Video Interview: https://youtu.be/-2YXPmu-dBk
References Mentioned in this Episode:
-The Nuremberg Code
“The voluntary consent of the human subject is absolutely essential. This means that the person involved should have the legal capacity to give consent; should be so situated as to be able to exercise free power of choice, without the intervention of any element of force, fraud, deceit, duress, overreaching, or another ulterior form of constraint or coercion; and should have sufficient knowledge and comprehension of the elements of the subject matter involved as to enable him to make an understanding and enlightened decision.”
-Moderna FDA Letter of Authorization
“It is an investigational vaccine not licensed for any indication.”
“it is reasonable to believe that Moderna COVID‑19 Vaccine may be effective in preventing COVID-19”
-Not FDA approved, companies do not have to abide by Anti-kickback Statute, False Claims Act, HIPAA regulations.
-Can make false claims, bribe medical professionals, patients, without repercussion.
“If we obtain FDA approval for any of our investigational medicines and begin commercializing those products in the United States, our operations will be directly, or indirectly through our prescribers, customers, and purchasers, subject to various federal and state fraud and abuse laws and regulations, including, without limitation, the federal Health Care Program Anti-Kickback Statute, the federal civil and criminal False Claims Act, and Physician Payments Sunshine Act and regulations. These laws will impact, among other things, our proposed sales, marketing, and educational programs. In addition, we may be subject to patient privacy laws enacted by both the federal government and the states in which we conduct our business.”
See pg 108-110
No true pre-clinical trials done
-Preclinical (animal) trials are normally done over 1-5 years to assess the safety and long-term risk. Pfizer and Moderna injected animals and checked for “efficacy” (meaning if the injection would cause the immune system to respond). None were tested for safety and there has been no peer review of the data. Only 1-2 months later were Phase 1 trials begun for both. See the timeline in the attached article.
See also FDA explanation of Preclinical Trials
“Before testing a drug in people, researchers must find out whether it has the potential to cause serious harm, also called toxicity… these studies must provide detailed information on dosing and toxicity levels. After preclinical testing, researchers review their findings and decide whether the drug should be tested in people.”
True Animal studies of SARS-CoV-1, all showed “efficacy” like the 73-79% similar SARS-CoV-2(COVID) vaccine, but when exposed to the virus after injection there was inflammation found in the lungs caused by a hypersensitivity caused by the injection.
“These SARS-CoV vaccines all induced antibody and protection against infection with SARS-CoV. However, the challenge of mice given any of the vaccines led to the occurrence of Th2-type immunopathology suggesting hypersensitivity to SARS-CoV components was induced. Caution in proceeding to application of a SARS-CoV vaccine in humans is indicated.”
VAERS data as of 7/30/21
23,413 life-threatening/permanent disability
516,442 all other adverse events
About Dr. Aimee Trammell
Currently, Pharmacy Manager in California, got my undergraduate in Biochemistry (graduated Summa Cum Laude), got my Doctorate in Pharmacy both from the University of Illinois at Chicago.
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* If you enjoyed this episode you may also enjoy Episode 88.