Back in 1987 Dr. Anthony Fauci was responsible for the deaths of thousands of AIDS sufferers, just as he is responsible for the
deaths of hundreds of thousands of Americans infected with COVID-19 [as of 3-22-21 well over half a million dead],
through the same unreasonable demand for a randomized blinded controlled trial (
which would be tantamount to mass murder of elderly COVID participants in the control or placebo group), of another cheap, generic, already well known and widely established and administered medication - Bactrim (which like hydroxychloroquine, is also on the World Health Organization's List of Essential Medicines).
As AIDS sufferers died from a treatable bacterial pneumonia, Fauci set his eye toward approval of AZT, which cost the user $10,000 per year (in 1987 dollars! It was the highest cost drug in the world at the time).
https://www.npr.org/sections/health-shots/2019/05/30/727731380/old-fight-new-front-aids-activists-want-lower-drug-prices-nowAny surprise then that Fauci's NIH gave the FDA the nod to give emergency use authorization to Gilead Sciences' experimental patented drug Remdesivir, that costs
$3,200 per course of treatment (double that for 10-day course),
that NIH and WHO studies both determined did not result in a statistically significant reduction in mortality, while it also has dangerous side effects that can permanently damage the liver, kidneys and heart?
https://www.covid-19forum.org/index.php?board=8.0But Fauci could only give Remdesivir emergency use authorization, after removing EUA from hydroxychloroquine, even though HCQ
has been shown to be 99-100% effective - even among elderly and high-risk individuals - in fighting COVID-19 in the
early outpatient setting, the HCQ portion of which
costs about $3.60 per course of treatment, that has a 65-year track record of being one of the safest drugs on earth.
https://www.covid-19forum.org/index.php?topic=276.0Crimes against humanity? Wrongful death? Negligent homicide? Mass murder?
Following transcript begins at the 12:53 mark in the video below:Levin: "What do you make of this?"
Highly esteemed and heavily published
Yale School of Public Health professor of epidemology Dr. Harvey Risch:
"So
the FDA is a very strange organization that
has a history of not making science based, rational based decisions about its approvals. It,
this, was started most noticably in 1987 when people with AIDS in New York City were dying of what is called pneomocystis pneumonia - PCP - and the clinical experience that had been amassed of a large number of cases who were prevented from dying by use of the antibiotic Bactrim. This is, even then was a generic medication and cheap and activists obtained a meeting with Dr. Fauci and 15 of his selected scientists at FDA at NIH and asked Dr. Fauci just to make guidelines to physicians that they consider using Bactrim to treat preventively AIDS people so that they wouldn't die of this pnemonia.
Dr. Fauci refused he said "I want randomized blinded controlled trial evidence that's my gold standard, that or nothing." The activists left.
The NIH did not fund any randomized trials. They raised money themselves from their own AIDS patients to collect the data to do a randomized trial. It took them two years. They came back to Dr. Fauci.
During those two years the FDA approved AZT as a treatment for AIDS. AZT works, but not completely, it needs other medications as well and
during the two years that it took them to get this data to come back to Dr. Fauci to support using Bactrim, 17,000 people with AIDS died because of Dr. Fauci's insistence on not allowing even a statement supporting consideration of the use.
This has gone on before.
Now we have Dr. Fauci denying that any evidence exists of benefit (of hydroxychloroquine) and that pervaded the FDA. The FDA has relied on Dr. Fauci and his NIH advisory group to make the statement saying that there is no benefit of using hydroxychloroquine in outpatients.
And this is counter to the facts of the case, the evidence is overwhelming. The FDA has also said that there is the harm of using these medications in outpatients overweighs the benefit, and
in fact they said this with no information, no evidence whatsoever of any harm in outpatient use and this is provable both by the fact that the FDAs webpage says as a warning against outpatient use, but says it relies on inpatient hospital data which means that they don't have any outpatient data. As well as the fact that 90% of the cases of COVID this year have occurred since the time that the FDA restricted usage to inpatients only.
So the FDA knows that it has no data for outpatients and no data on harm and yet it denied the Henry Ford petition for outpatient usage. Dr. Fauci and the FDA are doing the same thing that was done in 1987 and that's led to the deaths of hundreds of thousands of Americans that could have been saved by usage of this drug. And this is the same thing that the FDA has done, it's outrageous, people need to be writing or calling their congressmen and senators and complaining that this is not the way this country should work. That a bureaucracy that is in bed with other forces that are causing them to make decisions that are not based in the science, that is killing Americans, is not acceptable.
