Now that Big Pharma can get rapid Emergency Use Authorisation or Provisional Approval or Conditional Approval (whatever you like to call it) without the need to generate the usual safety and efficacy data which usually takes many years and billions of dollars for full approval……the flood gates are open.
In the past, countries had various mechanisms whereby, on a limited basis a company could distribute very limited supplies of drugs under development for any particular individual named patient suffering from life threatening or seriously disabling conditions if it was thought the benefit might outweigh the risk. But these experimental drugs could not be sold. Australia has such a scheme and it is called the Special Access Scheme.
But since 2018 with the new Provisional Approval system, drugs under development such as the COVID so-called “vaccines” could be sold at huge profits without the need to produce the usual safety and efficacy data costing billions of dollars. Moreover, they could be sold to everybody. It is a marketing goldmine. Not only that, it has become easy to hide the serious adverse effects by simply waving away the avalanche of serious adverse effects reported following vaccination by simply claiming there is insufficient evidence to establish a cause-effect relationship. These cause-effect assessments are done largely in secret with only limited information being reported by unnamed individuals who often have connections with the Pharma industry in one way or another.
If you think the COVID “vaccine” nightmare is ending, have a read of Robert Malone’s Substack (he was a prime inventor of the mRNA technology) CLICK HERE. You will see there is a truckload of mRNA therapies in the pipeline waiting for you.
And….The dirty little secret has been out for months……..Pfizer and Moderna do not own the COVID “vaccines”……You would know from my previous Substacks and published papers that the real owner is the US Dept. of Defense. This is not in dispute. This explains why the usual safety testing was not done and such safety testing was deemed unnecessary. It also accounts for the lack of critical appraisal by our drug regulatory agency, the TGA. The drug evaluation process was all theatre.
And…. to our Australian Chief Health Officers who probably rarely, if ever, see a real patient, they should listen to the world’s most published cardiologist, Dr. Peter McCullough, who treats lots of patients when he says myocarditis in children has jumped from 4 per million to 25,000 per million! This estimate is based on an extrapolation of a prospective clinical trial of myocarditis in adolescents conducted in Thailand. I have previously reported on this study in my Substack. I urge my new subscribers to go back and read some of these Substacks.
We have clowns advising us - not “health experts. CLICK HERE.
No, clowns entertain us with skills and buffoonery.
The health experts are buffoon's, but of the malignant kind.
This insanity needs to stop. Patients health and safety is paramount. It is clear that there are some in the pharmaceutical industry with self-serving and nefarious puropses. Unfortunately, these people make it more difficult for others.