Zimbabwe approves J&J COVID-19 vaccine for emergency use



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Vials labeled “COVID-19 Coronavirus Vaccine” and a syringe can be seen in front of the Johnson & Johnson logo displayed in this illustration taken on February 9, 2021. REUTERS / Dado Ruvic / Illustration

HARARE, July 28 (Reuters) – Zimbabwe has cleared emergency use of the COVID-19 vaccine from Johnson & Johnson (JNJ.N), the first western-made vaccine to be approved by the southern African country, its drug regulator announced Wednesday.

Like many African countries, Zimbabwe is in the throes of a third wave of infections, with nearly half of its 101,711 cumulative cases and 3,280 deaths recorded in this month alone, according to official data.

So far, the Zimbabwe Medicines Control Authority (MCAZ) had only registered vaccines from India, Russia and China.

“MCAZ has reviewed the technical documentation that has been submitted by the manufacturer, and emergency use authorization has been granted and communicated to (Ministry of Health),” MCAZ spokesperson Shingai Gwatidzo said.

He declined to say when Zimbabwe would receive its first J&J vaccines, adding that the health ministry would confirm the vaccine rollout after reviewing cold chain storage requirements.

So far, more than 1.5 million Zimbabweans have received a first dose of a COVID-19 vaccine. Most have received injections from Chinese Sinovac and Sinopharm.

Zimbabwe has so far received more than five million doses from China, including purchases and donations.

Finance Minister Mthuli Ncube said on Sunday that the government had fully paid for a total of 12 million doses of the vaccine from China.

He said Zimbabwe expected 5 million vaccines under an African Union vaccine procurement mechanism after making a deposit of $ 7.5 million, while $ 1.15 million additional doses would be delivered as part of the COVAX global vaccine distribution program.

Reporting by MacDonald Dzirutwe; Editing by Joe Bavier

Our Standards: Thomson Reuters Trust Principles.

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