Dirty Truth About the Only FDA Approved COVID Prescription

In the early months of 2019, the pharmaceutical business was below fireplace from legislators and the media about the exorbitant costs being charged in the U.S. for medicine. According to at least one ballot reported by Ars Technica,1 58% of individuals in the U.S. held a damaging view of the business.

The value hike on one life-saving medicine — EpiPen — rose from $50 in 2007 for a single autoinjector to $600 in 2018 for a pack of two.2 One cause the value rose so dramatically was that the maker, Mylan, started promoting the injectors in two packs solely — leaving the door open to cost no matter they felt like for that double-dose package deal.3

The transfer subsequently led to a category motion lawsuit alleging “the two-pack sale of EpiPens is a pretense for charging unconscionable prices” and that Mylan is “misstating the science of EpiPen dosage in order to purportedly justify its price gouging,’ in violation of various state deceptive and unfair trade practice and consumer protection laws,” in accordance with MarketWatch.

Profits for the drug firm rose to $1.1 billion every year for the drug since it’s subsequent to unimaginable for individuals with extreme allergic reactions to go with out an EpiPen. But simply when it seemed like governmental businesses and legislators have been contemplating taking a look at pricing insurance policies, the pharmaceutical business used the 2020 pandemic to reverse their public picture once they have been known as upon to develop a vaccine for a viral an infection at “Warp Speed.”4

Now, regardless of the reality the business holds no accountability for opposed occasions related to the vaccine,5 together with loss of life, 2020 gave Big Pharma the wanted impetus to beat their lowest status rating since public opinion of the business started being measured in 2001.6

During 2020, Big Pharma as an entire labored onerous to painting itself as a benevolent business that poured billions of {dollars} into the creation of medication and vaccines with the intent of defending public well being. As a part of that group, biotech big Gilead Sciences isn’t any totally different.

The firm manufactures remdesivir,7 which is the antiviral drug favored by Dr. Anthony Fauci, director of the U.S. National Institute of Allergy and Infectious Diseases, and the chief medical adviser to the president. However, whereas the chief medical officer of the U.S. promotes remdesivir, scientific proof demonstrates the drug has a darkish aspect, and it’s not efficient.

Fauci’s Favored Drug Has a Dark Secret

The FDA absolutely authorized remdesivir October 22, 2020, to be used in adults and youngsters in the therapy of COVID-19.8 This got here after the emergency use authorization was issued May 1, 2020, for remdesivir in sufferers who had “suspected or laboratory-confirmed COVID-19.”

Remdesivir is an antiviral drug that could be a nucleoside/nucleotide reverse transcriptase inhibitor. It was examined in primates as a therapy for Ebola and located to have some effectiveness towards the extreme acute respiratory syndrome (SARS) outbreak in 2002 and the Middle East Respiratory Syndrome (MERS) outbreak in 2012.9

Before this, Gilead had produced a remarkably related drug known as tenofovir for HIV.10 Remdesivir is sort of a replica of Gilead’s HIV drug and can be a reverse transcriptase inhibitor. According to a paper revealed in Molecules, “Reverse transcriptase is an enzyme in the human immunodeficiency virus (HIV) and many retroviruses that convert the RNA template to DNA.”11

The enzyme helps to synthesize a strand of DNA that enhances the RNA template. Several nucleoside reverse transcriptase inhibitors are anti-HIV brokers.12 This could help the speculation that the SARS-CoV-2 virus is a chimera.

The time period chimera comes from mythology and describes an organism or particular person through which the physique has cells from genetically distinct organisms. In Greek mythology,13 a chimera was a fire-breathing monster that had the face of a lion, the tail of a snake and the wings of a dragon. In a overview of the use of remdesivir for COVID-19, one analysis workforce wrote:14

“Other clinically approved nucleoside/nucleotide analogues, such as the hepatitis C drug sofosbuvir and HIV drugs alovudine and zidovudine, have also been shown to be active against the SARS RdRp [RNA dependent RNA polymerase] in in vitro biochemical assays and might have the potential to be repurposed against COVID-19.”

The Mountain View Voice15 stories Fauci believes the remdesivir trials have been paying homage to analysis that had been performed almost 34 years in the past when he and his colleagues have been analyzing the human immunodeficiency virus (HIV).

The relationship between SARS-CoV-2 and human retroviruses is advanced. To date, there are three retroviruses that scientists have recognized that infect people. Retroviruses are RNA genetic materials that modifications the host DNA. In 2019, the three identified retroviruses that will trigger human sickness have been HIV and kinds 1 and a pair of human T-cell lymphotropic viruses.16

In “The Many Ways in Which COVID Vaccines May Harm Your Health,” you may watch my interview with Stephanie Seneff, Ph.D., and Judy Mikovits, Ph.D., the place we focus on considered one of the extra harmful elements of SARS-CoV-2 — the spike protein envelope, frequent in retroviruses, that causes a lot of the illness challenges docs are combating from COVID-19.

Despite Negative Trial Results FDA Approved Remdesivir

Pharmaceutical firm Gilead Sciences was given at the least $70.5 million in taxpayer cash to develop remdesivir, and that quantity could also be larger.17 The really helpful therapy dose for remdesivir spans 5 to 10 days, all of which have to be administered in the hospital.18

Gilead Sciences fees the authorities $2,340 and personal insurance coverage $3,120,19 which is effectively above the drug maker’s estimated price for manufacturing, which is between $10 and $600 for a 10-day course.20

But the price ticket doesn’t mirror the effectiveness of the drug. There have been a number of damaging trial outcomes, and but the FDA authorized the drug anyway. Just a few trials were stopped early when contributors skilled important unwanted side effects. Some scientists believed the information urged the drug may shorten restoration time.21

However, the drug has not produced satisfactory outcomes or proved to cut back the potential for loss of life in these with extreme illness. Worse but, the therapy comes with an added price ticket of potential kidney harm.22

While Fauci known as the outcomes of research that had not been peer-reviewed from a pharmaceutical-sponsored scientific trial “highly significant” and referred to remdesivir as the “new standard of care,”23 the World Health Organization had a distinct advice. Based on proof from the SOLIDARITY trial, the WHO conditionally really helpful towards utilizing remdesivir in hospitalized sufferers.24

Fauci’s help of an antiviral drug that hasn’t lived as much as the hype helped help the firm’s falling revenues. During the first quarter of 2021, remdesivir grossed $1.5 billion in gross sales, serving to enhance Gilead’s whole backside line of $6.4 billion in income throughout that very same quarter — a 16% improve over the first quarter of 2020. But when income for remdesivir was excluded, income truly plummeted 11%, at a disappointing $4.9 billion.25

Remdesivir Not Backed by Results

The information from science trials for remdesivir have been disappointing. One examine revealed in The New England Journal of Medicine26 concluded that the drug labored higher than a placebo and so was stopped early for profit. However, as Peter Gotzsche from The Institute for Scientific Freedom wrote, this profit was not a discount in mortality from COVID-19, however reasonably shortened hospital days.27

The placebo-controlled examine demonstrated the drug may scale back hospital stays from 15 days to 11 days. Yet, different physicians have been discovering the drug was retaining individuals in the hospital longer. Although Dr. George Ralls with Orlando Health reported they noticed optimistic advantages with the drug, he additionally attributed it to longer hospital stays with a view to full the course of therapy.28

As I reported in “The New COVID-19 Medication Isn’t Backed by Results,” in the center of the examine (April 20, 2020), the researchers modified the major end result measures so sufferers solely needed to meet three of an unique eight classes,29 and none of the three included measurement of mortality.

In the final replace to Clinical Trials30 earlier than publication, the researchers had one major end result measurement — time to restoration. The concept for the drug was to maintain individuals from dying, however the researchers stopped measuring that necessary end result.

In one other examine revealed in The Lancet,31 researchers evaluated remdesivir in sufferers with extreme COVID-19. The major endpoint measurement was how lengthy it took for scientific enchancment. The drug was stopped early as a result of 12% of the sufferers skilled opposed occasions and researchers discovered there have been no statistically important scientific advantages.

Just earlier than the launch of the research in The New England Journal of Medicine and The Lancet, Bloomberg32 reported the WHO by accident posted outcomes of a 3rd examine. The abstract was eliminated, however particulars confirmed “the drug wasn’t associated with patients getting better more quickly; and 13.9% of patients getting the drug died, versus 12.8% getting standard care.”

Ivermectin Is Effective however Intentionally Suppressed

While researchers utilizing remdesivir battle to establish and show the drug is efficient towards COVID-19, information clearly present ivermectin can stop it and when used early can preserve individuals from progressing to the hyper inflammatory section of the illness.

In reality, ivermectin may even be used late in the illness to assist critically unwell sufferers recuperate. The drug has an extended historical past of use as an antiparasitic33 and has a identified security profile as in comparison with remdesivir, which has a brief historical past of use.

In the early months of COVID-19, a gaggle of physicians shaped the Frontline COVID-19 Critical Care Alliance (FLCCC).34 The collaboration of the 5 founding physicians in the group resulted in a protocol that can be utilized in the hospital and one other that can be utilized as an outpatient. Each of the 5 founding members has handled vital sickness for many years.

The two protocols can be found for obtain on the FLCCC alliance web site in a number of languages.35,36 Ivermectin was added to the outpatient and inpatient protocols. Although a lot of the medicine utilized in the protocols are actually accepted requirements of care in lots of locations, the identical just isn’t true of ivermectin.

It is necessary to keep in mind that as others clamor for randomized managed trials to exhibit that ivermectin is efficient, these develop into kind of unethical when you may see from scientific proof that one thing is working, and you already know you are condemning the management group to poor outcomes or loss of life.

In reality, that is the identical argument vaccine makers are utilizing now to justify the elimination of control groups by giving everybody the vaccine.

While the WHO really helpful that remdesivir not be utilized in hospitalized sufferers based mostly on a scientific overview and meta-analysis of pooled information from 4 randomized trials, the proof37 they used to suggest that ivermectin not be utilized in sufferers with COVID-19 besides in scientific trials is predicated on what they admit is a “high degree of uncertainty.”38

You can learn extra about the advantages of utilizing ivermectin and the way this information is being purposefully suppressed in “COVID, Ivermectin and the Crime of the Century.” In the article is a video from DarkHorse podcast host Bret Weinstein, Ph.D., through which he interviews Dr. Pierre Kory about the significance of early therapy of COVID-19 and the shameful censoring of information about ivermectin.

It’s no small irony, then, that YouTube deleted this interview, which is why I embedded a Bitchute model. How this interview may presumably be labeled as misinformation is a thriller, contemplating the whole dialog is about revealed analysis and they’re each credentialed medical science consultants.

Steps to Help Reduce the Severity of the Disease

As I’ve mentioned, fear is contagious and is getting used to regulate your conduct. One technique initially used to funnel the public into vaccination packages revolved round utilizing PCR testing to exhibit a rising variety of instances. However, as I’ve written a number of occasions, PCR testing doesn’t precisely diagnose an energetic an infection.

During lockdown, many individuals placed on pandemic pounds that contribute to rising your danger of getting sick. Instead of relying on medicine and vaccines, I like to recommend you proactively work to help your immune system utilizing methods that proof demonstrates reduces your danger of extreme illness.

It has develop into evident that optimizing your vitamin D stage could also be the least costly, best and most useful technique to reduce your danger. Making easy life-style modifications to normalize your blood sugar ranges may assist scale back your danger of coronary heart illness, Type 2 diabetes and viral infections resembling COVID-19 and flu.

Comorbid circumstances which are associated to extreme illness with COVID-19 embody heart problems and Type 2 diabetes. In “Nearly Half of American Adults Have Cardiovascular Disease,” I summarize methods that enhance the microcirculation in your coronary heart in addition to mitochondrial perform and insulin resistance, that are associated to sturdy coronary heart well being.

It is troublesome to regulate Type 2 diabetes while you rely strictly on medicine and don’t change the underlying life-style elements which have prompted the drawback. If correctly addressed, Type 2 diabetes could be totally reversible in most individuals. In “Diabetes Can Increase the Complications of COVID-19,” I focus on a few of these dietary and life-style selections and provide options for change.


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