HI ALL
WHILE JAN6’RS ROT IN SECRET AND OTHER JAILS, THE TRUTH OF WHAT HAPPENED IS OPPOSITE OF THE FORBIDEN ADMINISTRATION’S FINDINGS. IT HAS COME TO LIGHT THEY COVERED THAT UP TOO. THE PROBLEM HERE IS THAT IT IS NOT BEING RECOGNIZED BY THE COURTS. YET.
UNEARTHED JAN. 6 TRANSCRIPT COMPLETELY DEBUNKS HOUSE SELECT COMMITTEE’S NARRATIVE ABOUT TRUMP AND THE CAPITOL RIOT
In the final report of the House Select Committee to Investigate the January 6th attack on the United States Capitol, it claimed that it found no evidence supporting the idea that former President Donald Trump ordered 10,000 troops to be ready for Jan. 6, 2021. However, a previously hidden transcript has surfaced of an interview conducted by the U.S. House of Representatives panel that researched the breach of the U.S. Capitol that directly undermines the committee's claim.
https://www.newstarget.com/2024-03-21-j6-transcript-debunks-house-select-committees-claim.html
THE TRUTH CONTINUES TO COME OUT REGARDING COVID AND ITS PLANDEMIC WITH THE LEGAL SIDE TAKING FRONT AND CENTER STAGE.
MHRA, PFIZER AND UK OFFICIALS ACCUSED OF MISCONDUCT, FRAUD AND GROSS NEGLIGENT MANSLAUGHTER IN NEW CRIMINAL INVESTIGATION
On March 8, 2024, a new criminal investigation was launched against Pfizer, MHRA and UK officials. The investigating officer, Mark Sexton of the Acton Police Station in London, has charged UK officials with misconduct in public office, misfeasance in public office, fraud by false representation, corporate manslaughter and gross negligent manslaughter. Officer Sexton is backed by a team of lawyers, including Philip Hyland, Lois Bayliss and Dr. Sam White.
UK officials who mandated covid-19 “vaccines” charged for gross negligent manslaughter
Under crime number 6029679/21, the investigation specifically seeks to hold accountable a member of the British Parliament, Sir Graham Stuart Brady, and a British doctor, Dame June Munro Raine, who serves as the Chief Executive Officer of the UK’s Medicine and Healthcare products Regulatory Agency (MHRA). This investigation is part of a much larger investigation that Officer Sexton submitted back in 2021. Three years ago, Officer Sexton submitted 1100 pages of evidence to Hammersmith Criminal Investigation Department, which was signed off by two detectives.
https://www.newstarget.com/2024-03-22-mhra-pfizer-uk-officials-accused-misconduct-fraud.html
THE VERY LARGE EXPOSURE OF THE COVID PLANDEMIC AND THE DANGEROUS AND DEADLY VACCINES HAS COME TO ROOST IN THE SEAT OF THE DEEP STATE IN SWITZERLAND. THE HIGHLY RESPECTED CONSTITUTIONAL LAWYER PHILIPP KRUSE HAS FILED A CRIMINAL PROCEEDING AGAINST SWISSMEDIC, THE EQUIVALENT OF THE FDA. ALL SWISS WERE SUPPOSEDLY VACCINATED BASED ON THEIR RECOMMENDATIONS, AND DEATHS AND ADVERSE EVENTS SPIKED HORRIBLY. SWISSMEDIC DISREGARDED THE EVIDENCE AND CONTINUED PRESSURING ITS PEOPLE TO KEEP TAKING THE CLOT SHOT. THEY ARE IN VERY DEEP DOO DOO AND THE CRIMINAL FILING NOW IS SERVING AS A TEMPLATE FOR OTHERS TO PURSUE WITH THEIR COUNTRIES.
I INCLUDE MANY PAGES BELOW OF THE ACTION, AND THE FILING ITSELF IS 450 PAGES. FOR THOSE NOT PREDISPOSED TO GO TO THE NET TO READ THE SUMMARY, IT IS (IN PART) BELOW. IT IS COMPREHENSIVE.
CRIMINAL COMPLAINT VS. SWISSMEDIC/MRNA VAX
Swiss Lawyer Philipp Kruse provides a comprehensive summary of mRNA "vaccine" regulatory failures and lies
Robert W Malone MD, MS
Apr 02, 2024
On July 14, 2022, Philipp Kruse filed a carefully worded comprehensive legal complaint against the Swiss Regulatory authority known as Swissmedic for their role in enabling deployment of the COVID mRNA “vaccines” into the population of Switzerland. On 28 March 2024, the complaint was refiled with substantial updates and amendments. This complaint provides a comprehensive summary of the case against the official regulatory positions and activities promoted by Swissmedic, which closely parallel those taken by the US FDA, Health Canada, the European Medicines Agency and most other national regulatory authorities.
Swissmedic is the Swiss Agency for Therapeutic Products. More precisely, Swissmedic is the Swiss surveillance authority for medicines and medical devices, and is registered in Bern, Switzerland. Swissmedic fulfills a Swiss federal mission similar to the US HHS Food and Drug Agency (FDA).
Key complaints detailed in this filing include the following criminal acts, which appear to apply equally to many other national regulatory authorities:
Criminal acts performed by Swissmedic
Initial authorization that breaches the law and duties
Perpetuation of illegal authorizations that breach the law and duties
Disregard for all additional indications of risk
Absence of a "life-threatening or debilitating" disease
No benefits from ineffective to harmful mRNA injections
Omission of the most elementary safety and effectiveness tests
Swissmedic blocked effective alternative treatments
Benefit-risk analysis – Clearly a negative profile
Continuing despite an obviously negative benefit-risk ratio
No product monitoring proportionate to the risks
Misleading information not proportionate to the risks
Medical malpractice – lack of information, lack of reports
Swissmedic out of control and acting to the detriment of the state and the population
As summarized in his “X” bio (see image above and his academic CV which can be viewed here), Mr. Kruse is an experienced Swiss and International Law specialist. Having filed this legal complaint, he posted a PDF copy on “X” for download and review, promptly resulting in “X” designating his account “Temporarily Restricted” due to “unusual activity”.
UPDATE: Due to the censorship of the prior account, Philipp Kruse has now established a new “X” account at @KruseLawyer
I first met Mr. Kruse while visiting Stockholm to lecture on the COVIDcrisis and fifth generation warfare, and he told me of the legal case he was about to file in Switzerland regarding the governmental mismanagement of the response to COVID. Impressed with his knowledge of international law, I invited him to speak at the most recent Senator Johnson hearing in the US Senate regarding his understanding of the legal underpinnings of the proposed WHO pandemic treaty and International Health Regulation modifications. Below is a video of his brief testimony. As you can sense from the video, Mr. Kruse is a very meticulous, detail-oriented and fundamentally conservative (in the classical sense- cautious and non-flamboyant in demeanor and actions) Swiss attorney. He is committed to respect for human rights, but is certainly not a wild-eyed far-right radical. His positions are carefully researched and documented.
Mr. Kruse and his colleagues have addressed their reasons for taking these actions in a press release dated 24 March 2024.
Criminal complaint 2.0 against Swissmedic filed Zurich, 28 March 2024 –
In the name of and on behalf of six persons directly injured by mRNA vaccinations and for other persons, we hereby publish our criminal complaint against the Swiss regulatory authority Swissmedic and against vaccinating physicians ("Criminal complaint 2.0"), which has be filed on 7 February 2024 after comprehensive factual and legal updates, supplementation and clarification. This step became necessary because, since the first criminal complaint was filed on 14 July 2022, the legally relevant evidence had not only been fully confirmed in terms of the facts presented and the legal arguments, but had also been accentuated and aggravated in most cases. At the same time, the reported criminal activities were consistently continued by Swissmedic, without any sign of any constitutional correction on the part of the Swiss judiciary or the Swiss Parliament (Art. 169 et seq. Federal Constitution) - on the contrary: With the draft revision of the Epidemics Act, the Federal Council wants to further expand the current practice of emergency authorizations and the use of novel, experimental vaccines.
What's new?
Compared to the first version dated 14 July 2022, the criminal complaint 2.0 contains updated, supplemented and improved legally relevant evidence up to mid-2023 (in some cases beyond) and also comprehensively supplemented and clarified legal explanations, including with regard to
- Evidence that at no time was there a discernible threat to public health from SARSCoV-2 in the form of a debilitating or life-threatening disease within the meaning of Art. 9a para. 1 TPA;
- Evidence that available and long-established alternative prevention and treatment methods have been ignored by Swissmedic to date;
- Evidence that mRNA-based injections pose a particular risk to human health, especially that of children and adolescents (alarming mortality data and declining birth rates);
- Proof of the special experimental character of the mRNA-based preparations; - Evidence that a positive benefit/risk ratio of mRNA-based Covid-19 "vaccinations" was never proven;
- Extensive evidence that Swissmedic has consistently and permanently misled the entire population and Swiss key decision-makers regarding the actual risk content of mRNA preparations and the lack of evidence of a protective effect with regard to infection and transmission, which is why a criminal investigation into the offense of falsification of documents in office (Art. 317 SCC) can no longer be postponed.
Motive for new publication
As a consequence of the completion of our investigation since the end of 2021 (i.e. work by a larger team of both internal staff and a group of pro bono supporting scientists), there can no longer be any reasonable doubt that the risk to public health from mRNA substances, already sufficiently clearly demonstrated by the criminal complaint of 14 July 2022, is greater than that from SARS-CoV-2, and that this risk created by authorities continues to exist. For this reason, because Swissmedic is pursuing unperturbed it’s criminal behavior. Therefore, and because it is doing exactly the opposite of what Switzerland's highest authority for drug safety would be obliged to do by law, we feel compelled to make this criminal complaint 2.0 submitted on 7 February 2024 freely accessible to the public - and thus to all members of the Swiss Federal Assembly – ultimately to protect the public from high risk mRNA-based medicinal products and from misleading, deceptive information about the effective risk associated with the authorized mRNA-substances.
I suggest that the legal complaint which Mr. Kruse has compiled and submitted to Swiss legal authorities is the most comprehensive summary of the regulatory mismanagement and fraud which has taken place at virtually all western national regulatory authorities during the push for mandatory deployment and uptake of the COVID mRNA “vaccines”, and can serve as a template for both other complaints as well as expert witness testimony. Furthermore, I am struck by the parallels between the actions of the Swiss national regulatory authority, the US FDA/CDC, and virtually all other western national regulatory authorities. This strongly suggests close communication and/or collusion among these agencies and their political and bureaucratic State managers during the COVIDcrisis.
With that in mind, I have included key sections from the executive summary of the complaint below. A PDF copy of the full executive summary can be found here (independent archive) and here, and the press release together with both the summary and the full 450 page complaint document can be found here.
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SWISSMEDIC CRIMINAL CLAIM – "EXECUTIVE SUMMARY" (2.0)
(redacted for general legibility)
"All things are poison, and nothing is without poison; it is but the dosage that makes a thing not poison."
(Paracelsus [1493-1541], Swiss physician, alchemist and philosopher)
"Any person handling therapeutic products must take all measures necessary according to the state of the art to ensure that human or animal health is not endangered."
(Art. 3, Federal Act on Medicinal Products and Medical Devices, Therapeutic Products Act, TPA).
Suspicion
In the present case, we are dealing with the greatest danger to and violation of human health caused by medicinal products themselves and by misinformation from public officials in this regard that has ever occurred in the history of Switzerland. The mRNA "vaccines" against SARS-CoV-2 infections, which are largely ineffective and pose an above-average risk to human health, have been proven to pose a far greater threat to the healthy population than the SARS-CoV-2 pathogen itself, against which these "vaccines" were supposed to protect.
Swissmedic, or the persons acting on its behalf, are primarily responsible for the violation of human health already caused by mRNA-based substances and for the ensuing threat.
By law, Swissmedic is tasked with protecting the health of the Swiss population against ineffective or harmful medicinal products. According to the Swiss Therapeutic Products Act (TPA), it is obliged, on the one hand, to ensure that only high-quality, safe and effective therapeutic products are placed on the market. On the other hand, it must protect consumers of therapeutic products against fraud in this context (Art. 1 TPA). Other clear legal obligations as well as these were repeatedly and significantly not fulfilled by those acting on behalf of Swissmedic to the detriment of the injured persons making a report, which is why they have been under urgent suspicion from December 2020 until today.
• given that they, in the context of authorization, manufacture and batch testing and import, repeatedly breached the due diligence requirements under therapeutic products law.
• by granting a "temporary" marketing authorization for various mRNA-based preparations reserved only for special emergency situations in accordance with Art. 9a TPA for various mRNA-based preparations without need, maintaining them permanently and extending their scope of application to all age groups, although it was already adequately proven at the time of the initial authorization that a COVID-19 infection was neither "life-threatening" nor "debilitating" for the healthy population under 65 years of age within the meaning of the Therapeutic Products Act (and that even for those over 65 years of age a conspicuous mortality rate could only be established during short phases in 2020 – albeit without any evidence of a causal link with SARS-CoV-2
• by granting this de facto emergency authorization under Art. 9a TPA without actual need, maintaining this de facto emergency authorization permanently and extending its scope of application to all age groups, although suitable alternative treatment protocols were already available in the course of 2020 (N 1104 ff.),
• by granting – within the meaning of the TPA – the authorization of the mRNA "vaccines" under "temporary authorizations" in accordance with Art. 9a TPA despite the lack of sufficient proof of effectiveness, despite massive indications of risk and despite the absence of a life-threatening or debilitating disease for the population as a whole,
• by massively undercutting the already very low safety requirements applicable to the procedure under Art. 9a TPA, outside of the scope of their dutiful discretion instead of respecting the mandatory and otherwise usual requirements of the ordinary authorization procedure under the guise of "pandemic authorizations", thereby creating additional risks to public health that had never before been posed by a medicinal product,
• by, instead of carrying out a comprehensive risk-benefit analysis (N 807 ff.) and immediately revoking the authorizations or at least allowing the granted authorizations to expire, renewing their decision to act at the end of 2022 (i.e. having long since been against their better judgement) and perpetuating the new, still experimental mRNA therapy/prophylaxis from 2023 in the sole interest of the manufacturers as a new platform for broad-based use by means of allegedly "ordinary" authorizations,
• by not only permanently withholding key information from the public and the medical profession on the minimal to non-existent protective effect of the mRNA "vaccines" and on the actual risks of side effects, but also by permanently and systematically disseminating misleading information on these issues,
• of having failed to fulfill the obligation to monitor the product after marketing authorization (so-called "pharmacovigilance") in a manner that was proportionate to the risks involved, and instead seriously and permanently violated the obligation to provide notification of side effects under therapeutic product law (Art. 87 para. 1 lit. c TPA),
• of having seriously violated the prohibition on the advertising of medicinal products under therapeutic product law (Art. 87 para. 1 lit. b TPA),
• of having fulfilled the relevant elements of the Criminal Code ( N 1457 ff.) with respect to the undesirable side effects (death, damage to health) that were foreseeable from the authorization studies and then occurred after authorization,
• of having knowingly and persistently misled both the public and medical professionals in a criminal manner about facts that are essential for the risk-benefit assessment when making a vaccination decision (in particular: forgery of a document by a public official, Art. 317 SCC, N 1198 ff., 1427 ff.; see also ER N 1964 et seq., in particular).
Criminal acts performed by Swissmedic
Initial authorization that breaches the law and duties
The breaches of the law and duty of due diligence objected to here essentially consist of the fact that the authorized persons acting on behalf of Swissmedic provisionally authorized mRNA medicinal products for preventive purposes "on a temporary basis" within the meaning of Art. 9a TPA, although Swissmedic must have been aware of countless risk factors as early as December 2020, each of which would have individually stood in the way of granting a "temporary" authorization until the corresponding risk factors had been thoroughly clarified and eliminated under normal circumstances. The following should be emphasized at this point (for information on many other risk factors, see N 1291 ff.):
• The mRNA COVID-19 vaccines are based on the same mode of action as gene therapies and have therefore been categorized by regulators such as Swissmedic and the European Medicine Agency (EMA) as well as by the manufacturers themselves as an "Advance Therapy Medicinal Product" (ATMP), which poses a particular risk for the following reasons:
Until the end of 2020, mRNA technology had only been used in cancer patients at the pre-mortem stage, i.e. only to combat an existing life-threatening disease, but
had never before been used purely prophylactically to immunize an entire healthy
population (N 186 ff.; ER N 62, N 67 ff.). Compared to all other medicinal products
that have been authorized to date, either on an ordinary or "temporary" basis, the
authorization of this mRNA technology as an alleged "vaccine" for healthy people is completely unprecedented and therefore represents a considerable risk.
The mRNA technology used here is characterized by the fact that the production
process of the actual immunizing active substance (active pharmaceutical ingredient = the spike protein) is transferred into the human body. The end product of this internal "vaccine production" is completely unknown in terms of dosage and quality. To date, there is still not sufficient empirical data available to show that the body's own production of the spike protein can be controlled: (1) quantity of endogenous production; (2) duration of spike production; (3) location of production in the body (affected organs; (4) quality of the proteins produced; and with regard to (5) effectiveness and safety of the active substance produced for a healthy population treated purely prophylactically. The administration of a substance that proves to be uncontrollable with regard to all pharmaceutically relevant parameters must by definition be deemed an experiment on humans.
Both the Federal Office for the Environment and Swissmedic were aware of the particular problems associated with mRNA substances and recognized that these mRNA active substances are gene-modified organisms
(GMOs/GMMOs) and Advanced Therapy Medicinal Products (ATMPs). In doing
so, they implicitly recognized that both the Gene Technology Act must be observed and that, above all, the authorization of these products following the simplified authorization procedure would have been ruled out.
• In addition, Swissmedic abandoned the requirements for a standardized dosage of the (mRNA) preparations authorized for injection that are otherwise mandatory for all other medicinal products. For example, Swissmedic accepted an mRNA content per dosage in an arbitrarily wide range of 37% – 126% of the amount of active substance formally declared by the manufacturer, disregarding the most basic standards. Swissmedic thus accepted the corresponding risks of a high proportion of non-intact mRNA and a considerable risk of genotoxicity and carcinogenicity. The same applies to other toxic impurities such as nitrosamine and benzene.
• The manufacturing process for the mRNA products actually administered ("manufacturing process 2" with plasmid DNA) differed fundamentally from the manufacturing process used for the products authorized by Swissmedic ("manufacturing process 1") and the general public only became aware of this at the end of 2023 (while Swissmedic had known since the end of 2020). The products administered from manufacturing process 2 show a scandalously high level of bacterial self-replicating DNA impurities (so-called "plasmids"), such that all products made according to manufacturing process 2 should be regarded as "never authorized" as a consequence. However, Swissmedic tolerated this additional massive risk factor without informing the public and without suspending the mRNA authorizations.
• Initial animal studies – a mandatory prerequisite for clinical phase 2 and 3 trials and a key safety element – had not been carried out by the manufacturers at all or not to a sufficient extent, but they already showed disquieting results, for example with regard to the accumulation of toxic lipid nanoparticles.
• The subsequent studies on humans, on the basis of which the "temporary" authorizations were granted at the end of 2020, had only run for two months (instead of the usual 12–24 months) and were then de facto discontinued by the manufacturers by disbanding the control groups and were largely stripped of their medium and long-term significance.
Despite this alarming initial situation from a safety perspective, within the meaning of Art. 1 and Art. 3 of the Therapeutic Products Act, and despite numerous other circumstances that increased the risk, the first authorization of the mRNA "vaccines" was well and truly rushed through by Swissmedic. The applications for authorization were "reviewed" and approved in just 63 calendar days (an ordinary procedure would take 330 days, a procedure for "temporary" authorization usually takes 140 days), whereby important, mandatory, milestones were simply omitted.
As a result, these "temporary" authorizations within the meaning of Art. 9a TPA mean in actual fact that the entire Swiss population participated without their knowledge in the riskiest and largest clinical experiment ever to be conducted in Switzerland (and, by extension, the whole world). And this experiment has not been terminated to date (regarding the experimental character N 843 ff.).
Perpetuation of illegal authorizations that breach the law and duties
Disregard for all additional indications of risk
Without adequately addressing this immense risk created by Swissmedic itself (through the "temporary" authorization) and without at the very least informing the public of all the risks, Swissmedic proceeded unperturbed in June 2021 to extend its authorizations to adolescents aged 12 and over. This occurred although, in addition to all the other facts up to mid-June 2021 which increased the risk and were therefore legally relevant, it was known
• that regulatory authorities such as Swissmedic were flying completely blind due to a lack of strict batch testing and thus a lack of sufficient quality controls,
• that the dose authorized for adolescents was two times (Comirnaty) or five times (Spikevax) higher than the recommended dose, meaning that Swissmedic accepted an additional and again completely unnecessary risk among adolescents, an age group that was at no time seriously at risk during the pandemic year 2020 – i.e. just from COVID-19 without having been "vaccinated",
• that according to Pfizer's Post Marketing Pharmacovigilance Report, a total of 42,086 side effects and over 1,200 deaths had been reported for Comirnaty alone by February 2021 – i.e. within two and a half months, which should have led to the immediate termination of the trial,
• that according to this damning Pfizer report, as many as 13% of breastfed infants were affected by side effects and even Pfizer had identified a negative impact on male fertility as a potential risk,
• that, according to global adverse event reports, the alarm threshold of 50 deaths had already been exceeded by a factor of 150 by June 2021,
• that the COVID-19 "vaccines" had already proven in May 2021 to be significantly more dangerous than the flu, swine flu and measles vaccines– that were commonly administered up to that point – in view of the large numbers of adverse event reports.
Even these scandalous alarm bells did not prompt Swissmedic to seriously question the wrong path it had taken. Swissmedic neither limited the number of authorizations nor informed the public about the risks identified. Swissmedic did not even feel compelled to improve its own purely passive pharmacovigilance by recording the side effects identified in Switzerland. Instead, at the end of 2021, Swissmedic took the step of extending the authorizations to a third dose ("booster") and to children aged five and over, even though this youngest age group was not seriously at risk at any time during the pandemic year 2020 – i.e. from COVID-19 alone without having been "vaccinated" – and although by this point among other things (for information about many other risk factors) it was also known,
• that even representatives of the pharmaceutical industry were openly describing mRNA injections as what they really are – a form of gene therapy,
• that the toxic spike protein produced in the body of the vaccinated person is present in the body for much longer and in a much higher concentration than originally stated by Swissmedic and the manufacturers, which can lead to a number of serious side effects (including death),
• that data had been falsified and risk signals concealed in the context of the Comirnaty authorization study (Pfizer/BioNTech) (N 397 ff.), which should have led to the immediate withdrawal of the study,
• that Pfizer/BioNTech had presented an alarming interim report (PSUR) at the end of August 2021, according to which 46 cases had ended fatally in the clinical trials and 5,069 cases (1.6%) had already ended fatally in the so-called "postmarketing phase", which under normal circumstances should have led to an immediate revocationof the marketing authorizations,
• that Pfizer had delivered 7 batches with a massively increased number of adverse event reports to Switzerland – an alarm bell that should have led Swissmedic to immediately warn the population and even to recall the batches, but this has not yet happened,
• that at least 60 deaths were recorded of children in Switzerland, the EU and the USA for Comirnaty and Spikevax alone (N 438 f.), which means that the absolute alarm threshold of 50 deaths was clearly exceeded in this target group alone, which is in no way at risk from SARS-CoV-2, which should have led to the immediate suspension of this authorization extension at least, if not the suspension of all mRNA authorizations,
• that more than 2,000 premature births and stillbirths following mRNA injections had already been reported in the USA and the EU alone,
• that a worrying trend was already evident in Switzerland in 2021, namely a conspicuous and persistent death rate in younger age groups a short time after "vaccination activity",
• that the mRNA "vaccines" (Comirnaty and Spikevax) had received 60 times as many reports of serious side effects and 20 times as many reports of deaths per million doses administered in comparison with the influenza vaccines by the end of 2021.
Instead of finally suspending the mRNA authorizations, carrying out an in-depth analysis of the decisions taken, telling the public the truth about the risks that can actually be identified and improving the reporting system for recording vaccination side effects in line with these risks, Swissmedic continued to maintain all "temporary" authorizations in 2022. This occurred although, in addition to all the existing facts with risk and legal relevance (for information on many other risk factors, see N 1311), it was known
• that mRNA products belong to the group of ATMP high-risk products because "they contain nucleic acid, regulate gene expression and, as 'biologically active material' (i.e. RNA), are treated in the same way as genetically modified organisms (GMOs)", which even Swissmedic recognized,
• that for this reason alone and also in accordance with Art. 12 para. 5 lit. c and lit. e of the Ordinance of the Swiss Agency for Therapeutic Products on the Simplified Authorization of Medicinal Products and the Authorization of Medicinal Products in the Notification Procedure (Verordnung des Schweizerischen Heilmittelinstituts über die vereinfachte Zulassung von Arzneimitteln und die Zulassung von Arzneimitteln im Meldeverfahren; VAZV, SR 812.212.23), a temporary authorization under Art. 9a TPA was unlawful from the outset (see 530, N 916 ff., N 992 ff.),
• that almost four million adverse reactions to all COVID "vaccines" had already been reported worldwide (Switzerland, EU, USA) by May 2022 (N 538 ff.), with Comirnaty and Spikevax alone accounting for over 1.7 million reports, including 464,971 serious adverse reactions and 20,886 deaths (N 548 ff.), exceeding the alarm threshold of 50 deaths worldwide over 400 times at that time, and that these figures continued to rise,
• that an alarming interim report on Comirnaty had once again been published by Pfizer/BioNTech ("PSUR No. 3"), from which it emerged
that under 50-year-olds were excessively subject to side effects, i.e. a population group only minimally affected by COVID-19,
that guidance on the safe use of Comirnaty for pregnant women, breastfeeding
mothers and other patient groups was still lacking,
that there had been massive differences in quality between the individual batches
and that many dangerous batches had once again been delivered to Switzerland,
• that despite Swissmedic's statements that the mRNA "vaccines" had no effect on pregnancy, there were reports, without taking underreporting into account, of 2,135 stillbirths after vaccination with Comirnaty and 798 stillbirths after vaccination with Spikevax as well as 5,055 miscarriages after all COVID-19 "vaccines" by May 2022 in the EU and the USA alone, with the manufacturers still openly admitting in 2022 that, due to a lack of corresponding studies, "the safety profile of the vaccine in pregnant or breastfeeding women is not known",
• that there was a historic decline in live births amounting to 8.5% across the world and also across Switzerland in 2022, for which mRNA injections remain the only plausible cause after excluding all other hypotheses,
• that, according to a study on male fertility published in June 2022, sperm concentration 150 days after the second "vaccination" was still 15.9% below the initial value, which means that not only female fertility but also male fertility might be significantly negatively affected by the "vaccination",
• that an in-depth analysis of the FSO data by Professor Konstantin Beck revealed a conspicuous and persistent mortality rate in all age groups a short time after "vaccination activity",
• that based on the FSO data in Switzerland, there has been a significant increase in a wide variety of disease diagnoses, especially within age groups not threatened by COVID-19 in any way (damage to the nervous system: +29%; cancer diagnoses: +48%; pregnancy complications: +25%; pulmonary embolism, cardiac arrest, stroke and cerebral infarction in 0 to 14-year-olds: +125%) since the start of the "vaccination campaign",
• that, according to several autopsy results, the "vaccine" spike protein was proven to be the cause of death and that, contrary to Swissmedic's official statements, it is not only detectable in the human body for a short time, but for up to nine months,
• that the occurrence of myocarditis in connection with a COVID-19 mRNA injection, which can be fatal in the worst cases, is, according to a study from Basel that has now been peer-reviewed, much more frequent and up to 800 times more frequent than officially reported by the regulatory authorities (N 674 ff.),
• that with VAIDS , a serious side effect that has been suspected to exist for a long time and has been increasingly recognized since 2022 has become apparent, which constitutes damage to the immune system, which can lead not only to an increased onset of autoimmune diseases and cancer, but above all to an increased onset of infectious diseases – and, in particular, also to a greater susceptibility to COVID-19 infections ("Long COVID"),
• that by 1 March 2022, at least 128 peer-reviewed publications on heart problems, 216 peer-reviewed publications on life-threatening coagulation disorders (thromboses, etc.) and six peer-reviewed publications on possible deaths as a result of COVID vaccinations have been published.
With the "temporary" authorization of the mRNA "vaccines", Swissmedic therefore accepted an unprecedented and steadily increasing risk to public health. At best, this could only have been justified by the fact that it could have averted an unprecedented threat (from SARS-CoV-2) and in doing so outweighed the exceptionally high risk associated with the mRNA "vaccines". This is clearly not the case.
Absence of a "life-threatening or debilitating" disease
"COVID-19" is not and has never been a "life-threatening or debilitating" disease that threatens the public at large, this being the key prerequisite for the "temporary" authorization.
With an infection fatality ratio (IFR) of 0.15%–0.20%, COVID-19 was already discernibly no more dangerous than moderate influenza at the end of 2020; there was no historically conspicuous excess mortality in relation to the overall population and hospitals were never overcrowded.
• Even in 2021, when the vaccination was rolled out on a large scale, there was no historical excess mortality according to the official FSO methodology (N 774), the hospitals never reached over 80% capacity and "Delta" was a variant that corresponded to a normal mild case of influenza in terms of the danger it posed.
• In 2022, it was obvious that COVID-19 was not the "pandemic of the century", that despite the massive manipulation of the COVID "case numbers" in hospitals which was made public, the health care system was never overloaded, and that the IFR for "Omicron" was only 0.001–0.002%, i.e. at least 50 times lower than the IFR for normal influenza.
No benefits from ineffective to harmful mRNA injections
In view of the above, Swissmedic authorized a highly experimental and dangerous medicinal product to prevent a disease that poses no greater threat to the population as a whole than influenza does. The only remaining "lifeline" for Swissmedic would therefore be to prove that the target group comprising older and previously ill people, who were initially at somewhat higher risk, had at least been protected against SARS-CoV-2 in a reasonably effective manner. But this is also far from being the case. The "vaccination" clearly failed to achieve the "high" levels of effectiveness required by the end of 2020:
• The "vaccinations" should have protected against serious (fatal or debilitating) diseases. However, the authorization studies (still ongoing, but without the control group) primarily investigated whether the "vaccinations" protect against headaches, coughing, suffering a fever and other trivial side effects in combination with a positive PCR test result.
• Up to 100% of the reported figures on the effectiveness relate only to such minor side effects and are based on calculations that in no way reflect reality. Instead, one can assume that the effectiveness comes in at a low, single digit percentage, if at all.
• Not a single study has even come close to proving that it offers protection against serious illness. The few cases analyzed fall within the range of statistical chance.
• "Vaccinations", however, would have had to "immunize" for the long term, which was not an achievable goal given the "booster vaccinations" that were planned from the outset.
• The "vaccinations" undoubtedly offered no protection against the transmission of SARSCoV-2 either and were therefore simply unsuitable for "pandemic control".
In 2021 and 2022, this lack of effectiveness manifested itself in an obvious way:
• In February 2021, there were already signs that the mRNA injections were largely
ineffective because the most common side effects included the "vaccination" being ineffective and contracting the COVID disease itself.
• To date, no effective proof of effectiveness for immunization has been provided by the manufacturers, nor has protection against transmission been proven in any way.
• With regard to the "booster", a negative effect was observed early on, as the transmission time was not shortened but extended.
• There has also been an increased number of cases of illness and death worldwide, which correlates with the start of the "vaccination campaign" in 2021 (and not with the start of the "pandemic" in 2020), which clearly indicates that the mRNA injections were not effective.
Omission of the most elementary safety and effectiveness tests
To make matters worse, Swissmedic had not based its decision on the strictest legal requirements for the ordinary authorization of medicinal products, but had allegedly issued "temporary authorizations" in accordance with Art. 9a TPA. However, under the guise of an alleged "pandemic", Swissmedic had undermined even the minimum requirements of Art. 9a TPA. The "pandemic authorization" of the mRNA "vaccines" granted in the case at hand deviates from the ordinary authorization in all key safety aspects in a way that increases the risk, and even falls below the authorization hurdles of the simplified and temporary authorization.
Accordingly, the authorization of the mRNA "vaccines" was accompanied by a blatant omission of the most elementary safety and effectiveness tests, thus posing the greatest of possible risk to the health of the Swiss population.
Swissmedic blocked effective alternative treatments
Another complication is that Swissmedic has not yet authorized more effective and less harmful treatments that have been known about for a long time, such as treatment with Ivermectin or other suitable approaches for the treatment of COVID- 19. In doing so, Swissmedic has deliberately sidelined the authorization requirement of a lack of alternative treatment methods (see Art. 9a para. 1 lit. c TPA) and thus actively blocked demonstrably more effective protection against COVID-19 (than the mRNA "vaccinations").
Benefit-risk analysis – Clearly a negative profile
Any serious analysis carried out in accordance with the law and common practice to determine the net benefit of mRNA-based COVID-19 vaccines for the entire population would have had to take into account at the end of 2020 and in the following years the verifiable facts summarized above and presented in detail in the evidence report. Such an analysis would obviously have shown that Swissmedic had authorized a medicinal product on the Swiss market with a devastatingly negative benefit-risk profile (see also Benefit- risk analysis: N 807 ff.; ER N 1835 ff.):19 Swissmedic's plan to authorize the mRNA "vaccines" for all adults in Switzerland from December 2020 must be seen as an experimental project posing a significant, unprecedented risk. At the same time, it was clear from the outset that the mRNA "vaccines" were not effective – a fact that has become increasingly evident over time. An unprecedented risk, which has since already demonstrated its impact in the form of a large number of serious side effects, was and is therefore not offset by any proven benefit. This consideration alone should have long since led to the compelling conclusion that the mRNA "vaccines" should never have been authorized and that the authorizations that were nevertheless granted represent a massive breach of the law and of due diligence on the part of Swissmedic.
New risks created by Swissmedic: maximum….
https://rwmalonemd.substack.com/p/criminal-complaint-vs-swissmedicmrna
THERE ARE MANY MORE PAGES, AND THOSE WITH LEGAL BACKGROUNDS WILL APPRECIATE IT. IT IS SO WELL PUT TOGETHER AND DOES NOT MISS A THING.
MEANWHILE, PRICES ARE GOING UP AND THE BRIDGE DESTRUCTION IN BALTIMORE WILL NOT BE TRULY INVESTIGATED. WHY? BECAUSE BIDEN HAS SAID THAT THE GOVERNMENT WILL PAY FOR IT ALL. WHY? BECAUSE IF THE GOVERNMENT PAYS FOR IT ALL, THE INSURANCE COMPANY WILL NOT HAVE TO INVESTIGATE OR TAKE SAMPLES OF THERMITE CONTAMINATED STEEL. THE DEMOLITION WILL BE COVERED UP. THAT IS WHY BIDEN WENT IMMEDIATELY ON THE AIR AND TOLD EVERYBODY HE WILL PAY FOR IT FROM TAXPAYER’S POCKETS, INSTEAD OF THE INSURANCE COMPANY.
FROM 9/11 TO BLOWING UP FOOD FACILITIES TO THE BRIDGE, THE ADMINISTRATION OF THE DEEP STATE HAS DONE WELL TO BAMBOOZLE EVERYONE INTO THINKING THE OPPOSITE OF WHAT HAPPENED. NICE PEOPLE. MAYBE WE WILL HAVE A BRIDGE VACCINE AVAILABLE TO PREVENT FUTURE BRIDGE COLLAPSES. I BET THERE WOULD BE SOME THAT WOULD GO FOR IT.
BE SAFE BE WELL.
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LOVE AND LIGHT
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ZAP
APRIL 3, 2024
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