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Was a False Hydroxychloroquine Narrative Created to Destroy the Competition for Gilead’s Remdesivir?

by Vera SharavAlliance for Human Research Protection

Below, Dr. Meryl Nass reviews long a list of corrupt practices. The practices undermine the integrity of medical practice during the current  medical crisis; a crisis significantly made worse  by stakeholders who are focused on projected future profits from not-yet-developed “countermeasures” against  COVID-19.

The stakeholders include public health officials, global public health institutions,  government advisory committees, clinical trialists who design trials to provide commercially beneficial results, and editors of prestigious high impact, medical journals.

These collaborators engaged in an orchestrated effort to prevent physicians from utilizing an existing, off-patent, cheap and affordable drug, that thousands of clinicians attest to its therapeutic benefit.

  • The problem with Hydroxychloroquine is that there is no profit to be made from this off-patent drug!

It is remarkable that a series of events taking place over the past 3 months produced a unified message about hydroxychloroquine, and produced similar policies about the drug in the US, Canada, Australia, NZ and western Europe.  The message is that generic, inexpensive hydroxychloroquine is dangerous and should not be used to treat a potentially fatal disease, Covid-19, for which there are no (other) reliable treatments.

Were these acts carefully orchestrated?  You decide.

Might these events have been planned to keep the pandemic going?  To sell expensive drugs and vaccines to a captive population?   Could these acts result in prolonged economic and social hardship, eventually transferring wealth from the middle class to the very rich?  Are these events evidence of a conspiracy?

Here is a list of what happened, in no special order. Please help add to this list if you know of additional acts I should include.  This will be a living document.  I have penned this as if it is the “to do” list of items to be carried out by those who pull the strings.  The items on the list have already been carried out.  One wonders what else might be on their list, yet to be carried out, for this pandemic.

1.  You stop doctors from using the drug in ways it is most likely to be effective (in outpatients at onset of illness).  You prohibit use outside of situations you can control.

Situations that were controlled to show no benefit included 3 large, randomized, multi-center clinical trials (RecoverySolidarity and REMAP-Covid), which are generally believed to yield the most reliable evidence. However, each of them used excessive doses that were known to be toxic; see my previous articles here and here.

2.  You prevent or limit use in outpatients by controlling the supply of the drug, using different methods in different countries and states.  In NY state, by order of the governor, hydroxychloroquine could only be prescribed for hospitalized patients.  France has issued a series of different regulations to limit prescribers from using it.  France also changed the drugs’ status from over-the-counter to a drug requiring a prescription.

3.  You play up the danger of the drug, emphasizing side effects that are very rare when the drug is used correctly. You make sure everyone has heard about the man who died after consuming hydroxychloroquine in the form of fish tank cleaner.

4.  You limit clinical trials to hospitalized patients, instead of testing the drug in outpatients, early in the illness, when it is predicted to be most effective.

5.  You design clinical trials to give much too high a dose, ensuring the drug will cause harm in some subjects, sufficient to mask any possible beneficial effect.  You make sure that dozens of trials in dozens of countries around the world use these dangerous doses.

6.  You design clinical trials to collect almost no safety data, so any cause of death due to drug toxicity will be attributed to the disease instead of the drug.

7.  You issue rules for use of the drug based on the results of the unethical, overdosing Recovery study.

8.  You publish, in the world’s most-read medical journal, the Lancet, an observational study from a huge worldwide database that says use of chloroquine drugs caused significantly increased mortality.  You make sure that all major media report on this result. Then 3 European countries announce they will not allow doctors to prescribe the drug. And Sanofi announces it will no longer supply the drug for use with Covid, and will halt its own clinical trials, based on a fabricated study.

9.  Even after hundreds of people renounce this observational study due to easily identified fabrications–which, as James Todaro, MD, wrote was a “study out of thin air“–the Lancet held firm for two weeks, serving to muddy the waters about the trial, until finally 3 of its 4 coauthors (but not the journal) retracted the study. You make sure few media report that the data were fabricatedand the “study” a fraud.  You let people believe the original story: that hydroxychloroquine routinely kills.

10.  You ensure federal agencies like FDA and CDC hew to your desired policies.  For example, FDA advised use only in hospitalized patients (too late) or in clinical trials (which are limited, are difficult to enroll in, or use excessive doses).  As of mid June, FDA now advises patients and doctors to only use the drug in a clinical trial! Another example:  you have FDA make unsubstantiated and false claims, such as:  “Hospitalized patients were likely to have greater prospect of benefit (compared to ambulatory patients with mild illness)” and claim the chloroquine drugs have a slow onset of action. If that were really true, they would not be used for acute attacks of malaria or in critically ill patients with Covid. (Disclosure:  I once dosed myself with chloroquine for an acute attack of P. vivax malaria, and it worked very fast.). Providing no other treatment advice, CDC refers clinicians to the NIH guidelines, discussed below.

11.  You make sure to avoid funding/encouraging clinical trials that test drug combinations like hydroxychloroquine with zinc, with azithromycin, or with both, although there is ample clinical evidence that such combinations provide a cumulative benefit to patients.

12.  You have federal and UN agencies make false, illogical claims based on models rather than human data.  For example, you have the FDA state on June 15 that the dose required to treat Covid is so high it is toxic, after the Recovery and Solidarity trials have been exposed for toxic dosing.  This scientific double-speak gives some legal cover to the clinical trials that overdosed their patients.

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BobValdez
BobValdez
July 1, 2020

Was a False Hydroxychloroquine Narrative Created to Destroy the Competition for Gilead’s Remdesivir?
Yes.

The North remembers the feat of Soviet soldiers and sets an example for the whole Europe

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