This is a summary only. Ihr Arzt Manchmal wird der Impfstoff vor dem geplanten Termin einer Entfernung der Milz oder dem Beginn einer speziellen Krebstherapie verabreicht (normalerweise mindestens 2 Wochen vorher). Was sollten Sie beachten? PNEUMOVAX ® 23 is a vaccine indicated for active immunization for the prevention of pneumococcal disease caused by the 23 serotypes contained in the vaccine (1, 2, 3, 4, 5, 6B, 7F, 8, 9N, 9V, 10A, 11A, 12F, 14, 15B, 17F, 18C, 19F, 19A, 20, 22F, 23F, and 33F). Es kann Arzneimittel geben, mit denen Wechselwirkungen auftreten.
These bacteria can cause many types of illnesses, including pneumonia, which is an infection of the lungs. If you would like more information, talk to your health care provider. Wichtige Hinweise zu PNEUMOVAX 23 Injektionslösung. It helps protect you from infection by certain germs or bacteria which are called pneumococcus (pronounced "noo-mo-ca-cus"). Pneumococcal polysaccharide vaccine (PPSV23) can prevent pneumococcal disease. Reduction in type-specific pneumococcal bacteremia was 82%.A prospective study in France found a pneumococcal vaccine containing fourteen (types 1, 2, 3, 4, 6A, 7F, 8, 9N, 12F, 14, 18C, 19F, 23F, and 25) capsular polysaccharides to be 77% (95%CI: 51% to 89%) effective in reducing the incidence of pneumonia among male and female nursing home residents with a mean age of 74 (standard deviation of 4 years).In a study using a pneumococcal vaccine containing eight (types 1, 3, 6, 7, 14, 18, 19, and 23) capsular polysaccharides, vaccinated children and young adults aged 2 to 25 years who had sickle cell disease, congenital asplenia, or undergone a splenectomy experienced significantly less bacteremic pneumococcal disease than patients who were not vaccinated.In the United States, one post-licensure randomized controlled trial, in the elderly or patients with chronic medical conditions who received a 14-valent pneumococcal polysaccharide vaccine (types 1, 2, 3, 4, 6A, 8, 9N, 12F, 14, 19F, 23F, 25, 7F, and 18C), did not support the efficacy of the vaccine for nonbacteremic pneumonia.A retrospective cohort analysis study based on the U.S. Centers for Disease Control and Prevention (CDC) pneumococcal surveillance system, showed 57% (95%CI: 45% to 66%) overall protective effectiveness against invasive infections caused by serotypes included in Pneumovax 23 in persons ≥6 years of age, 65 to 84% effectiveness among specific patient groups (e.g., persons with diabetes mellitus, coronary vascular disease, congestive heart failure, chronic pulmonary disease, and anatomic asplenia) and 75% (95%CI: 57% to 85%) effectiveness in immunocompetent persons aged ≥65 years of age.
If you have any questions about the vaccine after you read this, you should ask your health care provider. Serious adverse experiences after placebo included heart failure and motor vehicle accident resulting in death.The most common local adverse reactions reported at the injection site after initial vaccination with Pneumovax 23 were pain/tenderness/soreness (60.0%), swelling/induration (20.3%), and erythema (16.4%). Im Impfstoff sind die folgenden 23 Typen von Pneumokokken-Polysacchariden enthalten: 1, 2, 3, 4, 5, 6B, 7F, 8, 9N, 9V, 10A, 11A, 12F, 14, 15B, 17F, 18C, 19F, 19A, 20, 22F, 23F und 33F.Die sonstigen Bestandteile sind: Phenol, Natriumchlorid, Wasser für Injektionszwecke.Der Impfstoff enthält weniger als 1 Millimol Natrium (23 Milligramm) pro Dosis, PNEUMOVAX 23 wird als Injektionslösung in einer Fertigspritze (0,5 Der Impfstoff ist in einer Packung mit 1 oder 10 Fertigspritzen ohne Kanüle erhältlich.Der Impfstoff ist in einer Packung mit 1 oder 10 Fertigspritzen mit je 1 beigepackten Kanüle erhältlich.Der Impfstoff ist in einer Packung mit 1 oder 10 Fertigspritzen mit je 2 beigepackten Kanülen erhältlich.Es werden möglicherweise nicht alle Packungsgrößen in den Verkehr gebracht.Merck Sharp & Dohme B.V., Waarderweg 39, 2031 BN Haarlem, Niederlande.Belgien, Bulgarien, Deutschland, Griechenland, Irland, Kroatien, Luxemburg, Malta, Niederlande, Österreich, Portugal, Rumänien, Slowakei, Slowenien, Spanien, Tschechische Republik, Vereinigtes Königreich, ZypernDänemark, Finnland, Frankreich, Island, Italien, Litauen, Norwegen, SchwedenGemäß § 22 Infektionsschutzgesetz müssen alle Schutzimpfungen vom Impfarzt mit dem Impfdatum, Handelsnamen, der Chargenbezeichnung, der Angabe der Krankheit, gegen die geimpft wurde, sowie Name, Anschrift und Unterschrift des impfenden Arztes in einen Impfausweis eingetragen werden.Häufig unterbleiben indizierte Impfungen, weil bestimmte Umstände irrtümlicherweise als Kontraindikationen angesehen werden. In patients who require penicillin (or other antibiotic) prophylaxis against pneumococcal infection, such prophylaxis should not be discontinued after vaccination with Pneumovax 23.Persons who are immunocompromised, including persons receiving immunosuppressive therapy, may have a diminished immune response to Pneumovax 23. Injection site reactions typically resolved by 5 days following vaccination.For subjects aged 50-64 years, the injection-site adverse reaction rate for revaccinees and initial vaccinees was similar (79.6% and 72.8% respectively).The rate of systemic adverse reactions was similar among both initial vaccinees and revaccinees within each age group. The rate of vaccine-related systemic adverse experiences was higher following revaccination (33.1%) than following primary vaccination (21.7%) in subjects ≥65 years of age, and was similar following revaccination (37.5%) and primary vaccination (35.5%) in subjects 50 to 64 years of age.Since elderly individuals may not tolerate medical interventions as well as younger individuals, a higher frequency and/or a greater severity of reactions in some older individuals cannot be ruled out.Post-marketing reports have been received in which some elderly individuals had severe adverse experiences and a complicated clinical course following vaccination.
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pneumovax 23 impfung