Interés Humano

Regulador europeo intenta apaciguar temores sobre la vacuna de AstraZeneca y Oxford

Tres países suspendieron uso debido a la aparición de coágulos de sangre en personas vacunadas con este inyectable

(FILES) In this file photo taken on March 09, 2021 a medical worker holds a syringe and a vial of the British-Swedish AstraZeneca/Oxford vaccine during a vaccination campaign at the National Museum of Science and Technology Leonardo Da Vinci. - Danish health authorities said on March 11, 2021 they were temporarily suspending the use of AstraZeneca's Covid-19 vaccine as a precaution after some patients developed blood clots since receiving the jab. The move comes "following reports of serious cases of blood clots among people vaccinated with AstraZeneca's Covid-19 vaccine", the Danish Health Authority said in a statement. (Photo by Miguel MEDINA / AFP)
(FILES) In this file photo taken on March 09, 2021 a medical worker holds a syringe and a vial of the British-Swedish AstraZeneca/Oxford vaccine during a vaccination campaign at the National Museum of Science and Technology Leonardo Da Vinci. - Danish health authorities said on March 11, 2021 they were temporarily suspending the use of AstraZeneca's Covid-19 vaccine as a precaution after some patients developed blood clots since receiving the jab. The move comes "following reports of serious cases of blood clots among people vaccinated with AstraZeneca's Covid-19 vaccine", the Danish Health Authority said in a statement. (Photo by Miguel MEDINA / AFP) MIGUEL MEDINA
AstraZeneca Un trabajador médico muestra un vial de la vacuna británico-sueca AstraZeneca/Oxford durante una campaña de vacunación en el Museo Nacional de Ciencia y Tecnología Leonardo Da Vinci. Foto: AFP (MIGUEL MEDINA/AFP)

La Haya. La Agencia Europea de Medicamentos (EMA) abogó este jueves por seguir administrando la vacuna de AstraZeneca, después que varios países de la región suspendieran su uso debido a la aparición de coágulos de sangre en personas vacunadas con este inyectable.

“Los beneficios continúan superando los riesgos y la vacuna puede continuar administrándose”, dijo la EMA, mientras se investigan presuntos casos de coágulos que derivaron en trombosis.

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