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

American Board of Internal Medicine Revokes Certifications of Drs. Marik and Kory Over COVID-19 Treatment Claims

The American Board of Internal Medicine (ABIM) revoked the certifications of Dr. Pierre Kory and Dr. Paul Marik for allegedly spreading misinformation. ABIM said that Kory and Marik’s “statements about the safety and efficacy of ivermectin and hydroxychloroquine” as treatments for COVID-19“ are false and inaccurate because they are unsupported by factual, scientifically grounded, andContinue reading American Board of Internal Medicine Revokes Certifications of Drs. Marik and Kory Over COVID-19 Treatment Claims

More news about Coronavirus

Health & Nutrition

Time Magazine Changes Headline About Ultra-Processed Foods After Online Backlash

Time Magazine received criticism and backlash for publishing an article originally titled, “What if Ultra-Processed Foods Aren’t as Bad as You Think?” The outlet has since changed the title to “Why One Dietitian is Speaking Up for Ultra-Processed Foods.” This comes after a Tucker Carlson segment about health issues in the United States has goneContinue reading Time Magazine Changes Headline About Ultra-Processed Foods After Online Backlash

More news about Health & Nutrition

Vaccines

FDA Renews Emergency Use Authorization for Updated COVID-19 Vaccines

The FDA has approved new formulations of the COVID-19 vaccines under Emergency Use Authorization (EUA). The fact sheet released by the FDA states, “An EUA is supported by a Secretary of Health and Human Services (HHS) declaration that circumstances exist to justify the emergency use of drugs and biological products during the COVID-19 pandemic. AContinue reading FDA Renews Emergency Use Authorization for Updated COVID-19 Vaccines

More news about Vaccines

Science & Tech

USDA Reopens Comment Period for Deregulation of Gene-Edited Plants

The deregulation of gene-edited plants is on the USDA agenda, and the public comment period has been extended by 21 days. The comment page has yet to be posted on the Federal Register. CRISPR is a new technology that is being used in agriculture to modify plants. “New Gene Technologies” or NGTs are how big agricultural companies like Bayer areContinue reading USDA Reopens Comment Period for Deregulation of Gene-Edited Plants

More news about Science & Tech

Environment

EPA Bans Herbicide Dacthal (DCPA) Over Fetal Health Risks

The EPA has banned Dacthal (DCPA), an herbicide commonly used on vegetables, following an assessment last year that showed severe risks for unborn babies. This is the first time the EPA has initiated an emergency order of this kind in 40 years. Michael Freehoff from the EPA Office of Chemical Safety and Pollution Prevention said,Continue reading EPA Bans Herbicide Dacthal (DCPA) Over Fetal Health Risks

More news about Environment

Policy

NTP Report Links Fluoride to Lower IQ in Children Amidst Ongoing EPA Lawsuit

A new report has found that water fluoridation levels at the World Health Organization’s (WHO) recommended levels are linked to lower IQ in children. The report was conducted by the National Toxicology Program (NTP), a division of the Department of Health and Human Services (HHS). The federal agency reviewed and analyzed previous studies before concludingContinue reading NTP Report Links Fluoride to Lower IQ in Children Amidst Ongoing EPA Lawsuit

More news about Policy