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    October 22, 2023
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    The nightmare continues....our drug regulator is silent.....most politicians either don't care or are incapable of understanding the problem

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    I’ve been distributing important information regarding international reports and opinion that the COVID-19 “vaccines” have been found to contain dangerous levels of toxic plasmid DNA. Readers of my Substacks should go to:

    Substack - 14 Oct. https://open.substack.com/pub/phillipaltman/p/more-on-dna-contamination-of-the?r=10pxn5&utm_campaign=post&utm_medium=web

    Substack - 5 Oct


    Substack - 25 September (Do COVID-19 “Vaccines” Cause Cancer?)



    The initial clinical trial batches of COVID-19 “vaccines” were made using a manufacturing method involving Real Time Polymerase Chain Reaction (PCR) which was able to produce limited quantities of mRNA no fermentation steps and involving no bacteria. In order to meet the projected worldwide demand for the COVID-19 “vaccines” the manufacturers had to resort to manufacturing circular pieces of DNA (plasmids) which coded for the production of mRNA and exposing these plasmids to large fermentation vats containing E. coli bacteria. The E. coli bacteria used the plasmid DNA to make mRNA in large quantities. The mRNA was extracted from the bacterial fermentation soup. But there was a problem. Some of the plasmids in the fermentation soup ended up with the mRNA used to make the COVID-19 “vaccines” and was not removed as it should have been. Plasmid DNA contamination in the “vaccines” have the potential to permanently integrate with your own DNA and may be passed on to future generations. Many experts believe this plasmid DNA can cause cancers to emerge. The potential harmful consequences to the world population are simply mind-blowing and our government and drug regulator is silent.

    Maybe they are silent because they use the bogus argument that the COVID-19 “vaccines” saved lives. Many believe there is no evidence that the COVID-19 “vaccines” actually saved net lives when you take into account the huge number of COVID “vaccine” related deaths, the extraordinary assumptions and extrapolations of the failed models predicting millions would die in the pandemic and the erroneous statistics reporting numbers of people who died WITH COVID as opposed to those who died DUE TO COVID.

    CLICK HERE to view The Defender – Children’s Health Defense: 20 Oct. 2023 by Michael Nevradakis PhD. Below are excerpts from the article:

    ‘An Admission of Epic Proportions’: Health Canada Confirms DNA Plasmid Contamination of COVID Vaccines

    Health Canada on Thursday confirmed the presence of DNA contamination in Pfizer COVID-19 vaccines and also confirmed that Pfizer did not disclose the contamination to the public health authority.

    The Defender – Children’s Health Defense: 20 Oct. 2023 by Michael Nevradakis PhD

    Patrick Provost, Ph.D., professor of microbiology and immunology at Laval University in Canada, told The Epoch Times “All it takes is a single integration [of SV40] at the wrong place in a single cell to initiate a cancerous process and kill a person.”

    In a recent articleDr. Angus Dalgleish, professor of oncology at St. George’s Hospital Medical School in London, said he has observed an increased incidence of cancer after COVID-19 vaccination, including an “epidemic of explosive cancers,” observing possible “DNA plasmid and SV40 integration in promoting cancer development.”


    It has been know for some time that the SV40 promoter nucleotide sequence used by Pfizer and Moderna can be used to insert genes into your DNA permanently in gene therapy.  This is not controversial. This is well known. See paper by David S. Strayer, 19 Oct. 1999 (https://onlinelibrary.wiley.com/doi/10.1002/(SICI)1097-4652(199912)181:3%3C375::AID-JCP1%3E3.0.CO;2-8)

    Here is a quote from that paper: “Effective genetic therapy requires both a fragment of genetic material to be used therapeutically and a means to deliver it. We began to study simian virus-40 (SV40) as a vector for gene transfer because available gene delivery vehicles did not provide for the full range of therapeutic uses. Other vectors are variably limited by immunogenicity, difficulties in production, restricted specificity, low titers, poor transduction efficiency, etc. In theory recombinant viral vectors based on SV40 (rSV40) should not, on the other hand, be similarly constrained. rSV40 vectors are easily manipulated and produced at very high titer, stable, lacking in immunogenicity, and capable of providing sustained high levels of transgene expression in both resting and dividing cells.”

    The danger is real - it is not hypothetical. Oncologists know the danger. Why is it being reported that cancers are on the rise? Do you know somebody who successfully had a cancer cure only to succumb to the cancer following COVID “vaccination”?

    Questions for our Therapeutic Goods Administration (TGA):

    1.    Did Pfizer and Moderna alert the drug regulator that the plasmid DNA used to make the mRNA contained the Simian Virus 40 ((SV40) promotor gene sequence?

    2.    When did the TGA know SV40 was used in the manufacturing process?

    3.    Did the TGA investigate the contamination of SV40 once it was aware of this possible contamination in the COVID “vaccines” at reported levels 18-70 times higher than the limits set by the FDA and the European Medicines Agency (EMA)?

    4.    Did the TGA question either Pfizer or Moderna on the potential for SV40 contamination?

    5.    Did the TGA conduct its own independent analysis to determine the level of contamination of SV40 or did it depend on information supplied by the manufacturers?

    6.    Is the TGA aware of international concern regarding the detection of plasmid DNA in the COVID-19 “vaccines” which contain SV40?

    7.    Have any batches of COVID-19 “vaccine” been released to the public with levels of plasmid DNA considered unsafe by international standards?

    8.    What plans does the TGA have to alert the population to the potential contamination of the COVID-19 “vaccines” so they can be fully informed?

    Good luck in obtaining answers.


    This is an example of a COVID Freedom of Information Request lodged by Senator Malcolm Roberts that he showed myself and others last Wednesday when we were in his offices to discuss the Excess Deaths symposium to be held later that day at Parliament House.  The question must have been a good one because the total response was redacted.  What a waste of printer toner.  What a waste of time.  This is the level of government censorship which is preventing people knowing the truth. Do you think the government is going to tell you the truth about plasmid DNA contamination in the jabs?

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    Phillip Altman

    Australian Pharmacologist - Clinical Trial and Drug Regulatory Affairs senior industry pharmaceutical consultant in drug research and regulatory approval with more than 40 years experience. BPharm(Hons), MSc, PhD. @PHILLIPALTMAN
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