Prospect: information for the user
Fluenz nasal suspension for inhalation
Influenza vaccine (live attenuated, nasal)
Read this prospect carefully before administering the vaccine, as it contains important information for you or your child.
1.What is Fluenz and for what it is used
2.What you need to know before administering Fluenz
3.How to administer Fluenz
4.Possible adverse effects
5.Storage of Fluenz
6.Contents of the package and additional information
Fluenz is a vaccine to prevent the flu. It is used in children and adolescents over24months andless than18years. Fluenz will help protect you from the virus strains contained in the vaccine and other closely related strains.
How Fluenz works
When the vaccine is administered to a person, the immune system (the body's natural defense system) produces its own protection against the flu virus. None of the vaccine components can cause the flu.
The Fluenz virus strains are grown in chicken eggs. Each year, the vaccine acts against three flu strains, following the annual recommendations of the World Health Organization.
You will not be given Fluenz:
If any of these conditions apply to you,inform your doctor, nurse or pharmacist.
Warnings and precautions
Inform your doctor, nurse or pharmacist before vaccination:
If any of these conditions apply to you,inform your doctor, nurse or pharmacist beforevaccination. They will decide if Fluenz is suitable for you.
Other medications, other vaccines and Fluenz
Inform your doctor, nurse or pharmacist if the person being vaccinated is using, has recently used or mayhave touse any other medication, including medications that do not require a prescription.
Your doctor, nurse or pharmacist will decide if Fluenz can be administered at the same time as other vaccines.
Pregnancy and breastfeeding
Driving and operating machinery
Fluenz will be administered under the supervision of a doctor, nurse, or pharmacist.
Fluenz should only be used as a nasal spray.
Fluenz should not be injected.
Fluenz will be administered as a spray into each nasal cavity. You can breathe normally while Fluenz is being administered. There is no need to inhale or actively aspirate.
Dosage
The recommended dosefor children and adolescents is0.2ml of Fluenz, administered at a rate of0.1ml into each nasal cavity.Children who have not been vaccinated against the fluwill receive a second dose offollow-up after a minimum interval of4weeks. Follow the instructions of your doctor, nurse, or pharmacist regarding whether your child should attend for the second dose and when.
If you have any other questions about the use of this medication, ask your doctor, nurse, orpharmacist.
Like all medicines, this vaccine may cause side effects, although not everyone will experience them. In clinical studies conducted with this vaccine, most side effects were brief and of mild nature.
Consult your doctor, nurse, or pharmacist if you wish to learn more about the possible side effects of Fluenz.
Some side effects may be serious.
Very rare
(may affect up to1in every10,000people)
Inform your doctor immediately or seek urgent medical attentionif you notice any of these symptoms.
Other possible side effects of Fluenz
Very common
(may affect more than1in every10people):
Common
(may affect up to1in every10people):
Uncommon
(may affect up to1in every100people):
Reporting of side effects
If you experience any type of side effect, consult your doctor, pharmacist, or nurse, even if it is a possible side effect that does not appear in this prospectus. You can also report them directly through thenational notification system included in theAppendix V. By reporting side effects, you cancontribute to providing more information about the safety of this medicine.
Keep this vaccine out of the sight and reach of children.
Do not use this vaccine after the expiration date that appears on the applicator label after the letters EXP.
Store in the refrigerator (between 2°C and 8°C). Do not freeze.
Keep the nasal applicator in the outer packaging to protect it from light.
Before use, the vaccine can be removed from the refrigerator once during a maximum period of 12 hours at a temperature of up to 25°C. If not used after this 12-hour period, the vaccine must be discarded.
Medicines should not be disposed of through the drains or in the trash. Ask your pharmacist how to dispose of the containers and medicines that you no longer need. This will help protect the environment.
Composition of Fluenz
The active principles are:
Influenza virus reaggregated* (live attenuated) from the following strains:
Strain similar to A/ Victoria/4897/2022 (H1N1)pdm09
(A/ Norway/31694/2022, MEDI 369815)107.0±0.5UFF***
Strain similar to A/ Thailand/8/2022 (H3N2)
(A/ Thailand/8/2022, MEDI 370626)107.0±0.5UFF***
Strain similar to B/ Austria/1359417/2021
(B/ Austria/1359417/2021, MEDI 355292)107.0±0.5UFF***
.......................................................................................................for a dose of0.2ml
*multiplied in fertilized chicken eggs from healthy chicken farms.
**produced in VERO cells by reverse genetic technology. This product contains genetically modified organisms (GMOs).
***Units of Fluorescent Foci
This vaccine meets the WHO (World Health Organization, Northern Hemisphere) recommendation and the EU decision for the 2024/2025 season.
The other components are sucrose, potassium dihydrogen phosphate, dihydrogen potassium phosphate, gelatin (pig, Type A), arginine chloride, monosodium glutamate monohydrate, and water for injection.
Appearance of Fluenz and packaging contents
This vaccine is presented in a nasal spray suspension in a single-use nasal applicator (0.2 ml) in a packaging size of 1 and 10 units. Only some packaging sizes may be available in your country.
The suspension is colorless to pale yellow, transparent to slightly turbid. It may present small white particles.
Marketing Authorization Holder
AstraZeneca AB,
SE-151 85 Södertälje,
Sweden
Responsible for manufacturing
AstraZeneca Nijmegen B.V.,
Lagelandseweg 78
Nijmegen, 6545CG
Netherlands
For more information about this medicinal product, please contact the local representative of the Marketing Authorization Holder:
België/Belgique/Belgien AstraZeneca S.A./N.V. Tel: +3223704811 | Lietuva UAB AstraZeneca Lietuva Tel: +37052660550 |
???????? ??????????? ???????? ???? ???.: +359 24455000 | Luxembourg/Luxemburg AstraZeneca S.A./N.V. Tél/Tel: +3223704811 |
Ceská republika AstraZeneca Czech Republic s.r.o. Tel: +420 222 807 111 | Magyarország AstraZeneca Kft. Tel.: +3618836500 |
Danmark AstraZeneca A/S Tlf: +4543666462 | Malta Associated Drug Co. Ltd Tel: +35622778000 |
Deutschland AstraZeneca GmbH Tel: +49 40 809034100 | Nederland AstraZeneca BV Tel:+31 85 808 9900 |
Eesti AstraZeneca Tel: +3726549600 | Norge AstraZeneca AS Tlf: +4721006400 |
Ελλ?δα AstraZeneca A.E. Τηλ: +30210 6871500 | Österreich AstraZeneca Österreich GmbH Tel: +431711310 |
España AstraZeneca Farmacéutica Spain, S.A. Tel: +34913019100 | Polska AstraZeneca Pharma Poland Sp. z o.o. Tel.: +48222457300 |
France AstraZeneca Tél: +33141294000 | Portugal AstraZeneca Produtos Farmacêuticos, Lda. Tel: +351214346100 |
Hrvatska AstraZeneca d.o.o. Tel: +38514628000 | România AstraZeneca Pharma SRL Tel: +40213176041 |
Ireland AstraZeneca Pharmaceuticals (Ireland) DAC Tel: +35316097100 | Slovenija AstraZeneca UK Limited Tel: +38615135600 |
Ísland Vistor hf. Sími: +3545357000 | Slovenská republika AstraZeneca AB, o.z. Tel: +421257377777 |
Italia AstraZeneca S.p.A. Tel: +39 02 00704500 | Suomi/Finland AstraZeneca Oy Puh/Tel: +3581023010 |
Κ?προς Αλ?κτωρ Φαρμακευτικ? Λτδ Τηλ: +35722490305 | Sverige AstraZeneca AB Tel: +46855326000 |
Latvija SIA AstraZeneca Latvija Tel: +37167377100 | United Kingdom (Northern Ireland) AstraZeneca UK Ltd Tel: +441582836836 |
Last review date of this leaflet:
Other sources of information
Further information on this medicinal product is available on the website of the European Medicines Agencyhttp://www.ema.europa.eu.
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