So I finally received the seasonal influenza vaccine yesterday. The vaccine contained three influenza viruses: one A (H3N2) virus, one regular seasonal A (H1N1) virus (not the 2009 H1N1 virus), and one B virus.
The influenza vaccine composition used in the 2009-2010 influenza season in the U.S. is identical to that recommended by the World Health Organization (WHO) on February 12, 2009, for the Northern Hemisphere's 2009-2010 influenza season.
It was recommended by the WHO that vaccines for use in the 2009-2010 influenza season (northern hemisphere winter) contain the following:
— an A/Brisbane/59/2007 (H1N1)-like virus;*
— an A/Brisbane/10/2007 (H3N2)-like virus;**
— a B/Brisbane/60/2008-like virus.#
* A/Brisbane/59/2007 is a current vaccine virus; A/South Dakota/6/2007 (an A/Brisbane/59/2007-like virus) is a current vaccine virus used in live attenuated vaccines.
** A/Brisbane/10/2007 and A/Uruguay/716/2007 (an A/Brisbane/10/2007-like virus) are current vaccine viruses.
# B/Brisbane/33/2008 is a B/Brisbane/60/2008-like virus.
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According to my documentation, the vaccine dose that I received was manufactured by Novartis Vaccines. I was given the vaccine in a single 0.5-mL intramuscular injection from a prefilled syringe.
According to the product information provided by Novartis on the FDA website, the shot in the prefilled syringe (0.5-ml) contains less than one microgram of mercury by 0.5-ml dose. Thimerosal, a mercury derivative used during manufacture, but removed by subsequent purification steps to a trace amount.
The 0.5-mL dose contained 15 micrograms (mcg) of influenza virus hemagglutinin (HA)
from each of the following 3 viruses: A/Brisbane/59/2007, IVR-148 (H1N1);
A/Uruguay/716/2007, NYMC X-175C (H3N2) (an A/Brisbane/10/2007-like virus); and
B/Brisbane/60/2008.
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Product information from the other licensed manufacturers of the seasonal flu vaccine can be found on the FDA website.
thanks ass
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