mFLUSIVA is a new mRNA flu vaccine produced by Moderna, which was approved by the US Food and Drug Administration on 5 August.
Do not allow these “vaccines” to be injected into you or your children.
Covid mRNA “vaccine” vials have reported residual plasmid DNA and other manufacturing-related materials that were undisclosed in the ingredient lists. There have also been discoveries of dangerous genetic sequences, rare earth metals, E. coli contamination and endotoxins.
The mFLUSIVA products should therefore be immediately investigated rather than assuming that the finished product contains nothing beyond what appears on the label, Dr. Mark Trozzi writes.
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Dangerous New mRNA Influenza Shots Coming Soon!
By Dr. Mark Trozzi, 21 August 2026
The FDA’s approval of Moderna’s mFLUSIVA marks another major expansion of modified mRNA technology. Approved on 5 August for adults aged 50 and older in the United States, the product is intended for use during the 2026–2027 influenza season and is expected to appear on shelves in the coming weeks.
This deserves immediate attention. Despite all of the harms we witnessed during the covid-19 “vaccine” rollout, the same dangerous technological platform is now being introduced into routine seasonal influenza inoculation. The United States may be first, but applications are also being considered elsewhere, making this an international issue. Please warn everyone of the dangers and do not take these injections.
From Covid to Seasonal Influenza
The covid-19 injections represented a dramatic departure from traditional vaccine technology. Rather than introducing an antigen directly, the mRNA products deliver tens of trillions of copies of foreign genetic code inside PEGylated lipid nanoparticles, intended to cause the recipient’s own cells to manufacture foreign proteins.
Many of us raised concerns about this technology before the covid-19 injection rollout began. Those concerns included the distribution of infinitely penetrating lipid nanoparticles throughout the body, the hyper-persistence of the modified mRNA, the continued production of foreign proteins and the high risk of serious adverse effects.
The safety signals reported following the covid-19 “vaccine” rollout only intensified those concerns. Before the covid-19 injections, there were typically only a few hundred deaths reported each year following vaccination in the United States. This is not accounting for underreporting. After the modified mRNA covid-19 injections were rolled out, this rose to tens of thousands of reported deaths within months, with higher numbers in those initial months than for all other vaccines, for all other diseases, over the previous 30 years combined. Not to mention, data shows the covid injections have a negative efficacy; they increase the risk of covid infection. They produced only harm, no benefit.
If we account for the underreporting factors, the covid-19 rollout has been an ongoing disaster, with upwards of a billion people injured and tens of millions already dead following the injections.
However, instead of stepping back from the technology and acknowledging their concerning risk profile, pharmaceutical companies are expanding its use.
What Is Actually Inside the Final Product?
Independent testing should be a priority as soon as commercial vials become available. Analyses by Kevin McKernan and others of covid-19 mRNA “vaccine” vials have reported residual plasmid DNA and other manufacturing-related materials that were undisclosed in the ingredient lists. There have also been discoveries of dangerous genetic sequences, rare earth metals, E. coli contamination and endotoxins. The mFLUSIVA products should therefore be immediately investigated rather than assuming that the finished product contains nothing beyond what appears on the label.
Qualified independent laboratories should examine commercially distributed vials and determine precisely what they contain, including the quantity and integrity of the mRNA, lipid nanoparticle composition, residual DNA, bacterial manufacturing residues and any other detectable contaminants.
The public must not rely exclusively on manufacturers and regulators for these answers, since they have already proven themselves untrustworthy.
The Existing Flu Shot Raises Its Own Questions
There is another important part of this story: how well do conventional influenza vaccines actually work?
A recent Cleveland Clinic study followed more than 50,000 employees during the 2024-2025 influenza season. In the study population, vaccinated employees experienced a higher cumulative incidence of influenza than unvaccinated employees. The researchers estimated vaccine effectiveness at approximately minus 27%.
This means even in the case of standard vaccination, there was a higher, rather than lower, risk of influenza following injection. That finding is particularly relevant when evaluating Moderna’s claims about mFLUSIVA.
Moderna did not establish that mFLUSIVA reduced influenza by 27% compared with receiving no vaccine. Instead, its trial compared the new mRNA product against an existing conventional influenza vaccine and reported roughly 27% greater relative efficacy against laboratory-confirmed influenza. That distinction matters.
Given that the comparator itself is associated with increased infection risk, outperforming it by 27% does not establish that the new product provides substantial protection compared with remaining unvaccinated. 27% better than -27% is essentially negligible.
Safety Matters as Much as Efficacy
Even a genuinely effective medical intervention must still justify its risks.
The adverse reactions that Moderna acknowledged in the mFLUSIVA trial were more frequent and intense than with the conventional flu vaccine comparator. This is an early warning sign of what is likely to come.
For a seasonal respiratory illness, the threshold for demonstrating safety should be exceptionally high. Regulators should demand compelling evidence of meaningful clinical benefit alongside careful long-term safety monitoring. This has not happened.
Demand Evidence Before Expansion
With FDA approval secured, people who have become accustomed to receiving an annual influenza injection may soon be offered an mRNA product instead; likely without their knowledge. The issue also extends far beyond the United States. Moderna has pursued regulatory approval for the product in other jurisdictions, including Canada, Europe and Australia.
This means urgent action is needed. Once millions of doses have been administered, any harms cannot simply be undone. Not only will injection recipients be at risk, but shedding is also a concern that could potentially affect those around them.
The expansion of mRNA technology from an “emergency” response that was an enormous failure into routine seasonal vaccination should not happen quietly. mFLUSIVA represents a worrying new stage in the normalisation of modified mRNA technology. We must do everything we can to warn everyone we can. Scrutiny needs to happen now, before widespread administration begins.
Contact Your Elected Federal Officials
If you live in the United States, contact your federal representatives today. Alert your Senators and Members of Congress that this is wrong and dangerous. Demand that they intervene to block the rollout of these mRNA flu injections and help warn their constituents about the risks of these genetic products. Find and contact them here: https://www.usa.gov/elected-officials
For everyone else – especially in countries where this product is under review – the time to act is now. Write to your Members of Parliament (“MPs”) or equivalent representative. Tell them your public health agency is considering these harmful, misrepresented genetic injections for approval as “vaccines.” Urge them to read this post and the links within it, and to do their part to stop this.
Here are links to contact MPs for the countries most immediately under threat:
- Canada: https://www.ourcommons.ca/members/en
- Australia: https://www.aph.gov.au/Senators_and_Members
Additional Material:
- New Cleveland Clinic Study Reveals Negative Efficacy of Influenza Vaccines
- Covid Science & Solutions: Your Starting Point
- Dr Trozzi | The True “Efficacy” of covid-19 “Vaccines”
- Dr Trozzi Alert | There’s DNA in the RNA Shots. Lots!
About the Author
Mark Trozzi is a 27-year veteran emergency physician and former trauma medicine instructor who practised in Canada before having his medical license revoked for his public criticism of covid public health mandates. He is one of the Directors of EBMCsquared CiC, an international steering committee member of the World Council for Health (“WCH”) and a founding member of WCH Canada.
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Categories: Breaking News, Latest News, World News
Never taken a flu vaccine, these products are just another example of tax fraud. That only the manufacturers benefit from.
What’s going to happen when everyone realises they’ve been trying to kill us all?
well there won’t be too many of us left by then … that being the plan
Adequate vitamin D is all that is required in the “flu season”, for example in northern latitudes in winter when there is little or no sunshine. Vitamin D is manufactured by sunlight on the sink, with only a few oily fish containing this vitamin. Vitamin D is a cheap and easy way to protect the population, but of course this is no good for big pharma profits. Are the technocrats trying to kill us all? Read “Turtles All The Way Down” by 2 anonymous authors for a deep dive into drugs and testing. I have never taken flu jabs and an mRNA version is deeply disturbing!
Moderna have just had a new mRNA jab approved called Nexspike. A friend of mine told me to look up what “nex” means in Latin – “The Latin word “nex” translates to concepts related to death and violence, specifically “violent death,” “murder,” or “slaughter.” This term is a noun and carries connotations of fatal violence, often associated with death caused by another person”….. Word on the street is that these people are all practising s*t*nists, but that even s*t*nists have rules they must abide by. The rule in this instance is that they can do whatever they want to you but they have to tell you first. They commonly do it through movies and other media but, as we see here, they do it in the names they give to the poisons they’re planning on forcing us to take. If you think that it’s just entertainment, or you don’t read the label and/or don’t understand Latin, that’s not their problem – they’ve fulfilled their side of the karmic bargain and the rest is on you. If you’ve ever seen the Deagal Predictions, you see there in black-and-white the proposed population reductions planned for every country in the world which is already under way. It’s why I often comment in support of Moslems – because Moslems are included in the population reduction that the global elites have planned ……. and I won’t elaborate on how they’re planning to do that but, suffice to say, it won’t be through an mRNA jab. I’ve attached here a screenshot from the CDC on ‘flu stats from 2018 – 2023 to add to the stats in the article. Study it well; it’s very revealing ….
….. 2018 – 2024 – sorry!
Agenda 2030, New World Order going to plan, if these MRNA “vaccines” aren’t stopped now.
All vaccines are an integrated depopulation strategy. They need to kill the majority of the people in order to take full control.
I never had a flu vaccine ( it simply doesn’t make sense….natural immunity is much better and effective and longer lasting). Needless to say, that I am the only one at work who hasn’t been sick in years.