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PROQUAD powder and solvent for injectable suspension

PROQUAD powder and solvent for injectable suspension

This page is for general information. Consult a doctor for personal advice. Call emergency services if symptoms are severe.
About the medicine

How to use PROQUAD powder and solvent for injectable suspension

Introduction

Package Leaflet: Information for the User

ProQuad

Powder and solvent for injectable suspension

Measles, mumps, rubella, and varicella (live virus) vaccine

Read all of this leaflet carefully before you or your child is vaccinated because it contains important information for you.

  • Keep this leaflet, you may need to read it again.
  • If you have any further questions, ask your doctor or pharmacist.
  • This vaccine has been prescribed for you or your child, do not pass it on to others.
  • If you experience any side effects, talk to your doctor or pharmacist, even if they are not listed in this leaflet. See section 4.

Contents of the pack

  1. What ProQuad is and what it is used for
  2. What you need to know before you receive ProQuad
  3. How to use ProQuad
  4. Possible side effects
  5. Storage of ProQuad
  6. Contents of the pack and other information

1. What ProQuad is and what it is used for

ProQuad is a vaccine that contains weakened viruses of measles, mumps, rubella, and varicella. When the vaccine is given to a person, the immune system (the body's natural defenses) will create antibodies against the measles, mumps, rubella, and varicella viruses. The antibodies help protect against infections caused by these viruses.

ProQuad is given to help protect your child against measles, mumps, rubella, and varicella. The vaccine can be given to people from 12 months of age.

ProQuad can also be given to children from 9 months of age under special circumstances (to comply with national vaccination schedules, in outbreak situations, or when traveling to a region with a high prevalence of measles).

Although ProQuad contains live viruses, they are too weak to cause measles, mumps, rubella, or varicella in healthy individuals.

2. What you need to know before you receive ProQuad

Do not use ProQuad

  • If the person to be vaccinated is allergic to any vaccine against varicella or measles, mumps, or rubella, or to any of the other components of this vaccine (listed in section 6), including neomycin.
  • If the person to be vaccinated has blood disorders or any type of cancer that affects the immune system.
  • If the person to be vaccinated is receiving treatment or taking medication that may weaken the immune system (except for low-dose corticosteroid therapy for asthma or replacement therapy).
  • If the person to be vaccinated has a weakened immune system due to a disease (including AIDS).
  • If the person to be vaccinated has a family history of congenital or hereditary immunodeficiency, unless the person's immune competence has been demonstrated.
  • If the person to be vaccinated has active untreated tuberculosis.
  • If the person to be vaccinated has any disease with a fever over 38.5 °C; however, a lower fever is not in itself a reason to delay vaccination.
  • If the person to be vaccinated is pregnant (also, pregnancy should be avoided for 1 month after vaccination, see Pregnancy and breastfeeding).

Warnings and precautions

If the person to be vaccinated experiences any of the following problems, consult their doctor or pharmacist before being vaccinated with ProQuad:

  • An allergic reaction to egg or any product containing egg.
  • Personal or family history of allergies or seizures (attacks).
  • An adverse effect after vaccination with measles, mumps, and/or rubella vaccines that involves bruising or bleeding more prolonged than usual.
  • HIV infection without symptoms of HIV disease. However, vaccination may be less effective than for uninfected individuals (see Do not use ProQuad).

If you have a coagulation disorder or low platelet count, the injection will be given under the skin.

In rare circumstances, it is possible to contract varicella, including severe varicella, from a person who has been vaccinated with ProQuad. This can occur in people who have not been previously vaccinated against varicella or who have had varicella, as well as in people who are in one of the following categories:

  • Individuals with low resistance to diseases.
  • Pregnant women who have never had varicella or have not been vaccinated against varicella.
  • Newborns whose mothers have never had varicella or have not been vaccinated against varicella.

Whenever possible, people who have been vaccinated with ProQuad should try to avoid close contact, until 6 weeks after vaccination, with anyone who is in one of the above categories. Inform your doctor if someone is in one of the above categories and is expected to be in close contact with the person being vaccinated.

As with other vaccines, ProQuad may not completely protect all vaccinated people. Additionally, if the person to be vaccinated has already been exposed to measles, mumps, rubella, or varicella viruses but has not yet developed the disease, ProQuad may not be able to prevent the onset of the disease.

Other medicines and ProQuad

Tell your doctor or pharmacist if the vaccinated person is using or has recently used other medicines (or other vaccines).

ProQuad can be given at the same time as other pediatric vaccines such as Prevenar and/or hepatitis A vaccine, or with vaccines that contain diphtheria, tetanus, pertussis, Haemophilus influenzaetype b, inactivated poliomyelitis, or hepatitis B. A different injection site will be used for each vaccine.

The doctor may delay vaccination for at least 3 months after a blood or plasma transfusion or after the administration of immunoglobulin (IG) or varicella-zoster immunoglobulin (VZIG). After vaccination with ProQuad, IG or VZIG should not be given for 1 month, unless your doctor tells you otherwise.

If a tuberculin test is to be performed, it should be done before, at any time, simultaneously with, or 4 to 6 weeks after vaccination with ProQuad.

Tell your doctor if the vaccinated person has recently received a vaccine or is scheduled to receive one in the near future. Your doctor will determine when to administer ProQuad.

The use of salicylates (e.g., acetylsalicylic acid, a substance found in numerous medicines used to relieve pain and reduce fever) should be avoided during the 6 weeks following vaccination with ProQuad.

Pregnancy and breastfeeding

ProQuad should not be given to pregnant women. Women of childbearing age should take precautions to avoid pregnancy for 1 month after vaccination.

Tell your doctor if you are breastfeeding or plan to breastfeed. Your doctor will decide whether you should receive ProQuad.

If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this vaccine.

ProQuad contains sodium

This medicine contains less than 1 mmol of sodium (23 mg) per dose; i.e., it is essentially "sodium-free".

ProQuad contains potassium

This medicine contains potassium, less than 1 mmol (39 mg) per dose; i.e., it is essentially "potassium-free".

ProQuad contains sorbitol

The additive effect of medicines containing sorbitol (or fructose) administered concomitantly and the intake of sorbitol (or fructose) in the diet should be taken into account.

3. How to use ProQuad

ProQuad should be injected into the muscle or under the skin, either in the outer aspect of the thigh or in the upper arm.

The recommended injection sites for intramuscular injections are the thigh area in young children, while for other ages, the upper arm is preferred.

If the person to be vaccinated has a coagulation disorder or low platelet count, the vaccine should be given under the skin because bleeding may occur after intramuscular administration.

ProQuad should not be injected directly into any blood vessel.

ProQuad is administered by injection as follows:

  • Children between 9 and 12 months of age:

ProQuad can be given from 9 months of age. To ensure optimal protection against varicella and measles, two doses of ProQuad should be given with an interval of at least 3 months.

  • Individuals 12 months of age and older:

To ensure optimal protection against varicella, two doses of ProQuad should be given with an interval of at least 1 month.

The appropriate time and number of injections will be determined by your doctor according to official recommendations.

Instructions for reconstitution intended for medical or healthcare professionals are included at the end of the leaflet.

If you miss a dose of ProQuad

Your doctor will decide when to give the missed dose.

4. Possible side effects

Like all vaccines and medicines, this vaccine can cause side effects, although not everybody gets them.

Allergic reactions (hives) can occur. Some of these reactions can be serious and can include difficulty breathing or swallowing. If the vaccinated person experiences an allergic reaction, call their doctor immediately.

Other side effects have been reported after the administration of ProQuad, and some of them were serious. These included:

  • Uncommon (may affect up to 1 in 100 people): febrile seizures.
  • Rare (may affect up to 1 in 1,000 people): bronchiolitis (difficult breathing with or without cough); unsteady walking.

The following side effects were most frequently reported with the use of ProQuad:

  • Very common (may affect more than 1 in 10 people): injection site reactions including pain/pain on touch/discomfort, redness, fever (38.9 °C or higher);
  • Common (may affect up to 1 in 10 people): injection site reactions including swelling or painful nodule; irritability; rash (including measles-like rash, varicella-like rash, and injection site rash); upper respiratory tract infection; vomiting and diarrhea.

Other side effects have been reported with the administration of at least one of the following vaccines: ProQuad, previous formulations of monovalent and combination vaccines against measles, mumps, and rubella manufactured by Merck & Co., Inc., or Varicella Virus Vaccine Live (Oka/Merck). These adverse events included:

  • Uncommon (may affect up to 1 in 100 people): cough
  • Rare (may affect up to 1 in 1,000 people): skin infection; varicella.
  • Unknown (cannot be estimated from the available data): unusual bleeding or bruising under the skin; testicular inflammation; tingling of the skin, herpes zoster (shingles); brain inflammation (encephalitis); inflammation of the membranes covering the brain and spinal cord not caused by a bacterial infection (aseptic meningitis), severe skin disorders; stroke; febrile seizures; joint pain and/or swelling (which may be transient or chronic); lung inflammation (pneumonia/pneumonitis).

Your doctor has a more comprehensive list of side effects for ProQuad and for the components of ProQuad (vaccines against measles, mumps, and rubella manufactured by Merck & Co., Inc., and Varicella Virus Vaccine Live (Oka/Merck)).

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 through the national reporting system included in Appendix V. By reporting side effects, you can help provide more information on the safety of this medicine.

5. Storage of ProQuad

Keep this vaccine out of the sight and reach of children.

Do not use this vaccine after the expiry date stated on the outer packaging after EXP. The expiry date refers to the last day of the month stated.

Store and transport refrigerated (between 2 °C and 8 °C).

Do not freeze.

Keep the vial in the outer packaging to protect it from light.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.

6. Container contents and additional information

ProQuad composition

After reconstitution, one dose (0.5 ml) contains:

The active ingredients are:

Measles virus1 Enders’ Edmonston strain (live, attenuated) ........at least 3.00 log10 CCID50*

Mumps virus1 Jeryl Lynn strain (Level B) (live, attenuated) ......at least 4.30 log10 CCID50*

Rubella virus2 Wistar RA 27/3 strain (live, attenuated) ...................at least 3.00 log10 CCID50*

Varicella virus3 Oka/Merck strain (live, attenuated) .........................at least 3.99 log10 PFU**

  • Dose that infects 50% of cell cultures

** Plaque-forming units

  1. Produced in chicken embryo cells.
  2. Produced in human diploid lung fibroblasts (WI-38).
  3. Produced in human diploid cells (MRC-5).

The other components are:

Powder

Sucrose, hydrolyzed gelatin, urea, sodium chloride, sorbitol (E-420), monosodium glutamate, sodium phosphate, sodium bicarbonate, potassium phosphate, potassium chloride, 199 medium with Hanks' salts, MEM, neomycin, phenol red, hydrochloric acid, and sodium hydroxide.

Solvent

Water for injectable preparations.

Product appearance and container contents

The vaccine is a powder for injectable suspension contained in a single-dose vial, which must be mixed with the supplied solvent.

The powder is a compact crystalline mass of white to pale yellow color and the solvent is a clear colorless liquid.

ProQuad is available in packs of 1 and packs of 10. Only certain pack sizes may be marketed.

Marketing authorization holder and manufacturer

Marketing authorization holder: MSD VACCINS, 162 avenue Jean Jaurès, 69007 Lyon, France

Manufacturer: Merck Sharp and Dohme, B.V., Waarderweg, 39, 2031 BN Haarlem, The Netherlands

For further information about this medicinal product, please contact the local representative of the marketing authorization holder.

België/Belgique/Belgien

MSD Belgium BVBA/SPRL

Tél/Tel: +32(0)27766211

dpoc_belux@merck.com

Lietuva

UAB Merck Sharp & Dohme

Tel.: +370.5.2780.247

msd_lietuva@merck.com

Text in Bulgarian language with contact information of Merck Sharp & Dohme Bulgaria including phone and email

Luxembourg/Luxemburg

MSD Belgium BVBA/SPRL

Tél/Tel: +32(0)27766211

dpoc_belux@merck.com

Ceská republika

Merck Sharp & Dohme s.r.o.

Tel.: +420 233 010 111

dpoc_czechslovak@merck.com

Magyarország

MSD Pharma Hungary Kft.

Tel.: + 36.1.888.5300

hungary_msd@merck.com

Danmark

MSD Danmark ApS

Tlf: + 45 4482 4000

dkmail@merck.com

Malta

Merck Sharp & Dohme Cyprus Limited.

Tel: 8007 4433 (+356 99917558)

malta_info@merck.com

Deutschland

MSD SHARP & DOHME GMBH

Tel: 0800 673 673 673 (+49 (0) 89 4561 2612)

e-mail@msd.de

Nederland

Merck Sharp & Dohme B.V.

Tel: 0800 9999000

(+31 23 5153153)

medicalinfo.nl@merck.com

Eesti

Merck Sharp & Dohme OÜ

Tel.: +372 6144 200

msdeesti@merck.com

Norge

MSD (Norge) AS

Tlf: +47 32 20 73 00

msdnorge@msd.no

Ελλ?δα

MSD Α.Φ.Β.Ε.Ε.

Τηλ: +30 210 98 97 300

dpoc_greece@merck.com

Österreich

Merck Sharp & Dohme Ges.m.b.H.

Tel: +43 (0) 1 26 044

msd-medizin@merck.com

España

Merck Sharp & Dohme de España, S.A.

Tel: +34 91 321 06 00

msd_info@merck.com

Polska

MSD Polska Sp. z o.o.

Tel.: +48.22.549.51.00

msdpolska@merck.com

France

MSD VACCINS

Tel:+ 33 (0)1 80 46 40 40

information.medicale@msd.com

Portugal

Merck Sharp & Dohme, Lda

Tel: +351 21 4465700

inform_pt@merck.com

Hrvatska

Merck Sharp & Dohme d.o.o.

Tel: +385 1 66 11 333

croatia_info@merck.com

România

Merck Sharp & Dohme Romania S.R.L

Tel: + 4021 529 29 00

msdromania@merck.com

Ireland

Merck Sharp & Dohme Ireland (Human Health)

Limited

Tel: +353 (0)1 2998700

medinfo_ireland@merck.com

Slovenija

Merck Sharp & Dohme, inovativna zdravila d.o.o.

Tel: +386.1.520.4201

msd.slovenia@merck.com

Ísland

Vistor hf.

Sími: + 354 535 7000

Slovenská republika

Merck Sharp & Dohme, s. r. o

Tel: +421 2 58282010

dpoc_czechslovak@merck.com

Italia

MSD Italia S.r.l.

Tel: +39 06 361911

medicalinformation.it@merck.com

Suomi/Finland

MSD Finland Oy

Puh/Tel: +358 (0)9 804 650

info@msd.fi

Κ?προς

Merck Sharp & Dohme Cyprus Limited

Τηλ: 800 00 673 (+357 22866700)

cyprus_info@merck.com

Sverige

Merck Sharp & Dohme (Sweden) AB

Tel: +46 77 5700488

medicinskinfo@merck.com

Latvija

SIA Merck Sharp & Dohme Latvija

Tel: +371.67364.224

msd_lv@merck.com

United Kingdom

Merck Sharp & Dohme Limited

Tel: +44 (0) 1992 467272

medicalinformationuk@merck.com

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 information is intended only for healthcare professionals:

Before mixing with the solvent, the vaccine powder is a compact crystalline mass of white to pale yellow color. The solvent is a clear colorless liquid. When fully reconstituted, the vaccine is a pale yellow to light pink liquid.

For reconstitution of the vaccine, use only the supplied solvent, as it does not contain preservatives or other antiviral substances that could inactivate the vaccine.

It is important to use a new sterile syringe and needle for each individual to prevent the transmission of infectious agents from one person to another.

A separate needle should be used for reconstitution and a different needle for injection.

ProQuad should not be mixed in the same syringe with other vaccines.

Reconstitution instructions

Withdraw the entire contents of the solvent from the vial into a syringe. Inject the entire contents of the syringe into the vial containing the powder. Gently shake to mix completely.

The reconstituted vaccine should be inspected visually for any foreign particles and/or variation in physical appearance before administration. If any of the above are observed, discard the vaccine.

The vaccine should be administered immediately after reconstitution to minimize loss of potency. Discard the reconstituted vaccine if not used within 30 minutes.

Do not freeze the reconstituted vaccine.

Withdraw the entire contents of the reconstituted vaccine from the vial into a syringe, change the needle, and inject the entire contents subcutaneously or intramuscularly.

Unused products or waste materials should be disposed of in accordance with local requirements.

See also Section 3 How to use ProQuad

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