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Don’t Be A Lab Rat




The European database of suspected drug reaction reports is EudraVigilance, which also tracks reports of injuries and deaths following the experimental COVID-19 “vaccines.”

Author: sheikyermami

A subscriber from Europe recently emailed us and reminded us that this database maintained at EudraVigilance is only for countries in Europe who are part of the European Union (EU), which comprises 27 countries.

The Drug Whose Name Must Not Be Uttered

Heart inflammation after COVID-19 shots higher than expected in study of U.S. military

Craig Kelly has been saying this for months, but I thought it was worth a simple summary of the current situation with regard to the use of Ivermectin to prevent/treat the Wuhan Flu. The Australian Department of Health website advises: There is currently insufficient evidence to support the safe and effective use of ivermectin, doxycycline and zinc (either separately, or in combination) for the prevention or treatment of COVID-19. More robust, well-designed clinical trials are needed before they could be considered an appropriate treatment option.
The National COVID-19 Clinical Evidence Taskforce, consisting of a large group of clinical experts, is continuously updating treatment recommendations based on the best available evidence. They have not made any recommendations for the use of ivermectin, doxycycline or zinc outside of properly conducted clinical trials with appropriate ethical approval.
Furthermore, there is insufficient data to recommend neither for nor against the use of zinc for the prevention or treatment of COVID-19.
That entry is dated 1 June 2021.
The US FDA says (my emphasis):
COVID-19. We’ve been living with it for what sometimes seems like forever. Given the number of deaths that have occurred from the disease, it’s perhaps not surprising that some consumers are looking at unconventional treatments, not approved or authorized by the Food and Drug Administration (FDA).
Though this is understandable, please beware. The FDA’s job is to carefully evaluate the scientific data on a drug to be sure that it is both safe and effective for a particular use, and then to decide whether or not to approve it. Using any treatment for COVID-19 that’s not approved or authorized by the FDA, unless part of a clinical trial, can cause serious harm.
There seems to be a growing interest in a drug called ivermectin to treat humans with COVID-19. Ivermectin is often used in the U.S. to treat or prevent parasites in animals. The FDA has received multiple reports of patients who have required medical support and been hospitalized after self-medicating with ivermectin intended for horses.
Here’s What You Need to Know about Ivermectin
FDA has not approved ivermectin for use in treating or preventing COVID-19 in humans. Ivermectin tablets are approved at very specific doses for some parasitic worms, and there are topical (on the skin) formulations for head lice and skin conditions like rosacea. Ivermectin is not an anti-viral (a drug for treating viruses).
Taking large doses of this drug is dangerous and can cause serious harm.
If you have a prescription for ivermectin for an FDA-approved use, get it from a legitimate source and take it exactly as prescribed.
Never use medications intended for animals on yourself. Ivermectin preparations for animals are very different from those approved for humans.
What is Ivermectin and How is it Used?
Ivermectin tablets are approved by the FDA to treat people with intestinal strongyloidiasis and onchocerciasis, two conditions caused by parasitic worms. In addition, some topical (on the skin) forms of ivermectin are approved to treat external parasites like head lice and for skin conditions such as rosacea.
Some forms of ivermectin are used in animals to prevent heartworm disease and certain internal and external parasites. It’s important to note that these products are different from the ones for people, and safe when used as prescribed for animals, only.
When Can Taking Ivermectin Be Unsafe?
The FDA has not reviewed data to support use of ivermectin in COVID-19 patients to treat or to prevent COVID-19; however, some initial research is underway. Taking a drug for an unapproved use can be very dangerous. This is true of ivermectin, too.
There’s a lot of misinformation around, and you may have heard that it’s okay to take large doses of ivermectin. That is wrong.
Even the levels of ivermectin for approved uses can interact with other medications, like blood-thinners. You can also overdose on ivermectin, which can cause nausea, vomiting, diarrhea, hypotension (low blood pressure), allergic reactions (itching and hives), dizziness, ataxia (problems with balance), seizures, coma and even death.
Ivermectin Products for Animals Are Different from Ivermectin Products for People
For one thing, animal drugs are often highly concentrated because they are used for large animals like horses and cows, which can weigh a lot more than we do—a ton or more. Such high doses can be highly toxic in humans.
Moreover, FDA reviews drugs not just for safety and effectiveness of the active ingredients, but also for the inactive ingredients. Many inactive ingredients found in animal products aren’t evaluated for use in people. Or they are included in much greater quantity than those used in people. In some cases, we don’t know how those inactive ingredients will affect how ivermectin is absorbed in the human body.
Meanwhile, effective ways to limit the spread of COVID-19 continue to be to wear your mask, stay at least 6 feet from others who don’t live with you, wash hands frequently, and avoid crowds.
The above, largely strawman, diatribe is dated May 3, 2021. Doctors advocating the use of Ivermectin, and those conducting clinical trials (none of which are detailed in either government website), are not suggesting that people should self-medicate, that they should binge on the stuff or that they should take versions designed for horses.
I don’t know how many clinical trials are currently underway (Craig Kelly says many) but the US National Institutes of Health National Library of Medicine has an article detailing the results of a number of successful trials. The summary of that article is:
To date, the efficacy of ivermectin in COVID-19 has been supported by the following:
Since 2012, multiple in vitro studies have demonstrated that Ivermectin inhibits the replication of many viruses, including influenza, Zika, Dengue, and others.
Ivermectin inhibits SARS-CoV-2 replication and binding to host tissue through several observed and proposed mechanisms.
Ivermectin has potent anti-inflammatory properties with in vitro data demonstrating profound inhibition of both cytokine production and transcription of nuclear factor-κB (NF-κB), the most potent mediator of inflammation.
Ivermectin significantly diminishes viral load and protects against organ damage in multiple animal models when infected with SARS-CoV-2 or similar coronaviruses.
Ivermectin prevents transmission and development of COVID-19 disease in those exposed to infected patients.
Ivermectin hastens recovery and prevents deterioration in patients with mild to moderate disease treated early after symptoms.
Ivermectin hastens recovery and avoidance of ICU admission and death in hospitalized patients.
Ivermectin reduces mortality in critically ill patients with COVID-19.
Ivermectin leads to temporally associated reductions in case fatality rates in regions after ivermectin distribution campaigns.
The safety, availability, and cost of ivermectin are nearly unparalleled given its low incidence of important drug interactions along with only mild and rare side effects observed in almost 40 years of use and billions of doses administered.
The World Health Organization has long included ivermectin on its “List of Essential Medicines.”
A summary of the statistically significant results from the above controlled trials are as follows:
Controlled trials in the prophylaxis of COVID-19 (8 studies)
All 8 available controlled trial results show statistically significant reductions in transmission.
Three RCTs with large statistically significant reductions in transmission rates, N = 774 patients.
Five OCTs with large statistically significant reductions in transmission rates, N = 2052 patients.
Controlled trials in the treatment of COVID-19 (19 studies):
♦Five RCTs with statistically significant impacts in time to recovery or hospital length of stay.
♦One RCT with a near statistically significant decrease in time to recovery, P = 0.07, N = 130.
♦One RCT with a large, statistically significant reduction in the rate of deterioration or hospitalization, N = 363.
♦Two RCTs with a statistically significant decrease in viral load, days of anosmia, and cough, N = 85.
♦Three RCTs with large, statistically significant reductions in mortality (N = 695).
♦One RCT with a near statistically significant reduction in mortality, P = 0.052 (N = 140).
♦Three OCTs with large, statistically significant reductions in mortality (N = 1688).
In addition to the trials, there are reports of actual widespread clinical usage in India and other parts of the world.
So why do the US and Australian governments continue to ignore what should be very welcome news? Let me quote Dr Jay Bhattacharya, a Stanford trained economist and physician:
The NIH exists to solve market failure’, however, the agency ‘has made comparatively little effort to catalyze randomized evaluations of off-patent drugs from Covid 19 therapeutics’, but ‘has devoted considerable resources to aid the Covid-19 vaccination randomized trial studies.
Argentinian doctor Hector Carvallo, the lead researcher in one preventive study – a study that resulted in all 788 people who received Ivermectin remaining uninfected, as opposed to 50 per cent of the control group who did – believes that ‘by now half of Argentina is using Ivermectin’. He says that his team faced pressure from ‘many doctors who worked for the pharmaceutical industry, because this was a very, very cheap treatment’.
That is one reason but, here in Australia, I believe there is another.
We are told that the vaccines will not prevent you from catching or spreading the disease but that they will prevent you from getting seriously ill. That’s good enough for me but not everyone is convinced. Government is desperate to get everyone vaccinated, despite the sluggish roll-out and the contrary and conflicting edicts and opinions from chief medical officers. And this has been exacerbated by “vaccination resistance” engendered by the news of blood clots and mixed messaging from the government. This leaves the government with the choice of forcing people to have a vaccine many don’t want, thus infringing on some very basic human rights, or allowing them to take a chance and refuse the vaccine and be it on their own head. In the latter case it would be a totalitarian state that denied those people an effective treatment. The knowledge that an effective treatment was available, would certainly inhibit the purported aim of getting 80 per cent of people vaccinated. To avoid this complication, I suspect the authorities are professional incurious about Ivermectin, which they are content to leave on the back burner.
Back in April 2020, researchers from Monash University’s Biomedicine Discovery Institute (BDI) with the Peter Doherty Institute of Infection and Immunity at Royal Melbourne Hospital recently published the results of a study revealing that Ivermectin, an approved anti-parasitic drug available worldwide, may actually treat against SARS-CoV-2 when applied to an infected cell culture. They also suggested Ivermectin be seriously investigated for possible use in humans.
The announcement that this research would be undertaken in Australia was covered on the Bolt Report. My impression then was that the research would involve clinical trials on humans, but I may be misremembering. As far as I’m aware, despite the recommendation from this trial, nothing further has been done in this country in over 12 months. And one wonders why the research team confined themselves to in vitro research in the first place, which, according to the NIH report above had shown promising results as early as 2012. Much must already have been known at this level. This is particularly odd, since the impetus for the trial initially came from representations by Dr Tomas Barody, who had already demonstrated the effectiveness of Ivermectin on human patients. I smell a large, laboratory rat.
And one final thought. Now that we have a number of vaccines, principally thanks to President Trump and his Operation Warp Speed, it is much easier for governments to sideline the Ivermectin treatment. But, given that development of a vaccine for a coronavirus was highly problematical – never having been done before nor in such haste – why was an effective treatment not fast-tracked as well? In April 2020, we had no guarantee a vaccine would be available by the end of the year and all the pundits were saying it would take at least 18 months.
Furthermore, according to Rebecca Weisser speaking to Alan Jones on Wednesday night, the incidence of adverse reactions to these vaccines – including fatalities – is considerably higher than we have been led to believe. This, we can safely assume, is because their development was fast-tracked and interim approval for emergency use was given in advance of full clinical trials. All of which suggests they should only be given to the most-at-risk group. Which, in turn, adds even more weight to the case for an effective prophylaxis and/or treatment viz ivermectin or hydroxychloroquine.
And now the big question: How many people died (or will die) that need not have, due to this politicised, mercenary and cavalier approach to public health? And who will pay?
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  1. I love the comment about Ivermectin, “More robust, well-designed clinical trials are needed before they could be considered an appropriate treatment option.”

    If only the same criteria where applied to the experimental mRNA immune programming treatment.



  2. My sister and her husband were feeling poorly after their second shot at being lab rats, she told me that if you have an adverse reaction its good!!!!! What could I possibly say? Fcuk you are so stupid? it was all I could think of but maybe not?



  3. Australia’s 4 phase plan.
    Seems to run parallel with the UK where follow up shots are talked about.

    The government will also look to implement the vaccine booster program at that time, or to be preparing it, depending on the time frame of hitting the vaccination threshold.

    That is quietly not mentioned in other news reports.
    New Zealand will not be far behind in following the UK’s and Australian plans.

    Minister Chris Hipkins told 1 NEWS New Zealand “has its own strategy” to reconnect with the world in the wake of the pandemic.

    Plan? plan? what is that? … umm umm
    Strategy? the one for complete control of the people.
    Punching above our weight in the world, following the sheeple.



  4. Talking on the Australian lock down, and then about the Australian vaccine roll out.

    Dr Peter McCullough Says We Must Shut Down the Vaccine Rollout Now.
    17 mins 56 secs : June 30, 2021 : ASIA PACIFIC TODAY with Mike Ryan.

    …… State Government leaders and their public health bureaucrats are again whipping up hysteria on Covid-19, this time based on mutation of the virus.

    They’re acting in concert in pursuit of narrow political ends, and to coerce and extend their control.

    How long can this punitive, unjust and dangerous behaviour go on?

    How long can community leaders and ethical members of the medical community remain silent, while these lies are peddled in the name of science? …..
    – – – – – – – – – – – – – – – – – – – – – –
    It is good as it touched on & dove tails in with where I threaded 2 comments on Dr. Richard Fleming and his 4 hour 30 mins lecture, where he also used FDA & Vaers figures showing how they came to those figures.
    Worth watching it, maybe in something like 20 minute parts?
    I like his attitude, Doctors should be allowed to be Doctors in the care & treatment of their patients with out the dictates of bureaucratic Doctors [like WHO Fauci etc.]!



    • Dr Peter McCullough in that video, does say, if you are going to get Covid, the delta one is the one to get, as hospitalizations are much lower, and the death rate is very low, as he mentions that about India, and the UK.
      – – – – – – – – – – – – – – – – – – –

      The next round coming now is Epsilon scariant, original from California.

      The data indicate that, with its three mutations, the Epsilon variant is resistant to both antibodies generated by messenger RNA vaccines and those generated by SarsCoV2 virus infection.


      So this would be behind the the “booster” vaccines that are being considered at the end of this year.

      What about the young people, who if had Covid, not to worry about the antigens, so much, but the built up T cells having gained the memory, would give the longer term protection.



  5. Former Victorian Police Commissioner Says There Was No Justification For Last Lockdown In Victoria
    15 mins 11 secs : Published July 1, 2021 : ASIA PACIFIC TODAY with Mike Ryan

    …. we are being thrown carrots and the very big stick of vaccination. Worse still, our public health officials are not following the science but enforcing, baseless and cruel rules. They are failing in their roles. Citizens have no idea about the true risk of experimental vaccines and extreme ignorance prevails amongst the very people charged with governing us.

    Former Victorian Police Commissioner Kel Glare AO, APM believes there was no justification for the last lockdown in Victoria. …..

    The former Police Commissioner shows how these bureaucrat powers grew.
    Talks reasonable commonsense, and does not pull his punches.
    Pity he could not do a stint as Commissioner here in New Zealand.
    His comments can be applied in New Zealand.
    Where in New Zealand can our people come out and speak commonsense, to be debated, discussed?



  6. This link has an article and there is below a rough transcript of the whole video, if you feel that it is quicker to peruse. 🙂

    MIT Scientist: Covid Vaccines May Cause Diseases in ’10 to 15 years’ (Exclusive Video)
    The video is 38 mins 14 secs. : July 2, 2021 : RAIR Foundation

    ….. Dr. Seneff serves as Senior research scientist at MIT’s Computer Science and Artificial Intelligence Laboratory…..
    ….. The MIT scientist wrote a research paper with Dr. Greg Nigh titled:
    “Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19”
    for the International Journal of Vaccine Theory, Practice, and Research. ……

    ….. Some of the major points of the RAIR exclusive interview:

    ( Dr. Seneff “anticipates that there will be long-term damage that won’t instantly be linked to the vaccine. Developments, such as an increase in auto-immune and neurodegenerative diseases, which may take 10 to 15 years before manifesting themselves.” “We are in for a big surprise down the road,” she predicts.

    ( Dr. Seneff believes the vaccine would exacerbate symptoms of those with Parkinson’s.

    ( Those who claimed that mRNA would not impact DNA are “wrong.”

    ( Spike protein “really has become the most toxic part of the virus” and exists when Covid is gone.

    ( “Among the possibilities she foresees is an increase in Creutzfeldt-Jacob disease (CJD), a prion disease (or protein misfolding disease) comparable to mad cow disease.”

    ( “There is an epidemic of Alzheimer disease, which people are getting at an increasingly younger age. The recklessly and haphazardly implementation of the vaccine roll-out will contribute to this trend.”……

    I am amazed at the people calling it safe, when it has not even been the time of gestation of a baby, and then takes time to see how the kid develops.
    Let alone the possible effects just on a human body.



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