Now comes another International Classification of Disease (ICD) billing code (Z28.310), complements of the World Health Organization, intended to inform the government and your insurer of your Covid vaccine status. The code will be required, no doubt, to receive full...
COVID Vaccine Stillbirths and Miscarriages
Pharma Today’s VACCINE Report exposes more of the shocking dangers of the experimental Covid shots, with toxicologist Dr. Janci Lindsay presenting new data on the alarming rise in stillborn babies and miscarriages following the COVID injections. Big Pharma supply chain and manufacturing expert Hedley Rees destroys Pfizer’s claims it didn’t cut corners in the manufacture of its vaccines in our show today.
Alexandra (Sasha) Latypova explains the recent statement “The FDA is impersonating a regulator” and exposes that it is actually the Department of Defense in control of the deployment of the COVID shots, and the FDA is not in charge of approval, safety oversight or manufacturing processes. She provides the legal framework that allows this major change to unleash this vast human experiment without adequate trials or safety testing.
Meet our experts for The Vaccine Report:
Alexandra Latypova has a career in research, toxicology, analysis, and research design. She is a former pharmaceutical research and development executive who co-founded and managed several contract research organizations in pharmaceutical clinical trials. She worked for sixty major pharmaceutical clients, including Pfizer. These pharmaceutical clients were her research and development partners. The area of her focus has been safety assessments, what was done in the Covid shots, and especially what Pfizer tried to cover up. She looks at not only the safety assessments but regulatory compliance and has interacted with the FDA and worked on FDA and Industry consortiums who are putting together the approaches proper approaches to clinical trials. Since 2014 she has focused on independent research and investigation of the regulatory oversight breakdown as our own taxpayer-funded agencies have failed in their duties, and she has worked to expose fraud and corruption associated with the Covid countermeasures. She has been looking at the variability in manufacturing from lots to lots in these mRNA injections, and why there is so much variation in adverse events and deaths varying with different lot numbers. Follow her research on www.trialsitenews.com and her videos and other publications on her Bitchute channel: https://www.bitchute.com/channel/7dNrFbLeGSev/.
Janci C. Lindsay, PhD., Toxicologist, Molecular Biologist. Director of Toxicology and Molecular Biology, Toxicology Support Services, LLC. Dr. Lindsay is a Toxicologist and Molecular Biologist with over 30 years of scientific research experience. She regularly consults as an expert witness in legal matters relating to the toxicity of chemicals, biologics and particulates as well as consults on biologic mechanism of action pathways in varying cancers and lung disease. She helped to develop what was meant to be a temporary contraceptive vaccine (the Zona vaccine) in the 1990’s that is now used as a sterility vaccine for animals due to its elicitation of auto-immune ovarian destruction. She regularly researchers and warns about the potential for acute and long-term reproductive toxicity of these shots and is known for her early and public warnings to the CDC ACIP committee that these shots could “sterilize an entire generation.”
Hedley Rees, based in the United Kingdom. Mr. Rees has been providing consultancy on the development, manufacture and distribution of drugs that are fully compliant with the GMP requirements of 21 CFR Title 21, since 2005 through his company, PharmaFlow. Prior to that, he spent 16 years in senior roles in Big Pharma (Bayer) and 10 years in biotech (British Biotech, Vernalis and OSI Pharmaceuticals (now Astellas). Read more on Facts about SARS-CoV-2 Injections (aka DNA vaccines) and advanced therapy medicinal products (ATMPs): https://open.substack.com/pub/hedleyrees/p/facts-about-sars-cov-2-injections?r=xoehy&utm_campaign=post&utm_medium=web. Watch his recent interview discussing the violations of manufacturing processes and regulations that are supposed to keep us safe: https://rumble.com/v1qe9nk-freeman-interviews-hedley.html.
Mr. Rees also authored Supply Chain Management in the Drug Industry: Delivering Patient Value for Pharmaceuticals and Biologics for Wiley, NJ in 2011. His expertise is in the area of anything to do with manufacture through the three phases of clinical trials (and preclinical if required) and ongoing distribution of the commercial supply. Where regulations have been breached, he has a duty to bring this to the attention of regulators, as has been happening with the frozen vials of COVID shots that were shipped only part way finished. Follow Hedley Rees on his Substack column, INSIDE PHARMA, where he shares all he can to expose the lies and deceptions that are costing lives and jeopardizing public safety. Watch his interview here: https://rumble.com/v14gou4-drug-development-expert-sounds-alarm-over-rushed-to-market-covid-19-vaccine.html.
Hedley joins Truth for Health Foundation Team: https://open.substack.com/pub/hedleyrees/p/hedley-joins-truth-for-health-foundation?r=xoehy&utm_campaign=post&utm_medium=web.
Whistleblower Report with the Truth For Health Team on America Out Loud Talk Radio can be heard weekdays at Noon ET. Listen on iHeart Radio, our world-class media player, or our free apps on Apple, Android, or Alexa. Listen to other episodes of the Whistleblower Report, available on podcast.
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