Pharmacokinetic, not applicable – we have been lied to in deadly cold blood

We have been assured that after mRNA injection the genetic code only stays in the shoulder and degrades rapidly. The product label for mRNA injections [1]under pharmacokinetics says “not relevant”. It should be noted that mRNA injections are not vaccines. They trigger the production of a toxic spike protein by the genetic code in the cells themselves. [1]This is why pharmacokinetics is particularly important. We are told that it is not known, but the pharmacokinetics of mRNA injection is opened up in this article. It is known in the EMA papers and it the story is not pretty.

RNA in the vaccine breaks down rapidly in the body

It’s been a familiar phrase for three years now. Hanna Nohynek and Mika Rämet have [3]confirmed that the mRNA, or genetic code, in the injection stays locally in the shoulder and degrades rapidly in the body. Experts say that cells are harnessed locally in the shoulder to produce the transiently toxic pathogen, the SARS-CoV-2 spike protein, according to reports.

In the article “Does the vaccine label disclose all ingredients – The answer is NO!” (article in Finnish) published on 17 August 2021, an extensive analysis of what ingredients the mRNA injection contains has been done. All internet search engines were used to compile it and the pharmacokinetics paper was not found by the search engines at the time. It was already proven to be online at the time, but not accessible to search engines.

“ALC-0315 gamma radiation” Google search turns up European Medicines Agency document

I came across a study with a list of radioactive vaccines. According to it, SARS-CoV-2 spikes have a possible 25-50 kGy of gamma radiation. Western mRNA injections do not have inactivated pathogens. The carrier is ALC-0315 nanofibres. The Astra Zeneca needle uses a chimpanzee adenovirus as a carrier. I was looking for information on the possible gamma irradiation or irradiation of ALC-0315.

Source:Ionizing Radiation Technologies for Vaccine Development – A Mini Review

Is 25-50kGy a lot? The “Risks of Using Sterilization by Gamma Radiation: the Other Side of the Coin” article gives some indication.

A search on gamma radiation, however, brought up the European Medicines Agency’s [6]Assessment report” file, which I could not find a year ago despite my best efforts. It contains section 2.3.2. Pharmacokinetics!

The pharmacokinetics of mRNA injection contains information that everyone should have absolutely known before taking the injection! It has been blacked out!


For traditional vaccines, pharmacokinetics is always marked as “not relevant”. In a conventional vaccine, a small amount of the inactivated pathogen is injected into a human. It is like a small amount of poison to which the human reacts by forming antibodies to the poison. It does not multiply or penetrate the cell. Quite harmless in principle.

mRNA injection is not a vaccine

mRNA injection is by no means a traditional vaccine. A single injection contains billions of nanofibre particles, which in turn contain the genetic code of the messenger RNA. ALC-0315 is the actual transporter, containing the mRNA code. It carries the code inside the cell and triggers the production of the SARS-CoV-2 toxic pathogen in its own cells. It is absolutely essential to know how long and where the production of the toxin takes place. Do you agree?

How long does ALC-0315 in mRNA persist in the body according to the EMA file?

[6]Wistar Han rats were IV bolus injected with LNP formulated luciferase-encoding RNA at 1 mg/kg and ALC-0315 and ALC-0159 concentrations at 15,3 mg/kg and 1,96 mg/kg respectively. ALC-0315 and ALC-0159 levels in plasma, liver, urine and faeces were analysed by LC-MS/MS at different time-points up to 2-weeks.

ALC-0315 and ALC-0159 were rapidly cleared from plasma during the first 24 hours with an initial t½ of 1.62 and 1.72 h, respectively. 24 hours post-dosing, less than 1% of the maximum plasma concentrations remained. This means that the nanofat bound to cells and was no longer present in the bloodstream.

Following plasma clearance, the liver appears to be to major organ to which ALC-0315 and ALC-0159 distribute. The applicant has estimated the percent of dose distributed to the liver to be ~60% for ALC0315 and ~20% for ALC-0159.

For ALC-0315 (aminolipid), the maximum detected concentration in the liver (294 μg/g liver) was reached 3 hours after IV injection. ALC-0315 was eliminated slowly from the liver and after 2-weeks the concentration of ALC-0315 was still ~25% of the maximum concentration indicating that ALC-0315 would be eliminated from rat liver in approximately 6-weeks. BOOM!

This has been a concern!

The applicant (Pfizer) was asked to discuss the long half-life of ALC-0315 and its effect, discussion on the comparison with patisiran, as well as the impact on the boosts and post treatment contraception duration. The applicant considered that there were no non-clinical safety issues based on the repeat dose toxicity studies at doses (on a mg/kg basis) much greater than administered to humans; this was acceptable to the CHMP.

Which organs does it accumulate in?

When I previously did an article on the components of mRNA injection, I found a [7]Pfizer leaked document (now censored from the internet). However, it contained a table, which is the equivalent of the European Medicines Agency paper. There is an image of the table below. The organs to which ALC-0315 accumulates the most are highlighted.

The pdf file is commonly censored online, but can be found on the web archive.

Concerning the liver the concentration matches the EMA paper, although only at 48 hours. In the EMA paper, the dosing was intravenous, or IV, where the effect is more rapid because the substance is put directly into the venous circulation.

ALC-0315 nanofibre, or mRNA transporter, does not stay in the shoulder

This shows that mRNA injected into the shoulder accumulates in the organs at exactly the same concentrations as IV administration, only slightly slower.

Do you understand? The substance in an mRNA injection DOES NOT STAY LOCAL, but spreads to major organs and stays there for about six weeks!

It is quite clearly stated in this [6]EMA paper. This has been a CONCERN!

This is shocking!

Medical experts have assured us that the mRNA injection is only local and quickly disappears from the body. No. It accumulates in major organs and remains in the liver of a rat for an estimated six weeks. The rat is a master at handling and tolerating toxins. It has many times the DNA repair capacity of humans. Human pharmacokinetics have not been studied!

All the media “experts” like Rämet, Nohynek, Kiuru, Marin Lasse Lehto et al. have lied in cold blood! ALC-0315’s long half-life has been a CAUTION and they have known it for sure!

But mRNA is unstable!

On 27 December 2013, Stephane Bancel, CEO of Moderna, says that mRNA instability is no longer a problem. That problem has been solved. At this point, it’s worth remembering that [8]Moderna made the injection within two days of the SARS-CoV-2 genome was released. Is that warp speed or something even faster? No, it was ready.

Here we are – the circle closes

In the first article in the Injection Guide on 8 June 2021, the video above was posted. I thought it was very important and I hoped that one day someone would make a mistake. Now it has happened! The EMA paper proves that the mRNA carrier accumulates in major organs and wreaks havoc for at least six weeks after each injection.

What this could mean – six weeks of hits to the liver and major organs

After the vaccine, there has often been talk of brain fog, sticky thoughts and extreme fatigue. I’m sure everyone knows that. The table mentions the pituitary gland, where some (small amount of toxin) accumulates. The pituitary gland has no large blood vessels and therefore has a relatively small blood supply compared to the rest of the brain. The pituitary gland is mainly supplied by blood flow through small blood vessels (capillaries) and lymphatic vessels.

The main concern in the brain is the [9]capillary or hypophysis, which is rich in blood vessels and has the second highest blood circulation after the kidneys. The pineal gland is not protected by a blood barrier and will take quite a hit due to its massive blood supply after mRNA injection. Basically, after just a few minutes, the pineal gland in the centre of your forehead receives its share of mRNA carrier lipids.

The pineal gland is responsible for daily circadian rhythms and the functioning of the internal clock, and its function affects hormone production, stress levels and physical performance. It is important for intuitive thinking. [10]The French philosopher Renee Descartes called it “the seat of the soul”. The pineal gland naturally contains N,N-dimethyltryptamine, a molecular compound that has been a hallucinogen for millennia.

The function of the pineal gland affects thinking and mood. It also produces a hormone called melatonin, the amount of which affects the quality and length of sleep. So if you feel very tired after the shot, it is because the dose affects the pineal gland with the toxin.


It has been shown that the ALC-0315 transporter, which contains the mRNA code, accumulates in the liver and remains there for an estimated six weeks. The Swedish study “SARS-CoV-2 Spike Impairs DNA Damage Repair and Inhibits V(D)J Recombination In Vitro” in October 2021 was concerned about the effect of the spike protein on V(D)J recombination, or in short, the body’s ability to repair things like DNA damage.

The study has now been withdrawn for some reason, but it can be found in the [12]web archive. There is an article based on the study written by Injection Medicine. [11]

If there is production of a spike protein in the liver after an injection that prevents DNA repair, it means that the chance of cancer cells potentially increases.

Study showing mRNA becomes part of the genome in liver cells

The [13]Intracellular Reverse Transcription of Pfizer BioNTech COVID-19 mRNA Vaccine BNT162b2 In Vitro in Human Liver Cell Line” study published in February 2022 presents extremely disturbing conclusions.

Some [14]huh-7 (a type of liver cancer cell) were exposed to Pfizer’s mRNA injection.

Our study is the first in vitro study on the effect of COVID-19 mRNA vaccine BNT162b2 on human liver cell line. We present evidence on fast entry of BNT162b2 into the cells and subsequent intracellular reverse transcription of BNT162b2 mRNA into DNA.


This means that mRNA will turn into part of the genome if the conditions are right and suitable cancer hosts are available. If boosters are forced every four months and the transporter persists for about six weeks, it is likely that at some point this may happen.

I hope you understood the article

Everything I wrote can be found in the sources list, check them. So far I have said you should wait before you take the mRNA injection until more information is available.

Now I say don’t take it. Under no circumstances should you let your child take it. You must protect your child´s life so that no foreign genome of any animal is injected into your child. Whether it comes from a bat or a snake.

Share this writing if you know any child or parent of a child. Parents need to know and protect their children. We have been lied to in cold blood!

P.S. There’s a lot of stuff coming up. I’ll write more about them soon. They’re horrible, but you need to know about them. Pretty soon it will all start again with a multiple force. We must soon unite and take care of each other.



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[1] Comirnaty product information

[2] Pharmacokinetics

[3] Can the Covid vaccine cause infertility or cancer? Experts answer 19 claims about vaccines

[4] Ionizing Radiation Technologies for Vaccine Development – A Mini Review!po=27.8409

[5] Risks of Using Sterilization by Gamma Radiation: The Other Side of the Coin

[6] Assessment report

[7] Does the vaccine label reveal all the ingredients – The answer is NO!

[8] We Had the Vaccine the Whole Time

[9] Pineal gland

[10] Human pineal physiology and functional significance of melatonin

[11] Swedish study: possible adverse effects of spike protein on DNA repair and adaptive immunisation

[12] SARS-CoV-2 Spike Impairs DNA Damage Repair and Inhibits V(D)J Recombination In Vitro

[13] Intracellular Reverse Transcription of Pfizer BioNTech COVID-19 mRNA Vaccine BNT162b2 In Vitro in Human Liver Cell Line


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