FDA grants EUA for Russia's Sputnik V vaccine

The Food and Drug Administration (FDA) has granted an emergency use authorization (EUA) for Russia's Sputnik V vaccine against COVID-19.

Interim data from ongoing phase three trials, published in The Lancet, indicate an overall efficacy rate of 91.6% in preventing COVID-19 across all age groups 18 and older.

The Sputnik V vaccine is administered as two intramuscular injections of 0.5 ml each, given 21 days apart.

Reported adverse events from the vaccine are mostly mild and transient, comparable to common vaccine reactions.

Following the EUA grant, the Philippine government plans to order approximately three million doses of the Sputnik V vaccine, with initial deliveries expected in April or May.

Negotiations are also underway to allow local government units and private companies to procure the Sputnik V vaccine.

Over 20 to 30 countries are reportedly using the Sputnik V vaccine.

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