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Notice to Readers: Availability of Additional Trivalent
Inactivated Influenza Vaccine for Adults
(Afluria®)
On September 28, 2007, CSL Biotherapies, Inc., (King of Prussia, Pennsylvania) received approval from the Food
and Drug Administration for use of
Afluria®, a trivalent inactivated influenza vaccine (TIV) administered intramuscularly
in persons aged >18 years (1). Afluria can be used for any adult influenza vaccine indication
(2).
The addition of Afluria brings to six (five TIVs and one live, attenuated influenza vaccine) the number of
seasonal influenza vaccines licensed for the U.S. market. CDC
estimates that manufacturers of the six vaccines will supply
a record 132 million doses of influenza vaccine for the
2007--08 influenza season.
Afluria is available in a 0.5 mL preservative-free, single-dose, prefilled syringe and in a 5 mL multidose vial
containing 10 doses. Thimerosal, a mercury derivative, is added as a preservative to the multidose vial; each 0.5 mL dose
contains 24.5 µg of mercury. Additional information is available from the manufacturer's package insert
(3) and CSL Biotherapies, Inc., telephone 888-435-8633.
References
Food and Drug Administration. Additional influenza vaccine approved for upcoming influenza season: approval increases available doses to
record level. Rockville, MD: Food and Drug Administration; 2007. Available at
http://www.fda.gov/bbs/topics/news/2007/new01714.html.
Afluria [package insert]. King of Prussia, PA: CSL Biotherapies, Inc.; 2007. Available at
http://www.afluria.com/pi.pdf.
Use of trade names and commercial sources is for identification only and does not imply endorsement by the U.S. Department of
Health and Human Services.References to non-CDC sites on the Internet are
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Department of Health and Human Services. CDC is not responsible for the content
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