Last week, the United States Food and Drug Administration (FDA) revoked the Emergency Use Authorization for Johnson & Johnson coronavirus shots. Peter Marks, the director of the FDA’s Center for Biologics Evaluation and Research, noted in a Thursday letter that the FDA made the revocation at the request of Janssen Biotech, a Johnson & Johnson subsidiary, that had related that the company would not be updating its shots, the latest “lots” purchased by the US government have expired, and “there is no demand for new lots.”
Tag: Johnson & Johnson
On Thursday, the Food and Drug Administration (FDA) further restricted the use of Johnson & Johnson coronavirus shots, again pushing Americans to use just the coronavirus shots from Pfizer-BioNTech and Moderna.
Yet again. The United States government’s Food and Drug Administration (FDA) this week warned of a danger — this time the bleeding disorder immune thrombocytopenia — from Johnson & Johnson’s experimental coronavirus vaccine shot, while, as usual, remaining silent about dangers from competing shots from Moderna and Pfizer-BioNTech.
It does not seem fair. This week, Johnson & Johnson was called out by the Food and Drug Administration (FDA) for problems with Johnson & Johnson’s experimental coronavirus vaccine. While experimental coronavirus vaccine competitors Moderna and Pfizer-BioNTech skated by without censure despite their shots appearing likely to cause the same problems, the FDA put out a warning regarding the Johnson & Johnson shot.
When the United States government’s Food and Drug Administration earlier this week called for temporarily halting the giving of Johnson & Johnson’s experimental coronavirus vaccine shots because of the developing of blood clots in people who have received the shots, I asked if we were seeing an example of regulatory favoritism for the new mRNA technology shots over more traditional vaccine shots such as the Johnson & Johnson shots. The question arises because the US government is still encouraging everyone to take experimental mRNA “vaccines” from Moderna and Pfizer-BioNTech regarding which there are also many reports of injury and death.
While a variety or injuries and deaths have been reported after people have taken experimental coronavirus vaccine shots developed respectively by the three companies, if you focus in on just blood clot problems, those problems appear to arise after Moderna and Pfizer-BioNTech experimental coronavirus shots as well as after Johnson & Johnson shots.
On Tuesday, the United States government’s Food and Drug Administration asked states to temporarily halt the giving of Johnson & Johnson’s experimental coronavirus vaccine shots, pointing to the developing of blood clots in people who have received the shots as the justification for halting.
This is like something out of a Three Stooges movie.
“Human error” is being blamed for contamination of Johnson & Johnson experimental coronavirus vaccine being produced at a Baltimore, Maryland, manufacturing plant that resulted in 15 million doses having to be thrown away. And the error sure is a doozy.