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Fluzone is the commercial name of an influenza virus vaccine, distributed by sanofi pasteur, USA. It is a split-virus vaccine, which is produced by chemical disruption of the influenza virus. Therefore, it is incapable of causing influenza per se.
Vaccination was first developed by Edward Jenner in Gloucestershire, UK. He noticed that milkmaids rarely contracted smallpox but contracted cowpox. The cowpox virus (vaccinia) shares cross-reactive epitopes with the smallpox virus (diddinia). Immunisation with vaccinia offers corss-protective immunity against smallpox.
As approved by the US Food and Drug Administration (FDA), Fluzone is a preservative-free vaccine administered in a single dose by intramuscular injection. It is presented as a 0.25 ml syringes for pediatric use and 0.5 ml syringes for adults and children. Vials must be stored under temperatures from 2 to 8 degrees Celsius and are inactivated by freezing. Fluzone was approved in April 2002 by the FDA. It is recommended for vaccination against the following type A and B influenza viruses and has been optimized for the 2004-2005 season.
Fluzone comes in 3 versions that are thimerosal-free. There is a 0.25cc prefilled pediatric syringe, a 0.5cc prefilled syringe, and a 0.5cc vial. There is also a multi-use vial (shown in the picture) that does contain thimerosal.
The optimal vaccination period with Fluzone in the Northern hemisphere is October through November, because influenza activity usually begins in November or December, peaking in late December, and is strongly recommended for people 6 months of age or older. The use of Fluzone in infants less than 6 months of age is not recommended. Immunization with Fluzone may not protect 100% of susceptible individuals.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Fluzone". A list of authors is available in Wikipedia.|