FDA & AAPS in War Over Proven, Safe CV-19 Treatment
This weeks marks the beginning of an all-out legal war between the FDA and medical doctors over a successful treatment for COVID-19.
A new FDA’s statement doubles down in opposing the Hydroxychloroquine (HCQ) treatment praised by President Trump. While the Association of American Physicians and Surgeons (AAPS), files a lawsuit against the FDA claiming bias and misinformation. [1]
A screenshot below of the AAPS lawsuit now filed in the federal court, Michigan:
Since President Donald Trump rightly praised the safety and efficacy of a cheap and readily-available protocol (Hydroxychloroquine with zinc and Z-pac) the FDA and media cronies have been all out to decry the remedy.
As correctly reported in the Washington Post (April 02, 2o2o):
“An international poll of more than 6,000 doctors released Thursday found that the antimalarial drug hydroxychloroquine was the most highly rated treatment for the novel coronavirus.
The survey conducted by Sermo, a global health care polling company, of 6,227 physicians in 30 countries found that 37{154653b9ea5f83bbbf00f55de12e21cba2da5b4b158a426ee0e27ae0c1b44117} of those treating COVID-19 patients rated hydroxychloroquine as the “most effective therapy” from a list of 15 options.” [2]
Worldwide there have been hundreds of thousands, if not millions, successfully treated. Indonesia, the world’s fourth most populous nation, told doctors to use the drugs to treat all COVID-19 patients with symptoms from mild to severe. The country has ramped up production of HCQ since March, granting two dozen licenses to local manufacturers, who have churned out millions of doses. [3]
Among the dirty tricks is a deliberate failure to report and explain that Hydroxychloroquine (HCQ) ON ITS OWN is not the treatment widely endorsed by doctors and practitioners. Indeed, the correct protocol is a combination of HCQ, zinc + Z-pac treatment.
Veterans’ Today (March 31, 2020) reported the correct combination as follows:
“Dr. Vladimir Zelenko, a board-certified family practitioner in New York successfully treated 350 coronavirus patients with 100 percent success using a cocktail of drugs: hydroxychloroquine, in combination with azithromycin (Z-Pak), an antibiotic to treat secondary infections, and zinc sulfate.” [4]
But fighting back against this great news is the FDA. It has now issued a statement intended to discredit further HCQ. As Breitbart reports in ‘FDA Cancels Emergency Use of Hydroxychloroquine: ‘Unlikely to Be Effective’ Against Coronavirus’ (June 15, 2020) [5]:
“In a statement issued Monday, the FDA, a component of the U.S. Department of Health and Human Services (HHS), announced the anti-malaria drugs “are unlikely to be effective in treating COVID-19 for the authorized uses in the EUA,” [6] adding:
Additionally, in light of ongoing serious cardiac adverse events and other potential serious side effects, the known and potential benefits of chloroquine and hydroxychloroquine no longer outweigh the known and potential risks for the authorized use.”
As with the climate fraud, this FDA claim relies on secret, unproven ‘science’ to smear independent scientists (and doctors).
The AAPS states [7]:
“In its lawsuit (http://aapsonline.org/hcqsuit), filed in June in federal court in the Western District of Michigan, AAPS asks the court to enjoin the enforcement of the restrictions in the Mar 28 EUA; to make available and distribute promptly, for the benefit of the public, HCQ from the SNS; and to enjoin FDA, the Biomedical Advance Research & Development Authority (BARDA), and HHS from impeding the distribution, sale, or purchase of HCQ by members of the public during the COVID-19 pandemic.
Through a biased, improper process, FDA officials from prior administrations acted contrary to the wishes of President Donald Trump by arbitrarily limiting use of HCQ. Rick Bright, Ph.D., former head of BARDA, who is an outspoken critic of President Trump and is personally opposed to making HCQ widely available, distorted the agency process to unjustifiably limit access.”
It doesn’t just stop with the bias of Rick Bright, it goes far wider and deeper. Readers may check for themselves just how many members of the FDA board also have connections to Gilead by viewing here: https://defyccc.com/covid-1… [8]
Why is this important? Because Gilead is the company pushing the (now failing) rival drug, Remdesivir. Remdesivir would expensive – a huge money-maker for Big Pharma.
Meanwhile, the UN WHO has also recommended that use of chloroquine (CQ) and HCQ for COVID-19 be suspended, and is also suspending their use in a global clinical trial called Solidarity. [9]
The goals of WHO and FDA members (in cahoots with Big Pharma) are the same: (i) to enrich themselves;(ii) reduce the global population and (iii) to enslave us economically and intellectually.
Yet again, corrupted government agencies go public citing secret data from unpublished studies to hoodwink the public and hide the scientific truths.
In response, the AAPS are learning from how climate skeptics defeated government secret science in the courts (by using common law rules of evidence to compel disclosure of all data). As with the Big Green rich corporations, elite billionaires, corrupt politicians and activists have all come together to share in common cause – to do down humanity.
The AAPS lawsuit continues:
“Harvey A. Risch, professor of epidemiology at the Yale School of Public Health and Yale School of Medicine, stated: “Hydroxychloroquine+azithromycin has been used as standard-of-care in more than 300,000 older adults with multicomorbidities, with estimated proportion diagnosed with cardiac arrhythmias attributable to the medications 47/100,000 users, of which estimated mortality is <20{154653b9ea5f83bbbf00f55de12e21cba2da5b4b158a426ee0e27ae0c1b44117}, 9/100,000 users.” He noted that 10,000 Americans are dying each week from COVID-19. Five studies, he writes, including two controlled clinical trials, have demonstrated significant major outpatient treatment efficacy. He concluded that “these medications need to be widely available and promoted immediately for physicians” (Am J Epidemiol, May 27, 2020, https://tinyurl.com/y9yfb2h9).”
Just like the man-made global warming scam, these crooks rely on a biased (sold out) media to hoodwink the scientifically-illiterate. The average citizen gets duped by trickery, misrepresentation and strawman argumentation.
But my colleagues and I would argue, whenever government or big corporation science impacts larger society, we must retain our natural right to see all the evidence.
It is imperative that the FDA publishes the studies they rely on to dismiss the HCQ, zinc + Z-pac treatment. It must be open to public scrutiny.
But we fear, just as with the climate fraud, such ‘studies’ either don’t exist or, if they do, are the usual junk science garbage, as was witnesses last week with the discredited (now retracted) Lancet study. [10]
By contrast, the HCQ protocol relies on a long-standing, generic medicine used for 65 years already and on the World Health Organization’s list of the world’s safest medicines is very low cost by comparison.
We urge readers to open their eyes, look behind the glib media facades and understand that major academic institutions, including medical schools, are a key element of the fraud.
As with university climatology departments, medical schools hike up overhead charges on every NIH or NSF research grant to fund their large staffs and build new campus buildings. In modern academia it is common knowledge the granting of tenure to science and medical academics depends chiefly on how much money they bring in.
As with climate scientists, medical researchers are prone to human failings, too. The real pandemic is the corruption within the science/medical industrial complex. Until we face up to it on a societal level we are doomed to endure a medical and scientific dystopia.
[1] https://aapsonline.org/judicial/aaps-v-fda-hcq-6-2-2020.pdf
[3] https://tinyurl.com/yaq5edq2
[4] Veterans’ Today (March 31, 2020) https://www.veteranstoday.com/2020/03/31/dr-vladimir-zelinko-has-699-cv19-cures-with-hq-z-pak-zinc/
[5] ‘FDA Cancels Emergency Use of Hydroxychloroquine: ‘Unlikely to Be Effective’ Against Coronavirus’ (June 15, 2020)
[7] http://aapsonline.org/hcqsuit
[8] https://defyccc.com/covid-19-panel-gilead-ties/
[10] https://principia-scientific.com/evidence-exposes-fraudulent-lancet-hcq-covid-19-study/
About the author: John O’Sullivan John is CEO and co-founder (with Dr Tim Ball) of Principia Scientific International (PSI). John is a seasoned science writer and legal analyst who assisted Dr Ball in defeating world leading climate expert, Michael ‘hockey stick’ Mann in the ‘science trial of the century‘. O’Sullivan is credited as the visionary who formed the original ‘Slayers’ group of scientists in 2010 who then collaborated in creating the world’s first full-volume debunk of the greenhouse gas theory plus their new follow-up book.
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Joseph Olson
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The CDC, FDA, NIH are involved in Racketeering Influenced and Corrupt Organizations Act violations for their liability protected, monopolist vaccine peddlers. These organizations are a threat to humanity and must be disbanded. (They are far more dangerous than rogue policemen)
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