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  1. Intanza® 9 μg is considered satisfactory by at least 95% of both vaccinees and prescribers, especially because of the short needle and rapid administration. Because Intanza® 9 μg ofers an alternative to intramuscular vaccines, it might help increase influenza vaccine coverage rates.

  2. INTANZA is at least as immunogenic as the comparator trivalent inactivated influenza vaccine administered by intramuscular route for each of the 3 influenza strains in subjects from 60 years of age and over.

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  3. 其他人也問了

  4. 2013年1月1日 · Intanza 9 µg is considered satisfactory by at least 95% of both vaccinees and prescribers, especially because of the short needle and rapid administration. Because Intanza® 9 µg offers an alternative to intramuscular vaccines, it might help increase influenza vaccine coverage rates.

    • Isabel Leroux-Roels, Françoise Weber
    • 2013
  5. Seasonal influenza causes annual epidemics in temperate climates and is associated with economic costs, morbidity and mortality. Vaccination is the primary method of prevention. Intanza (®) (Sanofi Pasteur, Lyon, France) is a newly licensed, trivalent, inactivated influenza vaccine that is delivered ….

    • Robert L Atmar, Shital M Patel, Wendy A Keitel
    • 2010
  6. Intanza. Active substance. influenza virus (inactivated, split) of the following strains:A/California/7/2009 (H1N1)pdm09 - like strain (A/California/7/2009, NYMC X-179A)A/Hong Kong/4801/2014 (H3N2) - like strain (A/Hong Kong/4801/2014, NYMC X-263B)B/Brisbane/60/2008 - like strain (B/Brisbane/60/2008, wild type) International non-proprietary ...

  7. 2014年1月9日 · Intanza ® (Sanofi Pasteur, Lyon, France) is a newly licensed, trivalent, inactivated influenza vaccine that is delivered intradermally with a proprietary micoinjection system. Two dosage formulations have been approved for use in Europe and Australia.

  8. 2016年8月3日 · Fluzone® ID and intanza®. An ID trivalent split-virion influenza vaccine (Fluzone® ID, Sanofi Pasteur, Swiftwater, PA) has been approved by the Food and Drug Administration (FDA) on 10 th May 2011 and been available in the US since the 2011/2012 influenza season for adults aged 18–64 y.