Booster dose
- Recommended between 6 and 12 months after the primary dose†2
- Where this is not possible, booster can be delayed up to 3 years2 [LOCs to update the booster delay timeline as per local SmPC]
- Given as a single dose, intramuscularly2
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59
Up to 50 years’ predicted long-term protection when administered in paediatric populations*3
100% seroconversion within 14 days of vaccination**1 (acute hepatitis A incubation period usually 15–50 days)4
[LOCs to update number of days in seroconversion claim when appropriate, to align with local SmPC]
[LOCs to check coadministration options against their local PI]
Havrix Junior has a two-dose regimen2
For children/adolescents aged 1–15 years2
[LOCs to update as per the therapeutic indication of Havrix Junior in the local SmPC]
Primary immunisation schedule
Given as a single dose, intramuscularly2
Booster dose
Havrix (Adult and Junior) has extensive clinical and real-world experience6,7
CI, confidence interval; UV, universal vaccination; mIU/mL, milli-international units per millilitre
*A descriptive analysis was used to predict long-term seropositivity results for children based on studies of vaccines containing inactivated hepatitis A antigen either as standalone hepatitis A vaccine or combination hepatitis A and B vaccine. In order to extrapolate outcomes in children using data in adults, studies with data on adult vaccine doses of hepatitis A and B vaccine 720 EU or hepatitis A vaccine 1,440 EU were selected3
**138 mIU/mL (95% CI: 120–159). In a comparative trial in which 332 seronegative children from 1–15 years of age were randomised to receive two doses of hepatitis A vaccine 6 months apart1
†Havrix Junior can be administered to children and adolescents aged 1–15 years.2 Havrix Junior is administered in a primary dose with a booster dose recommended 6 to 12 months after primary immunisation. Havrix Junior provides active immunisation against infections caused by hepatitis A in both age groups2
††In both paediatric and adult populations7
References
For more information, please refer to the prescribing information or contact GlaxoSmithKline
via gcc.medinfo@gsk.com
To report Adverse Event/s associated with the use of GSK product/s, please contact us via
gulf.safety@gsk.com
To report quality complaint/s associated with the use of GSK product/s, please contact us via
Gulf.ProductQualityComplaints@gsk.com
GlaxoSmithKline Biologicals SA. Rixensart, Belgium
© 2023 GSK group of companies or its licensor
Trademark is owned by or licensed to the GSK group of companies
PM-RCH-HAV-WCNT-230002 | Date of preparation: November 2023