“If it ain’t broke, don’t fix it.”
The Food and Drug Administration’s advisory committee voted on Tuesday to change the strain composition of COVID-19 vaccines as immunity continues to wane and more people suffer from adverse reactions from the experimental shots.
FDA’s panel of independent vaccine experts voted 19 to 2 to recommend redesigning the COVID vaccines to fight the Omicron variants this fall.
“It is the first time the panel has proposed that vaccine makers modify the shots to target a different variant. The FDA will likely accept the committee’s recommendation and authorize a vaccine change,” CNBC reported. “However, the panel did not make a recommendation on which omicron subvariant the shots should target.”
Both Moderna and Pfizer have claimed that their respective redesigned experimental shots generate a better immune response against BA.1 than their current shots that were designed for the original virus that emerged from China, according to Toronto Sun.
“During the Omicron-predominant period, VE against COVID-19–associated ED/UC visits and hospitalizations was 87% and 91%, respectively, during the two months after a third dose and decreased to 66% and 78% by the fourth month after a third dose. Protection against hospitalizations exceeded that against ED/UC visits.” the CDC said.
According to the Danish study published in JAMA Network in May, the researchers found a rapid decline in Omicron-specific serum neutralizing antibody titers only a few weeks after the second and third doses of Pfizer’s Covid-19 vaccine.
Data from around the world show just how ineffective the COVID-19 vaccines are.
For several months, the US public health regime and the bootlicking media have been downplaying the risk of developing myocarditis and other life-threatening reactions after taking the vaccine, calling the occurrence “mild” and “rare,” and systematically burying any evidence to the contrary.
However, myocarditis – a potentially life-threatening inflammation of the heart – is in no way a ‘mild’ adverse reaction to the vaccine – especially when 90% of cases that have been recorded in VAERS ended up hospitalized – so, in other words, that half of the narrative was just an outright lie.
The VAERS website has recorded 1,307,926 Reports of adverse reactions through June 17, 2022.