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 a health journalist and featured in his weekly segment, ’The Jaxen Report’, on The HighWire. As an investigative journalist, researcher, and compelling writer, Jefferey serves as Lead editor of The HighWire News and Opinion Team.

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

New Fluoride Study Ignores Neurotoxicity and Sugar Intake in Cost Analysis

A new fluoride study has been criticized for being a tool of the industry to promote continued water fluoridation following the banning of the practice in Utah and Florida. The authors conducted a simulation model and cost-effectiveness analysis with data from 8484 children with a mean age of 9.6 years. The authors concluded eliminating fluorideContinue reading New Fluoride Study Ignores Neurotoxicity and Sugar Intake in Cost Analysis

More news about Health & Nutrition

Vaccines

HHS Terminates Moderna Contract For Bird Flu Vaccine; Calls mRNA Technology “Under-Tested”

HHS has terminated a $766 million contract with Moderna to develop an mRNA bird flu vaccine. HHS spokesman Andrew Nixon said the decision is about “safety, integrity, and trust.” He added that “mRNA technology remains under-tested, and we are not going to spend taxpayer dollars repeating the mistakes of the last administration, which concealed legitimateContinue reading HHS Terminates Moderna Contract For Bird Flu Vaccine; Calls mRNA Technology “Under-Tested”

More news about Vaccines

Science & Tech

Humanoid Robots Malfunction and Attack; Sparks Debate Over AI Safety and Liability

A viral video released from an undisclosed Chinese factory shows a humanoid robot malfunctioning and attacking the factory workers. The Unitree H1, a product of the Chinese company Unitree Robotics, can be seen flailing its arms as workers move away to protect themselves. The robot was hung on a crane, and the workers were notContinue reading Humanoid Robots Malfunction and Attack; Sparks Debate Over AI Safety and Liability

More news about Science & Tech

Environment

CDC Advised Health Care Providers Not to Test East Palestine Residents for Chemical Illnesses, Lawsuit Alleges

Newsnation reported this week that the CDC advised local health care providers in East Palestine, OH, not to test local residents for chemical illnesses after the town was exposed to a toxic plume from a “controlled burn” after the Norfolk Southern train derailment in 2023. A lawsuit has been filed against Norfolk Southern and moreContinue reading CDC Advised Health Care Providers Not to Test East Palestine Residents for Chemical Illnesses, Lawsuit Alleges

More news about Environment

Policy

HHS and CMS Urge Changes to Gender-Affirming Care for Minors; Clinics Face Potential Loss of Federal Funding

HHS Secretary Robert F. Kennedy Jr. wrote a letter addressed to healthcare providers saying he expects them to update their “treatment protocols and training to ensure that care for children with gender dysphoria is evidence-based.” The letter was also addressed to healthcare risk managers and state medical boards. The letter refers to the report publishedContinue reading HHS and CMS Urge Changes to Gender-Affirming Care for Minors; Clinics Face Potential Loss of Federal Funding

More news about Policy