By Jefferey Jaxen

According to their now-preferred method of scientific communication, the U.S. Food and Drug Administration’s (FDA) press release has recently dictated to the medical community and public at large that it has authorized a second booster dose of both Moderna and Pfizer COVID shots for various groups and ages.

The agency has now amended its Emergency Use Authorization (EUA) to include a second booster dose of Moderna or Pfizer for 50 years of age and older at least 4 months after a first booster dose, a second dose of Pfizer for individuals 12 years of age and older with certain kinds of immunocompromise at least 4 months after a first booster dose, and a second dose of Moderna 4 months after the first booster dose for 18 years of age and older who are immunocompromised.

This was all done without convening its expert voting committee adding further division and contention among the medical and scientific community. It was exactly the agency’s [first] expedited booster push, sans robust data, in August of 2021 that led two senior scientists to resign in protest.

The FDA appears to have adopted Plotkin’s commandment in stride by incorporating the wordplay into its latest press release by stating:

The FDA previously authorized a single booster dose for certain immunocompromised individuals following completion of a three-dose primary vaccination series. This action will now make a second booster dose of these vaccines available to other populations at higher risk for severe disease, hospitalization and death.

In case you have lost count, the FDA’s new vaccine edicts gives the green light to shots/boosters four and five.

No one was speaking about a 3-shot series until after August 30, 2021 – the date of a CDC advisory committee meeting in which Stanely Plotkin called in to make a comment and effect vaccine policy – or as StatNews stated reported at the time ‘when Stanley Plotkin speaks, people listen.’

Calling the third dose a booster is immunologically incorrect and also gives the wrong impression that somehow the vaccines failed…” stated Plotkin.

So if you are immunocompromised, two shots plus a (third) booster is your primary series and the added (forth) booster previously meant you fell under the ‘fully vaccinated’ definition. Now, today’s FDA decision makes a second (fifth) booster available, which, minus the medical doublespeak, would be the fifth shot being injected into your arm presumably making you fully vaccinated once again.

Rather than being transparent and linking to the data the FDA used to inform their decision, the press release gave a basic summary. For safety, the FDA relied on open population surveillance imported from Israel’s Ministry of Health along with one study of 120 people. For immunogenicity data, the FDA looked at a publication provided to them from an ongoing study in healthcare workers at a single center in Israel.

In Janurary 2022, The Financial Times reported about the dismal findings of an Israeli study at the Sheba Medical Center writing:

Healthcare workers at the Sheba Medical Center who received a fourth dose of the vaccine continued to get infected even though blood tests showed an increase in two key kinds of antibodies, according to professor Gili Regev-Yochay who led the research.

Enough of them tested positive for coronavirus two weeks after their fourth jabs to indicate that the level of antibodies needed to protect against infection from Omicron was “probably too high” for the vaccine to induce, said Regev-Yochay.

Moving into the vote, professor of epidemiology and biostatistics at the University of California, San Francisco Vinay Prasad observed that the FDA vaccine regulation was sliding further into the abyss by writingIf the FDA moves forward on authorizing either product, it will cement a dangerous precedent: inadequate evidence being used to justify widespread vaccination for years to come.”

Meanwhile, Johns Hopkins Marty Makary, M.D. took to Twitter for a series of comments:

The U.K. appears to be heading in the same direction with its Health Minister Sajid Javid recently saying it was ‘possible’ there would be an autumn booster ‘probably for those that are 50 and over.’ Currently in the U.K., over-75 year olds, care home residents and patients with weak immune systems are receiving invitations for a spring boosters.

If they are offered another jab in the autumn, it will be their fifth. Some immunocompromised adults will have already had five by then according to a Daily Mail report.

Jefferey Jaxen

Jefferey Jaxen is an investigative journalist and researcher, best known for his weekly segment The Jaxen Report on The HighWire. With a sharp eye for detail and a talent for clear, compelling storytelling, he has exposed major issues in medicine, science, and public health policy, earning recognition as a trusted voice in independent journalism.

Other Headlines

Coronavirus

ICAN Releases Recordings of FDA’s Peter Marks; Vaccine Official Dismissed Vaccine Injuries

The Informed Consent Action Network (ICAN) and REACT 19 held a joint press conference today to reveal a trove of secret recordings and FOIA documents of Peter Marks, the former Director of the Center for Biologics Evaluation and Research. The press conference included ICAN Founder Del Bigtree, Attorney Aaron Siri, and REACT 19’s Brianne Dressen.Continue reading ICAN Releases Recordings of FDA’s Peter Marks; Vaccine Official Dismissed Vaccine Injuries

More news about Coronavirus

Health & Nutrition

US Labs Create Tick Colonies To Study Foreign Highly Pathogenic Disease With 30% Mortality

The White Coat Waste Project uncovered 10 existing USDA contracts to work on mRNA vaccines, including one that is studying Crimean-Congo Hemorrhagic Fever (CCHF), a highly pathogenic tick-borne disease with a 10-40% case fatality rate. The research grant is given to the Agricultural Research Service in Manhattan, Kansas, in combination with researchers at the NationalContinue reading US Labs Create Tick Colonies To Study Foreign Highly Pathogenic Disease With 30% Mortality

More news about Health & Nutrition

Vaccines

“Revolution In Vaccine Regulation” Following FDA Acknowledgement Of COVID-19 Vaccine Child Deaths

Dr. Robert Malone, ACIP vaccine advisory member, declared that there is a “revolution in vaccine regulation and approval” following the release of an internal FDA letter stating  “at least 10 children have died after and because of receiving COVID-19 vaccination.” The letter was written by Dr. Vinay Prasad, the FDA Director of the Center forContinue reading “Revolution In Vaccine Regulation” Following FDA Acknowledgement Of COVID-19 Vaccine Child Deaths

More news about Vaccines

Science & Tech

US Labs Create Tick Colonies To Study Foreign Highly Pathogenic Disease With 30% Mortality

The White Coat Waste Project uncovered 10 existing USDA contracts to work on mRNA vaccines, including one that is studying Crimean-Congo Hemorrhagic Fever (CCHF), a highly pathogenic tick-borne disease with a 10-40% case fatality rate. The research grant is given to the Agricultural Research Service in Manhattan, Kansas, in combination with researchers at the NationalContinue reading US Labs Create Tick Colonies To Study Foreign Highly Pathogenic Disease With 30% Mortality

More news about Science & Tech

Environment

Whistleblower: Dioxin Contamination in Roseland, LA Pond 18x Higher Than East Palestine

Independent toxicity expert and Government Accountability Project whistleblower Scott Smith has warned of high dioxin contamination in Roseland, Louisiana, that is more than 18 times higher than the highest reading he got while testing in East Palestine, Ohio, during the first week after the train derailment. Smith said his testing revealed 165 parts per quadrillionContinue reading Whistleblower: Dioxin Contamination in Roseland, LA Pond 18x Higher Than East Palestine

More news about Environment

Policy

Pfizer Settles AG Paxton Lawsuit For $41.5 Million; Adulterated ADHD Drugs 2012-2018

Pfizer and Tris Pharma agreed to a $41.5 million settlement in a case filed by the Texas Attorney General Ken Paxton in 2023, alleging the pharma companies violated the Texas Health Care Program Fraud Prevention Act (THFPA) by selling adulterated ADHD drugs to children. Quillivant is an ADHD drug that was first developed by NextWaveContinue reading Pfizer Settles AG Paxton Lawsuit For $41.5 Million; Adulterated ADHD Drugs 2012-2018

More news about Policy