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The 2011-2012 seasonal trivalent inactivated influenza vaccine is a biological preparation designed to provide active acquired immunity against three specific strains of the influenza virus: A/California/7/2009 (H1N1)pdm09-like, A/Perth/16/2009 (H3N2)-like, and B/Brisbane/60/2008-like. Developed for the 2011-2012 influenza season in the Northern Hemisphere, this specific formulation was evaluated by the Instituto Nacional de Salud Publica in Mexico for its safety and immunogenicity in pregnant women. It is an unadjuvanted, inactivated vaccine administered via intramuscular injection, containing 15 µg of hemagglutinin per strain to stimulate a protective immune response.
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