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5 cases of NEW blood condition in AstraZeneca Covid vaccine recipient

EU drug regulator reviewing 5 cases of NEW blood condition in AstraZeneca Covid vaccine recipients amid possible link to jab 9 Apr, 2021 17:25 Vials labelled “AstraZeneca coronavirus disease (COVID-19) vaccine” placed on displayed EU flag are seen in this illustration picture taken March 24, 2021. © Reuters / Dado Ruvic 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.

Johnson & Johnson COVID-19 vaccine under review by European Medicines Agency over blood clots

Johnson & Johnson COVID-19 vaccine under review by European Medicines Agency over blood clots Posted 4 AprApril 2021 at 12:52am Nearly 5 million people in the United States had received J&J s vaccine as of Thursday morning. Share Print text only Cancel Europe’s drug regulator says it is reviewing rare blood clots in four people in the United States who received Johnson & Johnson’s COVID-19 vaccine. Key points: Johnson & Johnson said it was aware of the rare reports of blood clots, and was working with regulators to assess the data The US Food and Drug Administration said it was aware of the reports, but they had  not found a causal relationship with vaccination

European regulators are watching J&J s vaccine for unusual blood clots -- Health & Wellness -- Sott net

Fri, 09 Apr 2021 16:39 UTC European regulators are watching J&J s vaccine for unusual blood clots.The European Medicines Agency is investigating reports of clots in people who received J&J s vaccine. The shot has not yet been given out in Europe. European regulators are investigating whether Johnson & Johnson s COVID-19 vaccine caused unusual blood clotting after four cases were reported in vaccine recipients, including one fatality. The European Medicines Agency s Pharmacovigilance Risk Assessment Committee disclosed Friday that they are reviewing the vaccine after three people who received J&J s vaccine in the US and another who was involved in a clinical trial developed blood clots. It s currently not clear if the vaccine caused these clots.

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