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This document provides information to California Vaccines for Children Program Providers regarding the availability, administration, and recommendations for the new rotavirus vaccine, RotaTeq™,
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How to fill out pentavalent bovine-human reassortant rotavirus
How to fill out PENTAVALENT, BOVINE-HUMAN REASSORTANT ROTAVIRUS VACCINE IS NOW AVAILABLE FROM VFC
01
Obtain the PENTAVALENT, BOVINE-HUMAN REASSORTANT ROTAVIRUS VACCINE from your local VFC provider.
02
Ensure the vaccine is stored at the appropriate temperature before administration.
03
Review the patient’s vaccination history to confirm eligibility for this vaccine.
04
Prepare the vaccine according to the manufacturer's instructions.
05
Administer the vaccine to the eligible patient following standard vaccination protocols.
06
Document the vaccination in the patient's medical record.
07
Provide any necessary information to the patient’s guardian about possible side effects and follow-up.
Who needs PENTAVALENT, BOVINE-HUMAN REASSORTANT ROTAVIRUS VACCINE IS NOW AVAILABLE FROM VFC?
01
Infants and young children who are at risk of rotavirus infection.
02
Children under 5 years of age to prevent severe gastroenteritis caused by rotavirus.
03
Children who are receiving routine immunizations through the VFC program.
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People Also Ask about
What are the 4 types of rotavirus vaccines?
Types Rotarix. Rotarix vaccine for oral administration. Rotateq. Rotateq is a live, oral pentavalent vaccine that contains five rotavirus strains produced by reassortment. Rotavac. Rotavac was licensed for use in India in 2014 and is manufactured by Bharat Biotech International Limited. Rotavin-M1. Lanzhou lamb. Rotasiil.
Is the rotavirus vaccine available in the US?
CDC recommends that infants get rotavirus vaccine to protect against rotavirus disease. Two rotavirus vaccines are currently licensed for use in infants in the United States. RotaTeq® (RV5) has been approved for use since 2006, and is given in three doses at 2 months, 4 months, and 6 months of age.
Can humans get bovine rotavirus?
Bovine G6 strains were reported in many countries to be associated with P[1], P[5], and P[11] (11, 12, 14–16). Two G8P[1] strains, NIC522 and B12, were described as evidence of direct transmission of bovine rotaviruses to humans (18, 19).
What is the pentavalent rotavirus vaccine?
This vaccine is used to help prevent a certain virus infection (rotavirus) in infants and young children. The infection can cause fever, vomiting, and diarrhea, which can lead to severe (rarely fatal) dehydration. Vaccination is the best way to protect against this infection.
What is the pentavalent human bovine reassortant rotavirus vaccine?
Pentavalent human-bovine rotavirus vaccine (HBRV) is an oral vaccine containing five live attenuated human-bovine reassortant strains containing the human serotypes responsible for the majority of rotavirus cases worldwide.
What is a pentavalent rotavirus vaccine?
Indications and Usage for RotaTeq® (Rotavirus Vaccine, Live, Oral, Pentavalent) 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.
What is the controversy with the rotavirus vaccine?
Some studies suggest that rotavirus vaccination possibly causes a small increase in the risk of intussusception, a type of blockage.
What is the new pentavalent rotavirus vaccine?
Indications and Usage for RotaTeq® (Rotavirus Vaccine, Live, Oral, Pentavalent) 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.
What is the controversy with the rotavirus vaccine?
Some studies suggest that rotavirus vaccination possibly causes a small increase in the risk of intussusception, a type of blockage.
What is the current rotavirus vaccine?
RotaTeq® (RV5) has been approved for use since 2006, and is given in three doses at 2 months, 4 months, and 6 months of age. Rotarix® (RV1) has been approved for use since 2008, and is given in two doses at 2 months and 4 months of age.
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What is PENTAVALENT, BOVINE-HUMAN REASSORTANT ROTAVIRUS VACCINE IS NOW AVAILABLE FROM VFC?
PENTAVALENT, BOVINE-HUMAN REASSORTANT ROTAVIRUS VACCINE is a vaccine designed to protect children from severe rotavirus gastroenteritis. It is now available through the Vaccines for Children (VFC) program to ensure that eligible children receive this important vaccination at no cost.
Who is required to file PENTAVALENT, BOVINE-HUMAN REASSORTANT ROTAVIRUS VACCINE IS NOW AVAILABLE FROM VFC?
Healthcare providers who administer the PENTAVALENT, BOVINE-HUMAN REASSORTANT ROTAVIRUS VACCINE are required to file necessary documentation with the VFC program to record vaccine administration and inventory management.
How to fill out PENTAVALENT, BOVINE-HUMAN REASSORTANT ROTAVIRUS VACCINE IS NOW AVAILABLE FROM VFC?
To fill out the documentation for the PENTAVALENT, BOVINE-HUMAN REASSORTANT ROTAVIRUS VACCINE, healthcare providers should accurately record patient information, vaccination date, vaccine lot number, and any reactions or follow-ups necessary as per VFC guidelines.
What is the purpose of PENTAVALENT, BOVINE-HUMAN REASSORTANT ROTAVIRUS VACCINE IS NOW AVAILABLE FROM VFC?
The purpose of the PENTAVALENT, BOVINE-HUMAN REASSORTANT ROTAVIRUS VACCINE is to provide immunity against rotavirus, which can cause severe diarrhea, dehydration, and even hospitalization in young children. The VFC makes it accessible to those in need.
What information must be reported on PENTAVALENT, BOVINE-HUMAN REASSORTANT ROTAVIRUS VACCINE IS NOW AVAILABLE FROM VFC?
Providers must report information including patient demographic details, vaccination date, vaccine manufacturer and lot number, and any adverse events following vaccination as required by the VFC program policies.
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