C19 weekly news – including confirmation of monkey DNA in the mRNA injections, a secret trial of actual (not Phase 3) doses with 3 times more harms and a NINTH C19 wave in Japan

Although, globally, the Public Health Emergency of International Concern (PHEIC, pronounced FAKE) is over and injections have slowed to around 60,000 a day, the back story of a global genocide remains with us. Proof of INTENT and PRE-MEDITATION abounds – as does the threat of ceding control to an unelected and incompetent bunch of bureaucrats TO REPEAT THE GENOCIDE controlled by and at the whim of an ex-Ethiopian terrorist – Tedros of the WHO.

Just how any world leader can be “OK” with this is beyond me – unless of course it reflects a similar mind set amongst world leaders (Cult of Moloch anyone?).

Anyway, lots of content this week, so grab a coffee and settle in.

You can buy me one too if you like, or even take a paid subscription, it’s my birthday in two weeks!

I have dropped the update on deaths and harms from VAERS. It is now almost useless as an indicator of anything timely and/or relevant.

There are, to all intents and purposes, no more injections in the US. The majority of reports will relate to events between 10 December 2020 and later dates. The completeness of reporting to VAERS for deaths is somewhere between just 5% and 10% of deaths suffered and adverse events are somewhere between 1% and 2.5%.

Those seeking the latest VAERS data can access it here or here.

Broadly speaking, 670 million doses of C19 mRNA injections were administered in the US over two and a half years, with 270 million (allegedly) injected at least once (81% of all Americans) giving an average number of 2.5 doses per person.

VAERS has 17,615 reports of death associated with C19 injections and almost a million adverse events.

The European equivalent of VAERS is called EUDRA. According to the latest data published on the website linked below, (compiled by a subscriber to that website) there have been over 50,000 deaths and 5.3 million “events” for 976 million injections administered in the EU:

50,663 DEAD and 5,315,063 Injured Following COVID-19 Vaccines in European Database of Adverse Reactions - Vaccine Impact

Anecdotal estimates for the level of reporting are around 1.5% events that actually get reported (an under-reporting factor of 70).

The CDC/FDA were not capable of handling the volumes of adverse events reported to VAERS and so spent around an initial 30 million bucks  hiring General Dynamics IT to do their work for them. There has probably been a further 20 million bucks of taxpayers money spent on getting these sub-contractors to process VAERS reports.

This is, of course, on top of the salaries paid for around the existing staff complement of 25,000 CDC/FDA employees who could not be spared during a national health emergency to monitor the plethora of safety signals that should have resulted in the withdrawal of the toxic C19 injections,

One can’t help but wonder who the auditors of VAERS and EUDRA are, and how they answered the requirements for “complete and accurate” records of adverse events. Any auditor being paid any money at all for an audit of these adverse event reporting systems in the face of the massive scale of under-reporting needs to be asked some serious questions. I doubt that saying “we put a signpost in the middle of the desert saying “water, 10 miles that way>>>” is going to cut it.

Japan is encountering its NINTH C19 wave, though the lethality and whatever variant is circulating is not clear. “Drbeen” covers it here.

Japan Wave 9 - What's Going On? - YouTube

And The Japan Times here.

Concerns growing over COVID-19 surge in Japan this summer | The Japan Times

Flu in summer in Japan in one of the world’s most highly injected countries, who would have thought it possible!

Still no information on the interaction of C19 mRNA injections on other treatments for heart disease, cancer, diabetes, Alzheimer's, ADHD, PTSD etc.

Western Australia just published a report on adverse events from C19 mRNA injections for calendar year 2021. The State auditor only had nice things to say about the State government in November 2021.

WA's COVID-19 Vaccine Roll-out - Office of the Auditor General

20 months after that audit report we have the release of the 2021 adverse event report. Dr John Campbell covered the report in a 15 minute video here:

Bad Australian vaccine data - YouTube

Suffice to say, Dr Campbell is appalled at the rate of serious adverse events. Even without any adjustment for under-reporting (which will be AT LEAST 90% given the UK experience) the rate of adverse events is double that reported to VAERS – with many types of adverse event being more than sufficient to result in the withdrawal of the C19 mRNA injections.

On a side note, the C19 mRNA manufacturers have exemption from prosecution because of a state of emergency in the US – but – this same immunity does not apply anywhere else in the world.

Of course the smart and expensive lawyers employed by Pfizer and Moderna covered this in supply contracts like this one for Slovenia:

(100) 25 Page Pfizer contract to EU member state, Slovenia (substack.com)

(Fun fact: the Argentinian government pledged its air force bases to Pfizer to secure supplies of the toxic injections. What on earth would Pfizer want with those? Oh wait, Pfizer are a DoD sub-contractor, right?)

Key question – the contract allows Pfizer to vary the contents of the vials without notice AND confers no liability for any emerging harms. How can that possibly be legally authorized by any government or not challengeable by its legal system! “We will supply you with Zyklon C, (or D, E or F) but if any Zyklon version kills or maims anyone, now or in the future, that is your problem, not ours”.

The difference between that sort of contractual immunity and US EUA law? We know the answer – both are immoral, unethical and otherwise unjustifiable – except, PERHAPS, in law. You should not be able to get immunity from causing death and harm IN ADVANCE – and WITH INTENT!

DEVELO[ING AND ONGOING MASSIVE SCANDAL!!!!

A bombshell revelation that Pfizer and Moderna doses contained contaminants from shoddy manufacturing, was confirmed this week. Historically, the presence of the same contaminants resulted in the immediate withdrawal of injections that contained them.

See here:

Breaking: DNA plasmid contamination replicated by a USC Professor of Molecular Biology & Genetics and several others. (substack.com)

Followed up here:

Cancer-causing agent SV40 found in Pfizer Covid-19 Vaccine alongside DNA Contamination – The Expose (expose-news.com)

“The World Council for Health (“WCH”) stated that a red line has been crossed.  “DNA contamination of mRNA ‘vaccines’ poses a risk to everyone on the planet,” WCH said. “Replicable DNA, so-called plasmids, in both the monovalent and bivalent vaccines, which should not be there at all … We can only speculate how it will end, but what needs to happen today after the publication of the paper by McKernan et al (2023) is an immediate stop of the ‘covid-19 vaccine’ program.”

Any correlation between the contamination of monkey DNA in the injections and “monkey pox” is purely coincidental, of course!

A reminder of another bombshell from last week. “inject people with one version in clinical trials - use a different version in the roll-out to the world at large”.

Pfizer (and Moderna) Phase 3 clinical trials in 2020 used “ingredients” that were described as part of “Process 1” ny the manufacturers, These ingredients WERE NOT USED during the roll-out of injections to the general population.

The ingredients of the doses actually manufactured and rolled out, had different ingredients. The lethality of these different doses were subject to another smakker trial – described as “Process 2”.

The “Process 2” trial was conducted on a much smaller subset of people – just 250 aside in injected v placebo groups - compared to around 21,900 in the injected v placebo groups in the Process 1 (Phase 3) clinical trials of Pfizer.

See here for details:

Executive Summary of the FDA VRBPAC presentation on dsDNA contamination in mRNA vaccines (substack.com)

“A recent analysis of Pfizer's pivotal study (Levi and Guetzkow) found 1.5-3 fold higher rates of adverse events in patients after crossover and presumably receiving Process 2 material, compared with patients before crossover, presumably receiving Process 1 material.”

Question: the CDC/FDA were aware of these up to three times worse results and did nothing. The Phase 3 clinical trials had already FAILED the sole end point of preventing symptoms of C19 disease. The Process 2 results were far worse.

WHEN IS A PLACEBO NOT A PLACEBO?

The other major talking point about different coloured dots resulting in disproportionate harms remains bubbling away on a very hot plate. One of many questions asked “Were placebos used to “dilute” the frequency of an alarming number of adverse events for doses administered in Denmark”?

Testimony is required from the Danish authorities as to why, at least, the blue dot vials were extensively tested, found to be harmful and left “on the market”, whilst the yellow dots were not tested so thoroughly.

I like Dr Rose’s take here:

(100) Is the placebo story a distraction? - by Jessica Rose (substack.com)

Here is my take. The issue of placebos is concerning and goes all the way back to the clinical trials. Given the number of “Related Adverse Events” suffered by the placebo group in those Phase 3 Clinical Trials back in 2020, one can’t help but wonder if the placebo  actually had the other toxic components of the injections – such as PEG coating or were actually just saline. I don’t buy any “placebo” effect as those in the trial would have been conditioned to think they had a chance of being saved by the “miraculous” injections – and were unblinded after just 7 weeks anyway. “Related Adverse Events” were more than likely the result of getting the treatment injection, following unblinding, not any saline placebo injection.

Recall that the Pfizer Phase 3 clinical trial was terminated (unblinded) just 47 days into a 6 month trial scheduled to end in January 2021 – with the injections approved for EUA on 10 December 2020, more than 50 days prior to the scheduled completion date of the clinical trial. Don’t forget all the whistle blowers revealing the appalling standards within the clinical trial.

A detailed summary of the FAILED Phase 3 (Process 1) Pfizer clinical trials, with increased harms and deaths in the injected group v the placebo group is below:

The COVID-19 Inoculations - More Harm Than Good FINAL Video & Print (canadiancovidcarealliance.org)

Here is a case made that there was no pandemic.

2023-06-22 There Was No Pandemic essay - Denis Rancourt

Here is a hint of the relative lethality of the Oxford/AstraZeneca injection:

(100) EUDRA shows 4-5 times more deaths and adverse events reported per million doses for viral vector C19 "vaccines" compared to mRNA C19 "vaccines" - media silence continues (substack.com)

We have this table taken from EUDRA by VaccineImpact.com from a few months ago (prior to the VaccineImpact link above):

As you can see, Pfizer/BioNTech was the “safest” injection (cleanest dirty shirt). Moderna was worse and AstraZeneca was appalling, indicating why it has been withdrawn globally – except for countries like India. Russia had close ties to AstraZeneca when developing its Sputnik injection.

India has administered around 2 billion doses of the Oxford/AstraZeneca injection via a licensing agreement with the Serum Institute of India.

The numbers in the above table DO NOT adjust for any under-reporting.

Here is a table of the last five weeks of US C19 cases and deaths using data from here:

Odd, isn’t it. These cases are likely an over-reporting – or rather, over emphasis – of the significance of C19 in the US. During 2020-2021, a faulty RT-PCR test that could not distinguish between the flu and C19 probably over-reported by a factor of 40 – and the VAERS system probably under-reports by the same factor of 40.

Dominant variants are here: CDC COVID Data Tracker: Variant Proportions

Over the week, XBB 2.3 remained at 13.4% and EG.5 at 13.0%.

Note that XBB 1.5 variants make up around one fifth of the estimates of circulating variants. Guess what injection formulation the FDA is asking big pharma to concoct? You guessed it, a “treatment” for XBB 1.5.

XBB 1.16’s and 1.9’s already dominate along with the XBB 2.3 and EG.5 and will increasingly do so.

FDA VRBPAC Hopelessly Chasing Outgoing XBB.1.5 as Fall Target (substack.com)

“On June 16, the FDA announced that it had advised manufacturers planning to update their COVID-19 vaccines that they should specifically target XBB.1.5. Scientists from Moderna, Novavax, and Pfizer had told the FDA and its advisory committee that their XBB.1.5 monovalent vaccines could be ready to inject into arms by late July or early fall.”

You cannot fix stupid – or corrupt, captured and compromised.

Did I mention it was my birthday in two weeks?

Onwards!

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