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Cross-species prediction of human survival probabilities for accelerated anthrax vaccine absorbed (AVA) regimens and the potential for vaccine and antibiotic dose sparing

Anthrax vaccine adsorbed (AVA, BioThrax) was recently approved by the Food and Drug Administration (FDA) for a post-exposure prophylaxis (PEP) indication in adults 18–65 years of age. The schedule is three doses administered subcutaneous (SC) at 2-week intervals (0, 2, and 4 weeks), in conjunction w...

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Detalhes bibliográficos
Publicado no:Vaccine
Main Authors: Stark, G.V., Sivko, G.S., VanRaden, M., Schiffer, J., Taylor, K.L., Hewitt, J.A., Quinn, C.P., Nuzum, E.O.
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5130595/
https://ncbi.nlm.nih.gov/pubmed/27558619
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.vaccine.2016.06.041
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