A trove of newly released documents detailing U.S.-funded coronavirus research in China prior to the COVID-19 pandemic shows that Dr. Anthony Fauci was “untruthful” when he claimed that his agency did not finance gain-of-research in Wuhan, an infectious disease expert said Sunday.
Documents published by The Intercept on Sunday show that Fauci’s organization, the National Institute of Allergy and Infectious Diseases (NIAID), provided federal funds to the U.S. nonprofit group EcoHealth Alliance and the Wuhan Institute of Virology to construct laboratory-generated SARS and MERS-related coronaviruses that demonstrated enhanced pathogenicity in humanized mice cells, according to Rutgers University professor of chemical biology Richard Ebright.
“The documents make it clear that assertions by the [National Institutes of Health] Director, Francis Collins, and the NIAID Director, Anthony Fauci, that the NIH did not support gain-of-function research or potential pandemic pathogen enhancement at WIV are untruthful,” Ebright said in a tweet Sunday evening.
The two leading European health agencies determined Thursday that COVID-19 booster shots are not necessary for fully vaccinated individuals who do not have compromised immune systems.
The European Centre for Disease Prevention and Control and the European Medicines Agency issued a statement saying the current priority should be vaccinating all eligible individuals. Booster shots should be considered only for those with compromised immune systems.
Top U.S. health officials told the White House pandemic coordinator on Thursday to scale back the Biden administration’s plan to administer the coronavirus booster shots to individuals in September, The New York Times reported.
Dr. Janet Woodcock, the acting commissioner of the Food and Drug Administration (FDA), and Dr. Rochelle P. Walensky, the director of the Centers for Disease Control and Prevention (CDC), told White House Coronavirus Response Coordinator Jeffrey D. Zients that they need more time to collect and analyze the necessary data relating to the booster shots, The New York Times reported.
The doctors told Zients that their agencies might be able to determine whether to recommend boosters for recipients of the Pfizer-BioNTech vaccine in the coming weeks, according to the Times.
The two doctors presented their argument to Zients at a meeting on Thursday. It is unclear how Zients responded to the news.
The U.S. Centers for Disease Control and Prevention changed course Tuesday, reversing its previous COVID-19 guidance by urging Americans to wear masks, regardless of their vaccination status. Critics quickly denounced the reversal, saying it undermines vaccine confidence.
The CDC said all students and teachers should wear masks, even if they are vaccinated, and that all Americans, including those with the vaccine, should wear masks in public places where the virus has a significant presence. The agency cited the delta variant of COVID, which is more transmissible.
The CDC had previously announced in May that vaccinated individuals did not have to wear masks. The White House fended off questions from reporters at the White House press briefing on the reasoning behind that reversal.
The Georgia Access to Medical Cannabis Commission will pick six companies to start producing the plant for medical uses in the state.
Nearly 70 companies applied for licenses to grow marijuana and convert it to oil to treat various illnesses. Once the commission approves them, the companies could be looking at paying up to $200,000 in licensing fees to the state. They will have one year to get product to thousands of Georgians who have been waiting for more than five years.
Patients with a Low THC Oil Registry card legally can purchase up to 20 fluid ounces of the THC oil from licensed dispensaries or pharmacies under legislation signed into law by former Gov. Nathan Deal in 2015. However, without guidelines and a medical marijuana marketplace, the 14,000 registered patients in Georgia have no way of legally obtaining the oil.
The Center for Disease Control updated federal COVID guidance Friday with several major changes as schools around the country grapple with policies for students’ return in the fall.
The CDC urged schools to allow students to return to in-person classes whether or not they are vaccinated as most studies showed significant learning loss during remote-only or hybrid teaching models.
The agency also said teachers and students should wear masks unless they have gotten the vaccine, a recommendation that is certain to drive controversy.
The U.S. Food and Drug Administration is asking for an internal review of its own approval process that gave a greenlight to a drug to treat Alzhiemer’s, a move that could shed more light on the controversial chain of decision-making that led to the drug’s being okayed for use.
The FDA last month approved drug company BioGen’s product Aduhelm, the first medicine greenlit in the U.S. to slow the cognitive decline of those living with Alzhiemer’s.
Yet that decision was shrouded in controversy: The approval went against the advice of an outside panel of FDA experts and even led to the resignation of several of those experts in protest.
The COVID-19 pandemic has taken a financial toll on Georgia’s long-term care facilities, officials said.
Devon Barill, communications director for the Georgia Health Care Association and Georgia Center for Assisted Living (GHCA/GCAL), said the facilities have faced increased expenses and revenue losses from caring for the state’s most vulnerable population.
While COVID-19 can lead to severe complications in older people and those with underlying issues, the congregated facilities are often home to the elderly and people who require supportive care.
The president of the largest union of health care workers in the U.S. says it will fight companies requiring its members to have mandatory COVID-19 shots as a condition of employment.
The announcement came one day after Houston Methodist announced that 153 employees had been fired or resigned for refusing to get the shots as a condition of employment. Those suing argue requiring employees to receive a vaccine approved only through Emergency Use Authorization violates federal law. After a recent court dismissal, their attorney vowed to take the case all the way to the Supreme Court.
George Gresham, president of 1199SEIU United Healthcare Workers East, is weighing the organization’s legal options.
Georgia’s public health state of emergency will end on July 1 under an executive order signed by Gov. Brian Kemp.
Kemp first declared a public health state of emergency on March 14, 2020, in response to the COVID-19 pandemic. The declaration helps the state easily access supplies and other resources needed to combat the spread of the coronavirus. It lifts certain medical and commercial transportation regulations.
Tuesday’s order extends the declaration by one day and one minute.
The Department of Health and Human Services will invest $3.2 billion to develop and manufacture COVID-19 antiviral medicines, it announced Thursday.
The initiative, funded as part of the American Rescue Plan, is designed to accelerate research into antivirals as well as build platforms for urgent response to future viral threats, the Department of Health and Human Services (HHS) said in a statement Thursday. Specifically, the plan expands antiviral clinical trials, forms partnerships between health agencies and pharmaceutical companies, and funds “drug discovery groups” tasked with innovating new antiviral medicines.
“New antivirals that prevent serious COVID-19 illness and death, especially oral drugs that could be taken at home early in the course of disease, would be powerful tools for battling the pandemic and saving lives,” said chief medical adviser Dr. Anthony Fauci in the statement.
Children and young adults are experiencing increased mental health issues, and suicide also is on the rise within the age group at least in part because of ongoing state shutdowns, according to several reports.
Within months of governors and local authorities shuttering schools, children were increasingly brought to emergency room doctors and specialists, according to a by the Centers for Disease Control and Prevention (CDC).