FDA approves Sanofi Pasteur's meningococcal vaccine

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FDA approves Sanofi Pasteur's meningococcal vaccine

news-medical.net

Sanofi Pasteur, the vaccines division of the sanofi-aventis Group, announced today that the U.S. Food and Drug Administration has granted licensure to expand the indication for its meningococcal conjugate vaccine, Menactra, to include a two-dose schedule for infants and children 9 months through 23 months of age.

View full resource at news-medical.net

Tags: Vaccination, Meningitis, Diet and Nutrition, Drug, FDA, Vaccine, Sanofi-Aventis, News

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Most Recently Shared on April 25, 2011 at 11:44 am By:

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Meningitis News: FDA approves Sanofi Pasteur's meningococcal vaccine: Sanofi Pasteur, the vaccines division of t... http://bit.ly/eCrvvc

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Microinjection Flu Vaccine Product Approved by FDA -- AAFP News Now -- American Academy of Family Physicians

aafp.org — “Family physicians soon may have a new weapon in their armamentarium to prevent influenza. Pharmaceutical manufacturer Sanofi Pasteur said in a May 10 news release that the FDA has approved the company’s license application for Fluzone Intradermal, making it the first influenza vaccine that uses a microinjection system to be licensed in the United States.View full resource at aafp.org

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empr.com — “Sanofi Pasteur announced that the FDA has approved Fluzone Intradermal (influenza virus vaccine) for the active immunization of adults 18--64 years old against influenza disease caused by influenza virus subtypes A and type B contained in the vaccine.View full resource at empr.com

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Fluzone Intradermal Vaccine Approved for Influenza Immunization - ONA

oncologynurseadvisor.com — “Sanofi Pasteur announced that the FDA has approved Fluzone Intradermal (influenza virus vaccine) for the active immunization of adults 18--64 years old against influenza disease caused by influenza virus subtypes A and type B contained in the vaccine.View full resource at oncologynurseadvisor.com

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Most Recently Shared on May 10, 2011 at 2:51 pm By:

Sanofi Pasteur Announces FDA Approval of Menactra Meningococcal Conjugate Vaccine Indication for Infants - Apr 22, 2011

sanofipasteurus.mediaroom.com — “Welcome to sanofi pasteur, Sanofi Pasteur US Media Center, the vaccines division of sanofi-aventis Group, is the largest company in the world devoted entirely to human vaccines.View full resource at sanofipasteurus.mediaroom.com

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Menactra Gains Indication for Immunization of Infants - ONA

oncologynurseadvisor.com — “The FDA has expanded the indication for Menactra (meningococcal [Groups A, C, Y and W-135] polysaccharide diphtheria toxoid conjugate vaccine; Sanofi Pasteur) to include a two-dose schedule for infants and children 9--23 months old.View full resource at oncologynurseadvisor.com

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FDA Approval Of Menactra Meningococcal Conjugate Vaccine Indication For Infants Announced By Sanofi Pasteur

medicalnewstoday.com — “Sanofi Pasteur, the vaccines division of the sanofi-aventis Group (EURONEXT: SAN and NYSE: SNY), announced today that the U.S. Food and Drug Administration (FDA) has granted licensure to expand thView full resource at medicalnewstoday.com

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Menactra Gains Indication for Immunization of Infants - MPR

empr.com — “The FDA has expanded the indication for Menactra (meningococcal [Groups A, C, Y and W-135] polysaccharide diphtheria toxoid conjugate vaccine; Sanofi Pasteur) to include a two-dose schedule for infants and children 9--23 months old.View full resource at empr.com

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Sanofi Pasteur receives FDA approval for Menactra to prevent meningococcal disease

news-medical.net — “The U.S. Food and Drug Administration today approved the use of Menactra in children as young as 9 months for the prevention of invasive meningococcal disease caused by Neisseria meningitidis serogroups A, C, Y and W-135. Menactra already is approved for use in people ages 2 through 55 years.View full resource at news-medical.net

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FDA accepts Sanofi Pasteur's Menactra vaccine sBLA for active immunization of infants and toddlers

news-medical.net — “Sanofi Pasteur, the vaccines division of the sanofi-aventis Group, announced today that the U.S. Food and Drug Administration (FDA) has accepted for review a supplemental Biologics License Application (sBLA) for use of Menactra® (Meningococcal [Groups A, C, Y and W-135] Polysaccharide Diphtheria Toxoid Conjugate Vaccine) for active immunization of infants and toddlers for the prevention of invasive meningococcal disease caused by serogroups A, C, Y, and W-135.View full resource at news-medical.net

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Meningitis News: FDA accepts Sanofi Pasteur's Menactra vaccine sBLA for active immunization of infants and toddler... http://bit.ly/doRVE7

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FDA accepts sBLA for Menactra for immunization of infants and toddlers - MPR

empr.com — “Sanofi Pasteur announced that the FDA has accepted for review a supplemental Biologics License Application (sBLA) for the use of Menactra (Meningococcal [Groups A, C, Y and W-135] polysaccharide diphtheria toxoid conjugate vaccine) for active immunization of infants and toddlers for the prevention of invasive meningococcal disease caused by serogroups A, C, Y, and W-135.View full resource at empr.com

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fiercepharma.com — “FDA Accepts Sanofi Pasteur's Application to Expand Indication of Menactra® Vaccine to Infants and Toddlers New Indication Seeks to Help Protect Infants and Toddlers Against Meningococcal... Read more...View full resource at fiercepharma.com

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FDA Accepts Sanofi Pasteur's Application to Expand Indication of Menactra® Vaccine to Infants and Toddlers. http://bit.ly/bnN5Cn

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FDA accepts sBLA for Menactra for immunization of infants and toddlers - ONA

oncologynurseadvisor.com — “Sanofi Pasteur announced that the FDA has accepted for review a supplemental Biologics License Application (sBLA) for the use of Menactra (Meningococcal [Groups A, C, Y and W-135] polysaccharide diphtheria toxoid conjugate vaccine) for active immunization of infants and toddlers for the prevention of invasive meningococcal disease caused by serogroups A, C, Y, and W-135.View full resource at oncologynurseadvisor.com

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