EU inombundira piritsi nyowani yeMerck yeLagevrito seCOVID-19 kesi kuvhiya

NeChishanu, European Union drug regulator yakapa 'mazano' anotsigira kushandiswa kwekukurumidzira kwemushonga mutsva we-anti-coronavirus wakagadzirwa nekambani yeAmerica yemarudzi akawanda yemishonga. Merck mukubatana neRidgeback Biotherapeutics, kunyangwe isati yapihwa mvumo nevakuru veUS.

The European Medicines Agency (EMA) yakakurudzira kushandiswa kwechimbichimbi kwe Merck'Piritsi rekurapwa kwevarwere vari munjodzi yeCCIDID-19 sezvo nyaya nyowani dzekoronavirus dzichikwira mukondinendi yeEurope.

Mutsamba, EMA akadaro mushonga unonzi Lagevrio - unozivikanwawo semolnupiravir kana MK 4482 - "unogona kushandiswa kurapa vanhu vakuru vane COVID-19 vasingade okisijeni yekuwedzera uye vari panjodzi yakawedzera yeCOVID-19."

EU regulator akati kurapwa kunofanirwa kuitwa nekukurumidza mushure mekunge COVID-19 yaonekwa uye mukati memazuva mashanu kutanga kwezviratidzo. Mushonga unofanirwa kutorwa kaviri pazuva kwemazuva mashanu.

The EMA yakanyora zvingangoitika papiritsi, kusanganisira manyoka ari pakati nepakati, kusvotwa, dzungu uye musoro. Mushonga haukurudzirwi kuvakadzi vane pamuviri.

Mutongi akazivisa kare neChishanu kuti anga atanga kuongorora mushonga wePfizer Paxlovid weCCIDID-19 aine chinangwa chimwe chete "kutsigira zviremera zvenyika" zvinogona kusarudza nezvekushandiswa kwayo kwekutanga kusati kwapihwa mvumo yekushambadzira nekuda kwekukwira kwenyaya uye kufa muEurope.

Nhasi, Austria yakazivisa kuti ichapinda mukuvhara kutsva kwenyika kubva Muvhuro uye kuita vaccine, ukuwo vakuru vehutano kuGermany vachiti nyika yaita "denda guru."

Vese Pfizer naMerck vakakumbira mvumo yemishonga yavo yekoronavirus kubva kuUS Food and Drug Administration, asi hazvizivikanwe kuti ingapihwa riini.