FDA Approves New CONvid-1984 Shot - Healthketeers Complicit

Article posted with permission from the author, Suzanne Hamner

While Secretary of the Department of Health and Human Services (HHS) Robert F. Kennedy, Jr. and Food and Drug Administration (FDA) head Marty Makary have been spouting rhetoric regarding the “Make America Health Again” (MAHA) agenda in the media, the “machine” of HHS and FDA has been functioning along the same “status quo”. Nothing has changed except the “heads” of the agency and departments. In fact, it has been reported the FDA has approved a new CONvid-1984 bioweapon available for adults age 65 and over and individuals 18 – 64 with at least one underlying condition placing them at risk for severe CONvid-1984.

The U.S. Food and Drug Administration (FDA) has granted full approval to the adjuvanted COVID-19 vaccine Nuvaxovid, produced by Novavax, according to a May 16, 2025, approval letter obtained by this publication.

But while headlines tout the vaccine as a safer, more traditional alternative to mRNA injections, the FDA’s approval rests on alarmingly thin evidence—including just 14 moderate-to-severe COVID-19 cases recorded in the placebo group and zero in the vaccine group during the pivotal phase 3 trial published in the New England Journal of Medicine.

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In other words, this “100% efficacy” claim against severe disease—the centerpiece of Novavax’s approval—was based on just 14 cases.

There are important aspects to consider about this injection.

First, this injection contains “recombinant spike protein produced in insect cells (from Spodoptera frugiperda, or fall armyworm) and is combined with the Matrix-M adjuvant derived from saponin extracted from tree bark.” This raises questions of DNA contamination.

Second, trial participants were followed for a total of only three months, with all cases of severe disease occurring in the normal saline placebo arm. The “placebo arm” consisted of 9868 participants while those who received the injection totaled 19,714, a ratio of 2 to 1. Moreover, the “placebo arm” did not include any vaccinated individuals over 65 experiencing severe disease. Since this injection was also created under a PREP Act declaration,

Third, the trial ended before any “variants” emerged. There was zero measurement of transmission or infection rates.

Fourth, the “post-marketing” red flags of myocarditis, anaphylaxis and menstrual issues were noted.

Australia’s post-market surveillance study, cited in Eurosurveillance, revealed serious concerns not seen in trials:

• Pericarditis (inflammation around the heart): 19.4 per 100,000 doses.
• Chest pain: 91.3 per 100,000 doses.
• Anaphylaxis: 7 cases—all in women—despite no anaphylaxis in trials.
• Menstrual disturbances: reported but not tracked in the trial at all.
• Death temporally linked to vaccination: 4 reported, but all dismissed as unrelated without detailed investigation.

Despite this information, Kennedy and Makary’s FDA approved this new injection for the CONvid-1984.

Fifth, how this injection is made raises serious concerns.

Nuvaxovid (NVX-CoV2373) uses a recombinant protein vaccine platform, which is fundamentally different from mRNA vaccines—but still raises serious biological and regulatory questions.

Nearly all Sf9 cell lines are persistently infected with Sf-rhabdovirus, an RNA virus recently discovered to be nearly universal across global supplies.

1. Insect Cells as Factories

• The spike protein in Nuvaxovid is produced inside insect cells from the Spodoptera frugiperda species (a moth), specifically a cell line called Sf9.
• These cells are cultured in large bioreactors to act as biological “factories” that churn out massive quantities of protein.

2. Genetically Engineered Baculovirus Infection

• The Sf9 insect cells are intentionally infected with a recombinant baculovirus—a virus that’s been genetically modified to carry the code for the SARS-CoV-2 spike protein.
• Once infected, the insect cells begin producing the full-length, prefusion-stabilized spike protein, which is then harvested and purified for use in the vaccine.
• Contamination from these insect cells makes it into the vaccine and therefore the vaccinated. [Emphasis mine.]

3. Protein + Adjuvant = Final Vaccine

• The harvested spike proteins are combined with Matrix-M, a saponin-based adjuvant derived from the bark of the Quillaja saponaria tree, which is said to boost immune response.

Residual DNA Contamination Risk: Even with purification steps, it’s possible for fragments of insect cell DNA or baculoviral DNA to end up in the final product. This is a known issue with recombinant protein biologics and must be monitored due to theoretical risks of insertional mutagenesis or immune activation.

Genetic Modification: The baculovirus used is a genetically engineered organism (GMO). This process qualifies Nuvaxovid as a genetically modified biologic, even if it’s not based on mRNA.

Regulatory Transparency: Most people have no idea they’re receiving a product derived from insect-virus genetic engineering, raising serious informed consent concerns.

Spike Protein Concerns: The vaccine still introduces the SARS-CoV-2 spike protein—the same spike many researchers link to vascular inflammation, immune dysregulation, and long COVID–like symptoms.

Not surprisingly, this injection skipped the FDA advisory committee review. According to the FDA, the advisory committee was not convened because the data “did not raise concerns or controversial issues.” Who made that decision when the data clearly raises concerns and controversial issues?

Long-term studies for risks have been deferred for several years: pediatric studies until 2026 -2031; myocarditis until 2032; atrial fibrillation and strokes until 2028; and, pregnancy safety outcomes until 2027.

Despite risks to pregnant women seen with previous CONvid-1984 injections, the government continues to move forward with approving and recommending CONvid-1984 shots for pregnant women – a group who should not be taking any injections/vaccinations due to risk to the unborn baby.

Because RFK Jr. has not rescinded the emergency declaration for the CONvid-1984, development of injections for this hoax “virus” continues to fall under the PREP Act and controlled by the Department of Defense. The PREP Act does not require proper testing, good manufacturing processes, nor FDA approval. If there is any doubt about this, review the works of Sasha Latypova, Due Diligence and Art, and Katherine Watt, Bailiwick News – both on Substack. Makary, head of the FDA, continues to participate with Kennedy in this sham.

But, this is not surprising as both are controlled opposition, placed in positions to subvert the medical freedom movement and instill the government MAHA agenda, which has nothing to do with making Americans healthy. Bones are thrown to the public as these charlatans target low-hanging fruit to maintain support of the deceived Trumpites. The machinations (policy, regulation, legislation – pretended and otherwise, executive orders) put in place to implement PREP Act violations against the public continues to operate unimpeded. You can add Bhattacharya and Oz to the members of the controlled opposition club.

Remember, this “new” CONvid-1984 injection enjoys PREP Act immunity from liability for injury and death associated with its administration. The Four “Healthketeers”, along with Dr. Vinay Prasad, who replaced Dr. Peter Marks, know this and capitulate to this.

These “Healthketeers”, along with Environmental Protection Agency head Lee Zeldin, remain silent on chemtrails spraying the entire population of the united States with harmful elements, chemicals, parasites, and possible pathogens. Stopping the intentional poisoning of Americans, the air, the water, the soil, the plants, and the animals would certainly fall under the MAHA agenda. Alas, the public hears crickets from RFK, Jr., Makary, Bhattacharya, Oz, Prasad, the Center for Disease Control (CDC) and Zeldin.

It’s time to flood HHS and RFK Jr. with petitions to rescind the emergency declaration for CONvid-1984; the FDA and Makary to recall the CONvid-1984 shots in all forms; and, Congress to repeal the PREP Act and any legislation, regulation, or policy connected to the PREP Act. The public should demand the ceasing of all research and development of all mRNA products currently in development and prohibiting of all future research and development of those same products. In the meantime, all residents within the united States should refuse all vaccines and products wrongly dubbed vaccines.

Continue to be vigilant and do your own research. Question everything and refuse to give any government employee your confidence. Your very life is dependent upon it.

Article posted with permission from Sons of Liberty Media