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FDA halts Valneva's Chikungunya vaccine sales in U.S. due to adverse events reported abroad.
The FDA has suspended Valneva's Chikungunya vaccine, IXCHIQ®, in the US following four new serious adverse events reported outside the country.
This immediate suspension halts all shipments and sales of the vaccine in the US.
Valneva is investigating the cases and assessing the financial impact, given the vaccine's contribution to sales.
The company remains committed to the vaccine's global availability for chikungunya outbreak prevention.
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La FDA detiene las ventas de la vacuna Chikungunya de Valneva en los EE. UU. debido a los eventos adversos reportados en el extranjero.