective COVID-19 medications or cures exist.

CHD explained that nations using HCQ have “only one-tenth the mortality rate in countries where there is interference with this medication, such as the United States.”

As the saying goes, follow the money. A potential bonanza of revenues and profits awaits drug and biotech companies whose COVID-19 vaccines are approved for sale by the FDA in the months ahead.

CQ has been around since 1934, HCQ since the mid-1940s, the latter drug approved by the FDA in 1955 to treat autoimmune-inflammatory conditions.

HCQ especially was shown to be effective prophylactically and therapeutically in treating COVID-19 as explained above.

The CHD reported that through late July,

“65 studies around the world indicated that 100% of the studies that assessed HCQ for Covid-19 pre-exposure prophylaxis (PrEP), post-exposure prophylaxis (PEP) or early use showed ‘high effectiveness,’ as did 61% of the studies examining HCQ use in later stages of illness.”

When properly used, HCQ can prevent or cure COVID-19 most often.

The alternative is going along with mass-vaxxing, risking potentially hazardous to human health side effects that may include contracting coronavirus disease and/or something more serious.

Note: If HCQ was widely promoted and used by the public, no lockdowns, social distancing, face masks, or other self-protective actions would be needed.

Economic and social life could resume normally without fear of contracting COVID-19.

Responsible government would promote the above, prioritizing public health, safety and welfare.

Not the US, acting in cahoots with Big Pharma’s aim to cash in big from hazardous to human health vaccines when available.

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Award-winning author Stephen Lendman lives in Chicago. He can be reached at lendmanstephen@sbcglobal.net. He is a Research Associate of the Centre for Research on Globalization (CRG)

His new book as editor and contributor is titled “Flashpoint in Ukraine: US Drive for Hegemony Risks WW III.”

http://www.claritypress.com/LendmanIII.html

Visit his blog site at sjlendman.blogspot.com.