The question is: When medicines are approved to be safe and effective, why can’t they be sold like any other safe and effective product? Why are they placed behind the counter like tobacco products? Why does one have to pay a service fee to bring the medicines from behind the counter to the front of the counter? Why cannot they be sold through vending machines, online, or chemical stores (medicines being chemicals) and reviewed by users and independent, knowledgeable third parties?
They cannot be because everything associated with authorities’ approved (allopathic) medicines will go bankrupt in no time, as no substantiated and independent scientific evidence is available to support their claims of their quality (by extension, safety and efficacy). Authentication (valid scientific testing) is not part of the medicines development and manufacturing system.
I have been saying this for the past 20 years about pharmaceutical products such as tablets and capsules. mRNA vaccines are the current and the best-documented example of this fraud. Medicines are sold on an as-is basis – with priesthood-type claims, i.e., science has been done, viruses exist, and vaccines work. When the fact is – that no science has been done, the virus does not exist, and vaccines cannot work. Science, its training and practice, is not part of the medical and pharmaceutical professions and practice. The public and “experts” have been living with lies for the past some decades.
No wonder developers and manufacturers require strong legal protection/immunity from expected damages (“adverse effects”) as medicines/chemical products are developed primarily under the guidance and supervision of (medical and pharmaceutical) experts who lack the needed expertise in science/chemistry.
Auditing by independent third parties, such as those having analytical chemistry-based expertise, considering medicines are chemicals, is urgently needed (more).