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FDA 2006 Guidance on Gene Therapy, Cancer Risks, and DNA Alteration
Tom Renz cites a 2006 FDA industry guidance document that allegedly predicted high likelihoods of delayed adverse reactions, such as cancer and autoimmune issues, from gene therapy products three to five years after administration. Renz argues that the current COVID-19 shots are "mod RNA" (modified RNA) rather than messenger RNA and contain excessive plasmid DNA. He claims the FDA knew these long-term effects were inevitable but proceeded with the rollout.

