Moderna’s updated COVID vaccine approved by British regulators
NEWYou can now listen to Fox News articles! British drug regulators have become the first in the world to authorize […]
vaccine
Bharat Biotech completes trials for India’s first intranasal Covid vaccine, says it’s safe, immunoge-
By Express News Service HYDERABAD: City-based Bharat Biotech on Monday announced it had completed clinical development for phase III trials
UK becomes first country to approve Covid booster vaccine targeting original and Omicron strains-
By PTI LONDON: The UK has become the first country to approve a so-called ‘bivalent’ COVID vaccine that targets both the
Cincinnati Open 2022 Novak Djokovic out from tournament due to not having covid vaccine | Cincinnati Open: कोरोना वैक्सीन को लेकर फिर हुआ जोकोविच का विवाद, अब इस बड़े टूर्नामेंट से किया गया बाहर
Cincinnati Open: 21 बार के ग्रैंडस्लैम चैम्पियन नोवाक जोकोविच कोरोना का टीका नहीं लगवाने के कारण अमेरिका की यात्रा नहीं
Punjab to procure 3.3 lakh more doses of goat pox vaccine-
By PTI CHANDIGARH: The Punjab government on Friday said it will procure 3.3 lakh more doses of goat pox vaccine
1.16 lakh doses of goat pox vaccine administered to cattle in Punjab-
By PTI CHANDIGARH: Around 1.16 lakh doses of goat pox vaccine have been administered to cattle in Punjab as the
Spain proposes ‘dose-sparing’ for monkeypox vaccine due to low supply and rising cases
NEWYou can now listen to Fox News articles! Spain has asked the European Medicines Agency (EMA) for permission to give
COVID vaccine production from South Africa’s Aspen Pharmacare to end due to low demand
NEWYou can now listen to Fox News articles! South Africa’s Aspen Pharmacare will stop making COVID-19 vaccines from the end
Polio vaccine campaign underway in London as the virus spreads in the city
NEWYou can now listen to Fox News articles! Britain is launching a polio vaccine booster campaign for children in London
Monkeypox vaccine authorization expanded by FDA to increase dose supply
NEWYou can now listen to Fox News articles! The Food and Drug Administration (FDA) expanded its emergency use authorization (EUA)