Prevention of rotavirus disease: guidelines for use of rotavirus vaccine

Pediatrics. 2007 Jan;119(1):171-82. doi: 10.1542/peds.2006-3134.

Abstract

On February 3, 2006, a bovine-based pentavalent rotavirus vaccine (RotaTeq, Merck & Co Inc, Whitehouse Station, NJ) was licensed by the US Food and Drug Administration for use in infants in the United States. The American Academy of Pediatrics recommends routine immunization of infants with 3 doses of pentavalent rotavirus vaccine administered orally at 2, 4, and 6 months of age. The first dose should be administered between 6 and 12 weeks of age; immunization should not be initiated for infants older than 12 weeks of age. Subsequent doses should be administered at 4- to 10-week intervals, and all 3 doses of vaccine should be administered by 32 weeks of age. Pentavalent rotavirus vaccine can be coadministered with other childhood vaccines. Pentavalent rotavirus vaccine is contraindicated for infants with a serious allergic reaction to any vaccine component or to a previous dose of vaccine.

Publication types

  • Clinical Trial, Phase III
  • Practice Guideline

MeSH terms

  • Administration, Oral
  • Feces / virology
  • Gastroenteritis / prevention & control*
  • Gastroenteritis / virology
  • Humans
  • Immunization Schedule*
  • Immunocompromised Host
  • Infant
  • Infant, Newborn
  • Infant, Premature
  • Risk Factors
  • Rotavirus / isolation & purification
  • Rotavirus Infections / epidemiology
  • Rotavirus Infections / prevention & control*
  • Rotavirus Vaccines / administration & dosage*
  • Rotavirus Vaccines / adverse effects
  • Rotavirus Vaccines / immunology
  • United States / epidemiology
  • Vaccines, Attenuated / administration & dosage*
  • Vaccines, Attenuated / adverse effects
  • Vaccines, Attenuated / immunology

Substances

  • RotaTeq
  • Rotavirus Vaccines
  • Vaccines, Attenuated