Dr. Marik, Founder of the FLCCC, spoke Monday to Senator Ron Johnson’s Discussion Panel on the Deadly Approach to Covid-19 with Vaccine Mandates, Poisonous Protocols, and Restricted Therapeutics.
Dr. Paul Marik, FLCCC
See his full remarks here.
“Almost 850,000 poor souls have died. These have been unnecessary, needless deaths. The NIH Guidelines for the treatment of hospitalized COVID include Remdesiver and low-dose Dexamethasone. Consequently, almost every single patient in this country, in this country is treated with the combination Remdesivir and low-dose Dexamethasone.
The Palm Study Group investigated four drugs for the use of Ebola. The results were published December 12, 2019, in the New England Journal of Medicine. That date is particularly important because that signaled the beginning of Covid. The Data Safety Monitoring Board of that study terminated the study of Remdesivir. TERMINATED, because Remdesivir INCREASED THE RISKS OF DEATH AND RENAL FAILURE. It was SUCH A TOXIC DRUG the Data Safety Monitoring Board terminated the use of REMDESIVIR.
Yet, in January and February of 2021 the NIH, in the ACTT 1 Study, enrolled patients in a study looking at Remdesivir for the treatment of Covid-19. The last patient was enrolled April 19, 2020. Ten days later, before the study had actually terminated, Dr. Fauci sat in the Oval Office of the White House and he said, “The trial was good news.”
What Dr. Fauci did not tell you was that the primary endpoint of the study was changed half-way during the study. We all know, that is scientific misconduct. Because the study was not going to be positive, they changed the primary endpoint.
The original endpoint was an 8-point scale that included death and a requirement for mechanical ventilation. Knowing that Remdesivir would not affect those endpoints, they invented a bogus endpoint called, “Time to Recovery.” Which they showed, in this study, was statistically significant. And based on this bogus endpoint, Remdesivir was approved by the FDA on October 20th, 2020.
So, if one does a meta-analysis looking at the studies of Remdesivir, the two studies, which were sponsored by Gilead, show a reduction in mortality. However, if you look at the four independent studies, including the large study by the WHO, it shows the opposite effect. Remdesivir increases the risk of death. Let me say that again. Remdesivir increases the risk of death by 3%. It increases your chance of Renal Failure by 20%. This is a toxic drug.
But, just to make the situation even more preposterous, the Federal Government will give hospitals a 20% bonus on the entire bill, if they prescribe Remdesivir to Medicare Patients. The Federal Government is incentivizing hospitals to prescribe a medication which is toxic.
So, it should be noted that Remdesivir costs about $3,000 a course. Dr. Kory spoke about Ivermectin. Ivermectin reduces the risk of death by about 50%. It costs the WHO two cents. Two cents.
So as regards dexamethasone, this is the wrong drug, in the wrong dose, for the wrong duration of time. Yet, every clinician in this country will absurdly use this homeopathic dose of dexamethasone. Why?! Because the N I H tells them to do this.
So, what the NIH and other agencies have ignored are multiple FDA approved drugs. These are FDA approved drugs. These are not experimental drugs, which are cost-effective, and safe, and have unequivocally been shown to reduce the death of patients in ICU and in hospital.
For example, there are 25 high quality studies (some people complain about the quality of these studies – so if you select out the high quality, randomized controlled trials) they show that Ivermectin reduces the risk of death by 26%. This is an extremely safe and cheap drug. In fact, it is one of the safest drugs on this planet. You are more likely to die from taking Tylenol…..
(This is just to the 7-minute mark. There are 8 more minutes of truth left. Watch the video
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