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Izvršna direktorica Europske agencije za lijekove (EMA) Emer Cooke na konferenciji za medije rekla je kako u ovom trenutku EMA nema indikacije da cjepivo AstraZenece uzrokuje povećan rizik od nastanka krvnih ugrušaka.

"Broj incidenata s ugrušcima krvi nije veći od broja koji je zabilježen u općoj populaciji", rekla je Cooke.

Cooke je rekla kako se zgrušavanje krvi dogodilo kod malog broja ljudi te da se to godišnje događa tisućama ljudi. "Želimo utvrditi je li to povezano s cjepivom", rekla je i najavila da će EMA proučiti svaki pojedinačni slučaj nakon čega će se opet sastati u četvrtak i donijeti odluku.

"I dalje smo uvjereni da je korist cjepiva AstraZenece veća od nuspojava", dodala je.

Cooke se osvrnula i na navode da je možda problem u nekim određenim pošiljkama cjepiva.

“Određene pošiljke cjepiva bile su sumnjive i s njima su bile povezane ove nuspojave. Mobilizirali smo radni odbor zadužen za analizu toga jesu li neke pošiljke povezane s ovim incidentima i je li došlo do nekih incidenata tijekom same proizvodnje koji su mogli dovesti do razlike u cjepivima”, pojasnila je Cooke, prenosi N1 i jutarnji.hr.

Rekla je i da ih ovi incidentni dosta zabrinjavaju. "Tek kad obavimo ovu analizu moći ćemo to procijeniti”, istaknula je Cooke, dodajući kako smatraju da su prednosti cjepiva i dalje veće od rizika.

Europska agencija za lijekove (EMA), europska regulatorna agencija za lijekove, sastat će se u četvrtak kako bi razgovarala o prikupljenim informacijama te službeno odlučila je li cjepivo pridonijelo tromboemboliji kod cijepljenih osoba.

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Izvršna direktorica Europske agencije za lijekove (EMA) Emer Cooke na konferenciji za medije rekla je kako u ovom trenutku EMA nema indikacije da cjepivo AstraZenece uzrokuje povećan rizik od nastanka krvnih ugrušaka.

"Broj incidenata s ugrušcima krvi nije veći od broja koji je zabilježen u općoj populaciji", rekla je Cooke.

Cooke je rekla kako se zgrušavanje krvi dogodilo kod malog broja ljudi te da se to godišnje događa tisućama ljudi. "Želimo utvrditi je li to povezano s cjepivom", rekla je i najavila da će EMA proučiti svaki pojedinačni slučaj nakon čega će se opet sastati u četvrtak i donijeti odluku.

"I dalje smo uvjereni da je korist cjepiva AstraZenece veća od nuspojava", dodala je.

Cooke se osvrnula i na navode da je možda problem u nekim određenim pošiljkama cjepiva.

“Određene pošiljke cjepiva bile su sumnjive i s njima su bile povezane ove nuspojave. Mobilizirali smo radni odbor zadužen za analizu toga jesu li neke pošiljke povezane s ovim incidentima i je li došlo do nekih incidenata tijekom same proizvodnje koji su mogli dovesti do razlike u cjepivima”, pojasnila je Cooke, prenosi N1 i jutarnji.hr.

Rekla je i da ih ovi incidentni dosta zabrinjavaju. "Tek kad obavimo ovu analizu moći ćemo to procijeniti”, istaknula je Cooke, dodajući kako smatraju da su prednosti cjepiva i dalje veće od rizika.

Europska agencija za lijekove (EMA), europska regulatorna agencija za lijekove, sastat će se u četvrtak kako bi razgovarala o prikupljenim informacijama te službeno odlučila je li cjepivo pridonijelo tromboemboliji kod cijepljenih osoba.

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Yves Herman
European Medicines Agency (EMA) Executive Director, Emer Cooke, appears on screen during a videoconference in Brussels, Belgium on March 16, 2021. - The European Medicines Agency remains ”firmly convinced” of the benefits of AstraZeneca's coronavirus vaccine despite several countries suspending its use over blood clot fears, the head of the regulator said. (Photo by YVES HERMAN/POOL/AFP)

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Hrvatska i svijetSPORNO CJEPIVO

Izvršna direktorica EMA-e: ‘Zasad nema indikacije da AstraZeneca uzrokuje stvaranje ugrušaka krvi‘

Piše dv

16. ožujka 2021. - 15:32

European Medicines Agency (EMA) Executive Director, Emer Cooke, appears on screen during a videoconference in Brussels, Belgium on March 16, 2021. - The European Medicines Agency remains ”firmly convinced” of the benefits of AstraZeneca&#39;s coronavirus vaccine despite several countries suspending its use over blood clot fears, the head of the regulator said. (Photo by YVES HERMAN/POOL/AFP)

European Medicines Agency (EMA) Executive Director, Emer Cooke, appears on screen during a videoconference in Brussels, Belgium on March 16, 2021. - The European Medicines Agency remains ”firmly convinced” of the benefits of AstraZeneca's coronavirus vaccine despite several countries suspending its use over blood clot fears, the head of the regulator said. (Photo by YVES HERMAN/POOL/AFP)Yves Herman

Izvršna direktorica Europske agencije za lijekove (EMA) Emer Cooke na konferenciji za medije rekla je kako u ovom trenutku EMA nema indikacije da cjepivo AstraZenece uzrokuje povećan rizik od nastanka krvnih ugrušaka.

"Broj incidenata s ugrušcima krvi nije veći od broja koji je zabilježen u općoj populaciji", rekla je Cooke.

Cooke je rekla kako se zgrušavanje krvi dogodilo kod malog broja ljudi te da se to godišnje događa tisućama ljudi. "Želimo utvrditi je li to povezano s cjepivom", rekla je i najavila da će EMA proučiti svaki pojedinačni slučaj nakon čega će se opet sastati u četvrtak i donijeti odluku.

"I dalje smo uvjereni da je korist cjepiva AstraZenece veća od nuspojava", dodala je.

Cooke se osvrnula i na navode da je možda problem u nekim određenim pošiljkama cjepiva.

“Određene pošiljke cjepiva bile su sumnjive i s njima su bile povezane ove nuspojave. Mobilizirali smo radni odbor zadužen za analizu toga jesu li neke pošiljke povezane s ovim incidentima i je li došlo do nekih incidenata tijekom same proizvodnje koji su mogli dovesti do razlike u cjepivima”, pojasnila je Cooke, prenosi N1 i jutarnji.hr.

Rekla je i da ih ovi incidentni dosta zabrinjavaju. "Tek kad obavimo ovu analizu moći ćemo to procijeniti”, istaknula je Cooke, dodajući kako smatraju da su prednosti cjepiva i dalje veće od rizika.

Europska agencija za lijekove (EMA), europska regulatorna agencija za lijekove, sastat će se u četvrtak kako bi razgovarala o prikupljenim informacijama te službeno odlučila je li cjepivo pridonijelo tromboemboliji kod cijepljenih osoba.

#CJEPIVO ASTRAZENECA