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  Vol. 287 No. 5, February 6, 2002 TABLE OF CONTENTS
  JAMA
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  From the Centers for Disease Control and Prevention: Morbidity and Mortality Weekly Report
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Supply of Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine

JAMA. 2002;287:579.

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

MMWR. 2002;50:1159

Diphtheria and tetanus toxoids and acellular pertussis vaccine (DTaP) remains in short supply, and the shortage will continue into mid-2002.1 Shortages are greatest in the public sector. Despite high vaccination rates, pertussis continues to cause serious illness and death, particularly among infants aged <6 months who are too young to have completed the 3-dose primary series of DTaP. In 2000, a total of 1,873 pertussis cases (rate: 99 per 100,000 infants aged <6 months) and 16 deaths were reported among infants aged <6 months. Vaccinating infants on time with the 3-dose primary series of DTaP to protect them from serious disease remains a priority during this vaccine shortage.

The shortage began in 2000 when two manufacturers (Wyeth Lederle, Pearl River, New York, and Baxter Hyland Immuno Vaccines, Baltimore, Maryland) stopped production of DTaP.1 Aventis Pasteur (Swiftwater, Pennsylvania) and GlaxoSmithKline (Philadelphia, Pennsylvania), producers of Tripedia® and InfanrixTM, respectively, . . . [Full Text of this Article]







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