Havrix vaccine is used to help prevent this disease in adults. Havrix works by exposing you to a small amount of the virus, which causes the body to develop immunity to the disease. This vaccine will not treat an active infection that has already developed in the body. Like any vaccine, Havrix may not provide protection from disease in every. Immunogenicity of HAVRIX was studied in subjects with chronic liver disease of various etiologies. 189 healthy adults and 220 adults with either chronic hepatitis B (n = 46), chronic hepatitis C (n = 104), or moderate chronic liver disease of other etiology (n = 70) were vaccinated with HAVRIX 1440 EL.U. on a 0- and 6-month schedule
Havrix 1440 (pro dospělé) Vakcína Havrix 1440 proti žloutence typu A je určena pro dospělé a mladistvé starší 16 let. Vakcína se očkuje do horní části paže. Objednat očkování online Kde očkujem havrix-1440-spc.pdf: NR - Rozhodnutí o registraci: PIL - Příbalová informace: havrix-1440-pil.pdf: PAR - Veřejná zpráva o hodnocení Text na obalu: havrix-1440-obal.pdf: Braillovo písmo: Výjimka Havrix 1440 Inj Sus 1x1ml+st+sj. Vakcína Havrix je indikována k aktivní imunizaci proti infekci vyvolané virem hepatitidy A (HAV) u jedinců vystavených riziku nákazy HAV HAVRIX 1440 U/1 ml ADULTES, suspension injectable en seringue pré-remplie. Vaccin inactivé de l'hépatite A adsorbé : Date de l'autorisation : 18/08/1994 . Cliquez sur un pictogramme pour aller directement à la rubrique le concernant. Pour plus d'information sur les pictogrammes, consultez l'aide..
Details for Havrix 1440 vaccine and its components Havrix 1440 and Havrix Junior are available as a monodose vial in packs of one or ten and as a pre-filled syringe. Not all presentations and pack sizes may be marketed in Australia. 6.6 Special Precautions for Disposal. In Australia, any unused medicine or waste material should be disposed of by taking to your local pharmacy HAVRIX 1440 Inj Susp: Hepatitis-A-Impfstoff; Fertigspritze 1 ml: Liste B, SL (LIM), CHF 56.5 Also, Havrix has been found to be efficacious in a clinical study of children at high risk of HAV infection [see Clinical Studies (14.1)]. Immunogenicity in Adults. Over 400 healthy adults 18 to 50 years of age in 3 clinical studies were given a single 1440 EL.U. dose of Havrix. All subjects were seronegative for hepatitis A antibodies at baseline
1 HAVRIX® 1440 and HAVRIX® Junior Inactivated Hepatitis A Virus Vaccine Consumer Medicine Information Leaflet. In this leaflet, HAVRIX refers to the use of both HAVRIX 1440 for adults and HAVRIX Junior for children A single dose of HAVRIX 1440 (hepatitis A vaccine, inactivated) (1 mL suspension) is used for primary immunization. Page 8 of 24 Children and adolescents from 1 year up to and including 18 years of age . A single dose of HAVRIX 720 Junior (0.5 mL suspension) is used for primar
HAVRIX 720 susp inj: Hépatite A, vaccin; seringue préremplie 0.5 ml: Liste B, LS (LIM), CHF 44.7 HAVRIX Vaccines HAVRIX Product information: HAVRIX product monograph. Patient information: Important information for patients. Healthcare Professional Information: May 1, 2018 - Important Safety Information for several GlaxoSmithKline Inc. vaccines: Potential Risk of Underdosing Trademarks are owned by or licensed to the GSK group of companies Kód SÚKL: 0056573: Registrovaný název LP: HAVRIX 1440: Název LP i: HAVRIX 1440: Doplněk názvu: 1440EU INJ SUS 1X1ML: Síla: 1440EU: Léková forma: Injekční. HAVRIX ®1440 AND HAVRIX® JUNIOR PRODUCT INFORMATION (Inactivated Hepatitis A virus Vaccine) DESCRIPTION HAVRIX, hepatitis A vaccine, is a sterile suspension containing formaldehyde - inactivated hepatitis A virus (HM 175 hepatitis A virus strain) adsorbed onto aluminium hydroxide. The virus is propagated in MRC5 human diploid cells
Havrix (PF) 1,440 ELISA unit/mL intramuscular suspension. color white shape No data. imprint No data. This medicine is a white, vial ‹ Back to Gallery Tradename: HAVRIX Manufacturer: GlaxoSmithKline Biologicals Indication: For active immunization against disease caused by hepatitis A virus (HAV) for persons 12 months of age and older. Product. Adult dose (persons 19 years of age and older): 1440 EL.U./mL Recommended dosing: A single 1-mL dose and a 1-mL booster dose administered between 6 and 12 months later: 90632: HAVRIX is available in single-dose vials and prefilled disposable Tip-Lok ® syringes (packaged without needles) (Preservative Free Formulation). Z23: Vial in Package of 1 HAVRIX prescription and dosage sizes information for physicians and healthcare professionals. Pharmacology, adverse reactions, warnings and side effects
The safety of HAVRIX has been evaluated in 61 clinical trials involving approximately 37,000 individuals receiving doses of 360 EL.U. (n = 21,928 in 3- or 4-dose schedule), 720 EL.U. (n = 12,274 in 2- or 3-dose schedule), or 1440 EL.U. (n = 2,782 in 2- or 3-dose schedule) 341 vaccinated with HAVRIX 1440 EL.U. on a 0- and 6-month schedule. The last group consisted of 342 alcoholic cirrhosis (n = 17), autoimmune hepatitis (n = 10), chronic hepatitis/cryptogeni Havrix 1440 dále obsahuje tyto pomocné látky: hydroxid hlinitý, polysorbát 20, aminokyseliny, hydrogenfosforečnan sodný, dihydrogenfosforečnan draselný, chlorid sodný, chlorid draselný, voda na injekci. Obsahuje stopové množství neomycin-sulfátu (Havrix 1440: méně než 20 ng) months after the first dose of HAVRIX 1440 or HAVRIX 720 Junior. During clinical trials, all the vaccinated subjects were virtually seropositive one month after the booster dose. However, if the booster dose was not administered between 6 and 12 months after the first dose, it can be administered up to 5 years at the latest
Vaccine Trade Name: Havrix™ 1440 Adult, One dose vial Vaccine Type: Havrix™ 1440 Adult Manufacturer: GlaxoSmithKline Country of Manufacture: Belgium Date of prequalification: 19 July 2013 NRA of Record: Federal Agency for Medicines and Health Products Product Description. Pharmaceutical form: liquid, ready to use Presentation: 1 dose vial Route of administration: intramuscula Jak Havrix 1440 vypadá a co obsahuje toto balení. Havrix 1440 je bílá mléčně zakalená suspenze. Během uchovávání se může vytvořit jemná bílá usazenina s bezbarvým supernatantem. Vakcína Havrix 1440 může být buď v lahvičce, nebo v předplněné injekční stříkačce. Velikost balení. 1 x 1 ml v lahvičce
HAVRIX 1440 EL.U. is only indicated for ages 19 and older. Some study subjects were under age 19. Reference: Prescribing Information for HAVRIX. Indication for HAVRIX. HAVRIX is a vaccine indicated for active immunization against disease caused by hepatitis A virus (HAV). HAVRIX is approved for use in persons 12 months of age and older HAVRIX is manufactured with 360 (for pediatric use), 720 (for pediatric and adult use) and 1440 (for adult use) EU (ELISA units) suspended in 0.5-1.0 ml. It is difficult to compare the exact HAV protein content of the two vaccines, since the viral protein content of HAVRIX is not reported
Consumer Medicine InformationWHAT IS IN THIS LEAFLETThis leaflet answers some of the common questions about HAVRIX vaccine. It does not contain all the available information. It does not take the place of talking to your doctor, nurse or pharmacist.All medicines and vaccines have risks and benefits. Your doctor has weighed the possible risks of you or your child having HAVRIX against the. Havrix ® Junior is approved for use for children from 1 year of age and adolescents to 16 years of age. Havrix ® 1440 is approved for use for adolescents from 16 years of age and adults. Havrix is not given as part of the routine immunisation schedule. Special groups. Havrix is recommended and funded for: Transplant recipients (two doses Havrix is not recommended for children less than one year old. For adults (19 years of age and older), one adult dose (1.0 mL) is injected into a muscle (preferably in the outer upper arm) with a repeat (booster) dose 6 to 12 months later
Registered for use in people aged 2-15 years. Each 0.5 mL monodose vial or pre-filled syringe contains: 720 ELISA units of inactivated hepatitis A virus (HM175 strain); 0.25 mg aluminium as aluminium hydroxid Havrix Monodose can be given concomitantly with monovalent and combination vaccines comprised of measles, mumps, rubella and varicella. When concomitant administration is considered necessary the vaccines must be given at different injection sites. Havrix Monodose must not be mixed with other vaccines in the same syringe
In an open-label, randomised trial, 520 adults of both sexes aged 18-30 years were allocated to receive one of two inactivated hepatitis A vaccines; Vaqta ™ or Havrix ™, at 0 and 24 weeks.Doses used were 50 or 100 antigen units (U) of Vaqta ™ and 1440 enzyme linked immunosorbent assay U of Havrix ™ given as 1 ml intramuscular injections. For each trial group safety data were. One hundred and eighty-five subjects were randomized to receive a booster dose of either Avaxim (n=92) or Havrix (n=93), 6 to 7 months after a primary dose of Havrix. Subjects were observed for 30 minutes for immediate reactions and subsequently completed a diary card for a further 2 weeks Ceník. SLUŽBY : konzultace, poradenství 200-400: aplikace 1. dávky 1 druhu vakcín HAVRIX - SUS IM 1440 ELISA UNITS/ML: Common or Proper name: hepatitis A vaccine, inactivated: Company Name: GLAXOSMITHKLINE INC: Market Status: MARKETED: Active Ingredient(s) HEPATITIS A VACCINE, INACTIVATED: Strength(s) 1440UNIT: Dosage form(s) SUSPENSION: Route of administration: INTRAMUSCULAR: Packaging size: 1's (prefilled syringe.
Notice to Readers: FDA Approval of Havrix ®. (Hepatitis A Vaccine, Inactivated) for Persons Aged 1--18 Years. On October 17, 2005, the Food and Drug Administration approved an application to allow use of the pediatric/adolescent formulation of Havrix ® (hepatitis A vaccine, inactivated) (GlaxoSmithKline Biologicals, Rixensart, Belgium) for persons aged 1--18 years WebMD provides common contraindications for Havrix Intramuscular. Find out what health conditions may be a health risk when taken with Havrix Intramuscula Vakcíny Havrix 720 Junior Monodose a Havrix 1440 jsou registrované léčivé přípravky vázané na lékařský předpis. Očkování provádí lékař, vakcíny se aplikují do svalu formou injekce (obvykle do stehna nebo horní části paže). Před použitím si předem pečlivě prostudujte příbalovou informaci dostupnou též na www. Havrix 1440 vyvolá ochranu proti hepatitidě A po 2 až 4 týdnech po očkování. K zabezpečení dlouhodobé ochrany (nejméně na dobu 10 let) se doporučuje podat posilovací dávku, a to kdykoli v době od 6 do 12 měsíců po první dávce
Havrix 1440 (pro dospělé) Vakcína proti žloutence typu A určená pro dospělé a mladistvé starší 16 let. Vakcína se očkuje do horní části paže. Očkovací schéma. Očkuje se dvěma dávkami v následujícím rozestupu: první dávka se aplikuje ve zvolený den, druhá dávka se aplikuje za 6 až 12 měsíce Havrix 1440 je očkovací látka určená k očkování dospělých proti virové hepatitidě A. Účinná látka: Účinnou látkou je plně inaktivovaný virus hepatitidy A, jde tedy o neživou vakcínu.Vakcína obsahuje stopové množství neomycinu Hrazení ze zdravotního pojištění: Vakcína Havrix 1440 není hrazena ze zdravotního pojištění, očkování je dobrovolné a zájemce.
Havrix Havrix 1440. Vakcína Havrix 1440 je určena pro osoby nad 16 let a chrání před onemocněním hepatitidou typu A. Zvláště je vhodná pro osoby pohybující se v rizikových oblastech. Dávkování je způsobem: jedna dávka a následná dávka posilující. Cenově je vakcína Havrix dobře dostupná, pohybuje se okolo 1500 Kč Havrix 1440, injekční suspenze Havrix 720 Junior monodose, injekční suspenze Vakcína proti hepatitidě A inaktivovaná adsorbovaná Injekční suspenze. Přečtěte si pozorně celou příbalovou informaci dříve, než budete očkován(a)/Vaše dítě bude. očkováno, protože obsahuje pro Vás důležité údaje Havrix: made by GlaxoSmithKline. Inactivated hepatitis A virus produced in MRC-5 cells. Each adult dose contains 1440 ELISA units of viral antigen adsorbed on aluminium hydroxide (0.5 mg Al). The pediatric (child) doses contain half the amount of viral antigen and aluminium
Overall, 65.6% of the subjects in the Twinrix group and 67.9% in the Havrix + Engerix‐B vaccine group reported at least one local symptom. General symptoms were also reported with similar frequency in the Twinrix (58.0%) and the Havrix + Engerix‐B vaccine groups (60.6%) Check Point Infinity architecture delivers consolidated Gen V cyber security across networks, cloud, and mobile environments Hepatitis A vaccine can prevent hepatitis A.. Hepatitis A is a serious liver disease.It is usually spread through close personal contact with an infected person or when a person unknowingly ingests the virus from objects, food, or drinks that are contaminated by small amounts of stool (poop) from an infected person Havrix 1440. Dotaz z 2.9.2016: Dobrý den, z obavy z nákazy žloutenkou A, jsem se minulou středu nechala naočkovat látkou havrix 1440. Chtěla jsem se zeptat jestli jsou s tím spojena nějaké rizika nákazy. Od tohoto úterý mě chytila průjem, není mi dobře. Může to mít spojitost Havrix 1440 Adult Monodose (1 dávka v inj.stříkačce) inaktivovaná vakcína proti hepatitidě typu Last updated: 6 December 2020 URL:https://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent&id=CP-2010-CMI-06704-