The exterior of the European Medicines Agency is seen in Amsterdam, Netherlands, December 18, 2020. REUTERS/Piroschka van de Wouw/File Photo
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- US, UK have already authorised Pfizer shot in same capacity
- Recommendation comes soon after global cases surpass 500 mln
April 22 (Reuters) – A European Medicines Agency (EMA) committee on Friday recommended approving the use of Pfizer (PFE.N) and BioNTech’s COVID-19 vaccine, Comirnaty, as a booster for adults who have previously been inoculated with other vaccines.
The recommendation from Europe’s drug regulator comes days after global COVID-19 cases surpassed 500 million, according to a Reuters tally, as the highly contagious BA.2 sub-variant of Omicron surges in many countries.
Some European countries are now seeing a slower uptick in new cases, or even a decline, but the region is still reporting over 1 million cases about every two days, according to the Reuters tally published on Thursday. read more
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In the United States and the United Kingdom, Comirnaty has already been authorised as a booster following two shots of any other type of vaccine.
Some countries have also begun rolling out second boosters in certain groups, such as the immunocompromised and the elderly. In March, the EMA said that there was not yet enough data to support a recommendation on the need for a second booster shot in the general population.
Last week, Pfizer and BioNTech showed that three doses of their shot produced significant protection against the Omicron variant of the coronavirus in healthy children aged five to 11. read more
Analysts have forecast sales of $33.79 billion for the vaccine in 2022, according to Refinitiv data. The two companies have already delivered more than 3.1 billion vaccine doses globally.
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Reporting by Natalie Grover, Editing by Louise Heavens and Elaine Hardcastle
Our Standards: The Thomson Reuters Trust Principles.