(Republican Insider) – According to a new report from Infowars, a panel of health advisors to the Centers of Disease Control and Prevention conducted a vote on Thursday where they decided unanimously that adult patients seeking booster shots should take either the Pfizer or Moderna shots rather than the vaccine produced by Johnson & Johnson.
The Advisory Committee on Immunization Practices ended up voting 15-0, a very, very decisive vote, that the mRNA vaccines are “preferred” to the J&J vaccine because, according to them, they are the safest and most effective vaccines on the market.
“CDC Director Rochelle Walensky is expected to decide whether to adopt the panel’s advice as agency policy later today,” the report said, adding, “Johnson & Johnson’s COVID-19 vaccine has been linked to rare forms of blood clotting.”
Gee, it’s almost like putting a foreign substance inside your body without proper long term testing, isn’t a very good idea. Who would’ve thought, right?
“A panel of experts who advise the Centers for Disease Control and Prevention (CDC) on vaccines is meeting Thursday to discuss updates to a severe condition linked to Johnson & Johnson’s COVID-19 vaccine,” a report from the Epoch Times said.
“The panel will listen to presentations by CDC officials on thrombosis with thrombocytopenia syndrome (TTS), which U.S. drug regulators say has a ‘causal relationship’ with the jab, according to a draft agenda for the meeting,” the report continued.
The syndrome mentioned above is a combo of blood clots and low blood platelet levels.
Concern over the possibility of those being vaccinated getting the syndrome was so high at one point that it caused a near-nationwide pause in the administration of the shot back in the spring, however, the pause was lifted once the Food and Drug Administration (FDA) determined that the benefits of taking the vaccine outweighed the potential risks.
However, more evidence has come out since that time linking the syndrome directly to the vaccine.
Researchers working for the CDC uncovered last month that individuals who received the Johnson & Johnson jab were a lot more likely to experience the syndrome than those who took the Moderna or Pfizer shots.
“The reporting rate to the Vaccine Adverse Event Reporting System (VAERS), a system run by the CDC and the FDA, was 3.55 per million doses administered for the Johnson & Johnson vaccine, compared to 0.0057 per million doses administered after one of the other vaccines,” the Infowars report said.
The rate was the highest among women belonging to the 30 to 39 age group.
“According to the American Society of Hematology, symptoms of blood clots typically occur about six to 14 days after injection with the Johnson & Johnson vaccine. The symptoms include severe headaches, abdominal pain, back pain and nausea,” a report from WND revealed.
According to the WND report, the shot developed by Johnson & Johnson is a viral vector vaccine.
“The vaccine replaces a small piece of the genetic instructions in the adenovirus with genetic instructions for the SARS-CoV-2 spike protein, producing antibodies to fight it. The Pfizer and Moderna mRNA technology ‘teaches’ cells to make a protein that triggers an immune response rather than inserting a live virus,” WND said.
“A study published in the journal Nature Medicine on Tuesday from Oxford University showing the COVID-19 vaccines can cause myocarditis, an inflammation of the heart, in young people at a rate higher than the incidence of COVID-19,” the report added.
There have been all kinds of issues with all of the vaccines being produced and administered. There is so much we do not know about the kind of effects these shots and the seemingly endless boosters the government wants to pump into your veins, when it comes to the long term.
Each person has to decide for themselves whether or not to get the jab. It’s imperative, however, that all individuals have access to complete information and data about the risks and potential benefits of taking the vaccine before getting the shot.
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