Topic: Safety Trials

Vaccine manufacturers are accused of "cheating" by using extremely short safety trial periods, sometimes as brief as five days, to avoid capturing long-term injuries. Bigtree references testimony from Stanley Plotkin regarding the use of tissue from 76 aborted fetuses in vaccine development. The discussion lists various "disgusting" ingredients in vaccines, including cancer cell lines, mercury, and formaldehyde, comparing the mixtures to a "witch's cauldron."

Brooke Jackson is described as a 20-year industry veteran who originally believed in vaccines but was horrified by the "systemic criminality" she witnessed. Barnes uses an analogy of a basketball referee being told to count points differently for different teams to explain the fraud. He argues Pfizer rushed the trials to secure billions in taxpayer money while falsely claiming immunity.

A caller named Cobra, claiming 20 years of experience in the pharmaceutical industry, expresses grave concern over the lack of long-term Phase 3 trials for COVID-19 vaccines. He explains that typically, drugs are shut down if short-term deaths occur because long-term effects are usually worse. He characterizes the skipping of these trials as intentional mass murder by globalist entities.

A randomized trial in Bangladesh involving 606 individuals demonstrated that povidone-iodine nasal washes significantly reduced the number of PCR-positive cases compared to a control group. The treatment "knocked the crud" out of the virus, showing much faster clearance than warm water washes. Travelers and those attending large gatherings are encouraged to use nasal irrigation once a day as a preventative measure.

The discussion reviews the history of vaccine testing, including the 1960s RSV trials and the swine flu vaccine. Dr. Stock asserts that all standard safety steps, including long-term animal trials and representative human trials, were bypassed for the current COVID-19 vaccines, leading to a lack of data on long-term organ damage.

Karen Kingston highlights Pfizer's Phase One trial protocols, which required male participants to use two forms of protection and avoid contact with pregnant women. She argues these precautions prove the manufacturers were aware of the risks of shedding and transmission. The segment notes that no clinical studies were conducted to verify the actual production or duration of spike protein in the vaccinated.

Sky and Jones discuss the lack of long-term safety data for COVID-19 vaccines, noting they have not passed standard human clinical trials or received full FDA approval. Sky encourages the public to ask their doctors specific questions about these facts to expose the lack of scientific foundation for the mandates. They characterize the push for universal vaccination as a form of cult-like religious programming.

India has officially refused emergency use authorization for the Pfizer COVID-19 vaccine, citing a lack of local studies. This follows reports that the British military previously advised against the vaccine for pregnant women due to miscarriage risks. Claims are made that standard animal trials were skipped in the rush for human distribution under emergency protocols.