(2) a box of 10 vials of diluent (package B). This is a summary only. If your child is 12 months to 12 years old and your doctor gives a second dose, the second dose must be given at least 3 months after the first shot. If you would like more information, talk to your healthcare professional, visit the web site at www.merckvaccines.com, or call 1-800-Merck-90. There were no reports of breakthrough varicella in 83% (63/76) of exposed vaccinees, while 17% (13/76) reported a mild form of varicella. At least 1 month should elapse between a dose of measles-containing vaccine and a dose of Varivax if the vaccines are not given concurrently [see Clinical Studies (14.1)]. : Varicella Vaccine Trials in Healthy Children. by: Merck Sharp & Dohme Corp., a subsidiary of Varicex Benda all’ossido di zinco Campi di applicazione - bendaggi semirigidi di lunga durata nel trattamento di edemi, insufficienza venosa cronica, ulcera venosa, tromboflebiti - trattamento riabilitativo in seguito a fratture Proprietà - impregnata di pasta all’ossido di zinco - pronta all’uso, pratica nell’utilizzo CATALOGOPRODOTTI SERVISANSPA–VIAG.VERDI8–20050VERANOBRIANZA(MI) Tel.0362992051–Fax0362992052–info@servisan.it–www.servisan.it SPORT Varivax does not treat chickenpox once you or your child have it. MedlinePlus en español también contiene enlaces a sitios web no gubernamentales. trace quantities of neomycin. : The Safety Profile of Varicella Vaccine: A 10-Year Review. Varivax, when reconstituted as directed, is a sterile preparation for subcutaneous injection. Severe disease and serious complications are more likely to occur in adolescents and adults. € 15,50. Stevens-Johnson syndrome; erythema multiforme; Henoch-Schönlein purpura; secondary bacterial infections of skin and soft tissue, including impetigo and cellulitis; herpes zoster. For information or a copy of the vaccine reporting form, call the VAERS toll-free number at 1-800-822-7967, or report online at www.vaers.hhs.gov. Consultare sempre le avvertenze e le indicazioni prima dell’utilizzo dei prodotti. The study enrolled healthy individuals 1 to 14 years of age (n=491 vaccine, n=465 placebo). Varivax is contraindicated for use in pregnant women because the vaccine contains live, attenuated varicella virus, and it is known that wild-type varicella virus, if acquired during pregnancy, can cause congenital varicella syndrome [see Contraindications (4.5) and Patient Counseling Information (17)]. Il prodotto è conforme allo Standard Internazionale Stop ai test su animali - Garantito da LAV Modalità d'uso: Applicare La Pasta all'acqua Baby Anthyllis in strato spesso, dopo ogni cambio ed in particolare prima di mettere il bambino a dormire, sulla pelle perfettamente pulita ed asciutta con un leggerissimo e breve massaggio per sfruttare appieno … varicella virus vaccine live injection, powder, lyophilized, for suspension, We comply with the HONcode standard for trustworthy health information -, measles virus vaccine / mumps virus vaccine / rubella virus vaccine / varicella virus vaccine, (pain/soreness, swelling and/or erythema, rash, pruritus, hematoma, induration, stiffness), (soreness, erythema, swelling, rash, pruritus, pyrexia, hematoma, induration, numbness). Oka/Merck Strain. These products may contain antibodies that interfere with vaccine virus replication and decrease the expected immune response. This translates to a 3.4-fold lower risk of developing varicella >42 days postvaccination during the 10-year observation period in children who received 2 doses than in those who received 1 dose (2.2% vs. 7.5%, respectively). Vendita di farmaci e parafarmaci su FarmaciaDiFiducia.com, spedizione rapida in tutta Italia in 24-48 h. Varivax works by helping the immune system protect you or your child from getting chickenpox. people who have a weakened immune system. Gershon, A.A.; et al. Avoid use of salicylates (aspirin) or salicylate-containing products in children and adolescents 12 months through 17 years of age for six weeks following vaccination with Varivax because of the association of Reye syndrome with salicylate therapy and wild-type varicella infection [see Drug Interactions (7.1)]. Withdraw the entire amount of reconstituted vaccine, inject the total volume and discard vial. Use a sterile syringe free of preservatives, antiseptics, and detergents for each reconstitution and injection of Varivax because these substances may inactivate the vaccine virus. Rates of breakthrough disease were significantly lower among children with VZV antibody titers ≥5 gpELISA units/mL compared with children with titers <5 gpELISA units/mL. N Engl J Med. Anaphylaxis (including anaphylactic shock) and related phenomena such as angioneurotic edema, facial edema, and peripheral edema. Efficacy Trial in Healthy Children. 78(suppl): 723-727, 1986. Questa pagina Web contiene informazioni sui prodotti destinate esclusivamente agli operatori sanitari. - compressione in flebologia. When reconstituting the vaccine, use only the sterile diluent supplied with Varivax. Kuter, B.J. It is meant to help prevent chickenpox. Among the subset of vaccinees who were actively followed in these early trials for up to six years, 76 individuals had household exposure to varicella. See the ingredient list at the end of this leaflet.). In clinical trials involving healthy children monitored for up to 42 days after a single dose of Varivax, the frequency of fever, injection-site complaints, or rashes were reported as shown in Table 1: In addition, adverse events occurring at a rate of ≥1% are listed in decreasing order of frequency: upper respiratory illness, cough, irritability/nervousness, fatigue, disturbed sleep, diarrhea, loss of appetite, vomiting, otitis, diaper rash/contact rash, headache, teething, malaise, abdominal pain, other rash, nausea, eye complaints, chills, lymphadenopathy, myalgia, lower respiratory illness, allergic reactions (including allergic rash, hives), stiff neck, heat rash/prickly heat, arthralgia, eczema/dry skin/dermatitis, constipation, itching. Two cases reported <50 lesions and none reported >75. Pagina 1 di 1. There are insufficient data to assess the rate of protective efficacy of Varivax against the serious complications of varicella in adults (e.g., encephalitis, hepatitis, pneumonitis) and during pregnancy (congenital varicella syndrome). Overall, 9454 healthy children (12 months to 12 years of age) and 1648 adolescents and adults (13 years of age and older) have been vaccinated with Varivax in clinical trials. A single dose after reconstitution is 0.5 mL. Varicex Benda all’ossido di zinco Campi di applicazione - bendaggi semirigidi di lunga durata nel trattamento di edemi, insufficienza venosa cronica, ulcera venosa, tromboflebiti - trattamento riabilitativo in seguito a fratture It is not known if these rare side effects are related to the vaccine. Clinical studies of Varivax did not include sufficient numbers of seronegative subjects aged 65 and over to determine whether they respond differently from younger subjects. The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records. Use of dry ice may subject Varivax to temperatures colder than –58°F (–50°C). Tuberculin skin testing, with tuberculin purified protein derivative (PPD), may be performed before Varivax is administered or on the same day, or at least 4 weeks following vaccination with Varivax, as other live virus vaccines may cause a temporary depression of tuberculin skin test sensitivity leading to false negative results. MedlinePlus en español contiene enlaces a documentos con información de salud de los Institutos Nacionales de la Salud y otras agencias del gobierno federal de los EE. : Live Attenuated Varicella Virus Vaccine. Utilizing the previously reported historical attack rate of 87% for wild-type varicella following household exposure to varicella among unvaccinated children in the calculation of efficacy, this represents an approximate 80% reduction in the expected number of cases in the household setting. : Live Attenuated Varicella Vaccine in Healthy 12- to 24-Month-Old Children. 10125410158 Autorizzazioni: Decreto Presidente Regione Lombardia n°1906 del 18.04.1996 Direttore Sanitario: dott. In a clinical study involving 307 children 12 to 18 months of age, 150 received an investigational varicella-containing vaccine (a formulation combining measles, mumps, rubella, and varicella in one syringe) concomitantly with a booster dose of PedvaxHIB [Haemophilus b Conjugate Vaccine (Meningococcal Protein Conjugate)], while 130 received M-M-R II concomitantly with a booster dose of PedvaxHIB followed by Varivax 6 weeks later. Do not take aspirin or aspirin-containing products for 6 weeks after getting Varivax. Although no placebo-controlled trial was carried out in adolescents and adults, the protective efficacy of Varivax was determined by evaluation of protection when vaccinees received 2 doses of Varivax 4 or 8 weeks apart and were subsequently exposed to varicella in a household setting. The 2-dose regimen of varicella vaccine had a safety profile comparable to that of the 1-dose regimen. In the US general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4%, and 15% to 20%, respectively. Abstracts of the 1988 Inter-Science Conference Antimicrobial Agents and Chemotherapy: 237(Abstract #731). Composizione For adolescents and adults, 2 doses of Varivax may be separated by 1 month [see Dosage and Administration (2.1)]. Less common but very serious complications can occur. In a clinical trial, a total of 2216 children 12 months to 12 years of age with a negative history of varicella were randomized to receive either 1 dose of Varivax (n=1114) or 2 doses of Varivax (n=1102) given 3 months apart. The overall incidence of injection-site clinical complaints (primarily erythema and swelling) observed in the first 4 days following vaccination was 25.4% Postdose 2 and 21.7% Postdose 1, whereas the overall incidence of systemic clinical complaints in the 42-day follow-up period was lower Postdose 2 (66.3%) than Postdose 1 (85.8%). Pediatrics. Bende impregnate di ossido di zinco, con differenti strutture tessili, pronte all'uso per un'applicazione rapida di bendaggi semirigidi nelle tromboflebiti, trattamento di edemi, insufficienza venosa cronica, ulcera venosa, come anche nel trattamento successivo all'ingessatura in seguito a fratture. 23: 132-37, 2004. Before reconstitution, protect from light. 04.1 Indicazioni terapeutiche. : Clinical Survey of Natural Varicella Compared with Breakthrough Varicella After Immunization with Live Attenuated Oka/Merck Varicella Vaccine. The ACIP has specific recommendations for intervals between administration of antibody-containing products and live virus vaccines. ; et al. ; et al. (This includes gelatin or neomycin. Indicazioni Bendaggi compressivi: in caso di trombo-flebite, flebotrombosi e loro conseguenze; vene varicose, ulcus cruris. What should I tell my healthcare professional before getting Varivax? Inject the vaccine subcutaneously into the outer aspect of the deltoid region of the upper arm or into the higher anterolateral area of the thigh. Arbeter, A.M.; et al. Acquista su Amazon. Further passage of the virus for varicella vaccine was performed at Merck Research Laboratories (MRL) in human diploid cell cultures (MRC-5) that were free of adventitious agents. In clinical trials involving healthy adolescents and adults, the majority of whom received two doses of Varivax and were monitored for up to 42 days after any dose, the frequencies of fever, injection-site complaints, or rashes are shown in Table 2. Ordina per: Varicex Benda Anelastica f - 10 x 5 1pz € 8,90 Iva inc. PAGINA PRECEDENTE. Bende di supporto: per il post-trattamento di fratture, lussazioni, operazioni delle articolazioni delle gambe. Contains no preservatives. Any freezer (e.g., chest, frost-free) that reliably maintains an average temperature between –58°F and +5°F (–50°C and –15°C) and has a separate sealed freezer door is acceptable for storing Varivax. How to use varix in a sentence. Guess, H.A. (This includes allergies to neomycin or gelatin.). Varicex F è una benda rigida all'ossido di zinco e ad alto contenuto di umidità utilizzata per l'applicazione di bendaggi ad asciugatura rapida. Vaccine. 92(6): 833-837, 1993. Benda Varicex F con ossido di zinco 10x500 Cm 1 Pezzo Benda Varicex F per bendaggi semirigidi di lunga durata nel trattamento di edemi, insufficienza venosa cronica, ulcera venosa, tromboflebiti € 9,36 € 10,40 -10% It can't be played in your browser. Tell your healthcare professional if you or your child: Varivax is given as a shot to people who are 12 months old or older. 310(22): 1409-1415, 1984. It is not known whether varicella vaccine virus is excreted in human milk. Before reconstitution, the lyophilized vaccine is a white compact crystalline plug. Wild-type varicella is known to cause fetal harm [see Use in Specific Populations (8.1) and Patient Counseling Information (17)]. Concomitant Administration with Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed (DTaP) and Oral Poliovirus Vaccine (OPV). : Oka/Merck Varicella Vaccine in Healthy Children: Final Report of a 2-Year Efficacy Study and 7-Year Follow-up Studies. Each 0.5 mL dose of Varivax is administered subcutaneously. Varicex Benda all’ossido di zinco ... Versione F - cotone/viscosa - benda rigida - alto contenuto di umidità - per bendaggi ad asciugatura lenta ... (previe altre indicazioni). Ortopedia e medicazione Medicazione. Pagina 1 di 1. In addition, adverse events reported at a rate of ≥1% are listed in decreasing order of frequency: upper respiratory illness, headache, fatigue, cough, myalgia, disturbed sleep, nausea, malaise, diarrhea, stiff neck, irritability/nervousness, lymphadenopathy, chills, eye complaints, abdominal pain, loss of appetite, arthralgia, otitis, itching, vomiting, other rashes, constipation, lower respiratory illness, allergic reactions (including allergic rash, hives), contact rash, cold/canker sore. BENDA DURELAST 6X500CM. If you have any questions about the vaccine after reading this leaflet, you should ask your healthcare professional. Do not administer Varivax to individuals with an active febrile illness with fever >101.3°F (>38.5°C). No. To reconstitute the vaccine, withdraw the total volume of supplied sterile diluent and inject into the lyophilized vaccine vial. In the first year, 8.5% of placebo recipients contracted varicella, while no vaccine recipient did, for a calculated protection rate of 100% during the first varicella season. MERCK & CO., INC., Whitehouse Station, NJ 08889, USA, For patent information: www.merck.com/product/patent/home.html, Patient Information Copyright © 1995-2020 Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. During shipment, maintain the vaccine at a temperature between –58°F and +5°F (–50°C and –15°C). A total of 50 clinical varicella cases were reported >42 days following 2-dose vaccination. Varicella, also commonly referred to as “chickenpox”, is an acute and highly contagious disease. pregnant women who have never had chickenpox. The vaccine virus (Oka/Merck strain) contained in Varivax may establish latency of varicella zoster virus in immunocompetent individuals, with the potential for later development of herpes zoster [see Clinical Pharmacology (12.2)]. € 20,60. Varicex F - benda rigida all'ossido di zinco . È pronta all’uso, consente di applicare velocemente bendaggi a lunga durata e semi-rigidi, in caso di: tromboflebite; trattamento di edemi; insufficienza venosa cronica; ulcera venosa in fase di guarigione; come trattamento dopo fratture. Le bende impregnate di zinco non esercitano pressione, se utilizzate con bende elastiche applicate con la tecnica circolare o a semi-arco, e sono disponibili in diversi modelli. It can be passed to others. A pregnancy exposure registry was maintained from 1995 to 2013 to monitor pregnancy and fetal outcomes following inadvertent administration of Varivax. Varivax® is a vaccine indicated for active immunization for the prevention of varicella in individuals 12 months of age and older. BENDE ALLA COLLA DI ZINCO Caratteristiche: benda di garza di cotone impregnata di pasta ad alto tenore di ossido di zinco con elevato potere antiflogistico. J Infect Dis. La tabella sotto riportata : è indicativa e parziale ; è stata elaborata sulla base delle informazioni riportate sui prodotti stessi; è stata elaborata sui prodotti che abbiamo … Tell your doctor or healthcare professional if you or your child expect to have close contact with someone who falls into one of these groups. For information regarding the product or questions regarding storage conditions, call 1-800-9-Varivax (1-800-982-7482). In a clinical study involving 822 children 12 to 15 months of age, 410 received COMVAX [Haemophilus b Conjugate (Meningococcal Protein Conjugate) and Hepatitis B (Recombinant) Vaccine] (no longer licensed in the US), M-M-R II, and Varivax concomitantly at separate injection sites, and 412 received COMVAX followed by M-M-R II and Varivax given concomitantly at separate injection sites, 6 weeks later. Varivax [Varicella Virus Vaccine Live] is a preparation of the Oka/Merck strain of live, attenuated varicella virus. - fissaggio di medicazioni. Chartrand, D.M. tissue culture origin containing Discard if the lyophilized vaccine cannot be dissolved. Among a subset of vaccinees who were actively followed in these later trials for up to 10 years postvaccination, 95 individuals were exposed to an unvaccinated individual with wild-type varicella in a household setting. Bende umide all'ossido di zinco con estensibilità in lunghezza; con pasta all'ossido … The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for Varivax, and any potential adverse effects on the breastfed child from Varivax or from the underlying maternal condition. UU. Some of them were serious. The protective efficacy of Varivax was established by: (1) a placebo-controlled, double-blind clinical trial, (2) comparing varicella rates in vaccinees versus historical controls, and (3) assessing protection from disease following household exposure. have active tuberculosis that is not treated. Indicazioni: particolarmente utilizzato per il taping sportivo e nell'immobilizzazione parziale con funzione di sostegno e scarico per articolazioni, muscoli e tendini. The first dose is administered at 12 to 15 months of age but may be given anytime through 12 years of age. Any freezer (e.g., chest, frost-free) that reliably maintains a temperature between -58°F and +5°F (-50°C and -15°C) and has a separate sealed freezer door is acceptable for storing VARIVAX.VARIVAX may be stored at refrigerator temperature (36°F to 46°F, 2°C to 8°C) for up to 72 continuous hours prior to reconstitution. The most common side effects reported after taking Varivax are: Other less common side effects have also been reported. are allergic to any of its ingredients. Varicella Virus Vaccine Live. Because the events are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to vaccine exposure. ; et al. Disseminated varicella disease and extensive vaccine-associated rash have been reported in individuals who are immunosuppressed or immunodeficient who were inadvertently vaccinated with a varicella-containing vaccine. Select one or more newsletters to continue. The U.S. Department of Health and Human Services has established a Vaccine Adverse Event Reporting System (VAERS) to accept all reports of suspected adverse events after the administration of any vaccine. In recipients of 1 dose of Varivax over 9 years of follow-up, the geometric mean titers (GMTs) and the percent of subjects with VZV antibody titers ≥5 gpELISA units/mL generally increased. Varivax, when reconstituted, is a clear, colorless to pale yellow liquid. Acquista online Benda Varicex F 10Cm X 7M Un Pezzo della categoria dei Parafarmaci e Medicazioni avanzate. The median of the maximum total number of lesions ranged from 15 to 42 per year. Aplastic anemia; thrombocytopenia (including idiopathic thrombocytopenic purpura (ITP)). Among a subset of vaccinees who were actively followed in these early trials for up to nine years postvaccination, 179 individuals had household exposure to varicella. Varivax is a suspension for injection supplied as a single-dose vial of lyophilized vaccine to be reconstituted using the accompanying sterile diluent [see Dosage and Administration (2.2) and How Supplied/Storage and Handling (16)]. In clinical trials {1-8}, Varivax was administered to over 11,000 healthy children, adolescents, and adults. Administration of immune globulins and other blood products concurrently with Varivax may interfere with the expected immune response [see Warnings and Precautions (5.4)] {9}. In this group there was considerable variation in varicella rates among studies and study sites, and much of the reported data were acquired by passive follow-up. Subjects were actively followed for varicella, any varicella-like illness, or herpes zoster and any exposures to varicella or herpes zoster on an annual basis for 10 years after vaccination. - morbida e piacevole sulla pelle. Visually inspect the vaccine before and after reconstitution prior to administration. Inform patient, parent, or guardian that vaccination with Varivax may not result in protection of all healthy, susceptible children, adolescents, and adults. The VAERS toll-free number is 1-800-822-7967 or report online to www.vaers.hhs.gov. White, C.J. JAMA. Agitate to dissolve completely. Weibel, R.E. Varivax® (pronounced "VAR ih vax") lunghezza non in trazione, confezionata singolarmente in busta in film di alluminio, Fissaggio, supporto e riduzione del carico, Raucodrape Sistema di copertura per sala operatoria, Setpack Sistema di medicazioni per sala operatoria, Kitpack Set a più componenti per sala operatoria, Percorso di trattamento L&R per le ulcere venose delle gambe, Imbottiture, medicazioni tubolari e accessori, confezionata singolarmente in busta in film di alluminio, confezionata singolarmente in busta in film di alluminio, sfusa nella scatola, bielastica (elastica in larghezza e lunghezza), effetto stretch, adatto anche a parti anatomiche affusolate, per applicare bendaggi a lunga durata e semi-rigidi nel trattamento di edemi, insufficienza venosa cronica, ulcera vascolare, tromboflebite, pronta all'uso e consente di risparmiare tempo. No cases of Reye syndrome have been observed following vaccination with Varivax. There were no reports of breakthrough varicella among the exposed vaccinees. Varicex® è una benda impregnata di zinco. Niltac sono salviette ipoallergeniche monouso al silicone per la rimozione delicata ed atraumatica di barriere cutanee (dispositivi per stomia), medicazioni, cerotti e residui di adesivo dalla cute. Hammerschlag, M.R. Prenota e Ritira ROSIDAL SOFT BEN10X0,4CM X2,5M. One case of herpes zoster has been reported in the adolescent and adult age group during 5410 person-years of follow-up in clinical trials, resulting in a calculated incidence of 18.5 cases per 100,000 person-years. ... BENDA VARICEX F 10X10 1PZ. Do not use the product if particulates are present or if it appears discolored. Advise the patient to read the FDA-approved patient labeling (Patient Information). Pediatrics. In another multicenter study involving adolescents and adults, 2 doses of Varivax administered 8 weeks apart induced a seroconversion rate of 94% in 142 individuals 6 weeks after the first dose and 99% in 122 individuals 6 weeks after the second dose.
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