Patient Leaflet Updated 28-Mar-2023 | Valneva UK Limited
IXIARO suspension for injection - Japanese encephalitis vaccine (inactivated, adsorbed)
IXIARO®
suspension for injection
Japanese encephalitis vaccine (inactivated, adsorbed)
1. What IXIARO is and what it is used for
2. What you need to know before you and/or your child receive IXIARO
3. How IXIARO is given
4. Possible side effects
5. How to store IXIARO
6. Contents of the pack and other information
IXIARO is a vaccine against the Japanese encephalitis virus. The vaccine causes the body to produce its own protection (antibodies) against this disease.
IXIARO is used to prevent infection with the Japanese encephalitis virus (JEV). This virus is mainly found in Asia and is transmitted to humans by mosquitoes that have bitten an infected animal (like pigs). Many infected people develop mild symptoms or no symptoms at all. In people who develop severe disease, JE usually starts as a flu-like illness, with fever, chills, tiredness, headache, nausea, and vomiting. Confusion and agitation also occur in the early stage of disease.
IXIARO should be given only to adults, adolescents, children and infants aged 2 months and older travelling to countries, where JE is endemic or who are at risk through work.
IXIARO must not be injected into a blood vessel.
Primary immunization should be completed at least one week prior to potential exposure to JEV.
Tell your doctor:
Your doctor will discuss with you the possible risks and benefits of receiving IXIARO.
Please note that:
Studies in humans to evaluate the effectiveness and safety of medicines (clinical trials) have shown that IXIARO can be given at the same time with hepatitis A vaccine and rabies vaccine.
Tell your doctor if you and/or your child are taking or have recently taken, or might take any other medicines, including medicines obtained without a prescription or have recently received any other vaccine.
There are limited amount of data from the use of IXIARO in pregnant or breast-feeding women.
As a precautionary measure, the use of IXIARO during pregnancy or breast-feeding should be avoided.
If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before receiving this vaccine.
IXIARO has no or negligible influence on the ability to drive and use machines.
This medicine contains potassium, less than 1mmol (39 mg) per 0.5 ml single dosage i.e. essentially ‘potassium-free’ and less than 1 mmol sodium (23 mg) per 0.5 ml single dosage, that is to say essentially ‘sodium-free’. This product might contain traces of residual sodium metabisulfite which is below detection limit.
The recommended dosage for adults, adolescents and children aged 3 years of age and older is a total of 2 injections of 0.5 ml each:
Adults aged 18 to ≤65 years can also be vaccinated as follows:
Babies and children aged 2 months to < 3 years of age
The recommended dosage for babies and children aged 2 months to < 3 years is a total of 2 injections of 0.25 ml each:
For instruction on the preparation of the 0.25 ml dose, please refer to the end of this package leaflet.
Make sure you and/or your child finish the complete vaccination course of 2 injections. The second injection should be given at least 1 week before you and/or your child will be at risk of exposure to JE virus. If not, you and/or your child may not be fully protected against the disease.
For adults, adolescents, children and infants aged 1 year and older a booster dose can be given within the second year (i.e. 12 - 24 months) after the first dose of the recommended primary immunization. In adults, a second booster can be given 10 years after the first booster. For elderly persons (>65 years) the first booster dose may be given earlier. Your doctor will decide on the requirement and timing for booster doses.
IXIARO is injected into your or your child’s upper arm muscle (deltoid muscle) by your doctor or a nurse. It must not be injected into a blood vessel. In case you and/or your child suffer from a bleeding disorder, your doctor may decide to administer the vaccine under the skin (subcutaneously).
If you have any further questions on the use of this product, ask your doctor or pharmacist.
If you and/or your child miss a scheduled injection, talk to your doctor and arrange another visit for the second injection.
Without the second injection you and/or your child will not be fully protected against the disease. There is data showing that the second injection can be given up to 11 months after the first one.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The majority of the side effects listed below have been observed during clinical trials. They usually occur within the first 3 days after vaccination, are usually mild and disappear within a few days.
Very common (affects more than 1 user in 10):
headache, muscle pain, injection site pain, injection site tenderness, tiredness
Common (affects 1 to 10 users in 100):
Nausea, influenza like illness, fever, other injection site reactions (e.g. redness, hardening, swelling, itching)
Uncommon (affects 1 to 10 users in 1,000):
vomiting, skin rash, changes in the lymph-nodes, migraine (throbbing headache, often accompanied by nausea and vomiting and sensitivity to light), dizziness, vertigo (spinning sensation), diarrhoea, belly pain, excessive sweating, itching, chills, general condition of feeling unwell, musculoskeletal stiffness, joint pain, weakness, abnormal laboratory liver test results (hepatic enzymes increased)
Rare (affects 1 to 10 users in 10,000):
palpitations, rapid heartbeat, difficulty to breathe, abnormal sensation of skin (for example pins and needles), hives, skin redness, pain in leg or arm, platelet deficiency, nerve inflammation, limb swelling and ankle swelling, taste disturbance, swelling of eyelid, fainting
In children aged 2 months to <3 years, the following side effects have been observed more frequently compared to children aged 3 years to <12 years, adolescents and adults:
Very common: fever (28.9%), diarrhoea (11.8%), influenza like illness (11.2%), irritability (11.0%)
Common: loss of appetite, vomiting, skin rash
Uncommon: cough
If you and/or your child get any side effects, talk to your doctor. This includes any possible side effects not listed in this leaflet.
You can also report side effects directly via the Yellow Card Scheme at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
By reporting side effects you can help provide more information on the safety of this medicine.
1 dose (0.5 ml) of IXIARO contains:
Japanese encephalitis virus strain SA14-14-2 (inactivated)1,2
6 AU3 corresponding to a potency of ≤ 460 ng ED50
1 produced in Vero cells
2 adsorbed on aluminium hydroxide, hydrated (approximately 0.25 milligrams Al3+)
3 Antigen Units
Aluminium hydroxide is included in this vaccine as an adjuvant.
The other ingredients are: Sodium chloride, potassium dihydrogen phosphate, disodium hydrogen phosphate, water for injections.
IXIARO is a suspension for injection (0.5 ml in a glass syringe with or without a separate needle, pack size of 1).
IXIARO is a white and slightly milky sterile suspension, which becomes homogenous on shaking.
Marketing Authorisation Holder:
Manufacturer:
For any information about this medicine, please contact the Marketing Authorization Holder by the following
e-mail address:
This leaflet was last revised in May 2021.
PS-GBE-01
A090630069355
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