WHO approves China’s Sinopharm COVID-19 vaccine for emergency use

World Health Organization (WHO) Director-General Tedros Adhanom Ghebreyesus, announced on Friday that the body had authorised the emergency use of a COVID-19 vaccine made by China’s Sinopharm.

It is the first non-Western vaccine to gain WHO emergency use approval.

“This afternoon, WHO gave emergency use listing to sign off on Beijing’s COVID-19 vaccine, making it the sixth vaccine to receive WHO validation for safety, efficacy and quality,” Ghebreysus said.

The WHO had already given such approval to vaccines developed by BioNTech-Pfizer, AstraZeneca, Johnson & Johnson and Moderna.

The WHO listing means the Sinopharm vaccine could eventually be included into the COVAX initiative in the coming weeks or months. The UN-backed scheme aims to provide vaccines to poorer countries.

“This expands the list of vaccines that COVAX can buy and gives countries confidence to expedite their own regulatory approval and to import and administer a vaccine.”

The jab would then be distributed via UNICEF and the WHO’s regional office in the Americas.

To date, Sinopharm has made very little data public, only publishing what it says are efficacy numbers for its two vaccine shots — one developed by the Beijing Institute of Biological Products and the other by the Wuhan Institute of Biological Products.

A document reviewed by Reuters news agency, however, showed that the Strategic Advisory Group of Experts, or SAGE, a separate group of WHO experts, voiced concern this week over Sinopharm data on the risk of serious side-effects in some patients after receiving the vaccine but said it was confident in the vaccine’s ability to prevent disease.