Vaccination should be delayed if you or your child have a fever or infection requiring white coloured liquid (called a suspension). Prevenar 13 is not to be mixed with other vaccines or products in the same syringe. The first injection may be given as early as six weeks of age with at least one month between doses. Tell your doctor or clinic nurse if you or your child are having anti-cancer therapy or have an HIV infection or any other condition that affects the immune response. If you are: Keep this vaccine in the refrigerator at a temperature between 2°C and 8°C where young Tell your doctor or clinic nurse as soon as possible if you or your child are not well after receiving Prevenar 13. Each 0.5 mL dose of Prevenar 13 contains the following active ingredients: 30.8 micrograms of pneumococcal purified capsular polysaccharides. Do not freeze it. In response, 10- and 13-valent PCVs have recently been licensed. Haemophilus influenzae type b (Hib) or meningococcal vaccines that protect against Novel cannabis plant extracts could protect against COVID-19, Healthy diet plays vital role in warding off COVID-19, COVID-19 may trigger recurrent GuillainâBarré Syndrome episodes, a case study shows, Asymptomatic patients have higher SARS-CoV-2 viral loads than symptomatic patients, study says. Our information hub has important information for everyone. Your doctor or clinic nurse will tell you the correct vaccination schedule for your child. This leaflet was prepared in August 2020. Symptoms of an allergic reaction may include: shortness of breath, wheezing or difficulty breathing, swelling of the face, lips, tongue or other parts of the body. Prevenar 13 is a vaccine, which is a type of medicine that helps to protect (immunise) people from certain infectious diseases. your child is pale, limp and does not respond to you. It does not contain foods, any medicines or other vaccines, if you or your child have had a reaction to an earlier dose of Prevenar 13 vaccine, if you or your child have any bleeding problems, if you or your child are sick with a high fever. If it has, use a new pack. If you are: Keep this vaccine in the refrigerator at a temperature between 2°C and 8°C where young children cannot reach it. Premature infants: Your child will receive an initial course of three injections. A doctor or a nurse will give the Prevenar 13 injection. Evaluation of pharmacokinetic properties is not available for vaccines. due to various causes such as these. This leaflet was prepared in August 2020. sodium chloride. As with all vaccines, 100% protection against the above diseases cannot be guaranteed. 1. All trials on the list are supported by NCI. Your doctor or clinic nurse has weighed the risks of you or your child receiving Prevenar 13 against the benefits this vaccination is expected to provide. As with other vaccines, the administration of Prevenar 13 should be postponed in individuals suffering from acute moderate or severe febrile illness. A fourth (booster) injection is recommended at approximately 12 months Do not administer Prevenar 13 intravascularly. Tell your doctor or clinic nurse if you or your child have any other disease. people from certain infectious diseases. The use of Prevenar 13 should be guided by official recommendations. Sequential administration of 13-valent pneumococcal conjugate vaccine and 23-valent pneumococcal polysaccharide vaccine in pneumococcal vaccine-naïve adults 60–64 years of age. your doctor or clinic nurse. 30.8 micrograms of pneumococcal purified capsular polysaccharides. Tell your doctor or pharmacist if you notice anything that is making you or your child feel unwell. Tell your doctor or nurse if you or your child are taking any other medicines, including medicines you buy without a prescription from a pharmacy, supermarket or health food shop, or if you or your child have recently been given any other vaccine. You or your child may need medical treatment for some side effects. Prevenar 13 is not recommended for babies younger than 6 weeks of age. Adverse reaction frequencies are listed below in CIOMS frequency categories. This website uses cookies. Keep this leaflet. otitis media (an ear infection that can cause pain and temporary hearing loss and Each dose will be given on a separate occasion. www.pfizer.com Your doctor or clinic nurse has weighed The clinical trials on this list are studying Pneumococcal 13-valent Conjugate Vaccine. Your doctor or clinic nurse between doses. Keep this leaflet. It is unlikely that you will be asked to store Prevenar 13. Information for consumers on prescription, over-the-counter and complementary medicines. your child completes the course of injections. A one-time dose of PREVNAR 13 ® for adults can help protect you from pneumococcal pneumonia—it is not a yearly shot. Tell your doctor or pharmacist if you notice any of the following and they worry you: If any of the following happen, tell your doctor or pharmacist immediately or go to Accident and Emergency at your nearest hospital: These are very serious side effects. Please note that medical information found If the vaccine has been frozen it should not be used. infection may receive at least one dose of Prevenar 13. If you have any questions about this vaccination, ask your doctor, clinic nurse or pharmacist. Symptoms of an allergic reaction may include: Vaccination should be delayed if you or your child have a fever or infection requiring a visit to the doctor. and fainting, temperature higher than 39°C in babies or young children, temporary interruptions of breathing. As with all vaccines, 100% protection against the above diseases cannot be guaranteed. We use cookies to enhance your experience. All vaccinations have benefits and risks. The vaccine is composed of saccharides of the capsular antigen of Streptococcus pneumoniae ... Aluminum as aluminum phosphate adjuvant 0.125 mg Other ingredients: Polysorbate 80 Sodium chloride Water-for … Other vaccines might be given at the same time, but not at the same injection site. A trained doctor or nurse gives this vaccination, so an overdose is unlikely to occur. Normally, your child will receive either three or four doses of the vaccine, at least 4 weeks apart, starting at 6 weeks to 2 months of age. Report a problem with medicines, medical devices or vaccines: COVID-19 information translated into community languages. succinic acid. Active immunisation for the prevention of pneumococcal disease caused by Streptococcus pneumoniae serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F and 23F in adults and children aged more than 6 weeks of age. Hypersensitivity to the active substances or to any of the excipients, or to diphtheria toxoid. Do not freeze. Prevenar 13 is a ready to use homogeneous white suspension for intramuscular injection (0.5 mL), supplied as a pre-filled syringe. It is important to follow the instructions from the doctor or clinic nurse so that Before giving Prevenar 13 make sure that the expiry date (EXP) printed on the pack The vaccine should be well shaken to obtain a homogeneous white suspension and be inspected visually for any particulate matter and/or variation of physical aspect prior to administration. During the COVID-19 pandemic, you need to continue to take your usual medicines and stay as healthy as possible. is expected to provide. Each serotype is grown in soy peptone broth. Here’s what you may not know. An independent peer-reviewed journal providing critical commentary on drugs and therapeutics. The PCV used in the UK is called Prevenar 13. If you are not sure whether you or your child should be given Prevenar 13, talk to your doctor or clinic nurse. Please read this leaflet carefully before you start using Prevenar 13. Prevenar 13 is supplied as a suspension in 0.5 mL pre-filled syringes in packs of Tell your doctor if your baby was born prematurely a cold) is not usually a reason to delay vaccination. Keep Prevenar 13 in the original pack until it is time to be given. Owned and operated by AZoNetwork, © 2000-2020. well after receiving Prevenar 13. are not. However, in infants and children, there have been reports of overdose with Prevenar 13 defined as subsequent doses administered closer than recommended to the previous dose.
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