U.S. regulators recommended pausing the use of the single-shot
earlier this month due to extremely rare cases of blood clots but on
Friday said the United States could restart vaccinations. Europe's
drug regulator has backed its overall benefits against any risk.
The Sisonke study is being carried out by the National Department of
Health, South African Medical Research Council and Johnson & Johnson
among others.
"It is much better to have the vaccine than to avoid taking it for
fear of getting a blood clot," Health Minister Zweli Mkhize said in
a statement released by the health ministry.
South African authorities would ensure "there is intensified
pre-vaccination assessment and post-vaccination monitoring" when the
Sisonke study resumes, the health ministry said.
Some 290,000 healthcare workers have been given J&J's vaccine in the
study so far out of a target of 500,000.
It comes as South Africa, the African country with the highest
number of recorded coronavirus infections and COVID-19 deaths, is
counting on J&J's vaccine to ramp up immunisations after a slow
start.
The suspension of the J&J study was the latest setback for South
Africa's immunisation efforts, after it ditched plans to kick-start
vaccinations with AstraZeneca's shot in February.
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A trial showed the AstraZeneca
vaccine had greatly reduced efficacy against the
dominant local coronavirus variant, and the
government has since sold its AstraZeneca shots
to other African countries.
The country's health regulator approved Johnson
& Johnson's COVID-19 vaccine in early April and
the government has ordered 31 million doses,
with the first commercial batch of 1.1 million
doses due to be dispatched in the coming days.
South Africa has also secured 30 million doses
of Pfizer's two-shot vaccine and expects the
first 650,000 doses to arrive before the second
phase of the country's vaccination programme,
which starts on May 17 and targets the elderly
and essential workers among others.
(Reporting by Alexander WinningEditing by Ana
Nicolaci)
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