Vaccine Johnson & Johnson, the OK of the FDA experts arrives at the ‘booster’ dose. The Advisory Committee of the American Medicines Agency Fda for vaccines and related biological products has in fact voted unanimously to recommend by the US regulatory body an authorization for the emergency use of a booster dose of the anti-vaccine. Covid of the American company Johnson & Johnson. J&J announced it last night via Twitter.
According to experts, reports the ‘Washington Post’, the booster of the single-dose vaccine developed by Janssen can be administered to the population over 18 after at least 2 months from the first dose.