The Tennessee General Assembly approved legislation on Thursday to label any food product with vaccine technology as a pharmaceutical drug. The bill is currently awaiting a signature from Governor Bill Lee.
HB 1894 was passed by the Tennessee House on Thursday and subsequently adopted by the Senate. It aims to define “food that contains a vaccine or vaccine material as a drug for purposes of the Tennessee Food, Drug and Cosmetic Act.”
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Three years after federal regulators granted emergency use authorization to COVID-19 mRNA vaccines for older teens and adults, mainstream scientific research is confirming suppressed warnings from two years ago that the novel technology has a problem with “translation fidelity.”
Translation: it tends to make a bunch of wacky “off-target” proteins whose effects and severity are unknown.
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The Centers for Disease Control and Prevention has updated the amount of time it recommends people isolate themselves after testing positive for COVID-19, shortening it from 10 days to five.
“Given what we currently know about COVID-19 and the Omicron variant, CDC is shortening the recommended time for isolation from 10 days for people with COVID-19 to 5 days, if asymptomatic, followed by 5 days of wearing a mask when around others,” the CDC said in a statement Monday.
The CDC changed the guidance because officials believe the data indicates the majority of COVID-19 transmission takes place early in the course of the illness, “generally in the 1-2 days prior to onset of symptoms and the 2-3 days after,” the statement said.
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Governor Ralph Northam announced Monday that Virginia has reached a key vaccination milestone: 70 percent of adult Virginians have received at least one dose of a COVID-19 vaccine.
“Virginia has reached a significant milestone in the fight against COVID-19,” Northam said in his announcement. “Thanks to the millions of Virginians who have rolled up their sleeves to get vaccinated, the virus is in retreat, our economy is growing, and we are closer to putting this pandemic behind us.”
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The Centers for Disease Control and Prevention will discuss reports of a rare heart inflammation following doses of mRNA-based COVID-19 vaccines in an emergency meeting, it announced Thursday.
The emergency meeting, set to take place on June 18, will include updates on mRNA COVID-19 vaccine safety with a specific focus on rare reports of myocarditis and pericarditis, Scott Pauley of the CDC told The Daily Caller News Foundation. The risks and benefits of administering the mRNA COVID-19 vaccines to adolescents and young adults will also be discussed, according to the meeting’s agenda.
The announcement comes following a presentation to the Food and Drug Administration by Dr. Tom Shimabukuro, deputy director of the CDC’s Immunization Safety Office, confirming 226 cases of myocarditis/pericarditis in people under 30. These cases are more than twice what was expected under the FDA’s safety assessment for COVID-19 vaccines.
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