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Varilrix

Common name:

Chickenpox vaccine, VV, varicella vaccine

Protects against varicella (chickenpox).

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Overview

In New Zealand, chickenpox is a common illness in childhood and most adults will have had the disease as a child. Adults who grew up in tropical countries are less likely to have had chickenpox in childhood. Adolescents and adults are at higher risk than children of severe disease and complications.

Varilrix® is a live vaccine containing a weakened form of the varicella-zoster virus to protect children and adults from chickenpox.

The National Immunisation Schedule varicella vaccine brand is changing from Varilrix to Varivax for eligible children and adults aged 12 months or older.

Varilrix will continue to be the funded varicella vaccine brand for infants aged 9–11 months who meet one of the special groups eligibility criteria.

In children aged from 9 months to under 13 years, a single dose of vaccine will protect around eight in 10 children. Up to two in 10 may still get chickenpox, but are usually protected against moderate to severe disease. Children aged 13 years and older, and adults up to 50 years who are not immune, require two doses of the vaccine for protection against moderate to severe disease. The vaccine may also prevent or reduce the severity of chickenpox in someone who has not previously had chickenpox or been vaccinated, if it is given within 3–5 days of exposure to the disease.

Extremely rarely a vaccine recipient with a vaccine-related rash could transfer the vaccine virus to another person. With more than 60 million vaccine doses given, 10 cases have been documented. There is no risk of the vaccine virus being transferred to another person if there is no vaccine-related rash. Vaccine recipients who develop a rash should avoid contact with women who are pregnant and not immune to chickenpox, newborn babies and people known to have weakened immune systems until the rash has gone.

Varilrix for eligible/funded infants aged 9–11 months is available from ProPharma.

Varilrix is also the vaccine available for purchase for childen and adults who are not eligible for funded varicella vaccine doses. Varilrix for non-funded child and adult doses is available from Healthcare Logistics.

Responses to vaccine

Varilrix (VV)

Common Responses

  • Headache and/or tiredness
  • Mild rash 6–43 days after immunisation

Rare Responses

  • High fever
  • Transfer of vaccine virus from a vaccine rash to another person

As with any medicine, very rarely a severe allergic reaction (anaphylaxis) can occur following immunisation.

References

  • Ampofo K, Saiman L, LaRussa P, Steinberg S, Annunziato P, Gershon A. Persistence of immunity to live attenuated varicella vaccine in healthy adults. Clin Infect Dis. 2002;34(6):774-9.
  • Baxter R, Ray P, Tran TN, Black S, Shinefield HR, Coplan PM, et al. Long-term effectiveness of varicella Vaccine: A 14-year, prospective cohort study. Pediatrics. 2013;131(5):138-1396.
  • Ezeanolue E, Harriman K, Hunter P, Kroger A, Pellegrini C. Centers for Disease Control and Prevention. General Recommendations on Immunization Recommendations of the Advisory Committee on Immunization Practices (ACIP);[updated 2020 July 27; cited 2020 September 28]. Available from: https://www.cdc.gov/vaccines/hcp/acip-recs/general-recs/downloads/general-recs.pdf 
  • Centers for Disease Control and Prevention. Prevention of varicella recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR Recomm Rep. 2007;56(RR-04):1-40.
  • Chaves SS, Haber P, Walton K, Wise RP, Izurieta HS, Schmid DS, et al. Safety of varicella vaccine after licensure in the United States: Experience from reports to the Vaccine Adverse Event Reporting System, 1995–2005. J Infect Dis. 2008;197(Suppl 2):S170-7.
  • Civen R, Chaves SS, Jumaan A, Wu H, Mascola L, Gargiullo P, et al. The incidence and clinical characteristics of herpes zoster among children and adolescents after implementation of varicella vaccination. Pediatr Infect Dis J. 2009;28(11):954-9.
  • Dennehy PH, Reisinger KS, Blatter MM, Veloudis BA. Immunogenicity of subcutaneous versus intramuscular Oka/Merck varicella vaccination in healthy children. Pediatrics. 1991;88(3):604-7.
  • Gershon A, Marin M, Seward J. Varicella vaccines. In: Plotkin S, Orenstein W, Offit P, Edwards K, editors. Plotkin’s Vaccines. 7th ed. Philadelphia: Elsevier; 2018. p. 1145-80.
  • Gillet Y, Steri GC, Behre U, Arsene JP, Lanse X, Helm K, et al. Immunogenicity and safety of measles-mumps-rubella-varicella (MMRV) vaccine followed by one dose of varicella vaccine in children aged 15 months-2 years or 2-6 years primed with measles-mumps-rubella (MMR) vaccine. Vaccine. 2009;27(3):446-53.
  • Goulleret N, Mauvisseau E, Essevaz-Roulet M, Quinlivan M, Breuer J. Safety profile of live varicella virus vaccine (Oka/Merck): Five year results of the European Varicella Zoster Virus Identification Program (EU VZVIP). Vaccine. 2010;28(36):5878-82.
  • Levin MJ, Murray M, Zerbe GO, White CJ, Hayward AR. Immune responses of elderly persons 4 years after receiving a live attenuated varicella vaccine. J Infect Dis. 1994;170(3):522-6.
  • Macartney K, McIntyre P. Vaccines for post-exposure prophylaxis against varicella (chickenpox) in children and adults. Cochrane Database Syst Rev. 2014;(6):Art. No.: CD001833.
  • Marin M, Marti M, Kambhampati A, et al. Global Varicella Vaccine Effectiveness: A Meta-analysis. Pediatrics. 2016;137(3):1-10.
  • Medsafe. New Zealand data sheet: Varilrix [Internet]. Wellington: New Zealand Medicines and Medical Devices Safety Authority; 1996 [updated 2019 September 2; cited 2020 July 1]. Available from: http://www.medsafe.govt.nz/profs/Datasheet/v/Varilrixinj.pdf
  • Ministry of Health. Immunisation handbook [Internet]. Wellington: Ministry of Health; 2020 [updated 2020 September 28; cited 2020 September 30]. Available from: https://www.health.govt.nz/publication/immunisation-handbook-2020
  • Schmid DS, Jumaan AO. Impact of varicella vaccine on varicella-zoster virus dynamics. Clin Microbiol Rev. 2010;23(1):202-17.
  • Strategic Advisory Group of Experts on Immunization. Systematic review of available evidence on effectiveness and duration of protection of varicella vaccines: WHO; 2014 [cited 2016 March 14]. Available from: http://www.who.int/immunization/sage/meetings/2014/april/presentations_background_docs/en/
  • World Health Organization. Varicella and herpes zoster vaccines: WHO position paper, June 2014. Wkly Epidemiol Rec. 2014;89(25):265-87.
  • Wutzler P, Knuf M, Liese J. Varicella: Efficacy of two-dose vaccination in childhood. Dtsch Arztebl Int. 2008;105(33):567-72.
In Depth

Other brands of varicella vaccine: Varivax®

Vaccine type:Live-attenuated virus vaccine

Vaccine schedule and administration

The National Immunisation Schedule varicella vaccine brand is changing from Varilrix to Varivax for eligible children and adults aged 12 months or older.

Varilrix will continue to be the funded varicella vaccine brand for infants aged 9–11 months who meet one of the special groups eligibility criteria.

    Special groups

    One dose of Varilrix for infants aged 9–11 months followed by one dose of Varivax from 12 months of age who meet one of the eligibility criteria below:

    • Who are HIV-positive with mild or moderate immunosuppression, on the advice of their specialist
    • Prior to elective immunosuppressive therapy that will be longer than 28 days
    • With chronic liver disease who may in future be candidates for transplantation
    • With deteriorating renal function before transplantation
    • Prior to solid organ transplantation
    • After a haematopoietic stem cell transplantation, on the advice of their specialist
    • After chemotherapy, on the advice of their specialist
    • With an inborn error of metabolism at risk of major metabolic decompensation
    • Who are a household contact of a child or adult patient who is immunocompromised or undergoing a procedure leading to immunocompromise, where the household contact has no clinical history of varicella infection or immunisation

    The vaccine brands Varilrix and Varivax are interchangeable within a two-dose course of vaccines.

      Varilrix vaccine for purchase

      Should children and adults have one or two varicella vaccinations?

      Children aged less than 13 years

      • Parents may choose to purchase a second dose of varicella vaccine, which can be administered a minimum of 4 weeks before or after the first dose.
      • Infants who receive their first varicella vaccine dose when aged under 12 months of age are recommended to have a second varicella vaccination from age 12 months. Maternal antibodies against chickenpox could be present in infants aged under 12 months and affect the infant's individual response to the vaccination.
      • In all children aged under 13 years, one dose gives good protection, two doses give optimal protection.

      Children aged 13 years or older and adults

      • The standard varicella vaccine schedule is two doses administered a minimum of 4 weeks apart for individuals in this age group receiving varicella vaccine for the first time.
      • Varicella vaccination is not routinely recommended for adults aged 50 years or older.

      Catch-up doses

      • All children and adults up to 50 years of age, as required.
      • Varicella vaccination is not routinely recommended for adults aged 50 years or older.

      Vaccine storage and preparation

      Store vaccine and diluent as per cold chain between 2°C to 8°C.

      Administration

      • The Ministry of Health recommends that varicella vaccine is administered via the IM route. However, administration of varicella vaccine by either the IM or SC injection route delivers a valid dose of vaccine. In the original clinical trials, varicella vaccine was given by SC injection and this became the recommended route of injection. Since then, data have shown that administration of varicella vaccine by IM injection generates an immune response equal to the response when the vaccine is given via the SC route, and the vaccine is also well-tolerated.
      • Varilrix and the alternative Varivax vaccine are interchangeable within a two dose course of vaccines. 

      For infants likely to require a liver or kidney transplanation who are on an accelerated vaccination schedule (refer to table 4.3 in the current Immunisation Handbook)

      • Varilrix can be administered concurrently with other Schedule vaccines, including MMR or hepatitis A. Separate syringes and different injection sites should be used.
      • If Varilrix is not given at the same visit as another live injectable vaccine e.g. MMR, a 4 week interval between the two live virus vaccines should be observed.

      Vaccine safety

      Varicella vaccine can be given to:

      • A person living with a newborn baby or a pregnant woman or a person who is immune suppressed.

      Immunisation should be postponed in individuals suffering from a fever over 38°C. However, the presence of a minor infection is not a reason to delay immunisation.

      Varicella vaccine should not be given to:

      • Anyone who has a severe weakness of the immune system
      • Anyone who had a severe allergic response (anaphylaxis) to a previous dose of this vaccine or a component of this vaccine.
      • Women who are currently pregnant. Women are advised to delay pregnancy for 4 weeks after receipt of a varicella vaccine dose.
      • People who have received another live injected vaccine within the previous four weeks

      Advice should be sought for the following groups:

      • People known to have a weakened immune system.
      • People receiving high-dose steroid medicine, e.g. prednisone, for more than 14 days. They should wait for at least four weeks after their treatment has finished before receiving the vaccine.
      • People taking antiviral medication, e.g. tablets for cold sores. These should be stopped for 24 hours prior to immunisation and not restarted for 14 days afterwards.
      • Children taking aspirin. Whilst there has been no association between chickenpox immunisation and Reye’s Syndrome, avoidance of aspirin around the time of immunisation and for six weeks afterward is advised as a precaution.
      • People who have received a blood product in the 11 months before immunisation.
      • People expecting to receive a blood product in the two months after immunisation. These should not be given for two months after immunisation unless their use outweighs the benefits of the immunisation.

      It is possible but extremely rare for a person with a vaccine related rash to transfer the vaccine virus to another person, only 10 cases have been reported from around 60 million vaccine doses in the U.S. There is no risk of the vaccine virus being transferred to another person if there is no vaccine-related rash.

      Vaccine effectiveness

      For optimal protection (99%) against all chickenpox disease in children aged nine months up to and including 12 years of age a vaccine course of two doses of Varilrix separated by at least four weeks is recommended. However, a single dose of vaccine offered from the age of 12 months can provide 70–90% protection against all chickenpox, and more than 95% will be protected from moderate-severe disease but may still get mild chickenpox (often fewer than 50 lesions).

      Available information suggests that chickenpox vaccinations may decrease the risk of developing shingles later in life compared with having the wild-type disease.

      Last updated: Sep 2020