Valneva Announces Removal of FDA-Recommended Pause on Use of Chikungunya Vaccine IXCHIQ® in Elderly and Updates to the Prescribing Information
UNITED STATES, AUG 7 – The FDA updated the chikungunya vaccine label to warn of serious adverse events mainly in older adults with underlying conditions after reviewing 17 global cases, including two deaths.
10 Articles
10 Articles
FDA Lifts Pause on Chikungunya Vaccine in Older Adults, With Revised Labeling
(MedPage Today) -- The chikungunya live-attenuated vaccine (Ixchiq) can once again be used in people ages 60 and older, after the FDA reversed a recommended pause spurred by serious adverse events in vaccinated older adults. "Based on the available...
FDA Ends Suspension of Chikungunya Vaccine, Adjusts Label - The Thinking Conservative
The FDA has lifted its hold on a vaccine against chikungunya, the agency announced on Aug. 6, as it adjusted the label for the shot. The post FDA Ends Suspension of Chikungunya Vaccine, Adjusts Label appeared first on The Thinking Conservative.
Valneva Announces Removal of FDA-Recommended Pause on Use of Chikungunya Vaccine IXCHIQ® in Elderly and Updates to the Prescribing Information
Saint Herblain (France), August 7, 2025 – Valneva SE (NASDAQ:VALN, PARIS:VLA), a specialty vaccine company, today announced that the FDA has removed its recommended pause in the use of IXCHIQ® in individuals 60 years of age and older and has approved updates to the Prescribing Information (PI) for IXCHIQ®. IXCHIQ® remains indicated in the United States for the prevention of disease caused by the Chikungunya Virus (CHIKV) in individuals 18 years …
Coverage Details
Bias Distribution
- 67% of the sources are Center
Factuality
To view factuality data please Upgrade to Premium