FDA hoarding 60 million doses of donated hydroxychloroquine that should be going to sick Americans9/12/2020 The American Association of Physicians and Surgeons (AAPS) is suing the U.S. Food and Drug Administration (FDA) for withholding from the public some 60 million doses of hydroxychloroquine (HCQ) that were donated by drug manufacturers to treat Wuhan coronavirus (COVID-19) patients.
Currently, these 60 million doses of HCQ are under strict lock and key at the Strategic National Stockpile because the FDA refuses to allow doctors to prescribe the drug to their ailing patients. Consequently, tens of thousands of Americans are needlessly suffering and dying from an illness that, quite frankly, is preventable. Because the medical deep state eventually wants everyone to get vaccinated for the Wuhan coronavirus (COVID-19), HCQ must remain off-limits because its widespread use would quickly prove that there is no need for a vaccine (RELATED: Learn more about how green tea and zinc can help support a healthy, COVID-free lifestyle). “[The FDA cares] more about [its] power over the HCQ Stockpile than the lives being lost daily without access to it,” the lawsuit against the FDA reads. “[T]he injunction plaintiff seeks would irreversibly overturn the status quo, by compelling the government to disburse the hydroxychloroquine in the Stockpile – a step that, once taken, cannot be undone.” The only thing that cannot be undone, the plaintiffs lament, is the “loss of life” that has come about due to the FDA playing politics with HCQ rather than simply doing the right thing to help sick people recover with this inexpensive, science-based remedy. Continue...
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HCQ works and ends this pandemic!!??
https://twitter.com/richardursomd/status/1294438462423273473 https://www.hitc.com/en-gb/2020/07/29/dr-richard-urso-hydroxychloroquine/ Open letter to Dr. Anthony Fauci regarding the use of Hydroxychloroquine for treating COVID-198/15/2020 By George C. Fareed, MD Brawley, California Michael M. Jacobs, MD, MPH Pensacola, Florida Donald C. Pompan, MD Salinas, California August 12, 2020
Anthony Fauci, MD National Institute of Allergy and Infectious Diseases Washington, D.C. Dear Dr. Fauci: You were placed into the most high-profile role regarding America’s response to the coronavirus pandemic. Americans have relied on your medical expertise concerning the wearing of masks, resuming employment, returning to school, and of course medical treatment. You are largely unchallenged in terms of your medical opinions. You are the de facto “COVID-19 Czar." This is unusual in the medical profession in which doctors’ opinions are challenged by other physicians in the form of exchanges between doctors at hospitals, medical conferences, as well as debate in medical journals. You render your opinions unchallenged, without formal public opposition from physicians who passionately disagree with you. It is incontestable that the public is best served when opinions and policy are based on the prevailing evidence and science, and able to withstand the scrutiny of medical professionals. As experience accrued in treating COVID-19 infections, physicians worldwide discovered that high-risk patients can be treated successfully as an outpatient, within the first five to seven days of the onset of symptoms, with a “cocktail” consisting of hydroxychloroquine, zinc, and azithromycin (or doxycycline). Multiple scholarly contributions to the literature detail the efficacy of the hydroxychloroquine-based combination treatment. Dr. Harvey Risch, the renowned Yale epidemiologist, published an article in May 2020 in the American Journal of Epidemiology titled “Early Outpatient Treatment of Symptomatic, High-Risk COVID-19 Patients that Should be Ramped-Up Immediately as Key to Pandemic Crisis." He further published an article in Newsweek in July 2020 for the general public expressing the same conclusions and opinions. Dr. Risch is an expert at evaluating research data and study designs, publishing over 300 articles. Dr Risch’s assessment is that there is unequivocal evidence for the early and safe use of the “HCQ cocktail.” If there are Q-T interval concerns, doxycycline can be substituted for azithromycin as it has activity against RNA viruses without any cardiac effects. Yet, you continue to reject the use of hydroxychloroquine, except in a hospital setting in the form of clinical trials, repeatedly emphasizing the lack of evidence supporting its use. Hydroxychloroquine, despite 65 years of use for malaria, and over 40 years for lupus and rheumatoid arthritis, with a well-established safety profile, has been deemed by you and the FDA as unsafe for use in the treatment of symptomatic COVID-19 infections. Your opinions have influenced the thinking of physicians and their patients, medical boards, state and federal agencies, pharmacists, hospitals, and just about everyone involved in medical decision making. Indeed, your opinions impacted the health of Americans, and many aspects of our day-to-day lives including employment and school. Those of us who prescribe hydroxychloroquine, zinc, and azithromycin/doxycycline believe fervently that early outpatient use would save tens of thousands of lives and enable our country to dramatically alter the response to COVID-19. We advocate for an approach that will reduce fear and allow Americans to get their lives back. We hope that our questions compel you to reconsider your current approach to COVID-19 infection. QUESTIONS REGARDING EARLY OUTPATIENT TREATMENT:
(IT WOULD BE VERY HELPFUL TO HAVE THE GRAPHS COMPARING OUR CASE FATALITY RATES TO OTHER COUNTRIES.)
Since the start of the pandemic, physicians have used hydroxychloroquine to treat symptomatic COVID-19 infections, as well as for prophylaxis. Initial results were mixed as indications and doses were explored to maximize outcomes and minimize risks. What emerged was that hydroxychloroquine appeared to work best when coupled with azithromycin. In fact, it was the president of the United States who recommended to you publicly at the beginning of the pandemic, in early March, that you should consider early treatment with hydroxychloroquine and a “Z-Pack.” Additional studies showed that patients did not seem to benefit when COVID-19 infections were treated with hydroxychloroquine late in the course of the illness, typically in a hospital setting, but treatment was consistently effective, even in high-risk patients, when hydroxychloroquine was given in a “cocktail” with azithromycin and, critically, zinc in the first five to seven days after the onset of symptoms. The outcomes are, in fact, dramatic. As clearly presented in the McCullough article from Baylor, and described by Dr. Vladimir Zelenko, the efficacy of the HCQ cocktail is based on the pharmacology of the hydroxychloroquine ionophore acting as the “gun” and zinc as the “bullet,” while azithromycin potentiates the anti-viral effect. Undeniably, the hydroxychloroquine combination treatment is supported by science. Yet, you continue to ignore the “science” behind the disease. Viral replication occurs rapidly in the first five to seven days of symptoms and can be treated at that point with the HCQ cocktail. Rather, your actions have denied patients treatment in that early stage. Without such treatment, some patients, especially those at high risk with co-morbidities, deteriorate and require hospitalization for evolving cytokine storm resulting in pneumonia, respiratory failure, and intubation with 50% mortality. Dismissal of the science results in bad medicine, and the outcome is over 160,000 dead Americans. Countries that have followed the science and treated the disease in the early stages have far better results, a fact that has been concealed from the American Public. Despite mounting evidence and impassioned pleas from hundreds of frontline physicians, your position was and continues to be that randomized controlled trials (RCTs) have not shown there to be benefit. However, not a single randomized control trial has tested what is being recommended: use of the full cocktail (especially zinc), in high-risk patients, initiated within the first 5 to 7 days of the onset of symptoms. Using hydroxychloroquine and azithromycin late in the disease process, with or without zinc, does not produce the same, unequivocally positive results. Dr. Thomas Frieden, in a 2017 New England Journal of Medicine article regarding randomized clinical trials, emphasized there are situations in which it is entirely appropriate to use other forms of evidence to scientifically validate a treatment. Such is the case during a pandemic that moves like a brushfire jumping to different parts of the country. Insisting on randomized clinical trials in the midst of a pandemic is simply foolish. Dr. Harvey Risch, a world-renowned Yale epidemiologist, analyzed all the data regarding the use of the hydroxychloroquine/HCQ cocktail and concluded that the evidence of its efficacy when used early in COVID-19 infection is unequivocal. Curiously, despite a 65+ years safety record, the FDA suddenly deemed hydroxychloroquine a dangerous drug, especially with regard to cardiotoxicity. Dr. Risch analyzed data provided by the FDA and concluded that the risk of a significant cardiac event from hydroxychloroquine is extremely low, especially when compared to the mortality rate of COVID-19 patients with high-risk co-morbidities. How do you reconcile that for forty years rheumatoid arthritis and lupus patients have been treated over long periods, often for years, with hydroxychloroquine and now there are suddenly concerns about a 5 to 7-day course of hydroxychloroquine at similar or slightly increased doses? The FDA statement regarding hydroxychloroquine and cardiac risk is patently false and alarmingly misleading to physicians, pharmacists, patients, and other health professionals. The benefits of the early use of hydroxychloroquine to prevent hospitalization in high-risk patients with COVID-19 infection far outweigh the risks. Physicians are not able to obtain the medication for their patients, and in some cases are restricted by their state from prescribing hydroxychloroquine. The government’s obstruction of the early treatment of symptomatic high-risk COVID-19 patients with hydroxychloroquine, a medication used extensively and safely for so long, is unprecedented. It is essential that you tell the truth to the American public regarding the safety and efficacy of the hydroxychloroquine/HCQ cocktail. The government must protect and facilitate the sacred and revered physician-patient relationship by permitting physicians to treat their patients. Governmental obfuscation and obstruction are as lethal as cytokine storm. Americans must not continue to die unnecessarily. Adults must resume employment and our youth return to school. Locking down America while awaiting an imperfect vaccine has done far more damage to Americans than the coronavirus. We are confident that thousands of lives would be saved with early treatment of high-risk individuals with a cocktail of hydroxychloroquine, zinc, and azithromycin. Americans must not live in fear. As Dr. Harvey Risch’s Newsweek article declares, “The key to defeating COVID-19 already exists. We need to start using it.” Very Respectfully, George C. Fareed, MD Brawley, California Michael M. Jacobs, MD, MPH Pensacola, Florida Donald C. Pompan, MD Salinas, California Source:www.thedesertreview.com/opinion/columnists/open-letter-to-dr-anthony-fauci-regarding-the-use-of-hydroxychloroquine-for-treating-covid-19/article_31d37842-dd8f-11ea-80b5-bf80983bc072.html
Comments by Brian Shilhavy
Editor, Health Impact News Medical journalist Del Bigtree of the weekly broadcast Highwire discussed on his show this week what he believes may be the primary reason why Fauci and the other political medical tyrants are so desperately trying to censor the positive results of Hydroxychloroquine (HCQ), a drug that has been around for over 65 years and is already FDA approved. The reason is probably because they want to force a COVID vaccine upon the public, and to do so, they need to fast-track the development of these vaccines, and then the FDA has to issue a an Emergency Use Authorization (EUA) to approve it. August 9, 2020 Print This Post Is the 100% Cure Rate of Hydroxychloroquine a Threat to Fast-Tracking the COVID Vaccines? Some of the doctors who are successfully curing COVID patients with Hydroxychloroquine that the Globalists are trying to silence. Why? Comments by Brian Shilhavy Editor, Health Impact News Medical journalist Del Bigtree of the weekly broadcast Highwire discussed on his show this week what he believes may be the primary reason why Fauci and the other political medical tyrants are so desperately trying to censor the positive results of Hydroxychloroquine (HCQ), a drug that has been around for over 65 years and is already FDA approved. The reason is probably because they want to force a COVID vaccine upon the public, and to do so, they need to fast-track the development of these vaccines, and then the FDA has to issue a an Emergency Use Authorization (EUA) to approve it. According to the “Qualifying Criteria” that allows the FDA to issue an EUA, there must be “No adequate, approved, and available alternative.” HCQ is an “adequate, approved, and available” alternative, which should then disqualify any EUAs issued for a vaccine to treat COVID. The problem, of course, is that the Trump Administration has already given over $8 BILLION to Big Pharma to develop the vaccine in “Project Warp Speed,” fast-tracking the vaccines development. In fact, this has already happened with Gilead’s anti-viral drug Remdesivir, which was fast-tracked as a treatment for COVID and then issued an EUA. See: Was a False Hydroxychloroquine Narrative Created to Destroy the Competition for Gilead’s Remdesivir?While the cost for the older HCQ medication is only about $20, Remdesivir’s cost is about $3200.00. And there is such a demand for it now, being the only “approved” medication for COVID, that other pharmaceutical companies are now stepping forward and offering to make it available as well, as Attorney Generals in 34 states this week sent a letter to the Federal Government requesting they “sidestep” Gilead’s patent. (Source.) These mass murderers who call themselves “doctors” and claim absolute authority on medical issues do not treat patients themselves, but they control the FDA, the CDC, the NIH, and pretty much the entire Government. They don’t value human life, and only want control so they can usher in their New World Order, and if a fast-tracked COVID vaccine ends up injuring and killing more people than COVID, it fits in perfectly with their plans for their New World Order and a One World Government as they seek to reduce the world’s population of those they deem “non-essential.” Watch the entire segment with Del Bigtree (who has now been banned from YouTube.) The Highwire Bitchute Video Channel is here. Connecting The Dots
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Doctors Adnan Munkarah and Steven Kalkanis.
Photo courtesy of Henry Ford Health System. by Brian Shilhavy Editor, Health Impact News As mass murder Dr. Anthony Fauci continues to appear in the corporate media to attack the use of hydroxychloroquine (HCQ), which thousands of doctors have now said can completely cure COVID, more doctors are coming forward to expose his lies. Fauci publicly attacked a recent positive study about HCQ published by the Henry Ford Health System, prompting two of the leading doctors of the study, doctors Adnan Munkarah and Steven Kalkanis, to publish an “Open Letter” refuting the lies of the mass murderer, Anthony Fauci. Dr. Munkarah works as the chief clinical officer of the Henry Ford Health System, and Dr. Kalkanis works as the chief academic officer. Here is an excerpt: We want to point out that scientific debate is a common occurrence with almost every published study. In part, this is what fuels the advancement of knowledge – challenging one another on our assumptions, conclusions and applications to get to a better place for the patients we collectively serve. You can read the original study here and the senior author’s letter to the editor here. Unfortunately, the political climate that has persisted has made any objective discussion about this drug impossible, and we are deeply saddened by this turn of events. Our goal as scientists has solely been to report validated findings and allow the science to speak for itself, regardless of political considerations. To that end, we have made the heartfelt decision to have no further comment about this outside the medical community – staying focused on our core mission in the interest of our patients, our community, and our commitment to clinical and academic integrity. (Full letter here.) Fauci’s main complaint about their study is that it was not a “double-blind, randomized clinical trial,” which is considered the “Gold Standard.” This is an interesting criticism, since almost all of the current new medical products being fast-tracked by the FDA to treat COVID, are also not “double-blind, randomized clinical trials.” This is especially true for the COVID vaccine drug trials, which do not even use a true placebo, but instead usually use another vaccine known for serious side effects, to make the new COVID vaccine appear to be more safe. Peter R. Breggin, MDAnother doctor who has come forward to criticize Fauci is Peter R. Breggin, MD, who published an article yesterday (August 3, 2020) titled: Why COVID-19 Clinical Trials Cannot Be Trusted: The “Gold Standard” for Science Is Gold for the Drug CompaniesExcerpts: Science! We have been told that science must be relied upon to make our decisions when dealing with the pandemic called COVID-19. We must in effect bow down to science, no matter how humiliating and painful it may feel. But science has an Achilles heel—a fatal flaw that can completely ruin it and frequently does. What is the fatal flaw of science? It is conducted by human beings. Science is only as dependable as the people who conduct and disseminate it. The adage for judging opinions still holds true—consider the source! When Anthony Fauci announced the rollout of his initial clinical trial for remdesivir as the great hope for knocking out the coronavirus epidemic, he boasted about the clinical trial’s importance: “A randomized, placebo-controlled trial is the gold standard for determining if an experimental treatment can benefit patients.” Since controlled clinical trials involving drugs and vaccines are very expensive, require access to sick and often highly infectious patients, and must be approved by the Institutional Review Boards (IRBs) and the FDA—they can only be conducted with funding from Big Pharma and Big Government or occasional other large institutions. We will see that the tragic result of this hegemony was remarkably demonstrated in Fauci’s government trial on behalf of his favorite drug company, Gilead. Meanwhile, the People’s Drug Is Running Ahead As we have documented in earlier reports, here and here and on our Coronavirus Resource Center, hydroxychloroquine and zinc as a prophylactic, and hydroxychloroquine plus azithromycin and zinc for patients developing COVID-19 could right now greatly improve the treatment of patients in the US, as it has done elsewhere. Doctors and entire nations have been and are continuing to use this drug successfully, especially in combination with azithromycin and zinc. The Association of American Physicians and Surgeons has shown that the countries which actively use hydroxychloroquine have significantly lower death rates than those that do not. (Full article.) Dr. Pascal SacréAnother doctor who has spoken out in an article published today (August 4, 2020) is French Dr. Pascal Sacré. The title of his article is: COVID-19: We have a Treatment: Hydroxychloroquine (HCQ). We do Not Need a Vaccine!Some excerpts: We have a treatment in COVID-19 and it doesn’t have the support of Big Pharma and their experts! Hydroxychloroquine (HCQ) is effective in treating COVID-19. It is effective in halting the progression of the disease, provided it is given early enough and provided it is given in accordance with “contraindications” and safety of use (cardiac). It costs nothing and the powerful pharmaceutical industry does not want to hear about it. Big Parma has done everything to outlaw and demonize it, including the publication in the most prestigious medical journal (Lancet) of a fraudulent article withdrawn 12 days later. Let’s stop saying that there is no treatment for COVID-19 or that only a vaccine will save us! There is a treatment for this disease, not in intensive care, where it is too late, but to prevent it from going to intensive care, so to be given early enough, by general practitioners or emergency doctors. The key to defeat COVID-19 already exists. We need to start using it. (Full Article.) Dr. Kevin R. Wheelan and Dr. Peter McCullough Texas doctors Dr. Kevin R. Wheelan, chief of cardiology at Baylor Heart and Vascular Hospital in Dallas and Dr. Peter McCullough, a clinical cardiologist and professor at the Texas A&M School of Medicine, have also made public comments and sent a letter to the FDA a few days ago. Reported in The Texan: The number of doctors publicly supporting the use of hydroxychloroquine for early treatment or prevention is growing. Recently, Dr. Kevin R. Wheelan, chief of cardiology at Baylor Heart and Vascular Hospital in Dallas and Dr. Peter McCullough, a clinical cardiologist and professor at the Texas A&M School of Medicine, issued a letter supporting the emergency use authorization (EUA) of hydroxychloroquine for outpatient treatment and prophylaxis for COVID-19. The letter dated July 6 was submitted in support of a petition by several other doctors asking the Federal Drug Administration (FDA) to reissue an emergency use authorization for hydroxychloroquine that has been donated to the national stockpile. Wheelan and McCullough say in their letter that “when started earlier in the hospital course…and in outpatients, antimalarials [hydroxychloroquine] may reduce the progression of disease, prevent hospitalizations, and are associated with reduced mortality.” They cite several studies for support. In response to concerns that have been raised about cardiac issues with patients using hydroxychloroquine, the doctors point out that even with heightened scrutiny of the use of hydroxychloroquine, no monitoring boards have declared safety concerns with the 65-year-old drug. They urge the FDA to allow physicians to assess the risk to their patients in determining whether hydroxychloroquine is an appropriate treatment. (Full article.) This is just a sampling of the doctors who are coming forward and speaking out, but don’t expect the national corporate media to give them any coverage, and don’t expect to find out anything about these doctors if you do a Google Search, as Google and the rest of Big Tech are accomplices to mass murder along with the big corporate media outlets, such as CNN, NBC, ABC, MSNBC, and also Fox News. See: Google Search is the Greatest Mind Control Brainwashing Tool in the History of MankindLaura Ingram and Tucker Carlson on Fox will at times give exposure to these doctors, but they will also probably politicize it and use it to attack Democrats and Joe Biden, even though this is clearly a non-partisan issue. In spite of this overt censorship, the news seems to be getting out, and as we reported yesterday, hundreds of thousands of people took to the streets to protest in Europe over the weekend. See: Hydroxychloroquine Scandal Spurs Hundreds of Thousands to Protest in Europe, While Americans Mostly Just Comply Because English is now the common language among the educated around the world, hundreds of thousands of readers from India and Africa have also been coming to Health Impact News to learn the truth about HCQ during the past few days. The question now is will Americans wake up in time to free themselves of this medical tyranny, or just mostly continue to willingly comply with their own destruction? |
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