Category: Analaytical Testing

People should know that PCR and PCR Tests are two completely different things. Dr. Mullis developed and worked with PCR and not PCR tests. The PCR test is an invention of medical or biology experts who do not know or understand testing science/chemistry. Hence, they created a fraudulent test, which has no value in detecting an unknown and imaginary virus. It is all fake and false.

One may explain the difference between PCR and PCR tests with an analogy. PCR is like a fermentation process. It cannot show if alcohol (ethanol) is produced. However, alcohol production in the broth is tested by an alcohol test or tester (PCR test).

A test can only be developed if the reference standard is available. An alcohol test or tester will be valid as its reference standard (alcohol) exists and is available. However, a PCR test is invalid because its reference standard (virus) is unavailable. The PCR test/testing is a fake and fraudulent concept and practice.

Laboratories would have been shut down, and people would have gone to jail if such practices had been done in science/chemistry (analytical) laboratories. Unfortunately, doctors and their science are protecting this fraudulent activity.

@ “Before widespread vaccines, disease killed nearly half of U.S. children under 5” (link)

The article, by a physician, is full of misinformation and false claims about science. Unfortunately, doctors do not study or are trained in science, so they make incorrect claims. For example;

@ “When a vaccine is developed, it is not immediately available to patients. It goes through many years of rigorous development before it is determined safe for human trials.”

Human or clinical trials are not science. It is a gross misunderstanding.

@ “Anyone can publish their opinion that is not based on science or expertise.”

This is true for physicians who do not study science and make false claims. Sorry! Doctors, please consider correcting your information and knowledge.


Clinical trials – misrepresentation of science (link)
COVID-19 Clinical trials: be watchful (link)
Understanding clinical trials and their outcomes – fake science at its best! (link).
Doctors Lie (link)  
Biology, Virology, Immunology, Medical Science, Etc. Cannot Be Considered Science Subjects (link)
The FDA Committee’s Review of Pfizer-BioNTech COVID-19 Vaccine: Unscientific, False and Deceitful (link).

Blog Article: Fake And False Science Of Illnesses And Diagnoses (link). FB (link). For convenience, questions are copied below the response.

Response:

@ “… is vacciantion build on the simmilar principle as homeopathy / administering a small doses of alleged poison to treat the illness/”

I have some knowledge and personal experience with homeopathy. Based on this, I would say that they are not similar. To me, they are as similar to comparing electric and gas-powered vehicles because they both require a (small) battery or electric power to start the car. So, they both could be considered electric-powered. However, they are very different in operation – there is no comparison.

Concerning “small doses/amount of alleged poison,” I do not think homeopathy injects poison. On the other hand, I am certain, based on what is available in the literature about vaccines, that they are not in small amounts (compared to homeopathic doses) but certainly significantly large amounts of filth/gunk (potentially poison). I would not suggest anyone take it, considering the science/chemistry aspect of it.

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Often, one hears such announcements, i.e., FDA approves, concerning drugs and drug products from the FDA and other similar regulatory authorities. People, including physicians, assume that the FDA independently evaluates the products and that the claims (safe and effective) are based on scientific studies or evidence.

Unfortunately, it is not true.

An approved drug product does not mean it is safe and effective, but it only means that it complies with the FDA requirements for putting its label or stamp for approval. In short, approval is for compliance mostly with arbitrary standards and requirements that do not reflect the products’ quality (by extension, safety and efficacy). Prove me wrong!

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I came across this article “Genetic tracing of market wildlife and viruses at the epicenter of the COVID-19 pandemic.” (link)

There are three at least issues with claims made:

  • Genetic virus tracing cannot be done because a virus has not been isolated and characterized. Therefore, the gene cannot be established or traced. The publication makes a false claim about the virus.
  • The virus cartoon in the abstract’s top left corner cannot be true because no sample of the isolated virus is currently available.

    As per the publication, “This study did not generate new unique reagents, but processed data generated for this study can be found in the supplementary files, and reconstructed genomes and phylogenies can be found at the data and code repository associated with this work.” No experimental work was done. But, computer-generated codes/” sequences” were used. Therefore, work was not done with the virus but with computing. (False claim about working with the virus)
  • The publication authors and institutions are related to medical and biological areas/subjects, not science, as commonly understood or implied. The publication may be understood as a science publication, which is incorrect. (link)

Therefore, I stamped it as certified BS’ (link)

medicine, healthcare and pharmacy concept – different pills and capsules of drugs

A drug dissolution test is a test used to establish the quality of a pharmaceutical product, such as a tablet or capsule. This test is conducted because the drug (often called active ingredient) needs to be released from the product for its absorption into the blood to elicit its therapeutic effect.

The test is conducted in place of a clinical test/study called bioavailability or bioequivalence, a pharmacology/pharmacokinetic study type. The test is the backbone of quality assessment of all tablet and capsule products. It is a requirement of worldwide authorities, including the FDA, Health Canada, etc., and pharmacopeias such as USP, BP, EP, etc.

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Pharmaceuticals/drugs/medicines are often pure (potent) chemicals that are nonphysiological and can be detrimental to normal body processes (reflected as adverse effects/reactions), as can natural products and ingredients, especially if taken in large amounts and for extended periods.

In general, allopathic drugs are developed and should be prescribed for their acute effect to minimize or avoid their serious effects. Further scientific research is needed to understand the mechanism of drug actions or interactions (good or bad) to address the harmful effects of drugs and, by extension, develop safe and efficacious medicines.

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