THE MCCULLOUGH REPORT Dr. Peter McCullough

The McCullough Report with Dr. Peter McCullough – With FDA warnings for heart damage, blood clots, neurological damage, and severe allergic reactions, one can imagine if the scope of information were restricted to that provided by the US FDA alone, a reasonable woman and her husband would decline an experimental injection...

The McCullough Report with Dr. Peter McCullough - With >3.5 million injuries and >40,000 deaths, a gross underestimate, the vaccines must be pulled. On this week’s show, we have a wonderful song from Emma Ohm (We are the World 2022) and an exclusive interview from World Council for Health, Dr. Kat Lindley...

The technology differs from Pfizer and Moderna’s shots, which were the first ones using messenger RNA technology to receive FDA approval and have resulted in catastrophic rates of injury, disability, and death. In the Novavax clinical trial experience, there were no hospitalizations or deaths due to COVID-19...

From a regulatory perspective, any death that occurs after an investigational product within 30 days is attributed to the article under investigation. For traditional vaccines, special adverse events of interest have a 24-month window of observation and potential concern. For genetic products (e.g., mRNA and adenoviral DNA), this window is extended to five years...

In a hyperbolic over-reaction, the US government announced the purchase of 13 million doses of the clinically unproven Jynneos vaccine. Some vaccine enthusiasts have proposed perimeter or rim vaccination of monkeypox contacts. This appears unjustified since the virus spreads by intensive physical contact (kissing, sex, touching blisters/pustules) and is not...

The COVID-19 vaccines, of which there are 16 in use or about to be deployed, under any conditions cannot improve human health. There is a strong body of evidence that they are leading to a marked decline in the well-being of humans and resulting in record numbers of serious adverse events, disability, and death...