MENVEO POWDER AND SOLUTION FOR INJECTABLE SOLUTION
How to use MENVEO POWDER AND SOLUTION FOR INJECTABLE SOLUTION
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This page provides general information and does not replace a doctor’s consultation. Always consult a doctor before taking any medication. Seek urgent medical care if symptoms are severe.
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Introduction
Package Leaflet: Information for the User
Menveo Powder and Solution for Solution for Injection
Meningococcal conjugate vaccine against serogroups A, C, W-135 and Y
Read all of this leaflet carefully before you or your child are given this medicine, because it contains important information for you.Keep this leaflet, you may need to read it again.
- Keep this leaflet, you may need to read it again.
- If you have any further questions, ask your doctor, pharmacist or nurse.
- This vaccine has been prescribed for you or your child only.
- If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4.
Contents of the Package Leaflet
- What is Menveo and what is it used for
- What you need to know before you or your child are given Menveo
- How to use Menveo
- Possible side effects
- Storage of Menveo
- Contents of the pack and further information
1. What is Menveo and what is it used for
Menveo is a vaccine used for active immunization of children (from 2 years of age), adolescents and adults at risk of exposure to Neisseria meningitidis serogroups A, C, W-135 and Y, to prevent invasive diseases. The vaccine works by making your body produce its own protection (antibodies) against these bacteria.
Bacteria from serogroups A, C, W-135 and Y of Neisseria meningitidis can cause serious infections that can be life-threatening, such as meningitis or septicemia (blood poisoning).
Menveo cannot cause bacterial meningitis. This vaccine contains a protein (called CRM197) from the bacteria that causes diphtheria. Menveo does not protect against diphtheria. Therefore, you (or your child) will need to receive other vaccines to protect against diphtheria when the time comes or if your doctor advises it.
2. What you need to know before you or your child are given Menveo
Menveo must not be given to you or your child if:
- You or your child have ever had an allergic reaction to the active substances or any of the other components of this vaccine (listed in section 6)
- You or your child have ever had an allergic reaction to diphtheria toxoid (a substance used in several vaccines)
- You or your child have a high fever. However, a mild infection or upper respiratory tract infection (such as a cold) is not in itself a reason to delay vaccination.
Warnings and precautions
Tell your doctor or nurse before you or your child are given Menveo if you or your child:
- Have a weakened immune system. There is limited information on the effectiveness of Menveo in people with weakened immune systems due to immunosuppressive medication, HIV infection or other possible causes. It is possible that the effectiveness of Menveo may be reduced in such individuals.
- Have hemophilia or any other condition that prevents blood from clotting properly. This is the case for people undergoing treatment with anticoagulants.
- Are receiving treatment that blocks part of the immune system known as complement activation, such as eculizumab. Even if you have been vaccinated with Menveo, you are still at increased risk of invasive disease caused by Neisseria meningitidis serogroups A, C, W-135 and Y.
Fainting, feeling of loss of consciousness or other reactions related to stress may occur in response to any injection with a needle. Tell your doctor or nurse if you have had such a reaction in the past.
This vaccine only protects against meningococcal bacteria of serogroups A, C, W-135 and Y. It does not protect against other types of meningococcal bacteria or other causes of meningitis or septicemia (blood poisoning).
As with any vaccine, it is possible that Menveo may not protect 100% of vaccinated individuals.
If you or your child received a dose of Menveo more than a year ago and are still at particular risk of exposure to meningococcal bacteria of serogroups A, a booster dose may be considered to maintain protection. Your doctor will advise whether you should receive a booster dose and when.
Using Menveo with other medicines
Tell your doctor or nurse if you are using, have recently used or might use any other medicines.
Menveo can be given at the same time as other vaccines, but it is preferable to administer the injection of other vaccines in the opposite arm to the one used for the Menveo injection.
These vaccines include: tetanus, reduced-dose diphtheria and acellular pertussis (Tdpa), human papillomavirus (HPV), yellow fever, typhoid fever (Vi polysaccharide), Japanese encephalitis, rabies, hepatitis A and B, and meningococcal group B (Bexsero).
There may be a reduction in the effect of Menveo if administered to individuals taking medications that suppress the immune system.
It is necessary to administer the injection in different locations if more than one vaccine is administered at the same time.
Pregnancy, breastfeeding and fertility
If you are pregnant or breastfeeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine. Your doctor or nurse may still recommend that you are given Menveo if you are at high risk of infection with meningococcal bacteria of serogroups A, C, W-135 and Y.
Driving and using machines
No studies on the effects on the ability to drive and use machines have been performed. A few cases of dizziness have been reported after vaccination. This may temporarily affect the ability to drive or use machines.
Menveo contains
This medicine contains less than 23 mg (1 mmol) of sodium per dose; i.e. essentially 'sodium-free'.
This medicine contains less than 39 mg (1 mmol) of potassium per dose; hence it is considered 'potassium-free'.
3. How to use Menveo
Your doctor or nurse will give you or your child Menveo.
The vaccine is usually injected into the muscle of the upper arm (deltoid) in children (from 2 years of age), adolescents and adults. Your doctor or nurse will make sure that the vaccine is not administered into a blood vessel and that it is injected into the muscle and not into the skin.
A single injection (0.5 ml) of the vaccine will be given to children (from 2 years of age), adolescents and adults.
The safety and efficacy of Menveo in children under 2 years of age have not been established. Data available for subjects aged 56-65 are limited, and there are no data available for persons over 65 years of age.
Tell your doctor if you or your child have previously been given an injection of Menveo or another meningococcal vaccine. Your doctor will decide whether you need another injection of Menveo.
For more information on reconstitution of the vaccine, see the section for healthcare professionals or doctors at the end of this leaflet.
If you have any further questions on the use of this medicine, ask your doctor or nurse.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Generally, the most common side effects reported during clinical trials lasted only one to two days and were not usually serious.
In children (2-10 years of age), the side effects reported during clinical trials are listed below.
Very common (may affect more than 1 in 10 people): somnolence, headache, irritability, feeling unwell, pain at the injection site, redness at the injection site (≤ 50 mm), induration at the injection site (≤ 50 mm)
Common (may affect up to 1 in 10 people): changes in eating habits, nausea, vomiting, diarrhea, skin rash, muscle pain, joint pain, chills, fever ≥ 38°C, redness at the injection site (> 50 mm) and induration at the injection site (> 50 mm)
Uncommon (may affect up to 1 in 100 people): itching at the injection site
In adolescents (from 11 years of age) and adults, the most common side effects reported during clinical trials are listed below.
Very common: headache, nausea, pain at the injection site, redness at the injection site (≤ 50 mm), induration at the injection site (≤ 50 mm), muscle pain, feeling unwell
Common: skin rash, redness at the injection site (> 50 mm), induration at the injection site (> 50 mm), joint pain, fever ≥ 38°C, chills
Uncommon: dizziness, itching at the injection site
Side effects reported during post-marketing use include:
Rare: swollen lymph nodes.
Frequency not known: allergic reactions, which can include severe swelling of the lips, mouth and throat (which can cause difficulty swallowing), difficulty breathing with wheezing (noisy breathing) or coughing, skin rash and swelling of the hands, feet and ankles, loss of consciousness, very low blood pressure; seizures (convulsions), including those associated with fever; balance disturbance; fainting; infection of the skin at the injection site; swelling at the injection site, including extensive swelling of the injected limb.
If you experience a severe allergic reaction, seek medical attention immediately or go to the emergency room, as you may need urgent medical attention.
Reporting of side effects
If you experience any side effects, talk to your doctor, pharmacist or nurse, even if they are not listed in this leaflet. You can also report side effects directly via the national reporting system listed in Annex V. By reporting side effects, you can help provide more information on the safety of this medicine.
5. Storage of Menveo
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the carton after EXP. The expiry date refers to the last day of that month.
Store in a refrigerator (2°C - 8°C). Do not freeze. Keep the vials in the original packaging to protect from light.
After reconstitution, the product should be used immediately. However, the chemical and physical stability after reconstitution has been demonstrated for 8 hours below 25°C.
Medicines should not be disposed of via wastewater or household waste. Your doctor or nurse will dispose of this medicine. This will help protect the environment.
6. Container contents and additional information
Menveo composition
A dose (0.5 ml of reconstituted vaccine) contains:
The active substances are:
(Original powder content)
- Meningococcal group A oligosaccharide 10 micrograms
Conjugated with CRM197 protein from Corynebacterium diphtheriae16.7 to 33.3 micrograms
(Original content of the injectable solution)
- Meningococcal group C oligosaccharide 5 micrograms
Conjugated with CRM197 protein from Corynebacterium diphtheriae7.1 to 12.5 micrograms
- Meningococcal group W-135 oligosaccharide 5 micrograms
Conjugated with CRM197 protein from Corynebacterium diphtheriae3.3 to 8.3 micrograms
- Meningococcal group Y oligosaccharide 5 micrograms
Conjugated with CRM197 protein from Corynebacterium diphtheriae5.6 to 10.0 micrograms
The other components (excipients) are:
In the powder: potassium dihydrogen phosphate and sucrose.
In the injectable solution: sodium chloride, sodium dihydrogen phosphate monohydrate, sodium hydrogen phosphate dihydrate, and water for injectable preparations (see also the end of Section 2).
Product appearance and container contents
Menveo consists of a powder and an injectable solution.
Each dose of Menveo is supplied with:
- 1 vial containing the conjugated component MenA as a white to off-white powder.
- 1 vial containing the conjugated component MenCWY as a clear solution.
- Container size for one dose (2 vials), five doses (10 vials), or ten doses (20 vials). Not all container sizes may be marketed.
Both contents (from the vial and the other vial) must be mixed before vaccination via1dose of0.5ml.
Marketing authorization holder and manufacturer
Marketing authorization holder:
GSK Vaccines S.r.l. –
Via Fiorentina 1, 53100 – Siena,
Italy.
Manufacturer:
GSK Vaccines S.r.l.
Bellaria Rosia, 53018 Sovicille (Siena),
Italy.
For further information about this medicinal product, please contact the local representative of the marketing authorization holder:
Belgium/België/Belgien GlaxoSmithKline Pharmaceuticals SA/NV Tel: + 32 10 85 52 00 | Lithuania GSK Vaccines S.r.l Tel: +370 80000334 |
Bulgaria GSK Vaccines S.r.l Tel: +359 80018205 | Luxembourg/Luxemburg GlaxoSmithKline Pharmaceuticals SA/NV Tel: + 32 10 85 52 00 |
Czech Republic GlaxoSmithKline s.r.o. Tel: + 420 2 22 00 11 11 | Hungary GSK Vaccines S.r.l Tel: +36 80088309 |
Denmark GlaxoSmithKline Pharma A/S Tel: + 45 36 35 91 00 | Malta GSK Vaccines S.r.l Tel: +356 80065004 |
Germany GlaxoSmithKline GmbH & Co. KG Tel: +49 (0)89 36044 8701 | Netherlands GlaxoSmithKline BV Tel: + 31 (0)33 2081100 |
Estonia GSK Vaccines S.r.l Tel: +372 8002640 | Norway GlaxoSmithKline AS Tel: + 47 22 70 20 00 |
Greece GlaxoSmithKline Μονοπρ?σωπη A.E.B.E Tel: + 30 210 68 82 100 | Austria GlaxoSmithKline Pharma GmbH. Tel: + 43 (0)1 97075 0 |
Spain GlaxoSmithKline, S.A. Tel: + 34 900 202 700 | Poland GSK Services Sp. z o.o. Tel: + 48 (22) 576 9000 |
France Laboratoire GlaxoSmithKline Tel: + 33 (0) 1 39 17 84 44 | Portugal GlaxoSmithKline - Produtos Farmacêuticos, Lda. Tel: + 351 21 412 95 00 |
Croatia GSK Vaccines S.r.l Tel: +385 800787089 | Romania GSK Vaccines S.r.l Tel: +40 800672524 |
Ireland GlaxoSmithKline (Ireland) Ltd Tel: + 353 (0)1 495 5000 | Slovenia GSK Vaccines S.r.l Tel: +386 80688869 |
Iceland Vistor hf. Tel: +354 535 7000 | Slovak Republic GSK Vaccines S.r.l Tel: +421 800500589 |
Italy GlaxoSmithKline S.p.A. Tel: +39 (0)45 7741 111 | Finland GlaxoSmithKline Oy Tel: + 358 10 30 30 30 |
Cyprus GSK Vaccines S.r.l Tel: +357 80070017 | Sweden GlaxoSmithKline AB Tel: + 46 (0)8 638 93 00 |
Latvia GSK Vaccines S.r.l Tel: +371 80205045 | United Kingdom(Northern Ireland) GSK Vaccines S.r.l Tel: + 44 (0)800 221 441 |
Date of last revision of this leaflet:
Other sources of information
Detailed information on this medicinal product is available on the European Medicines Agency website: http://www.ema.europa.eu
This leaflet can be found in all EU/EEA languages on the European Medicines Agency website.
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This information is intended only for healthcare professionals:
Reconstitution of the vaccine
Menveo must be prepared for administration by reconstituting the powder with the solution.
The contents of the two different vials (MenA powder and MenCWY solution) must be mixed before vaccination, resulting in 1 dose of 0.5 ml.
Withdraw the entire contents of the vial with the solution using a syringe and a suitable needle (21G, 40 mm in length or 21G, 1 ½ inches in length) and inject it into the vial with the powder to reconstitute the conjugated component MenA.
Invert and shake the vial vigorously, then withdraw 0.5 ml of the reconstituted product.
Note that it is normal for a small amount of liquid to remain in the vial after withdrawal of the dose. Before injection, replace the needle with one suitable for administration. Ensure that there are no air bubbles in the syringe before injecting the vaccine.
After reconstitution, the vaccine is a clear, colorless to slightly yellow solution without visible foreign particles. If any foreign particles or changes in physical appearance are observed, the vaccine must be discarded.
Menveo is administered as an intramuscular injection, preferably in the deltoid muscle.
Any unused vaccine or waste material should be disposed of in accordance with local regulations.
- Country of registration
- Active substance
- Prescription requiredYes
- Manufacturer
- This information is for reference only and does not constitute medical advice. Always consult a doctor before taking any medication. Oladoctor is not responsible for medical decisions based on this content.
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