FDA Suspends Valneva Vaccine’s License Following New Reports of Adverse Events

Valneva must immediately cease U.S. shipments and sales of Ixchiq, a vaccine for chikungunya virus. The FDA recently lifted a pause on dosing of Ixchiq, but the agency’s new safety alert is based on an assessment that found the vaccine appears to be causing chikungunya-like illness in recipients.

The post FDA Suspends Valneva Vaccine’s License Following New Reports of Adverse Events appeared first on MedCity News.

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