Pengwin » 27 Aug 2021, 5:40 am » wrote: ↑
Explain to us why a pill a used (mostly) to treat worms in animals would be the solution a new deadly virus?
BTW, the FDA does not approve your wonder-drug for Covid-19 making it - experiment (and not even approved on an emergency basis unlike the vaccines)...
Idiot!!! Look who funds the FDA...Look who funds the WHO. The old adage "follow the money" is very relevant to this issue.
Don’t mention Ivermectin; it’ll upset the vaccine rollout
12th May 2021 by
Editor
By Andrew Bannister*
What if there was a cheap drug, so old its patent had expired, so safe that it’s on the WHO’s lists of Essential and Children’s Medicines, and used in mass drug administration rollouts? What if it can be taken at home with the first signs COVID symptoms, given to those in close contact, and significantly reduce COVID disease progression and cases, and far fewer few people would need hospitalisation?
The international vaccine rollout under Emergency Use Authorisation (EUA) would legally have to be halted. For an EUA to be legal, “there must be no adequate, approved and available alternative to the candidate product for diagnosing, preventing or treating the disease or condition.” The vaccines would only become legal once they passed level 4 trials and that certainly won’t happen in 2021.
This would present a major headache for the big public health agencies led by the WHO.
The vaccine rollout, outside of trials, would become illegal. The vaccine manufactures, having spent hundreds of million dollars developing and testing vaccines during a pandemic, would not see the $100bn they were expecting in 2021. In a pandemic, and for the next one, we need
big pharma to react quickly, and the best way to that, is to reward them financially. Allowing any existing drug, at this time, well into stage 3 trials, to challenge the legality of the EUA of vaccines, is not going to happen easily. On the 31st of March 2021, the WHO recommended against
the use of Ivermectin for COVID treatment, citing safety and lack of large RCT proof.
The question of why the WHO would do this is difficult to answer, only if you ignore the importance of the legality of the EUA, and the time tested advice, of following the money. The WHO, a once noble organisation funded by the worlds countries, now receives less than 20% of its budget from member states. The
Bill and Melinda Gates Foundation is the second biggest sponsor after the USA.
The GAVI Alliance, a private/public organisation promoting vaccines, was founded by Gates, and now pushing for vaccine passports, are the 4th biggest sponsor to WHO.
Tedros Adhanom Ghebreyesus, the WHO Director-General, served on the GAVI board for several years. The WHO, in 2021 changed the definition of “
herd immunity”, to occurring only when the global population has been vaccinated.
The WHO has either made serious mistakes in their analysis or deliberately undermined Ivermectin and other early treatment drugs, in favour of vaccinating the world. Obviously this is a huge windfall for vaccine manufacturers, with
Pfizer set to receive over a trillion rand from vaccines over the next five years according to Morgan Stanley.
In January this year, the several months long, Ivermectin research, meta-analysis of Randomised Control Trials (RCT), commissioned by WHO was released. The paper showed that
Ivermectin reduces death by 74% and is 85% effective as prophylaxis. The trial leader,
Dr Andrew Hill, was on Zoom meetings saying that governments should secure their source before demand outstrips supply and that it would be immoral, not to roll it out. The same month, two other independent, unsponsored meta-analysis confirmed a similar range of effectiveness at various stages of the disease. While effective at all stages of the disease, Ivermectin is most effective as a prophylaxis and about 80% in early treatment, depending on dose used.
The WHO currently have no advice or recommendation’s for early treatment apart from recommending against self-medication. If you don’t heal in the first week, when symptoms are generally mild, by the time you have to go to the hospital with breathing problems, your chances of dying have increased significantly. The use of Ivermectin and other repurposed drugs, could prevent that. As its safer than paracetamol, it should be available over the counter. As is happening in Mexico City and some states in India, anyone testing positive or feeling sick should take it, and give it to those they are in close contact with. It may be possible, if you want to attend a large social event or travel in a plane, that you take a pill, four hours before, and you will have significant protection for a few days. Lockdowns could end.
Ivermectin has been used in humans for 35 years and over 4 billion doses have been administered.
Merck, the original patent holder, donated 3.7 billion doses to developing countries. 2015 the two individuals who developed Ivermectin were awarded a Nobel Prize for medicine. While known primarily as an anti-parasitic, Ivermectin has powerful anti-viral and anti-inflammatory properties. Its safety is documented at doses twenty times the normal. Only 19 deaths are known and side-affects are generally mild and short. As a comparison, approximately 450 US citizens die from paracetamol every year.
In January this year, the several months long, Ivermectin research, meta-analysis of Randomised Control Trials (RCT), commissioned by WHO was released. The paper showed that
Ivermectin reduces death by 74% and is 85% effective as prophylaxis. The trial leader,
Dr Andrew Hill, was on Zoom meetings saying that governments should secure their source before demand outstrips supply and that it would be immoral, not to roll it out. The same month, two other independent, unsponsored meta-analysis confirmed a similar range of effectiveness at various stages of the disease. While effective at all stages of the disease, Ivermectin is most effective as a prophylaxis and about 80% in early treatment, depending on dose used.
Ultimately what this means, is that if Ivermectin and other repurposed drugs (like the promising anti-depressant Fluvoxamine), work for early treatment, you won’t have to use a vaccine, that’s still in trial, with unknown long-term safety or ability to treat future variants, and for which, the manufactures accept no liability.
In case you get sick, keep Ivermectin close by for early, household treatment, and you will prevent viral replication early and almost certainly, avoid hospital. You would have also built an immune response that will provide natural protection against future infections. Its wide-spread use, should dampen waves of disease, while vaccines can use this time to prove themselves, with long term safety and efficiency.
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