Dr. Paul Marik at Ron Johnson Hearings - Fauci Knew Remdesivir was Deadly (1.24.22)

TRANSCRIPT: Dr. Paul E. Marik 03:45
Thank you, Senator Johnson. And it's a privilege to be here with my esteemed colleagues. So as you said, I'm a critical care doctor, I've practiced in the ICU for 35 years, until recently and before my job was terminated, I've been treating COVID patients in the ICU since March of 2020. I've treated hundreds and hundreds of COVID patients.
So, what I need to tell you is that between four to 10% of symptomatic patients with COVID-19 ever required hospitalization across the world. With omicron, it's about 2%. In this country, 4 million patients have been hospitalized with COVID. And of those 850,000 poor souls have died. 850,000 people have died. These have been unnecessary, needless deaths.
The NIH guidelines for the treatment of hospitalized patients for COVID include remdesivir and low dose dexamethasone. Consequently, almost every single patient in this country, almost every single patient in this country is treated with a combination of remdesivir and low dose dexamethasone. The PALM study group investigated four drugs for the use of ebola The results were published December the 12th, 2019, in the New England Journal of Medicine, and that date is particularly important,because that signaled the beginning of COVID.
The data safety monitoring board of that study terminated the study of RM 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 and the act one study enrolled patients in a study looking at remdesivir for the treatment of COVID-19.
The last patient was enrolled April 19, 2020. 10 days later, 10 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 halfway 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 eight point ordinal scale that included death, and the 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 the study was statistically significant. And based on this bogus endpoint, remdesivir was approved by the FDA on October the 20th, 2020.
So, if one does a matter 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 full 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 chances 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 hospital bow, 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 NIH 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, unequivocally been shown to reduce the death of patients in the ICU and in hospital. For example, there are 25 high-quality, so people complain about the quality of these studies, so if you select out the high-quality randomized control trials, they showed 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, you are more likely to die from taking Tylenol than ivermectin.
Yet, the FDA calls this a dangerous horse deworming medicine.
So, we have a whole host, as Dr. Urso and other clinicians have said, there are a whole host of drugs that have been proved highly effective for the treatment of hospitalized patients, including antiandrogen therapy, spironolactone, fluvoxamine, nitazoxanide, melatonin, vitamin C, and I can go on. So, the question is, why? Why have cheap, safe and effective drugs been ignored for the treatment of COVID- which could have saved maybe 500,000 lives? And I think Dr. Kory has told us exactly why. Thank you.

https://realfoodchannel.com/wp-content/uploads/2022/02/Transcript-of-Sen.-Johnson-COVID19-A-Second-Opinion-Hearing-1.pdf

Video First published at 17:08 UTC on January 25th, 2022.
Fauci Knew Remdesivir was Deadly, Submitted False Study – Modified Endpoint to FDA

'Watch this one. But dont sit close enough to the monitor to break it when you air punch. He details how evil and corrupt the entire Covid narrative is in terms of money for dangerous meds when cheap safe ones could have saved OVER HALF those who died of Covid19'

SOURCE: https://www.bitchute.com/video/kvTVkgrrnQEO/