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EU drug regulator reviewing 5 cases of NEW blood condition in AstraZeneca Covid vaccine recipients amid possible link to jab

Follow RT on Five cases of a very rare blood disorder in people who have received the Covid-19 vaccine developed by AstraZeneca are being reviewed by the European Medicines Agency (EMA), the EU s drug regulator has said. The cases of capillary leak syndrome, which can cause leakage of fluid from blood vessels, tissue swelling and a drop in blood pressure, were reported from across the European Economic Area, the EMA said on Friday. The regulator said it is The EMA said the five cases, all reported in the European Economic Area, warrant further investigation and potentially an update to the vaccine s product information, if deemed necessary by its Pharmacovigilance Risk Assessment Committee (PRAC).

AstraZeneca : J&J COVID-19 vaccine under EU review over blood clots

Four cases of blood clots in recipients of J&J shots J&J says working with regulators to assess data on its vaccine Probe of AstraZeneca vaccine and blood clots already ongoing April 9 (Reuters) - Europe s drug regulator said on Friday it is reviewing rare blood clots in four people in the United States who received Johnson & Johnson s COVID-19 vaccine. The European Medicines Agency s safety committee has also been looking at how AstraZeneca s COVID-19 vaccine is associated with very rare cases of unusual blood clots and said it was now reviewing reports of capillary leak syndrome in people given AstraZeneca s vaccine.

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