Nasal Vaccination Against SARS-CoV-2: Synergistic or Alternative to Intramuscular Vaccines?
Mattia Tiboni, Luca Casettari, Lisbeth Illum It is striking that all marketed SARS-CoV-2 vaccines are developed for intramuscular administration designed to produce humoral and cell mediated immune responses, preventing viremia and the COVID-19 syndrome. They have a high degree of efficacy in humans (70–95%) depending on the type of vaccine. However, little protection is provided […]
The High-Speed, Bivalent COVID Boosters are Here
Meryl Nass On Wednesday, August 31, the FDA issued emergency use authorizations for new Pfizer and Moderna mRNA booster vaccines for COVID. The next day, September 1, the CDC’s advisory committee and CDC Director approved the immediate rollout of the new vaccines. They will be administered in the US starting this week. Surprisingly, more than […]
China Approves World-first Inhaled COVID-19 Vaccine
Ben Turner China has approved the world’s first inhaled COVID-19 vaccine, the vaccine maker CanSino Biologics (CanSinBIO) in Tianjin, China has announced. The newly approved vaccine, named Convidecia Air, uses the same platform as the injectable COVID-19 vaccine by the same manufacturer — pieces of genetic material transported by a harmless adenovirus vector so the […]
Rapid Rollout of New COVID Boosters with nNo Human Trials – ‘A Tale of Recklessness’
Meryl Nass The U.S. Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) cooperated to issue Emergency Use Authorizations (EUA) and roll out new, bivalent Pfizer and Moderna COVID-19 vaccines this week, without any human trials, which is unprecedented. There is international coordination regarding bivalent boosters, and a major effort […]
Evidence of Risk, Harms Mount as FDA Forces new Covid Booster Without Human Testing
Jefferey Jaxen … Throughout the pandemic response, the US Food and Drug Administration (FDA) has become increasingly reckless rubber stamping Covid shots into circulation. At the start of the FDA’s vaccine vetting process, the agency promised transparency. We’ve went from rushing experimental vaccines onto the market with short, improper testing during an emergency to rushing […]
The End of Covid-19 Vaccine Safety Science in America
Toby Rogers On June 28, the FDA decided that henceforth THEY will choose the variants for reformulated Covid-19 shots and NO clinical trials will be conducted to evaluate safety. Because $cience.
Breaking News: FDA Expands Eligibility for Pfizer-BioNTech Covid-19 Booster Dose to Children 5 through 11 Years
The safety of a single booster dose of the Pfizer-BioNTech COVID-19 Vaccine in this age group was assessed in approximately 400 children who received a booster dose at least five months (range 5 to 9 months) after completing a two-dose primary series. The most commonly reported side effects were pain, redness and swelling at the […]
