Forwarded this email? Subscribe here for more FDA Orders Pfizer to Add PARALYSIS WARNING to RSV Vaccine Labels “FDA conducted a post-marketing observational study that assessed the risk of GBS (paralysis and muscle weakness) following vaccination with Abrysvo (Pfizer) and Arexvy (GSK) RSV vaccines." Karen Kingston Jan 15 ∙ Preview   READ IN APP   January 15, 2025: Last Wednesday, the FDA ordered Pfizer and GSK to add Guillain-Barre Syndrome (GBS) as a serious adverse event risk warning to both Pfizer’s Abrysvo and GSK’s Arexy Respiratory Syncytial Virus (RSV) vaccine labels. RSV is the leading cause of respiratory infection in adults over the age of 60. Prior to 2023, the CDC has not published data on the incidence of RSV death in babies and children. In 2023, the CDC estimates that approximately 100 children under the age of 5 died from RSV. Despite these low numbers, the CDC recommends that pregnant women receive an RSV vaccine to ‘protect’ their baby from RSV. Image: Pfizer’s Abrysvo RSV Vaccine website Share The FDA describes GBS as, “a rare disorder in which the body’s immune system damages nerve cells, causing muscle weakness and sometimes paralysis.”... Keep reading with a 7-day free trial Subscribe to The Kingston Report to keep reading this post and get 7 days of free access to the full post archives. Start trial A subscription gets you: Subscriber-only posts with references Post comments and join the community Access to ALL articles beginning in 2022. Without a paid subscription articles are not available after 3 weeks.   Like Comment Restack   © 2025 Karen Kingston miFight Inc, Karen Kingston, 960 Postal Way, #307 Vista, CA 92085 Unsubscribe