It says this with a caveat.I smell a cover-up. They have the deaths that were reported to the CDC missing from their chart. Besides this claim contradicts the development of past safer vaccines proclaiming so soon they are safe or effective. It still is not officially licensed by the FDA yet. But here these folks are saying these are safe. I wonder who paid them off to run with one of a Pfizer or Moderna press-release? I worked with PR firms, I know how they get glowing reports like this into the press. They don't know this yet. The CDC and FDA keep track of reports coming in from people who died just after being vaccinated and the numbers are on the CDC's site.
It is clear that coronavirus vaccines are safe and effective, but as more are rolled out, researchers are learning about the extent and nature of side effects.
Backed by decades of research and safety data for herpes-family viruses, U.S.-based researchers at Bio-Virus Research Inc, Reno, Nevada, report on the successful treatment of the first 30 frontline doctors and nurses and a thousand-plus patients given the amino acid lysine to prevent and even abolish COVID-19 coronavirus infections at a clinic in the Dominican Republic. Astonishingly, symptoms of COVID-19 are reported to have dissipated within hours of this natural treatment.
Arginine/lysine balance
Lysine therapy interrupts the replication of viruses, including COVID-19 coronavirus, by countering arginine, an amino acid that fosters the eruption of dormant viruses. Lysine has been safely used for decades to quell herpes virus outbreaks that cause cold sores on the lips (herpes labialis), a treatment pioneered by one of the Bio-Virus Research team members in 1974.
Third-party validation for lysine therapy
Writing in the International Journal of Infectious Diseases another research team based in New York and Texas reports that arginine depletion is a strategy to quell both coronaviruses and other herpes family viruses.
in 2016 In 2016 researchers documented that lysine impairs the growth of coronaviruses in a lab dish.
The Bio-Virus Research team are not loners nor out on a scientific limb. A report, published in the Journal of Antivirals & Antiretrovirals, is what prompted to the current discovery that was put into clinical practice in the Dominican Republic. The science was in place prior to the announcement a mutated coronavirus was sweeping the globe which no one had immunity towards.
https://www.lewrockwell.com/2021/02/...-for-vaccines/
Epidemiologists baffled by low rate of coronavirus infections in IndiaSame link as above.
Despite its large population and poor sanitation, disease trackers are baffled by India’s low rate of coronavirus infections. Maybe it is India’s lysine-rich diet of yogurt, lamb, chicken, fish curry that protects its population from viral disease. The striking difference in the country-to-country prevalence of Herpes Simplex-2 infections (only 9.6% in South East Asian countries and 10.7% in Europe vs. 24.0% in the Americas and 43.9% in Africa) could be explained by the lysine/arginine ratio in native diets.
Incredibly good news https://t.co/nN6AsY215M
— Ben Shapiro (@benshapiro) February 18, 2021
Pathologist: FDA ‘misled the public’ on Pfizer vaccine efficacyRemember, the PCR tests are now going to use a much lower cycle threshold which means less cases of of the virus will be reported. Watch, for the vaccines to be touted, albeit falsely to the lower level of Covid cases. What a scam!
In an amended reply to the FDA’s rejection of his concerns about Pfizer’s clinical trials, Dr. Sin Hang Lee says the FDA is glossing over potential risks of an mRNA vaccine while concealing its true efficacy.
https://www.lifesitenews.com/news/pa...ccine-efficacy
* They still suffer from regulatory capture issues, so it's not like they're always right. They have approved products later removed from the market.
Dr. Sin Hang Lee, a Connecticut pathologist, who questioned Pfizer’s methodology and asks the U.S. FDA to require accurate counts of COVID-19 cases in the Pfizer/BioNTech COVID-19 mRNA vaccine trial before granting the vaccine Emergency Use Authorization (EAU).
“Before an EUA or unrestricted license is issued for the Pfizer vaccine, or for other vaccines for which PCR results are the primary evidence of infection, all “endpoints” or COVID-19 cases used to determine vaccine efficacy in the Phase 3 or 2/3 trials should have their infection status confirmed by Sanger sequencing, given the high cycle thresholds used in some trials. High cycle thresholds, or Ct values, in RT-qPCR test results have been widely acknowledged to lead to false positives …
Same link as above.