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CRITICAL ALERT: Pfizer Hid Damning Biodistribution Data in COVID-19 Vaccine Submissions to FDA, Jeopardizing Global Trust A bombshell report, spotlighted by Dr. Robert Malone on October 4, 2025, has uncovered that Pfizer deliberately concealed critical biodistribution data in its COVID-19 vaccine submissions to the FDA, casting serious doubt on the integrity of the vaccine approval process. Canadian immunologist Dr. Byram Bridle’s detailed analysis reveals that Pfizer’s U.S. regulatory filings misrepresented the systemic spread of their mRNA vaccine, potentially undermining informed consent for billions worldwide. In preclinical studies using a luciferase-tagged surrogate mRNA in mice, data submitted to Japanese regulators showed the vaccine’s lipid nanoparticles and mRNA components rapidly dispersing beyond the injection site, accumulating in critical organs such as the liver, spleen, kidneys, adrenal glands, ovaries, testes, heart, lungs, brain, and cerebral arteries. These components remained detectable for at least nine days, with peak concentrations in the spleen and liver. Yet, Pfizer’s FDA submissions presented a sanitized version of this data: bioluminescent scans were cropped to exclude organ hotspots, graphs were manipulated to minimize systemic distribution, and key findings were redacted to falsely suggest the vaccine stayed primarily in the deltoid muscle and nearby lymph nodes. Dr. Bridle calls this a “bald-faced lie” crafted to evade rigorous scrutiny during a global health emergency. Moderna’s submissions mirrored this deception. Their studies, also using a surrogate mRNA, confirmed widespread organ distribution but were framed to regulators as evidence of localized action. Both companies perpetuated a narrative that the vaccines were confined to the injection site and cleared within days—a claim now thoroughly debunked. Human studies have since revealed alarming persistence: a 2025 Japanese study detected spike protein in cerebral arteries 17 months post-vaccination, while other research confirms its presence in lymph nodes, heart tissue, and the central nervous system for months or even years. This contradicts earlier assurances from the CDC and manufacturers that the spike protein was rapidly eliminated. These findings align with reports of “long COVID” symptoms potentially linked to persistent spike protein, prompting the CDC to withdraw vaccination recommendations for children and pregnant women in 2025 under pressure from advocates like RFK Jr. Dr. Charlotte Kuperwasser of Tufts University has called the absence of reproductive safety studies in pregnant animals “deeply troubling,” highlighting unaddressed risks to fertility and fetal development. Dr. Malone, a pioneer in mRNA technology, stated, “The data presented to the FDA was selectively edited to support a false narrative of localized action, eroding trust in the regulatory process.” The implications are profound: billions received a vaccine whose systemic effects were downplayed, potentially contributing to unexplained adverse events, including cardiovascular issues, neurological symptoms, and sudden deaths reported globally. The lack of transparency raises ethical concerns about the rush to approve these vaccines under emergency use authorization without fully disclosing their biodistribution profile. The public deserves unredacted data and independent investigations into regulatory oversights to restore confidence in public health systems.