The COVID experimental emergency medical countermeasures (EEMCs, as separate and distinct from pharmaceuticals) produced under the command and control of the US. of Defense (currently referred to as “COVID-19 vaccines) have caused more deaths and serious adverse events than any drug in the history of the pharmaceutical industry. Hundreds of thousands or even millions of people have likely died yet drug regulators (including the US FDA and the Australian Therapeutic Goods Administration, TGA) around the world continue to say they are “safe and efficacious” and usually produce only mild or only rare serious adverse effects (eg heart inflammation, blood clots, strokes, death etc)?
What allows the kabuki theatre to continue despite people of all ages, including children, dying in huge numbers since the introduction of the EEMCs? How can this go on any longer?
The trick has been to rely on passive, arbitrary, inefficient and corruptible post-marketing pharmacovigilance systems around the world to justify the claims of safety.
Normally, pharmaceuticals would be developed over maybe 7-10 years and during that time there are strict guidelines to determine the quality, safety and efficacy of new drugs. For any new drug many highly monitored and controlled clinical trials are necessary requiring enormous manpower, data analysis and reporting. Meticulous attention paid to any adverse event that might be associated with the research drug. Extensive investigation and follow up would be required to assess the probable association of the drug administration to the adverse event, its severity and implications. After all, drug companies want to avoid being sued for marketing unsafe drugs and this can cost billions of dollars. Pharmaceutical companies normally have considerable legal exposure.
But in the case of the EEMCs these are not defined legally as “pharmaceuticals” in the conventional sense of the word (in fact, they are not even “vaccines”) – they are EEMCs and are not required to be proven safe and effective nor are they required to meet the normal quality standards of pharmaceuticals. More importantly to the investors, there is absolutely no liability risk associated with EEMC under law.
Due to the rushed production of the EEMCs using many contractors operating under secret contracts, there was no time to adequately assess the safety of these serious injections before putting them to use. The overestimate of the treat of COVID, lack of safety the testing of the EEMCs and reckless use in healthy individuals including children, infants and even pregnant woman will go down in history as the greatest ever fraud perpetrated on the world. Without extensive and diligent highly monitored clinical trials, there is near total reliance upon various passive, ad-hoc and subjective adverse drug event reporting systems around the world to record the incidence of adverse reactions and death associated with the use of these EEMCs and to assess the probability that these EEMCs caused the adverse event or death.
Now, here comes the trick………Given that these EEMCs have caused more death and injury than any drug in history, how can the standing adverse drug reporting systems routinely used to record adverse events for all drugs be rigged to avoid reporting the catastrophic toll of the EEMCs? Easy. There are a number of ways:
- Install senior staff to manage these reporting systems with individuals who are connected or conflicted directly or indirectly with the vaccine industry or academic institutions which receive significant funding from Big Pharma and dedicated to the promotion of vaccines. The decisions on whether or not to ascribe causality of an adverse event to an EEMC can be left to the discretion of conflicted staff, perhaps a single unidentified person. Sometimes these staff members are ex-Big Pharma people.
- Slow the review of serious adverse events or deaths due to EEMCs to a crawl, claim poor resources to hire more staff or the need for training.
- Change definitions: eg define a person as “unvaccinated” within 14 days of injection. That way, if a person died suddenly and unexpectedly within the first few days of an injection (as they do), this death would be recorded as death of an “unvaccinated person”.
- Make it harder to generate statistics showing the EEMC caused the death by removing a data entry code to easily report a death or serious injury probably caused by the EEMC. The term “death” has also be removed in some reporting and replaced with “cardiac arrest” or something similar.
- Make the reporting of any adverse event by doctors and patients alike difficult eg no real person to answer questions by phone, long delays to answer phones or complicated forms to fill out which doctors are reluctant to complete due to time constraints.
- Ensuring there is no transparency, no critical assessment of the criteria for establishing the possible causal relationship of an adverse event with one of these EEMCs.
- Ensure, through draconian professional health regulations, that health professionals live in fear of retribution if they deviate from the government’s “safe” narrative on the EEMCs. It is widely known that any health professional who deviates from the government dogma may be subject to a professional investigation and possible loss of licence to practice. That should dampen the enthusiasm of health professionals from reporting.
- Doctors who now realise they have been misled by the so-called “health experts” and are now witnessing first hand the serious adverse effects and unexpected deaths of the vaccinated, are refusing to face reality and often gaslight their patients who return with serious injuries and refuse to submit legitimate adverse drug reaction incident reports for evaluation by the health authorities.
Undoubtedly, the adverse drug reaction reporting systems around the world (including VAERS, the Australian DAEN system, the British Yellow Card System and the Eudraviligance system) are broken and report or affirm only a tiny fraction of the deaths and serious adverse events which are caused by the EEMCs. It is the world’s greatest man-made disaster let alone the worst health policy disaster of all time.
If these last ditch safe-guard systems cannot be fixed with bias and vested interests removed, then any and all provisional approval and emergency use authorisation systems must cease to operate. There is no other way to keep us safe.
There is no justification now to claim the EEMCs are “safe”. They are not safe…They can be deadly.
The walls are closing in on those responsible and undoubtedly many minds in the halls of power are now turning to develop arguments and plans to extricate the so-called “health experts” and bureaucrats from the jaws of justice and pubic ridicule which inevitably will come as the body count mounts. The media will be essential for the cover up to succeed. Let’s see who is prepared to exhibit some integrity.
"drug companies want to avoid being sued for marketing unsafe drugs and this can cost billions of dollars." Their history shows that they really don't care how much they pay in fines, as long as they still turn a tidy profit on the drug, because regulators will continue to approve drugs produced by serially criminal pharmaceutical companies, and governments will continue to subsidise the cost of these drugs e.g. through the PBS. Their criminal behaviour is facilitated by the revolving door between pharma companies, regulatory bodies and other government entities.
Just as one example, it's now very well known that Merck knew that Vioxx was going to cause carnage, but their bean counters calculated that the drug would still be a great earner even after fines and compensation payouts (which turned out to be true), so they released it anyway. They then went on to unleash Gardasil on children and young adults, with not a prick of conscience (see A Midwestern Doctor's excellent write-up of this shameful behaviour, at https://rwmalonemd.substack.com/p/what-happens-to-vaccine-clinical).
Fines are just a cost of doing business to these psychopathic corporate entities.
The length of time it takes for drug/vaccine to be approved is irrelevant to its safety/effectiveness, as FDA approvals are based on feedback from criminal organizations, such as CDC & NIAID & fraudulent studies.
It was crucial for Trump to have vaccine available before "leaving" Office to prevent gov/globalists from locking down country until 2025. An extended lockdown would have destroyed America to point of no return & caused hundreds of millions of more deaths around world, in addition to deaths occurring today.
Trump's "vaccine" was harmless & created by DOD as countermeasure to globalist's plan to lock us down for years & destroy our country so they could usher in their New World Order. Although the Military Industrial complex is corrupt, there are many good Generals & Special Forces who took their oath to protect our Constitution seriously. That said, we've been under military occupancy since Trump took Office on January 20, 2017. Continuity Of Government (military COG) is currently taking place so that the global garbage can be taken out with as little civil unrest as possible. Biden 2.0 is a fake president - Part of COG - Elon Musk's name & Twitter account are being used by military to reveal truths to awaken people. This avoids appearance of hostile military takeover. Musk & Kevin McCarthy are part of COG.
Derek Johnson's website, TheDocuments.Info is great place to go to learn about what's really going on in our country.
Sorry this is so long - Just think it can bring people peace of mind.
When Trump said, "We caught them all" & "The best is yet to come", he meant it:)