Posted on 09/21/2020 6:45:22 AM PDT by SeekAndFind
MOSCOW: More than a month after becoming the first country to approve a coronavirus vaccine, Russia has yet to administer it to a large population outside a clinical trial, health officials and outside experts say.
The approval, which came with much fanfare, occurred before Russia had tested the vaccine in late-stage trials for possible side effects and for its disease-fighting ability. It was seen as a political gesture by President Vladimir Putin to assert victory in the global race for a vaccine.
It is not clear whether the slow start to the vaccination campaign is a result of limited production capacity or second thoughts about inoculating the population with an unproven product.
The Russian vaccine is one of nine candidates around the world now in the late-stage clinical trials that are the only sure means to determine whether a vaccine is effective and find possible side effects.
A vaccine is considered the only way to halt the spread of the coronavirus, which has sickened more than 30 million people globally and slowed economies around the world since it first appeared in China late last year.
In one example of the limited scope of distribution, the company financing the vaccine pointed to a shipment sent this past week to the Crimean Peninsula. The delivery contained doses for 21 people in a region with 2 million.
The Russian Ministry of Health has not said how many people have been vaccinated in all of Russia. The minister, Mikhail Murashko, said last weekend that the first small shipments were being delivered this past week to the Russian provinces.
He did not say how many doses were shipped, describing the shipments only as small amounts, and also did not say when they would become available.
(Excerpt) Read more at economictimes.indiatimes.com ...
Uh oh did Putin lose the antidote to the virus he planted in Xi’s lab. Bad Vlad very sloppy.
Translation:Bring Out Your DeadA. It doesn't provide immunity.
B. It has horrific side effects.
C. Both a and B
Post to me or FReep mail to be on/off the Bring Out Your Dead ping list.
The purpose of the Bring Out Your Dead ping list (formerly the Ebola ping list) is very early warning of emerging pandemics, as such it has a high false positive rate.
The false positive rate was 100%.
At some point we may well have a high mortality pandemic, and likely as not the Bring Out Your Dead threads will miss the beginning entirely.
*sigh* Such is life, and death...
If a quarantine saves just one child's or one old farts life, it's worth it.
The Wicked Witch of the East's death opened a whole new Hate the evil Orange man opportunity.
It will be, an anti-masker died yesterday from COVID and the boogeyman needs to remain active.
He died because he was put on a ventilator. That is the kiss of death as we learned in March and April.
My the time President Trump announces his selection, the Commie Media will be saying that he murdered the Wicked Witch so he could replace her.
The common cold is sometimes a rhinovirus and sometimes a corona virus. They’ve never been able to make a vaccine for the common cold in either rhino virus or corona virus form. What make them think COVID19 will be any different?
All the wishing in the world won’t make it happen. All we’ll hear is a constantly moving target. It’ll be ready in 3 months and when 3 months is over, it’ll be another 3 months; and that will repeat forever.
The death rate on ventilators is down to 25%. Try again
"scientists from US, Italian and other universities wrote an open letter to the Russian researchers on 7 September. In the open letter, they pointed out to certain statistical anomalies that were detected in some of the experiments depicted in article by the Russian scientists."
https://swarajyamag.com/insta/sputnik-v-russian-covid-19-vaccine-developers-respond-to-criticism-of-clinical-trial-data-in-medical-journal-lancet
A simple google search would show that the reason a vaccine for the common cold has not been developed is because the common cold is made up of over 200 different viruses, so that it's not feasible to developed a vaccine that gets them all, or even a small fraction of them. COVID19 is not like that at all.
From what I read, China and Korea figured out how bad ventilators were with the previous SARS viruses.
The very nature of the rna virus itself insists it will laugh at any vaxby the time trials roll out.
Is that just 200 for a single year? Or for life? 200 vaccines every year is rediculous you impractical, for a sickness that is mild for all but those who are severely compromised in their immune system.
Russians lie like Stalinists
One word: zombies.
VACCINE FAILURE
Why Are Moderna Executives Dumping Their Stock?
Article By: Dr. Joseph Mercola
Results from Modernas Phase 1 human trial revealed the 100-mcg dose vaccine which had a 100% side effect ratio after the second dose is proceeding to Phase 3 trial assessment
Moderna has no legal rights to a key patent for its vaccine delivery system. Moderna sought to invalidate the patent for lipid nanotechnology owned by Arbutus Biopharma but lost the challenge at the end of July 2020
Executives at Moderna have cashed in stock options, raking in about $90 million in personal profits since January. Two Moderna executives have now sold off all of their stock holdings in the company, and its general counsel has sold nearly all of hers
AstraZeneca has temporarily halted its Phase 3 vaccine trials due to a suspected serious and unexpected adverse reaction in a British participant
AstraZeneca did not divulge the nature of the adverse reaction, but an anonymous source claims the trial participant was found to have transverse myelitis, an inflammatory condition that affects the spinal cord and is frequently triggered by viral infections
The U.S. Health and Human Services’ Operation Warp Speed has pledged to deliver 300 million doses of a COVID-19 vaccine by 2021,1 if not sooner.2 However, developing a safe and effective vaccine normally takes years and begins with animal studies. The COVID-19 vaccines are all being rushed straight into human clinical tests, forgoing lengthy animal trials altogether.
Such fast-tracked vaccines pose unknown risks, which are further magnified since governments are granting COVID-19 vaccine makers immunity from liability for all vaccine injuries and deaths that occur after the vaccines are recommended (or mandated) by public health officials.3
At the end of July 2020, AstraZeneca announced4 most countries it expects to supply with COVID-19 vaccine will grant the pharmaceutical company complete liability protection if people are harmed.
In the U.S., vaccine makers already have something of a “free pass” when it comes to vaccine injury liability and lawsuits through the National Childhood Vaccine Injury Act of 19865 and the Public Readiness and Emergency Preparedness (PREP) Act, passed in 2005.6
The main concern is that the combination of COVID-19 vaccines being fast-tracked to market at “warp speed” with minimal testing, together with blanket liability protection against vaccine injuries could be a public health nightmare in the making.
Problems With Modernas Vaccine Are Becoming Apparent
Early warning signs that something might be amiss have already started emerging. As detailed in Gates Tries to Justify Side Effects of Fast-Tracked Vaccine, results7 from Modernas Phase 1 human trial revealed 100% of volunteers in the high-dose group suffered systemic side effects. Side effects included fatigue, chills, headache and myalgia (muscle pain); 21% suffered one or more severe events.
According to Bill Gates, those side effects are largely due to the high dosages Moderna had to use in order to achieve desired antibody levels. But, if high dosages are required to create a robust-enough immune response, and higher dosages also cause systemic side effects in nearly all people, just how safe will this vaccination campaign be?
In the 20 years that vaccine makers have tried to develop a coronavirus vaccine, efforts have failed due to dangerous, many times lethal, side effects.
In July, it was reported8 that the 100-mcg dose vaccine despite its 100% side effect ratio after the second dose would proceed to Phase 3 trial assessment. In a May 26, 2020, article9 in STAT news, Ian Haydon, one of the Phase 1 study participants who suffered severe side effects requiring hospitalization, stated that while he recovered, the inoculation left him feeling as sick as hed ever felt. As noted by Robert F. Kennedy Jr.:10
Three of the 15 human guinea pigs in the high dose cohort (250 mcg) suffered a serious adverse event within 43 days of receiving Modernas jab. Moderna acknowledged that three volunteers developed Grade 3 systemic events defined by the FDA as Preventing daily activity and requiring medical intervention.
Moderna allowed only exceptionally healthy volunteers to participate in the study. A vaccine with those reaction rates could cause grave injuries in 1.5 billion humans if administered to every person on earth. That is the threshold that Gates has established for ending the global lockdown.
Moderna did not explain why it reported positive antibody tests for only eight participants. These outcomes are particularly disappointing because the most hazardous hurdle for the inoculation is still ahead; challenging participants with wild COVID infection.
Past attempts at developing COVID vaccines have always faltered at this stage as both humans and animals achieved robust antibody response then sickened and died when exposed to the wild virus.
Vodka and valarian root.
Do people still get sent to Siberia to count trees?
It doesnt matter. People need to be scared of thinking incorrectly about COVID-19 by a slurry of select people dying because they didnt wear masks.
Disclaimer: Opinions posted on Free Republic are those of the individual posters and do not necessarily represent the opinion of Free Republic or its management. All materials posted herein are protected by copyright law and the exemption for fair use of copyrighted works.