Risk of heart attack in the next 5 years increases from 11% to 25% after the jab - peer reviewed study

[LordBrownTrout]

Thursday seems a good day for that.

That was comedy hour. But yeah, our govt is worthless. Tens of thousands have died from faucis gof virus and his snake elixir injection. Govt killing people. What a surprise.

 

[badger2]

Horse manure. Fau Chi's mistake is recorded in his youtube video where he mentions the D614G mutation backwards. His Freudian slip happened because he knew that it linked to Wuhan tick virus 1, which is vectored by Rhipicephalus microplus, basically a cattle tick, also on cattle in Brazil.

Wuhan tick virus 1 vectored by this tick is an unclassified Dimarhabdovirus, most closely related to Eel European X virus, which is closely related to the Vesiculovirus genus. As any reader can see, the SARS-CoV-2 spike page at Uniprot shows the D614G mutation linking to VSV, vesiculo stomatitis virus. The Indiana strain of this virus is used as basis for ebola vaccine.

R. microplus also attacks Odocoileus virginianus, White-Tailed deer. SARS-CoV-2 now infects white-tailed deer in the U.S. (northeastern Ohio).

 

[Fort Fun Indiana]

Clinical trials usually last from 5-12 years before the results are published and approval is sought.

No. You are a little confused, there. Mostly because you are just pulling things out of your ass.

They don't do large scale human Trials and then wait for years and years.

Please read:

Vaccine Research & Development - Johns Hopkins Coronavirus Resource Center

How can COVID-19 vaccine development be done quickly and safely?

coronavirus.jhu.edu

 

[LordBrownTrout]

No. You are a little confused, there. Mostly because you are just pulling things out of your ass.

They don't do large scale human Trials and then wait for years and years.

Please read:

Vaccine Research & Development - Johns Hopkins Coronavirus Resource Center

How can COVID-19 vaccine development be done quickly and safely?

coronavirus.jhu.edu

U.S. Vaccine Safety - Overview, History, and How It Works | CDC

Safety is a priority during the development and use of all vaccines in the United States. Learn more about the history of vaccine safety, current safety programs, and how they work.

www.cdc.gov

Vaccine licensing is a lengthy process that can take 10 years or longer. The FDA requires that vaccines undergo three phases of clinical trials with human subjects before they can be licensed for use in the general public:

• Phase 1 trials are small, involving only 20 to 100 volunteers, and last only a few months. The purpose of phase one trials is to evaluate basic safety and identify very common reactions.
• Phase 2 trials are larger and involve several hundred participants. These studies last anywhere from several months to two years and collect additional information on safety and efficacy. Data gained from phase two trials can be used to determine the composition of the vaccine, how many doses are necessary, and a profile of common reactions.
• Phase 3 trials are the next step, unless the vaccine is ineffective or causes health problems, and are expanded to involve several hundred to several thousand volunteers. Typically, these trials last several years. Because the vaccinated group can be compared to those who have not received the vaccine, researchers are able to identify true reactions. [1, 3, 7, 8, 9]

If the clinical trials demonstrate that the vaccine is safe and effective, the manufacturer submits a Biologics License Application (BLA) to FDA requesting two licenses: one for the vaccine (product license), and one for the production plant (establishment license).

 

[Fort Fun Indiana]

Vaccine licensing is a lengthy process that can take 10 years or longer

In my link explains how could be expedited. And no, they don't just sit around for five years after doing large-scale human trials. You are pulling shitt right out of your ass and you don't know what you're talkin about.

Go read my link.