Facebook Twitter YouTube Instagram Homepage
Latest Natural Health News

FDA Severely Limits Use of J&J COVID Shot

FDA Severely Limits Use of J&J COVID Shot
Share This Article

From MedPage Today

Use of Johnson and Johnson’s (J&J) COVID-19 vaccine should only be limited to certain adults, the FDA said on Thursday.

Due to an updated analysis of the rare cases of thrombosis with thrombocytopenia syndrome (TTS), which typically occur 1 to 2 weeks after vaccination, use of the J&J vaccine should be restricted to those for whom mRNA vaccines are “not accessible or clinically appropriate,” or who would not get vaccinated if not for the J&J vaccine, the agency said.

“Our action reflects our updated analysis of the risk of TTS following administration of this vaccine and limits the use of the vaccine to certain individuals,” said Peter Marks, MD, PhD, director of the FDA’s Center for Biologics Evaluation and Research, in a statement.

Read the full story.

Leave a Reply

Your email address will not be published. Required fields are marked *

Related Posts