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FDA and CDC recommend pausing use of chikungunya vaccine Ixchiq in people aged 60+ due to serious side effects.
The FDA and CDC recommend pausing the use of Valneva's chikungunya vaccine, Ixchiq, in people aged 60 and older due to serious adverse events, including neurological and cardiac issues, reported in recipients aged 62 to 89.
There have been 17 serious events, including two deaths, as of May 7.
The vaccine remains recommended for those aged 18 to 59 at risk of exposure, while the FDA conducts a new benefit-risk assessment for the older age group.
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La FDA y los CDC recomiendan interrumpir el uso de la vacuna contra la chikungunya Ixchiq en personas mayores de 60 años debido a efectos secundarios graves.