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Choose RotaTeq® (Rotavirus Vaccine, Live, Oral, Pentavalent) to help protect babies against RGE

RotaTeq is indicated to help protect against more types of rotavirus1,a

  • RotaTeq has broad coverage, indicated to help protect against RGE caused by five strains, including G2.
  • RotaTeq is the only rotavirus vaccine indicated to help protect against RGE caused by G2.1
    • Rotarix® (Rotavirus Vaccine, Live Oral) is not indicated to help protect against RGE caused by G2.1
    • Rotarix® is indicated for the prevention of rotavirus gastroenteritis caused by G1 and non-G1 types (G3, G4, and G9) when administered as a 2-dose series. Rotarix® is approved for use in infants 6 weeks and up to 24 weeks of age.1
  • Flexible dosing schedule aligns with well-baby visits.1,2

RGE, rotavirus gastroenteritis.

Rotarix is a registered trademark of GSK.

aCompared to Rotarix. Rotarix is indicated for the prevention of rotavirus gastroenteritis caused by G1 and non-G1 types[G3,G4, and G9] when administered as a 2-dose series. Rotarix is approved for use in infants 6 weeks and up 24 weeks of age.1

Most pediatricians chose
RotaTeq to help protect their patients3:

Based on Komodo claims data from January 2019 to December 2025 and defining the pediatrician as a RotaTeq user if they vaccinated at least 80% of their patients with RotaTeq annually.

Rotavirus strain variability

Review the strain coverage information for RotaTeq.

Explore strain coverage

Dosing and administration

Review the dosing schedule and administration of RotaTeq.

Learn more about dosing

References

  1. Rotarix. Prescribing information. GSK; 2024.
  2. MedlinePlus. National Library of Medicine (NLM). Well-child visits. Last reviewed January 1, 2025. Accessed January 22, 2026. https://medlineplus.gov/ency/article/001928.htm
  3. Data available on request from the Merck National Service Center via email at daprequests@merck.com. Please specify information package US-ROT-00933.
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Indications and Usage

RotaTeq is indicated for the prevention of rotavirus gastroenteritis in infants and children caused by Types G1, G2, G3, G4, and G9 when administered as a 3-dose series to infants between the ages of 6 to 32 weeks. The first dose of RotaTeq should be administered between 6 and 12 weeks of age.

The vaccination series consists of 3 ready-to-use liquid doses of RotaTeq administered orally starting at 6 to 12 weeks of age, with the subsequent doses administered at 4- to 10-week intervals. The third dose should not be given after 32 weeks of age.

Selected Safety Information

RotaTeq is contraindicated in infants with a demonstrated history of hypersensitivity to the vaccine or any component of the vaccine.

RotaTeq is contraindicated in infants with Severe Combined Immunodeficiency Disease (SCID). These infants should not receive RotaTeq. Post-marketing reports of gastroenteritis, including severe diarrhea and prolonged shedding of vaccine virus, have been reported in infants who were administered RotaTeq and later identified as having SCID.

RotaTeq is contraindicated in infants with a history of intussusception. These infants should not receive RotaTeq.

No safety or efficacy data are available from clinical trials regarding the administration of RotaTeq to infants who are potentially immunocompromised.

In a post-marketing observational study in the US, cases of intussusception were observed in temporal association within 21 days following the first dose of RotaTeq, with a clustering of cases in the first 7 days.

No safety or efficacy data are available for administration of RotaTeq to infants with a history of gastrointestinal disorders.

Vaccine virus transmission from vaccine recipient to nonvaccinated contacts has been reported. Caution is advised when considering whether to administer RotaTeq to individuals with immunodeficient contacts.

In clinical trials, the most common adverse events included diarrhea, vomiting, irritability, otitis media, nasopharyngitis, and bronchospasm.

In post-marketing experience, intussusception (including death) and Kawasaki disease have been reported in infants who have received RotaTeq.

RotaTeq may not protect all vaccine recipients against rotavirus.

Before administering RotaTeq, please read the accompanying Prescribing Information. The Patient Product Information also is available.

Indications and Usage
Selected Safety Information

RotaTeq is indicated for the prevention of rotavirus gastroenteritis in infants and children caused by Types G1, G2, G3, G4, and G9 when administered as a 3-dose series to infants between the ages of 6 to 32 weeks. The first dose of RotaTeq should be administered between 6 and 12 weeks of age.

The vaccination series consists of 3 ready-to-use liquid doses of RotaTeq administered orally starting at 6 to 12 weeks of age, with the subsequent doses administered at 4- to 10-week intervals. The third dose should not be given after 32 weeks of age.

Selected Safety Information

RotaTeq is contraindicated in infants with a demonstrated history of hypersensitivity to the vaccine or any component of the vaccine.

RotaTeq is contraindicated in infants with Severe Combined Immunodeficiency Disease (SCID). These infants should not receive RotaTeq. Post-marketing reports of gastroenteritis, including severe diarrhea and prolonged shedding of vaccine virus, have been reported in infants who were administered RotaTeq and later identified as having SCID.

RotaTeq is contraindicated in infants with a history of intussusception. These infants should not receive RotaTeq.

No safety or efficacy data are available from clinical trials regarding the administration of RotaTeq to infants who are potentially immunocompromised.

In a post-marketing observational study in the US, cases of intussusception were observed in temporal association within 21 days following the first dose of RotaTeq, with a clustering of cases in the first 7 days.

No safety or efficacy data are available for administration of RotaTeq to infants with a history of gastrointestinal disorders.

Vaccine virus transmission from vaccine recipient to nonvaccinated contacts has been reported. Caution is advised when considering whether to administer RotaTeq to individuals with immunodeficient contacts.

In clinical trials, the most common adverse events included diarrhea, vomiting, irritability, otitis media, nasopharyngitis, and bronchospasm.

In post-marketing experience, intussusception (including death) and Kawasaki disease have been reported in infants who have received RotaTeq.

RotaTeq may not protect all vaccine recipients against rotavirus.

Before administering RotaTeq, please read the accompanying Prescribing Information. The Patient Product Information also is available.