The Probe into the Israeli Vaccine Policy and its Outcome is beyond Damning.

 BY GILAD ATZMON

CP SIDE EFFECTS.jpg

Report by Gilad Atzmon

In Israel yesterday, an independent legal body that calls itself the Civilian Probe (CP)* published its finding regarding the catastrophic impact of the Pfizer vaccine on the nation.

In their report, which they submitted to the Attorney General and the Health Minister, the committee listed a chain of critical legal and ethical failures that point at a possible attempt to mislead not just Israelis but also the entire world. Since the beginning of January I have been reporting on an undeniable correlation between vaccinations, cases and deaths (here , here, here and here ). The CP confirms my suspicions but their study also presents alarming medical findings regarding the scale of lethal side effects.  

In the document the CP points at a government attempt to conceal its dealing with Pfizer. The document states that “the Pfizer-Israel agreement is suffocated with redacted segments, consequently, it is not possible to analyze it legally and/or fully grasp Its implications as far as public health is concerned… This concealment casts a heavy shadow over anyone who took part in the (Israeli/Pfizer) negotiations…”

The CP then continues arguing that “in order to generate demand (amongst the people) for the vaccine, the government and the Ministry of Health have launched an unprecedented aggressive campaign, aiming to make Israelis rush to ‘get vaccinated.’ During that campaign all the basic rules of medical caution and ethics were disregarded, and with them also key guidelines formed after WWII regarding participation in medical trials (the Nuremberg Code). Instead of transparent and clear explanations, the public was misled by repeated official statements that the (Pfizer vaccine) has been ‘approved by the FDA’ after passing ‘rigorous tests.’”

The CP is accusing the state of Israel of intentionally reckless conduct… “Monitoring systems that enable the detection of side effects are a basic and critical condition for granting a permission for mass use of any new medicine, certainly when a mass operation of treatment that is defined as experimental is given to millions, and especially when this treatment is given to an entire country…”.

But Israel failed to set such a monitoring system.

“On the one hand, the state did not inform the citizens that Pfizer’s vaccine is in experimental stages that have not yet been completed, and that at this stage they are actually taking part in the experiment. On the other hand, the state did not maintain transparent and open control and monitoring systems for the public. As a result, there is a serious concern that this critical and negligent omission stems from: (a) the fear that such disclosure could interfere with the fulfilment of the objectives that may be implied by the Israel-Pfizer agreement or (b) the fear of diminishing demand for the exceptional number of vaccines that were purchased by Israel in advance, and / or (c) the fear of revealing unflattering results of the ‘experiment’ being carried out in Israel.” 

The CP is brave to admit that the lack of a monitoring system isn’t just a potential crime against the Israeli people, it may also be a crime against the rest of the world (i.e., humanity):


“In the absence of a transparent monitoring system that reports on side effects, not only have the Israeli government and the Ministry of Health failed citizens by providing them with misleading information, the Israeli government have failed both Pfizer and the rest of the world awaiting the results of the (so called) ‘real world experiment’ (that is taking place in Israel).”

To remove any doubt, the CP alerts the Israeli Attorney General to the possible criminal act implied by Israel’s vaccine policy.

“This is an alleged deception, suspiciously criminal, which should be thoroughly examined before the Attorney General allows the Israeli government to continue the alleged campaign of deception of Israel’s citizens and the (rest of the) world.”

The CP extended their study well beyond the legal realm, as it also attempts to fill the wide hole created by the State’s lack of a monitoring system.

“What do we learn from the facts on the ground?” the CP report asks. “An examination of mortality data published by the government shows that there is a correlation between number of vaccinations and the number of deaths. The excess mortality is noticeable among people up to 70 and also among adults over the age of 70, and remains even after offsetting the deaths attributed to Corona. In the population over the age of 70 – in January 2021 an excess mortality of 19.5% was observed compared to October 2020 – the month when the corona data were highest, and 22.4% compared to January 2020. In the younger population – an excess mortality of 7% was observed in January 2021 compared to the month October 2020 – the month in which the corona death numbers were the highest, and 7% compared to January 2020. It should be noted that this trend continues in the following month as well.”

As mentioned above I have been writing about the devastating correlation between vaccines and deaths since early January. In Britain and the USA, we detect identical correlation between mass vaccination and death. However, far more problematic is the realm of side effects, something which governments, the WHO, the corrupted pharmaceutical industry, and of course social media giants attempt to suppress in the most Orwellian manner. The Israeli CP seems to have produced the first robust report on Pfizer’s vaccine side effects. They published a table of their findings, which they summarize here:

“As one can detect looking at the table – there are close to 200 deaths, and this – only by examining about 800 reports of cases of serious side effects. As mentioned, the CP is still working on analyzing side effects and we have hundreds of additional reports that are subject to analysis. Our study so far indicates that about 25% of deaths are from people under the age of 60. About 15% of them are under 50 years old. 7 of the deceased are at young ages – below age 30. Also, the study identified 27 cases of heart problems in people under the age of 60, of which 24 cases are among young people aged 17-30.  Regarding the issues to do with female medical complications (including labor-complication, delayed menstruation or irregular menstruation, etc.) – it should be noted that the committee has about 200 additional reports that have not yet been included in the final list of our findings.”

For many years, I doubted whether there was a force in the middle east that could face, let alone defeat, Israel. I am pretty convinced now that with Netanyahu at the helm and Pfizer taking care of the nation’s wellbeing, Israel doesn’t really need enemies. However, every world citizen who is concerned about the future of humanity should be alarmed by the CP’s findings and particularly by the desperate and relentless attempts to suppress free academic, scientific and ethical discussion about Covid, the so-called ‘vaccines’ or anything else.

*To read the CP report click here

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Dozens of Deaths from Covid Vaxxing

Stephen Lendman. US Waging Wars on Multiple Fronts...Majority In Favor of  War

By Stephen Lendman

Source

Virtually everything reported about covid, face masks, PCR tests, social distancing, and vaccines by Big Government, Pharma, and their Big Media press agents are bald-faced Big Lies or distortions.

An all-out mass deception campaign has been ongoing throughout most of 2020, continuing in the new year, to manipulate the public mind with rubbish that’s harmful to our health, well-being, safety and future.

Vaccines don’t protect. Too often, they cause diseases they’re promoted to protect against, along with risking illness from numerous others. 

High-risk, experimental Pfizer and Moderna DNA altering mRNA vaccines are especially dangerous.

The risk contraction of serious illnesses near-or-longer-term.

The especially risk death, notably to the elderly and infirm.

What government officials, Pharma, and Big Media suppress about the dangers of these vaccines is essential for everyone to know.

Around a month after mass-vaxxing for covid (aka seasonal flu/influenza) in the US began, at least 55 individuals died.

That’s what is known. Perhaps the true number is much higher to be learned later after widespread damage was done.

If dozens or more Americans died from vaxxing already, will thousand more suffer the same fate, notably among the elderly and infirm?

After all-out brainwashing to push mass-vaxxing, notably by Big Media, will what’s coming unleash a tsunami of serious illnesses and deaths ahead — including among normal adults who’d be alive and well if not vaxxed.

According to the US Vaccine Adverse Event Reporting System (VAERS) — that greatly downplays numbers of adverse health events — 55 Americans already died from covid vaxxing.

VAERS is disturbingly inaccurate. According to Robert F. Kennedy Jr.’s Children’s Health Defense:

“VAERS is an abysmal failure, (a) designed to fail” system.”

It lets “regulators and industry (maintain) their pretense that current vaccine risk profiles are acceptable.”

“A 2010 study funded by HHS concluded that VAERS captured ‘fewer than 1% of injuries.’ ” 

“In other words, the actual injury rates from mandated vaccines are more than 100x (greater than) what HHS has been telling the public!”

“The 2010 HHS study found that the true risk for serious adverse events was 26/1,000, or one in 37.”

The high risk applies to potential numbers ahead from covid vaxxing.

For Pfizer and Moderna experimental, inadequately tested, genetically modifying mRNA technology covid vaccines, the risk of serious illnesses and deaths may be much higher.

What’s already known is alarming. What’s yet to be known may reveal catastrophically large numbers of people harmed from mass-vaxxing for covid.

Even former FDA chief, incoming Biden/Harris regime chief science advisor Dr. David Kessler acknowledged that VAERS doesn’t work as claimed.

The VAERS website admits that reported adverse events “often lack details and sometimes can have information that contains errors.”

By letter to Kessler in December, Kennedy said the following:

“I am writing on behalf of Children’s Health Defense to request that you consider the long-overdue need for a comprehensive, high-integrity system to monitor adverse outcomes following” mass-vaxxing for covid.

“(A)s someone who has repeatedly called attention to the structural deficiencies of our nation’s (VAERS) drug adverse event (system), you are uniquely qualified to articulate (its) shortcomings and recommend badly needed improvements.”

VAERS “co-administered by FDA and CDC since 1990 is a well-documented public failure.”

“You have said yourself that the vaccine injury reports received by FDA ‘represent only a fraction of the serious adverse events’ that occur.” 

In your earlier “Journal of the American Medical Association (JAMA), “you noted that MEDWatch would not affect VAERS nor attempt to remedy underreporting of adverse events associated with vaccines.” 

“At the time, even vaccine manufacturers were estimating (confidentially) ‘a fifty-fold underreporting of (vaccine) adverse events.’ ”

Double this number is more accurate. Mass-vaxxing for covid poses an unacceptably high threat to public health and well-being.

ZeroHedge.com reported that large numbers of “calls (are urging) suspension of the use of mRNA-based COVID-19 vaccines” because of alarming numbers of reported deaths.

Norwegian health authorities said covid vaccines may be too high-risk for elderly individuals.

Pfizer’s mRNA vaccine is being used in the country.

A company statement downplayed numbers of deaths in Norway after vaxxing, saying:

“(T)he number of incidents so far is not alarming, and in line with expectations” — showing indifference toward public health and well-being, along with mass deception about the high risk its covid vaccine poses.

Along with increasing numbers of reported deaths from covid vaxxing, they’ve been thousands of reported adverse events, including life-threatening ones, in the US alone.

They’ve also been about two dozen reported cases of vaxxed individuals becoming permanently disabled, along with numerous emergency room visits and hospitalizations.

RT reported that over a dozen vaxxed Israelis experienced facial paralysis.

As of mid-January, over 10 million Americans were vaxxed for covid.

CDC National Center for Immunization and Respiratory Diseases director Nancy Messonnier’s claim that Pfizer and Moderna covid vaccines “are safe and effective” is part of a state-sponsored, Big Media mass deception campaign.

It’s more evidence that we’re being lied to by indifferent to public health and well-being government officials and their media press agents.

If mass-vaxxing for continues unchecked in the US and elsewhere without interruption — what’s most likely — the toll on public health and welfare may increase exponentially.

FDA Approves First COVID-19 Drug

FDA Approves First COVID-19 Drug

By Staff, Agencies

US regulators on Thursday approved the first drug to treat COVID-19: remdesivir, an antiviral medicine given to hospitalized patients through an IV.

The drug, which California-based Gilead Sciences Inc. is calling Veklury, cut the time to recovery by five days — from 15 days to 10 on average — in a large study led by the US National Institutes of Health.

It had been authorized for use on an emergency basis since spring, and now becomes the first drug to win full Food and Drug Administration approval for treating COVID-19. US President Donald Trump received it when he was sickened earlier this month.

Veklury is approved for people at least 12 years old and weighing at least 40 kilograms who are hospitalized for a coronavirus infection. For patients younger than 12, the FDA will still allow the drug’s use in certain cases under its previous emergency authorization.

The drug works by inhibiting a substance the virus uses to make copies of itself. Certain kidney and liver tests are required before starting patients on it to ensure it’s safe for them and to monitor for any possible side effects. And the label warns against using it with the malaria drug hydroxychloroquine, because that can curb its effectiveness.

“We now have enough knowledge and a growing set of tools to help fight COVID-19,” Gilead’s chief medical officer, Dr. Merdad Parsey, said in a statement.

The drug is either approved or has temporary authorization in about 50 countries, he noted.

Its price has been controversial, given that no studies have found it improves survival. Last week, a large study led by the World Health Organization found the drug did not help hospitalized COVID-19 patients, but that study did not include a placebo group and was less rigorous than previous ones that found a benefit. The FDA’s approval statement noted that, besides the NIH-led one, two other studies found the drug beneficial.

Gilead charges $2,340 for a typical treatment course for people covered by government health programs in the United States and other developed countries, and $3,120 for patients with private insurance. The amount that patients pay out of pocket depends on insurance, income and other factors.

So far, only steroids such as dexamethasone have been shown to cut the risk of dying of COVID-19. The FDA also has given emergency authorization to using the blood of survivors, and two companies are currently seeking similar authorization for experimental antibody drugs.

Trump’s COVID Infection Curable – Not by Toxic Experimental Drugs

By Stephen Lendman

Global Research, October 04, 2020

There’s nothing unusual about Trump falling ill from exposure to the SARS-CoV-2 virus that causes Covid disease — notably because of his close contact to numerous people daily.

Millions of Americans and countless others worldwide contract seasonal flu/influenza.

It happens annually with no fear-mongering mass hysteria, no mandated or voluntary house arrest, no mass shutdowns of businesses — no economic collapse that’s happening in the US and elsewhere.

According to Trump’s physician Dr. Sean Conley, he experienced a mild cough, nasal congestion, fatigue, and a low-grade fever that came down, adding:

He’s “cautiously optimistic” about his condition, saying as well that he’s “not yet out of the woods.”

According to medical experts, Covid disease can worsen days after contracting it.

Initial mild symptoms can become more serious.

According to reports by Trump’s doctors, he’s being treated with two experimental drugs — remdesivir and a neutralizing antibody cocktail.

If true, he’s playing Russian roulette with his health, notably because a proved effective Covid disease treatment exists.

When used as directed, hydroxychloroquine (HCQ) combined with either azithromycin or doxycycline and zinc is highly effective in treating Covid-infected individuals when administered within around 10 days of being diagnosed with the disease.

Everyone infected with Covid disease should be treated with this protocol.

No one should use potentially toxic experimental drugs. No responsible medical providers should prescribe them.

If reports are accurate, both drugs administered to Trump received emergency FDA authorization for his use.

Neither one cures Covid disease.

Earlier, Thailand Medical News (TMN) said “Americans are getting their lives placed (at) risk (because) the US FDA…rapidly approved remdesivir as a drug to treat COVID-19 despite conflicting study results, and the fact that the drug does not clearly demonstrate any specific efficacy against the SARS-CoV-2 coronavirus,” adding:

Use of the drug in trials “show(ed) hepatoxicity effects coupled with even slight indications of nephrotoxicity and even cardiotoxicity, and there are insufficient studies to demonstrate its safety on humans.”Big Pharma Controlled FDA Approves Inadequately Tested Drug for COVID-19

Claims by the US National Institute of Allergy and Infectious Diseases that use of the drug shortens hospitalizations for Covid-infected individuals are dubious at best.

The conclusion was based on use of the drug by small numbers of patients with the disease, far too few to be meaningful.

According to the WHO, remdesivir used in the study failed to improve patients’ health or reduce pathogens in their blood.

The FDA endorsed “an unproven but toxic drug,” TMN stressed — defying medical ethics and patient safety.

If widely marketed following its use by Trump, it’ll be a potentially large-scale experiment that may be harmful to countless numbers of Covid-infected patients.

The same may be true for Regeneron Pharmaceuticals’ experimental neutralizing antibody cocktail administered to Trump — if reports are accurate.

These drugs may potentially be more harmful by administering them in combination.

Big Pharma-controlled FDA has a history of approving inadequately tested drugs.

In her book titled “The Truth About the Drug Companies,” former New England Journal of Medicine editor Dr. Marcia Angell said the following:

Big Pharma is “primarily a marketing machine to sell drugs of dubious benefits, using its wealth and power to co-opt every institution that might stand in its way, including the US Congress, the (FDA), academic medical centers, and the medical profession itself.”

Maximizing profits is prioritized over human health.

Despite US federal law requiring that FDA approved drugs must be “safe and effective,” Public Citizen’s Health Research Group revealed otherwise, explaining:

Meds that “don’t work” get approved. Virtually all drugs have labels that warn of potential hazardous to human health side effects.

Enough drugs in combination with each other increase the risk more greatly.

An estimated 100,000 American die annually from the toxic side effects of prescription drugs.

On October 3, TMN warned that remdesivir “causes kidney problems,” adding:

“An urgent immediate safety review of…remdesivir (was) called by the European Medicines Agency after numerous COVID-19 patients taking the drug developed serious kidney problems.”

The EU regulator said the drug appears to cause “acute kidney disease.”

Medical authorities in some EU countries are halting remdesivir’s use until more safety studies are conducted.

So far, no longterm safety studies on the drug were conducted in the US or elsewhere.

According to TMN, profiteers in the US called “Scientists to Stop COVID-19” were behind remdesivir’s rapid approval.

Last week, Trump’s physician Dr. Sean Conley said he received a single dose of Regeneron’s antibody cocktail (REGN-COV2 – perhaps more at Walter Reed) along with remdesivir.

If Trump is being treated with these drugs in lieu of the HCQ combination explained above, he may or may not recover fully from Covid infection.

He’ll be vulnerable to other serious health issues that at his age (74) and obesity (around 240 lbs.) may be life-threatening over the short or longer-term.

*

Note to readers: please click the share buttons below. Forward this article to your email lists. Crosspost on your blog site, internet forums. etc.

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.The original source of this article is Global ResearchCopyright © Stephen Lendman, Global Research, 2020

Exempting Big Pharma from COVID-19 Vaccines Liability

By Stephen Lendman

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.

*

Note to readers: please click the share buttons below. Forward this article to your email lists. Crosspost on your blog site, internet forums. etc.

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.

Featured image is from Natural NewsThe original source of this article is Global ResearchCopyright © Stephen Lendman, Global Research, 2020

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