This post was published by Jon Fleetwood. Support him by subscribing at Substack and following at Instagram / X / Facebook.
All FDA-approved and emergency-use-authorized mRNA vaccines use E. coli to produce so-called starting DNA or other manufacturing materials, creating a lipopolysaccharide (LPS) endotoxin contamination risk that manufacturers test for in the finished shots. Endotoxin has been shown to drive cardiac injury and abnormal clotti…
Read with caution - this story is only being covered by one news source that has a ‘low factuality’ rating, which means the outlet has a history of poor reporting practices. Learn more about factuality ratings here.