Are the PCR Test Swabs Dangerous?

In my engineering work, an essential part of it is quality control. We are constantly testing our antimicrobial nutritional and surface-coating products in third-party laboratories to assure their safety.

Perhaps because of all the testing done over the years, it occurred to me very recently (just this month, January 2022) that since it seems almost all pharmaceutical ingredients come from China, the PCR test swabs might come from China as well. Unfortunately, it was just quite recently this occurred to me⏤and I wish I had thought of this earlier. But in any case, here is the information. 

Note that this relates to just one manufacturer and may not represent results from all manufacturers of the PCR swabs. However, the frightening results of the toxicological study is a clarion call for a study of the swabs from all manufacturers.

A recent internet search turned up some disturbing research on possible toxicity on the “cotton” part of the swabs. At least that of one manufacturer in China. The study concerns only one Chinese manufacturer, but the results lay a foundation for a very thorough study of ALL the PCR test swabs in use today.

Millions of people are tested daily, and this is part of a rush and panic to get massive testing done. I suppose rushing into anything in a panic is not a very sound principle.

To underscore the seriousness of this potential problem, I’d like to provide the background of the researcher who tested the swabs for possible toxicity. Dr. Antonietta M Gatti, Ph.D., is a heavyweight.

Antonietta M. Gatti, PhD, is the co-founder and principal investigator of Nanodiagnostics srl. She is an International Fellow of the Societies of Biomaterials and Engineering, and is the coordinator of the Italian Institute of Technology’s Project of Nanoecotoxicology, called INESE.

Dr. Gatti founded the association, Health, Law and Science, in Geneva, Switzerland. She is a Member of the NANOTOX Cluster of the European Commission. She is a selected expert of the Food and Agriculture Organization of the United Nations and the World Health Organization (FAO/WHO) for the safety in nanotechnological food.

Dr. Antonietta M. Gatti

Dr. Antonietta Gatti has an interdisciplinary background that ranges from physics, chemistry, biology, physiology, and pathology. Dr. Gatti has 30 years of experience in research in the field of biomaterials and biocompatibility at national and international levels in various capacities.

Dr. Gatti received her Ph.D. in Biomedical Technologies at the Faculty of Medicine of the University of Bologna, Italy, where she was on the faculty in the Laboratory of Bioengineering and at the Orthopaedic Institutes.

She is an undisputed expert in Nanopathology, Nanotoxicology, Environment, Ecotoxicity, Investigative and Personalized Medicine, Environmental Medicine, Forensic Pathology, Expert of Environment Sustainability, Nanotoxicology, Nanoecotoxicology, Risk assessment, Nanomaterials, Materials Biocompatibility, Biomaterials, Food Contamination, Scanning Electron Microscopy and x-ray microanalysis.

Now Let’s See What She Discovered:

Professor Antonietta Gatti examined various PCR test swabs and analyzed their ingredients. The results showed that they are made of tough materials and contain a large number of nano-particles, including silver, aluminum, titanium, and glass fibers. All of which are not declared on the PCR test package insert.

Prof. Gatti came to the following very frightening conclusions:

“The “porcupine” swabs are made from tough fibers. If they scrape on the nasal mucosa, they can damage it, causing a bleeding lesion or, in any case, trauma to the tissue.

“During the healing process of the mucous membrane, the broken fibers can penetrate the tissue without an opportunity to remove them, causing the formation of a granuloma or fibrotic tissue, as happens with any foreign body.

The medical devices examined are not completely biocompatible and therefore do not meet the requirements of ISO standard 10993 and the tests required to obtain the CE mark.

The summary of the professors’ findings is as follows:

>  Swabs are dangerous for the nasopharyngeal mucosa. The glassy fibers, hard and brittle, can scratch the mucous membrane and create lesions. The bleeding is an indication of the invasiveness of the test.

>  Repeated swab testing can produce chronic lesions. The release of fragments of the brittle, glassy fibers can cause biological reactions such as granulomas and/or fibrosis of the tissue.

>  These smears pose a risk to the health of infants and children. If the tests are necessary, small and mild smears must be carried out in children.”

COVID PCR Test Swabs are as dangerous as inhaling Asbestos

What about Dr. Fauci and Dr. Walensky? Working day and night as guardians of public health?

Fauci as director of the National Institute of Allergy and Infectious Diseases and the Chief Medical Advisor to our sock-puppet president…and Walensky, director of the CTC…

The possibility of a problem related to the safety of PCR tests may be shown after further research to be simply another pandemic disaster caused by or allowed to occur by health authorities.

A complete and ongoing quality control study of PCR test swabs of all manufacturers is called for on an urgent basis. And is something that can be added to the list of negligence attributable to Fauci’s National Institute of Allergy and Infectious Diseases and Walensky’s CDC, if it has not been carried out previously.

Please note: the toxicological study referred to in this article, was only of one manufacturer of the swabs, and that manufacturer is located in China. It is possible and hopefully the case, that this test result is unusual, and swabs are generally safe. And particularly, swabs that are manufactured in the US and EU fulfill safety requirements. However, a massive quality control effort is being called for to determine what the situation actually is relative to the safety of PCR swabs!

DISCLAIMER: No one in this post is being accused of a crime. Criminality in this matter can be determined only in a court of law. Furthermore, there is no medical advice in this article. Readers should consult with their own doctor and follow that advice. The article presents a political analysis, and an educational analysis only, and is based on varied sources of reliable publically available opinion.

New NIH COVID Treatment Guidelines: Real Questions Joel S Hirschhorn January 22, 2022

What our government is telling physicians boggles this author’s mind. Read the following from a publication aimed at doctors.

This was reported:

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“Due to the Omicron variant and the short supply of COVID therapeutics, NIH recommends certain therapies over others for patients at high risk of progressing to severe COVID, said federal officials on a call with clinicians Wednesday [January 12].

In order of preference, clinicians should use the oral antiviral nirmatrelvir-ritonavir (Paxlovid), the monoclonal antibody sotrovimab, the IV antiviral remdesivir (Veklury) and finally, the oral antiviral molnupiravir, said Alice Pau, PharmD, of the NIH COVID-19 Treatment Guidelines panel.

While the drugs were ranked from 1 to 4, she noted that nirmatrelvir-ritonavir, sotrovimab, and IV remdesivir three times a day all had similar clinical efficacy, with a relative risk reduction of 88%, 85%, and 87% in hospitalizations and deaths, respectively, versus placebo. However, molnupiravir, with its 30% efficacy, should be used only if the other three choices are not available, Pau noted.”

Here are the main reasons why the NIH list of preferred COVID treatments should not reassure the public:

1.  The first preferred action, using the Pfizer drug Paxlovid, makes little sense because there is nearly no availability of it.  And even if people could get prescriptions filled, would they be acting fast enough to get benefits.  In the clinical trials people had to start the drug within three days of symptoms; even though they now talk of starting within five days, that too is totally impractical and unrealistic.  Few people would be able to distinguish symptoms being COVID and not the flu or a bad cold quickly, getting an appointment with the doctor quickly and getting a prescription filled quickly.  And the safety has not been adequately assessed. A new article written for physicians details concerns about interactions with commonly used medicines.

2.  The monoclonal antibody sotrovimab is nearly impossible to get because of extremely limited supply.  And here too, a sick person would have to get medical attention quickly, that is extremely difficult.  Even your local hospital might not have it.

3.  The very expensive drug remdesivir has a terrible history of being both ineffective and having terrible side effects.  It is mostly given to very ill patients in hospitals.

4.  Then you get to the absolutely head-scratching fourth option, the new Merck antiviral that has a real question of effectiveness and that has not been proven safe.  An absolutely questionable choice.

Most troubling according to this author, the NIH continues to ignore ivermectin or hydroxychloroquine as real-world treatment options.  It disregards positive-impact, real-world treatment protocols of frontline doctors like Dr. Fareed and Dr. Zelenko that do NOT include any of the four NIH preferences.

Of special importance is that NIH has ignored a recent detailed study of ivermectin and aimed at informing clinical guidelines reached these conclusions: “…large reductions in COVID-19 deaths are possible using ivermectin.  Using ivermectin early in the clinical course may reduce numbers progressing to severe disease. The apparent safety and low cost suggest that ivermectin is likely to have a significant impact on the SARS-CoV-2 pandemic globally.”  An even newer study found remarkable benefits of using IVM, including a 68% reduction in mortality and 56% reduction in hospitalization.  NIH is not respecting positive results for IVM.  And their guidelines could make it difficult for states trying to make IVM easily available.

Is U.S. taxpayer money properly used for the benefit of the people?

The real message for the public: We must question the government and whether the present-day recommendations are in fact protecting human health. The pandemic has exposed the challenges with the present-day public health apparatus, evidencing greater risks to the broader population.  While agencies such as the NIH accuse others of propagating misinformation, in reality, that apex research institution in fact projects their own complicity in such an unfortunate ongoing undertaking.

Dr. Joel S. Hirschhorn, author of Pandemic Blunder and many articles and podcasts on the pandemic, worked on health issues for decades, and his Pandemic Blunder Newsletter is on Substack. As a full professor at the University of Wisconsin, Madison, he directed a medical research program between the colleges of engineering and medicine.  As a senior official at the Congressional Office of Technology Assessment and the National Governors Association, he directed major studies on health-related subjects; he testified at over 50 US Senate and House hearings and authored hundreds of articles and op-ed articles in major newspapers.  He has served as an executive volunteer at a major hospital for more than 10 years.  He is a member of the Association of American Physicians and Surgeons, and America’s Frontline Doctors.

U.S. Terrorist Network Left Untouched After Synagogue Attack

Current News

1) Record 360 million Christians persecuted in 2021 report states. See news report HERE.

2) Biden regime sued for Terrorist Financing. See news report HERE.

3) Former child bride says Biden regime "aiding and abetting" bringing sharia to U.S.  Read the article HERE.

4) China, Russia, and Iran hold their 3rd join naval operation in the Indian Ocean. Click HERE to read the report.

5) The UN gives $32 million to Taliban terrorists. Read more HERE.

6) Texas synagogue jihadi tied to Tabligi Jamaat (TJ). Read the story HERE. Note: UTT will post and article about TJ and their U.S. networks in the next couple days.

 

Featured Article:  U.S. Terrorist Network Left Untouched After Synagogue Attack 

by John D. Guandolo

The attack on a synagogue in Colleyville, Texas last Saturday again highlights the dangerous truth that the FBI and state authorities across America have done nothing - absolutely nothing - to rip down the terrorist support network in the United States, which is comprised of all of the most prominent Islamic organizations in America, as a matter of fact and evidence.

Despite the fact that nearly all Islamic terrorist attacks inside the United States can be directly tied to support from the U.S. Muslim Brotherhood (MB), Deobandi (Tabligi Jamaat/Dar ul Uloom), and other partnered Islamic Movements inside America, nothing has been done to systematically take these networks down by the very agencies charged with doing so.

Here are a few examples of jihadi Movements directly supporting terrorist attacks in the United States:

9/11: Islamic Center of San Diego (MB)

Boston Marathon bombing: Islamic Society of Boston (MB)

Orlando Nightclub Attack: Islamic Center of Fort Pierce (Tabligi Jamaat)

Fort Hood Attack: Dar al Hijra Islamic Center (MB)

Chattanooga Attack: Islamic Society of Chattanooga (MB)

San Bernardino: Dar al Uloom al Islamiyyah (Tabligi Jamaat)

Garland, Texas Draw Mohammed Event Attack: Islamic Community Center of Phoenix (MB)

Investigations always end when the perpetrators and individuals involved in the violence of the attack are discovered and arrested. The massive Islamic network in the United States that births, nurtures, and supports these terrorists and their operations are left alone.

To continue reading click HERE

Click HERE to listen to John Guandolo's radio interview with Frank Gaffney on "Who is Aafia Siddiqui"

 

Featured Video

Last weekend's jihadi attack in Texas serves as a reminder of how broken Mr. Biden's national security team is and how they are intentionally aiding and abetting terrorists in America.  This goes to explain why Mr. Biden, Ms Harris, and the entire democrat national security apparatus intentionally supported the Taliban terrorists and left Americans to die behind enemy lines.  Let's go back and listen to UTT's John Bennett as he broke it all down for Steve Bannon at the time.  Click HERE to watch.

 

Featured UTT Product

In light of the jihadi attack in Colleyville, Texas last weekend, UTT encourages all of you to understand the jihadi threats better.  Pick up your copy of "Typical Comments" - a document that will help you respond to the typical comments from detractors who do not understand Islam, jihadis, or their massive network in America.  Click HERE to get yours today.

For our TEXAS residents - and anyone who wants to see how deep and wide the jihadi and communist networks are at the local level - we encourage you to get your FREE copy of "The Takedown of Texas" now.  Just click HERE.

 

UTT Victories

UTT is gaining ground in our ability to get our message out.  Our team members are speaking at more larger venues, on more radio/TV interviews, and current events are helping people see the truth about the coordinated efforts by the jihadis and communists to take America down.

Last week's article entitled "Jihadi Attack on Synagogue Highlights Info War & Massive Islamic Movement Operations in Texas" has gained a significant amount of attention in Texas and beyond.

Today, UTT Vice President John Bennett is speaking at a Freedom Rally in Oklahoma.  Next Weekend John Guandolo is speaking at a Patriot Conference in Texas.  Peggy Mast has been making the round at numerous rallies, conferences, and speaking engagements.  UTT's Caleb Collier is a featured speaker at a Patriot Rally in Washington State expected to draw 10,000 people.

Thanks to all of you for spreading the word.  PLEASE continue to share UTT's work with everyone you know and encourage them to go to UnderstandingtheThreat.com and contact us to bring the INTO ACTION training to their town and/or donate any amount of recurring donation to UTT to keep this train rolling!

 

What Can You Do to Stay Informed?

1) Listen to John Guandolo's Weekly Radio Show. Click HERE

2) Join UTT's team live as they deliver interactive presentations every Tuesday at 7 PM CST/8 PM EST on EncouterTruth.com.  To join click HERE now!

3) Join John Guandolo on the "Understanding the Threat" TELEGRAM channel livestream every Wednesday evening at 9:15 PM CST for a short (15 minute) brief on pertinent current events, followed by your questions.

4) Subscribe to UTT's YouTube Channel. Click HERE

 

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Get trained and Get in the Fight OR Fund the War Effort!

GET TRAINED...

UTT's INTO ACTION Training is the portal for all citizens to empower you to take back your community, your county, and your state.  This 3-day program gives citizens an understanding of jihadi and communist threat doctrines, networks and modus operandi, and details where these hostile networks are in your local community, as well as helping identify those collaborating with them.  By the end of the 3 days the team will be assembled, organized, have priorities, and will have action items to begin working on immediately in your county.

You reach out to us when you have 20 or more Patriots ready to defend liberty, law, and the Constitution.

The objective is to FORTIFY your county by flushing all of the hostile organizations and leaders out, while simultaneously re-establishing a republican form of government at the county level.  By working with friendly adjacent counties and fortifying them as well, a LIBERTY STRONGHOLD is created from which the state can be retaken under law and the U.S. Constitution.

Go to the Contact Page at UnderstandingtheThreat.com or just click HERE and let us know you have a team who want to get INTO ACTION!

 

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Music Corner

"This was a ton of fun to record a cover song that is a classic.  I hope we did it justice.  I think we did."  John Guandolo, Boats Against the Current, regarding the band's cover of "Wicked Game."

Click HERE to watch and listen.

 

Quote of the Day

"If a man hasn't discovered something that he will die for, he isn't fit to live."

Martin Luther King, Jr.

Rwandans Vaccinated by Force, According to German Broadcaster

Rwandans say that local law enforcement authorities are rounding up individuals to physically force coronavirus vaccine doses injections without consent.

Police Go Door-To-Door to Deliver Shots Without Consent

Deutsche Welle (DW) reported this week that local Rwandan government officials, including local police in rural areas, went door-to-door to roust people from their homes and inject them without their consent.

The report said the practice primarily involved impoverished Rwandans including street children and suspected criminals in more remote Rwandan transit centers in the Western Province’s Ngororero district nearly 40 miles northwest of Kigali, the nation’s capital.

Rwanda: Africa’s mRNA Production Hub

Rwanda and BioNTech SE announced in October that the African nation would be home to the first state-of-the-art manufacturing site for mRNA-based vaccines in the African Union by mid-2022. 

“This is the next step in BioNTech’s efforts to implement sustainable end-to-end vaccine supply solutions on the African continent,” BioNTech said in a statement.

Low Vaccination Rates in Africa

Rates of vaccination in Africa are among the world’s lowest at about six percent continent-wide, or about 77 percent of the population. That is far fewer than the World Health Organization’s missed goal of 40 percent vaccination rates by the end of 2021.

The reasons for Africa’s slow pace of vaccination include supply-chain problems include logistical challenges like finding enough cold storage facilities across a vast, mostly rural landmass to poor perceptions of recent pandemic responses to diseases like human immunodeficiency virus and ebola.

African nations have also sought to deploy diverse methodologies to contain the pandemic including exploring use of ivermectin and other therapeutics and the use of so-called “vaccine bonds” to fund the manufacture of drugs that may not have a strong enough profit incentive.

Legacy Public Health Practices in Africa Inform Vaccine Hesitancy 

A recent PLOS One survey of 5,416 respondents across 34 African countries and the African diaspora found that only 63 percent were willing to take COVID vaccines “as soon as possible,” 79 percent were worried about side effects and 39 percent feared vaccine-associated infections.

Amid relatively low caseloads (about 10 million as of January 8) and slow COVID vaccine uptake across Africa, some nations have attempted to impose mandates.

Rwanda represents a troubling pandemic trend where emergency public health policies have been advanced by governments without strong rule of law or human rights safeguards.

Rwanda’s Fragile Social Order

Rwanda suffered one of history’s worst genocides in 1994 when as many as 800,000 killings took place, nearly all of them committed by machete-wielding members of the Hutu ethnic group against their ethnic rivals, the Tutsis, within only 100 days.

In the decades that followed, Rwandans have striven to reconcile and build one of Africa’s fastest-growing economies. But the landlocked nation has also struggled with bouts of authoritarian and sometimes violent government repression.

COVID Mandates and Human Rights

In 2020, a United Nations Development Programme report on COVID policies on Rwandan human rights cited infringement on freedom of expression, movement, assembly, and deterioration of rule of law. The international agency said it “strongly believes that there is still room for improvement in terms of human rights protection in relation to the challenges posed by of COVID-19.”

Forced vaccinations have been reported in other nations including China, which has also been accused of “disappearing” critics of the government’s vaccine policies.

The Ivermectin Wars Intensify as States Want Access Over the Counter and a Medical Freedom March Commences This Weekend

TrialSite recently shared that a handful of states have proposed bills to ensure ivermectin is available to treat COVID-19 via a legitimate physician’s prescription. Those states include Indiana, Kansas, and New Hampshire. Recently, a leading proponent of the use of ivermectin, Dr. Paul Marik, one of the co-founders of the Front Line COVID-19 Critical Care Alliance (FLCCC), discussed the pending New Hampshire ivermectin legislation with conservative news platform, America’s Voice Network.

Marik, board certified in Internal Medicine, Critical Care Medicine, Neurocritical Care, and Nutrition Science, is a key opinion leader who has worked in numerous hospitals and health systems from South Africa, UK, and of course, the United States where he is most recently affiliated with Eastern Virginia Medical School (EVMS) as well as other medical institutions. Not a stranger to controversy, or for that matter, pushing the comfort boundaries of the medical establishment, Marik isn’t a lightweight, with over 400 peer-reviewed journal articles, 50 book chapters, and author credits for four critical care books.

Recently, he filed a lawsuit against his hospital over the institution’s ban on various therapies including ivermectin, which happens to be a core therapy in his and his colleagues MATH+ Hospital Treatment Protocol for COVID-19. He and colleagues such as Dr. Pierre Kory experienced what they declare is censorship, as key journals had reviewed and accepted manuscripts, such as with the Journal of Intensive Care Medicine, only to see the approvals retracted. Physicians such as those affiliated with the FLCCC represent prominent figures at this weekend’s medical freedom march.

Background

In a recent interview DR. PAUL MARIK | NEW HAMPSHIRE IVERMECTIN BILL – Good News | 45 | Data Matter (tvwfc.co.uk) with the conservative media platform America’s Voice Network, Marik shared his opinions on pending legislation, the importance of repurposed therapeutics, and who he thinks has been involved in the attack on ivermectin as an off-label treatment option.

The alternative media reporter, Heather Mullins, shared that New Hampshire’s bill is now “sponsored” and must still “go through some hurdles to get passed,” but if done so will “essentially make ivermectin available over the counter.” According to the TrialSite report, the proposed bill would authorize access at the pharmacy via a “standing order” which generally indicates authorization for nurses, pharmacists, and other appropriately credentialed health care professionals that if directed by state law, empowers the direct care and admonition of a vaccine or therapy (in this case ivermectin) based on an approved medical doctor-based approved protocol.

TrialSite didn’t report that Paul Marik testified for the proposed bill in New Hampshire. Mullins reports that Marik and other front-line physicians have been on the record that if ivermectin had been allowed for use as an early at-home prophylactic treatment targeting COVID-19,  hundreds of thousands of lives could have been saved.

The Interview

Prior to the testimony in New Hampshire, Dr. Marik shared that 3.7 billion doses of ivermectin have been administered around the world, “changing the face of parasitic diseases on this planet.” Marik declared that ivermectin “is probably the second most important drug ever invented” [the drug’s inventors did win a Nobel Prize and the drug is on the World Health Organization Essential Drug List].

Declaring that the drug is cheap, safe, and “highly effective against SARS-CoV-2, and if used more widely this drug could have saved hundreds of thousands of lives.”

Referring to its use in many other countries, the critical care physician went on the record that it’s a “lifesaving drug.” 

Why the pushback against ivermectin? Marik, now somewhat liberated given he isn’t dependent on his employer Sentara, let loose declaring, “There are multiple reasons, and this is probably generated by Big Pharma, government, and big corporations who don’t like cheap repurposed drugs.”  He continued, “So this is a war on cheap, repurposed drugs.” Emphasizing the goals of ivermectin’s adversaries, Marik stated, “They want you to use expensive designer drugs which in fact don’t work.”

In clarifying his understanding of the New Hampshire bill, Marik declared it is proposing to make ivermectin available over the counter [again via standing order] and according to the critical care doctor, it makes sense given the drug’s safety profile— “the drug is safer than Tylenol,” stated Marik. Repeating again the drug’s safety profile makes it safer than Tylenol, he went on the record “People should be given access to this drug in order to prevent and treat COVID.”

Marik espoused the critical FLCCC view that early treatment for COVID-19 absolutely represents a critical care strategy: simply waiting at home for a symptomatic phase, prompting a trip to the hospital raises significant danger for severe disease and worse.

The Controversy

According to Heather Mullins’ report, there has been a coordinated effort to censor the robust data pointing to at least some ivermectin-based efficacy around the world. Ivermectin study watchers often point to the website which tracks all ivermectin studies in a clean, orderly series of tables and graphs. While the majority of the 75 completed studies point to positive data points, the mainstream media and medical establishments in North America, Europe, and Australia have limited the number of studies within the research portfolio that they even acknowledge to just a handful. The others? These studies are dismissed because of bad quality. 

A couple of prominent studies showed no benefit, yet, at least one of them became surrounded with controversy and allegations among some industry watchers of conflict of interest. TrialSite notes this hasn’t been proven, and one study in Egypt that was part of a couple of meta-analysis studies turned out to have manipulated data. Yet even with the questionable Egyptian study, TrialSite’s Sonia Elijah’s investigation raised some disturbing questions in “How Ivermectin became a Target for the Fraud Detectives.”

TrialSite has chronicled ivermectin studies all over the world, including the ICON study done in Broward County early on during the pandemic. Of course, this study wasn’t a randomized controlled trial, thus limiting its impact. Interviews with the head of the largest hospital in the Dominican Republic as well as a well-respected investigator in Dhaka, Bangladesh, and interactions with doctors in Nigeria, Zimbabwe, South Africa, and India found positive data points. TrialSite even sponsored an objective documentary in Peru, one of the first nations to accept the use of the drug for the novel coronavirus.

After numerous interviews, study write-ups, and real-world observations, the case for ivermectin should be taken seriously. The U.S. National Institute of Health is financing an ivermectin-based study called ACTIV-6, while the University of Minnesota led one of the largest ongoing ivermectin studies called COVID-OUT.

The drug does have a proven safety profile at doses currently approved for parasitic indications. However, claims that higher dosages are just as safe as Tylenol might be a stretch—rather that claim would be associated with currently approved indications. Yet, it’s not a stretch to declare the drug is generally safe if taken off-label under the guidance of a licensed, competent physician.

The FDA’s behavior during this pandemic in association with ivermectin has been questionable, to say the least. Issuing warnings to the public not to use the animal variety of the drug, they emphasized that for the human version, it should be used only in clinical trials. TrialSite’s Sonia Elijah’s piece on obtaining FDA emails suggested the possibility of some form of disinformation campaign emanating from the world’s most respected food and drug regulatory body—an activity, if true, is beneath this organization.

FDA letters to medical and pharmacy boards and medical societies have led to considerable pressure on doctors employed by health systems and pharmacies not to allow ivermectin prescriptions off-label for COVID-19. In addition to a survey substantiating this trend, TrialSite chronicles plenty of instances evidencing efforts to block access. The TrialSite survey evidenced the effectiveness of an ongoing purge.

While there has been much controversy following the drug, Marik, Kory, and others actually visited the National Institutes of Health COVID-19 Treatment Guidelines Panel to discuss the evidence of efficacy against SARS-Cov-2 in early 2021.

Just weeks after that meeting the NIH changes its ivermectin recommendation.

 from use only in clinical trials to the following recommendation:

  • There is insufficient evidence for the COVID-19 Treatment Guidelines Panel (the Panel) to recommend either for or against the use of ivermectin for the treatment of COVID-19. Results from adequately powered, well-designed, and well-conducted clinical trials are needed to provide more specific, evidence-based guidance on the role of ivermectin in the treatment of COVID-19.

Yet if the drug is generally safe and a licensed physician along with an appropriately consenting patient agree to an off-label regimen, why would this vary from other standard off-label use cases that no one makes a fuss about? What is it about COVID? TrialSite has observed based on the severity and intensity of the pandemic, more federal involvement, and intervention in healthcare. Concerns of ivermectin took off when government, industry, and regulators discovered that prescriptions skyrocketed from 3,000 per week pre-pandemic to nearly 90,000 per week during the second year of the pandemic.

TrialSite recently reported on a study led by a University of Michigan doctor showing that at least $130 million in insurance claims for the drug treating COVID-19 in 2021—that figure is probably more than double when counting all the cash-based prescriptions.

Perfect Storm: Vaccine Booster ‘Fatigue’ + Antiviral & mAb Shortages = Push to Introduce State Laws Ensuring Ivermectin Access

While TrialSite reported that a Brazilian rural state recently passed a law allowing the use of ivermectin and hydroxychloroquine for COVID-19, now in the United States, Republican lawmakers from New Hampshire, Kansas, and Indiana push to ensure access to such repurposed drugs in those states, despite a stance by the U.S. Food and Drug Administration (FDA) that such drugs should only be used for COVID-19 in clinical trials. In Concord, New Hampshire, some politicians seek to make it easier for patients to access ivermectin as an early-onset treatment for COVID-19. In the ‘Live Free or Die’ state, House Bill 1022 would enable pharmacists to dispense ivermectin via what’s known as a standing order, reports local media WMUR 9, despite the FDA’s declaration on the drug for off-label use against COVID-19. In Kansas, a growing Republican-led movement calls for a similar bill for early treatment to include ivermectin and hydroxychloroquine, while similar calls are heard in Indiana. Will 2022 be the year of the push for repurposed therapies at the state level? Prominent U.S. government-backed clinical trials that include ivermectin may help or hinder the momentum for state-level initiatives. Meanwhile, with record COVID-19 infection counts, health authorities become more intent on educating people about the benefits of vaccination versus the risks of COVID-19. A lack of early treatments combined with the concern that monoclonal antibodies may not work as well against Omicron leaves the sick fewer choices, as it appears only Sotrovimab works well against the latest variant of concern, according to some critical care doctors.

What to do?

With an explosion of Omicron COVID-19 cases across America, concerns grow that vaccination does not stop viral transmission, as observed with mounting breakthrough infections. TrialSite covered the recent study from Denmark’s Statens Serum Institut which reported in an uploaded preprint study that the second doses of Pfizer and Moderna mRNA-based vaccines may actually increase the likelihood of SARS-CoV-2 infection after 90 to 150 days.

It would be misleading to declare that the vaccines are not effective against Omicron. Rather, the investigators from Denmark found them to be effective, but the durability of the vaccines raised concerns. The study authors declared, “In light of the exponential rise in Omicron cases, the findings highlight the need for a massive rollout of vaccinations and booster vaccinations.” The latter was emphasized with the Pfizer vaccine, due to waning effectiveness but an identified rebound in positive efficacy with a booster.

Regardless, “booster fatigue” becomes a growing topic, as a confluence of forces increasingly indicate countries such as the USA, the UK, and perhaps soon Israel’s health authorities will signify a transition to an endemic stage of COVID-19.

Authorized Treatments in Short Supply

While both Pfizer and Merck have antiviral-like medications now coming to market there are still limited supplies amidst the historic rises in new infections due to the highly transmissible nature of Omicron.

Concerns with Merck’s Molnupiravir are mounting in some parts of the world—so much so that in the world’s second most populated nation, India, the apex research organization ICRM has cautioned against the use of the drug.

The antivirals, key for many as a tool to end the pandemic, are hard to come by in many locations. With Omicron raging, the timing of the shortages couldn’t be worse

In the meantime, although monoclonal antibodies have helped infected Americans fight off COVID-19, a crisis emerged with this class of treatment as well. A confluence of factors, including product shortages in part due to federal meddling of the supply chain combined with the fact that only one of the mAb products appears to work well with the new mutant version of SARS-CoV-2 (GSK and Vir’s Sotrovimab), makes access to these products exceedingly elusive.

Meanwhile, with vaccinated persons becoming infected all over America due to the highly transmissible mutant, concern and fear associated with breakthrough hospitalizations become a daily fear. Yes, it appears that the vaccines still protect people from more severe Omicron-based disease, but again, the effectiveness wanes and booster fatigue become a growing reality. What about other treatments?

Moves to Ivermectin?

Despite the incredible controversy surrounding ivermectin, TrialSite reports that elected officials are proposing bills to ensure access to this FDA-approved repurposed drug. Even though the FDA recommends only in clinical trials, a medical freedom movement thrusts forward with what is supposed to culminate in a large march in the nation’s capital Sunday, January 23. TrialSite follows proposed legislation involving ivermectin, and the even more controversial hydroxychloroquine.

New Hampshire’s Move

The medical freedom movement takes on steam in anticipation of a forthcoming march in Washington, DC (January 23), as several groups testified against the proposed New Hampshire Bill while others “say there should be more research.”

Recently tracked on local media, New Hampshire Republicans seek to guarantee access to the repurposed drug. Recently showcased on WMUR 9, a Hearst Media-owned station, Dr. Nick Perencevich, a retired surgeon was filmed on television declaring, “I would like to think that the standard of care in New Hampshire is that a patient can certainly have ivermectin prescribed off-label if that patient, ideally, gets put into some clinical trial, whether it’s a drug company, or whether it’s an academic institution like Dartmouth.”

Now before the House Health and Human Services Committee, the WMUR 9 report shared [the Bill] is expected to make it to the House floor for a vote in the weeks ahead. The broadcast ended with a segment on ivermectin indicated for horses. TrialSite notes that the media didn’t bother to interview the proponents of the bill nor hear their argument, indicating the possibility of bias.

Kansas Callings

Meanwhile, In Kansas, Sen Mark Steffan recently announced forthcoming bills to promote off-label use of approved FDA prescription drugs including hydroxychloroquine and ivermectin for COVID-19 patients. 

The bill was introduced in a special session, however, has not yet been acted upon in a recent Kansas Senate committee resolution, reports the Kansas Reflector, an independent non-profit-based media.

In the recent report, reporter Noah Taborda referred to the proponents of the forthcoming bill as driven to appease “anti-vaxxers,” and that would “undermine local health officials and promote off-label use of prescription drugs.”

An anesthesiologist, Sen. Steffen has been critical of the medical establishment’s efforts to block use of off-label early care treatments such as ivermectin and hydroxychloroquine. Taborda writes that “the Hutchinson Republican advocated for more avenues to use these treatments,” even though the FDA is on the record that ivermectin, for example, should only be used for COVID-19 in clinical trials. TrialSite reports a couple of sizable clinical trials including ivermectin have been underway in the United States.

Meanwhile, COVID-19 continues to rage in Kansas, breaking new daily case counts. The issue of off-label drug use continues to be positioned as an “anti-vaxxer” issue, yet this clearly isn’t the case for all proponents. In the case of Steffen, he is on the record that the risk-benefit analysis associated with the COVID-19 vaccine products favors avoidance for children who rarely end up hospitalized. Yet, according to the Kansas Reflector, while the movement for medical freedom gains momentum in parts of this plains state, there has been an explosion of cases, many of which are either Delta or Omicron-based, with a total of 7,162 deaths in a state with a population of 2.93 million residents. 

Tragically, Tim Carpenter writing for the local media reported child deaths—three children under ten years old and three additional adolescents between the age of 10 and 17. Hence, medical establishment proponents argue the risks of hospitalization and death are too high, justifying universal vaccination.

Hoosier Hope?

In the meantime, in the midwestern state of Indiana, Rep. Curt Nisly, R-Goshen, authored a bill that would allow for use of ivermectin to treat COVID-19. Like Kansas, this agricultural state has more access to the animal variety of the drug. Nisly went on the record for the Indy Star in an email declaring, “Why wouldn’t we make this available, especially if we want Hoosiers to stop using horse paste. Hoosiers should be able to care for their health safely and effectively.”

The proposed House Bill 1372 allows for a physician or advanced practice registered nurse to write a standing order for ivermectin ensuring the pharmacist would dispense the drug while stipulating that the pharmacist couldn’t try to dissuade the patent from accessing the drug.

Conclusion

The surge in Omicron cases, in a way, is the perfect bad storm, as a combination of vaccine booster fatigue and antiviral and monoclonal antibody shortages along with the rising medical freedom movement lead to state legislatures pushing for new bills to make economical repurposed drugs like ivermectin available on demand.

An imminent march on Washington this Sunday, January 23 possibly intensifies the medical freedom movement which very well may influence midterm elections. TrialSite predicts within a couple of weeks more proposed off-label bills will contribute to a growing clash of interests. Luckily, thus far, omicron infections appear milder but exponential numbers of cases, hospitalization rates, and deaths move higher, regardless.

Preventive Ivermectin: international scientific review confirms 68% efficacy in SUS study

Over the weekend, after reviewing the data by three independent groups of scientists, the 68% efficacy of the preventive ivermectin against deaths caused by COVID-19 was confirmed. The final results of the study were published in the prestigious scientific journal Cureus, based in San Francisco, USA, and with a chapter in Munich, Germany. 

Cureus has two esteemed editors-in-chief in the scientific community: Dr John Adler Jr, Professor of Neurosurgery and Radiation Oncology (Emeritus) at Stanford University in California, and Dr Alexander Muacevic, the medical director of the European Radiosurgery Center in Munich, Germany and a professor at the University of Munich Hospitals.

The medical research took place in Itajaí, a port city in Santa Catarina, in the southern region of Brazil, between July and December 2020. The lead scientist of the study is the Brazilian medical doctor Lucy Kerr. Other important scientists collaborated with the scientific article and co-signed the research. Among them are Jennifer Hibberd, from the University of Toronto, Canada, Fernando Baldi, professor at the State University of São Paulo (UNESP), Dr Pierre Kory, North American medical professor and one of the world’s leading experts in intensive care, among several others.

The largest ivermectin study in the world only occurred because of the excellence of SUS

UBS – Basic Health Unit Promonar was one of several health points used to distribute ivermectin, record data on comorbidities, previous diseases, perform COVID tests, and serve the population of Itajaí during the study. Photo: Google Street View.

The study was only possible due to the excellence of the Brazilian public health system. “The National Health System (SUS) functions as full healthcare support to the entire population allowed the city to establish a non-restricted population program,” the scientists explained in the study.

Only people over the age of 18 participated. “Children were excluded. And also people who have had COVID before,” Lucy Kerr explained. 

Thus, of the 223,128 citizens of Itajaí considered for the study, a total of 159,561 individuals were included in the analysis: 113,845 (71.3%) ivermectin users and 45,716 (28.7%) non-users.

The drug was offered by the municipal government to all citizens and only those residents who wanted it participated. “Patient preferences and medical autonomy were preserved,” the scientists explained.

SUS professionals in Itajaí monitored and recorded the data of both patients who took ivermectin and those who did not take the drugs. “The whole city had digital registration at SUS and it was being updated with the new consultations as people went to get their medication,” Kerr said.

The scientist praises the health professionals in Itajai. “They all collaborated very, very much,” said Dr. Lucy. “It wasn’t just data if they took it or didn’t take it. It was also knowledge of all people’s previous comorbidities and illnesses. Whether they had asthma, diabetes, cancer.”

“I don’t know if this would be possible in other countries, since Brazil, through SUS, is one of the most digitalized countries, and with accurate data, in the health system,” said Dr Flavio Cadegiani, one of the scientists involved in the data analysis.

Result: 44% reduction in chance of getting COVID-19, study concludes

The study was published in the journal Cureus (link)

Among all citizens over the age of 18 with no history of COVID, 113,845 volunteered to take Ivermectin every two weeks. Among those who did not volunteer, there were 45,716 people. 

Over the next six months, among those taking ivermectin, 3.7% became infected with the virus. Among non-users, 6.6%. There was a 44% reduction, therefore, in the chance of being infected with Sars-Cov-2, the virus that causes COVID-19.

Once infected, 56% reduction in chance of being hospitalized

Among the 113,845 who took ivermectin, 4,197 had Covid. Among the 45,716 who did not take it, 3,034 had Covid.

In the study, from this point on, there was an advanced statistical technique called Propensity Score Matching, where two groups were balanced to be similar with regard to age and risk factors, such as previous diseases and sex. Thus 3,034 citizens using ivermectin were matched and compared with 3,034 non-users.

The hospitalization rate among users of the preventive medicine was 1.6%. Among non-users, it was 3.3%. Therefore, ivermectin reduced the need for hospitalizations by 56%.

A 68% reduction in mortality among ivermectin users

Among the 3,034 with COVID not users of preventive ivermectin, 79 people (2.6%), died. Among the 3,034 in the comparison group, ivermectin users, 25 people (0.8%) died. So there was a 68% reduction in mortality.

“There was no early treatment established by the municipality, so there was no interference in the study regarding hospitalization and death. It’s just the effect of prophylaxis. With treatment after infection, the numbers tend to improve,” says Dr Flavio Cadegiani.

“The statistical technique used, the PSM, allows us to affirm that the study has the power close to a randomized clinical trial,” he added.

How peer review happened

Peer review, when other scientists review and attest to the scientific quality of articles, is an essential scientific process. In the case of this study, three independent groups had access to all the data and the manuscript. Subsequently, they contacted the authors anonymously via the Cureus journal communication system. Each group of reviewers was classified with a letter of the Greek alphabet: Alpha, Beta, and Gamma.

“In addition to peer review, the study goes through three editorial stages. And all three need to accept the work. In our case, due to the relevance of the study, we didn’t even have the opportunity to appoint reviewers. All were completely independent”, says Dr. Flavio Cadegiani.

Transparent and available data for the scientific community

Aerial photo of Itajaí. Photo by Eduardo Marquetti, under Creative Commons license, published in Wikipedia.

“Health status was assessed and data were entered prospectively throughout the period of the program, in a fully digitized system provided by the National Health System (SUS),” the scientists stated in the study.

“Since the system existed prior to the pandemic, a significant number of the population were already registered with their health information, including past and current diseases, use of medications, and other characteristics.,” they added.

Soon, in about two weeks, with the objective of total transparency with the national and international community, the raw data extracted from the SUS system of Itajaí, containing all the characteristics of the residents, preserving their identities, will be made available. The data will be publicly available on a platform. The electronic address will be announced on the blog of the journal Cureus.

“Unlike studies with vaccines and patent medicines, this is a unique opportunity in the pandemic where scientists from around the world will be able to analyze the data. To our knowledge this is unprecedented for a study of this level and importance in Covid-19,” said Cadegiani.

This was a decision of the team that produced the study. It comes at the same time as an editorial in the BMJ (British Medical Journal), one of the world’s most respected medical journals, published yesterday, calling for all raw data on vaccines and new treatments for COVID to be made public.

Official data from the epidemiological bulletin confirm the drop in mortality throughout Itajaí

Of the more than 220 thousand inhabitants of Itajaí, only a little more than 114 thousand volunteered to use ivermectin every two weeks. Even so, the impact on the entire city was quite significant, compared to the other cities in the state.

One of the study’s results tables shows a dramatic drop in mortality before and during the study, even with much of it not using the drug. Deaths dropped from 3.5% of those infected to 1.4%.

“The most basic confirmation that there can be of this whole result is to do an analysis on all the epidemiological bulletins of the state of Santa Catarina. The difference between hospitalizations and mortality, before and during the ivermectin program, was striking. Anyone can check this at any time with official numbers,” says Cadegiani.

Doses used

ivermectin was offered in biweekly doses of 0.2mg per kg per day for two days. In other words, a person weighing between 60 and 90 kg was given 3 ivermectin tablets a day every two weeks for two consecutive days. If the weight was greater than 90 kg, 4 tablets a day for two consecutive days were offered. 

“I believe the results could be even better if the use was weekly, in the same amount, while maintaining the same unquestionable level of safety,” Cadegiani explained.

Other possible uses of ivermectin

In addition to having identified no relevant side effects from the use of ivermectin citywide, the scientists wrote about promising data found: “Prophylactic use of ivermectin can be particularly impactful in older subjects. In addition, ivermectin seemed to reduce the exceeding risk of hypertension, T2D, and other diseases.,” they wrote in the study.

Dr Flavio Cadegiani, one of the authors, is excited about the possibility of other uses of the drug besides COVID-19. “Preliminary data surprised us. It helped for liver, kidney and inflammatory issues. In other words, ivermectin may help reduce fat in the liver, kidney problems, prevent inflammatory disease, and other potential metabolic benefits. It may work to control cholesterol and diabetes,” he says. “It would be a crime not to study it for those diseases,” he exclaimed.

Press attacked the action, but there was good reception among the citizens

The prophylactic action of ivermectin against COVID was proposed by Dr Volnei Morastoni, a medical doctor and mayor of the city of Itajaí. Soon after, he came under attack.

Among the various aggressions at the time, Dr Volnei was called a “witch doctor” by a local newspaper, the NCS total.  In the newspaper O Estado de S. Paulo, one of the most important in the country, biologist Natália Pasternak wrote an article with the following title: “Analysis: the case of Itajaí shows how the fight against the pandemic is marked by science denialism”. 

“The mayor of Itajaí seems to build public health policies based on social network fads and conspiracy theories,” she stated in the article. In her twitter, she classified the action concluded now as effective as “Itajaí madness.”

However, even at that time, the population was already suspicious of the excessive aggressiveness of the press. The positive result was felt by the population during the action, and they gave their answer in the ballot box. In October 2020, Marastoni was re-elected mayor of the city for another four-year term.

So far, four days after the international review confirming that lives were saved, there has been no apology to the mayor for the offenses. “The denialism came exactly at the person who colored himself as a defender of science. This is a great example of the catastrophe that occurs when science and political passions mix,” says Cadegiani.

“How many lives would be here today if it weren’t for the attacks devoid of logic and valid arguments?” he questions. “Vanity will never allow people to turn back. It would be to confess that they killed in the name of a false science.”

“It is important to make it clear that I did not believe in the effectiveness of ivermectin as a preventative. That doesn’t mean to say that I was against using it, because, after all, any scientist with the least humanity, knowing that there were no theurapeutic alternatives and the drug is safer than any medicine we use for headache, I would never smear or contraindicate it in a pandemic of intubated people,” Cadegiani said. “I was wrong in my bet of ineffectiveness and I assume it. That’s science.”

Journalists and science communicators got everything wrong, even the speculation that ivermectin would relax other measures

At the time, journalists and science communicators bet that the use of the drug would lead to the loosening of other measures to contain the pandemic. “The narrative that using preventive and early treatment therapies will have people relax their caution of remaining socially and physically distanced to allow more COVID-19-related infections is not supported here,” the scientists concluded in the study.

“These study data demonstrate that the use of preventive ivermectin significantly lowers the infection rate and that benefits outweigh the speculated increased risk of changes in social behaviors. Hence, we can speculate that the prophylactic use of ivermectin could play an important role in the reduction of the pandemic burden.,” they added.

Other studies on the same data from Itajaí will be coming out soon

This study aimed to evaluate the impact of the whole preventive program in the city during five months. However, many residents who started with ivermectin, discontinued after some time of use and did not complete the five months.

Now, in a phase two analysis of the data collected by the SUS, efficacy calculations are being done only on those residents who kept using the drug for the full five months. “At first, looking at the data, those who used more than 75% of the doses had zero deaths. That’s surprising. Too bad it was a minority. We are calculating the data to hand over to reviewers,” Cadegiani said.

“In the third month, of the more than 100,000 who volunteered to take ivermectin, only a little more than 8,000 continued, and even then we had this 68% reduction in deaths. Even the most optimistic were shocked.”

Daughter of a fish, a little fish is (a Brazilian saying, when sons follow their fathers)

Dr Lucy Kerr, during the World Council for Health

The father of Lucy Kerr, the main scientist of the Itajaí study, was Warwick Stevam Kerr, a Brazilian scientist who died in 2018, at age 96, in the city of Ribeirão Preto, where he developed most of his brilliant career.

Warnick, with a worldwide career, besides several Brazilian universities, lectured in North American universities (Louisiana, California, Wisconsin and Columbia University in New York.). In Brazil he held important positions, such as Scientific Director of FAPESP.  He was also president of the prestigious Brazilian Society for the Advancement of Science.

With relevant scientific productions, he was a member of the “National Academy of Sciences”, in the USA, besides being admitted by President Itamar Franco in the National Order of Scientific Merit in the “Grã-Cruz” class in 1994.

Lucy confesses to be inspired by her father: “I used to accompany him whenever I could. He didn’t bother to help”, she says.

There are 15 other studies on ivermectin prophylaxis. All are unanimously positive.

The Itajaí study is the largest in the world with ivermectin. Besides it, there are 15 other studies on prophylaxis, all finding positive effects of the drug against COVID-19. However, because it was with a large number of patients and uses the statistical technique PSM – Propensity Score Matching, due to the data having great precision, there is a greater weight in this study as scientific evidence. That is, Itajai only confirmed other studies.

Check out the complete list here.

Final note: Nostradamus against anxious fact-checkers

Hello, fact-checker. You are now going after some expert to refute the study, right? I know. Your goal is to say that the study proves nothing. There is one thing left for your expert to say: that the study is not randomized and double blind. He is in the mood to shout: “observational studies do not prove effectiveness”.

If he says that, throw in his lap the Anglemeyer study, published in Cochrane in 2014, and watch him have a sudden malady. This study says that there are no significant differences between observational studies with “gold standard” RCT study, especially when the difference is greater than 8% efficacy, as is the case. In other words. It says that observational studies do prove efficacy. 

Was that not enough?  Show Kjell Benson’s study, published in 2000 in the New England Journal of Medicine, where the author reached the same conclusions. He will run out of answers. He will have a stroke.

Don’t even make up an answer, think that you are refuting the study with two or three sentences, without mentioning Anglemeyer and Benson. Are we agreed?