SA’s medicines regulator expects the US Food & Drug Administration (FDA) will approve the release of Johnson and Johnson’s (J&J) Covid-19 vaccines later this week, clearing the way for the government to rapidly scale up its mass inoculation drive.

The government’s plans to use the shot as the workhorse of its vaccination programme were dealt an unexpected blow in early May, after the FDA flagged problems at a US company contracted by J&J to make a key vaccine ingredient. The development put a hold on millions of doses of J&J’s shots made by contractors that relied on the components made by Emergent BioSolutions, including SA’s Aspen Pharmacare, which at that stage had 1.1-million doses of the vaccine ready for dispatch. And it left the government with only limited quantities of Pfizer’s double-shot vaccine with which to begin the national vaccination programme on May 17, forcing it to get off to a slower than anticipated start...

Subscribe now to unlock this article.

Support BusinessLIVE’s award-winning journalism for R129 per month (digital access only).

There’s never been a more important time to support independent journalism in SA. Our subscription packages now offer an ad-free experience for readers.

Cancel anytime.

Would you like to comment on this article?
Sign up (it's quick and free) or sign in now.

Speech Bubbles

Please read our Comment Policy before commenting.