The vaccine advisory committee of the Centers for Disease Control and Prevention is scheduled to meet Dec. 4 and 5. On the agenda: the hepatitis B vaccine, the overall childhood vaccine schedule and specific vaccine ingredients. We’ll summarize what we’ve written about these topics and what the committee has said about them in recent meetings.
A presentation by scientists on a work group for the Centers for Disease Control and Prevention’s vaccine advisory panel highlighted various alleged “safety uncertainties” of the mRNA COVID-19 vaccines, including those about cancer and changes to the immune system. Scientists, however, told us that many of the cited studies are either misconstrued or of poor quality.
The COVID-19 vaccines have saved millions of lives, according to multiple studies. Despite this, Florida Surgeon General Dr. Joseph Ladapo issued a statement on Jan. 3 calling for a halt in the use of mRNA COVID-19 vaccines, made by Pfizer/BioNTech and Moderna.
The mRNA COVID-19 vaccines — like many other vaccines — can contain small amounts of DNA left over from the manufacturing process. There’s no evidence this residual DNA causes “turbo cancer,” or very aggressive cancer. Nor did Moderna admit that “mRNA Jabs Cause Turbo-Cancer,” contrary to an online article that misconstrues a line from a patent application.
As with many medical products, the mRNA COVID-19 vaccines may contain trace amounts of residual DNA from the manufacturing process. It is not considered adulteration, and the Food and Drug Administration is not “required” to pull the vaccines from the market, contrary to viral claims online.