Svizzera -
italiano -
Swissmedic (Swiss Agency for Therapeutic Products)
fsme-immun 0.25 ml junior sospensione iniettabile in una siringa preriempita
pfizer ag - virus fsme inactivatus (stamm neudörfl) - sospensione iniettabile in una siringa preriempita - virus fsme inactivatus (stamm neudörfl) 1.19 µg, aluminii hydroxidum hydricum ad adsorptionem corresp. aluminium 0.17 mg, albuminum seri humani, natrii chloridum, dinatrii phosphas dihydricus, kalii dihydrogenophosphas, aqua ad iniectabile q.s. ad suspensionem pro 0.25 ml corresp. natrium 0.71 mg et kalium 0.007 mg, residui: saccharum, formaldehydum, protamini sulfas, neomycinum, gentamicinum. - immunizzazione attiva contro l'encefalite da zecche, di età 1. fino all'età di 16. anni - vaccini
Svizzera -
italiano -
Swissmedic (Swiss Agency for Therapeutic Products)
fsme-immun cc sospensione per iniezione intramuscolare
pfizer ag - virus fsme inactivatus (stamm neudörfl) - sospensione per iniezione intramuscolare - virus fsme inactivatus (stamm neudörfl) 2.4 µg, aluminii hydroxidum hydricum ad adsorptionem corresp. aluminium 0.35 mg, albuminum seri humani, natrii chloridum, dinatrii phosphas dihydricus, kalii dihydrogenophosphas, aqua ad iniectabile q.s. ad suspensionem pro 0.5 ml corresp. natrium 1.42 mg et kalium 0.013 mg, residui: saccharum, formaldehydum, protamini sulfas, neomycinum, gentamicinum. - immunizzazione attiva contro l'encefalite da zecche, che abbiano compiuto il 16. anni - vaccini
Svizzera -
italiano -
Swissmedic (Swiss Agency for Therapeutic Products)
fsme-immun 0.25 ml junior sospensione per iniezione intramuscolare
pfizer ag - virus fsme inactivatus (stamm neudörfl) - sospensione per iniezione intramuscolare - virus fsme inactivatus (stamm neudörfl) 1.19 µg, aluminii hydroxidum hydricum ad adsorptionem corresp. aluminium 0.17 mg, albuminum seri humani, natrii chloridum, dinatrii phosphas dihydricus, kalii dihydrogenophosphas, aqua ad iniectabile q.s. ad suspensionem pro 0.25 ml corresp. natrium 0.71 mg et kalium 0.007 mg, residui: saccharum, formaldehydum, protamini sulfas, neomycinum, gentamicinum. - immunizzazione attiva contro l'encefalite da zecche, di età 1. fino all'età di 16. anni - vaccini
Svizzera -
italiano -
Swissmedic (Swiss Agency for Therapeutic Products)
influvac tetra 0.5 ml sospensione iniettabile
mylan pharma gmbh - haemagglutininum influenzae a (h1n1) (virus-stamm a/guangdong-maonan/swl1536/2019 (h1n1)-pdm09: reassortant virus cnic-1909 derived from a/guangdong-maonan/swl1536/2019), haemagglutininum influenzae a (h3n2) (virus-stamm a/hong kong/2671/2019 (h3n2)-like: reassortant virus ivr-208 derived from a/hong kong/2671/2019), haemagglutininum influenzae b (virus-stamm b/washington/02/2019 (victoria lineage)) - sospensione iniettabile - haemagglutininum influenzae a (h1n1) (virus-stamm a/guangdong-maonan/swl1536/2019 (h1n1)-pdm09: reassortant virus cnic-1909 derived from a/guangdong-maonan/swl1536/2019) 15 µg, haemagglutininum influenzae a (h3n2) (virus-stamm a/hong kong/2671/2019 (h3n2)-like: reassortant virus ivr-208 derived from a/hong kong/2671/2019) 15 µg, haemagglutininum influenzae b (virus-stamm b/washington/02/2019 (victoria lineage)) 15 µg, haemagglutininum influenzae b (virus-stamm b/phuket/3073/2013 (yamagata lineage)) 15 µg, kalii chloridum, kalii dihydrogenophosphas, dinatrii phosphas dihydricus, natrii chloridum, calcii chloridum dihydricum, magnesii chloridum hexahydricum, aqua ad iniectabile q.s. ad suspensionem pro 0.5 ml corresp. natrium 2.0 mg, kalium 0.1 mg, residui: cetrimidum, formaldehydum, gentamicini sulfas, polysorbatum 80, ovalbuminum. - aktive immunisierung gegen influenza, ab 3 jahren - vaccini
Svizzera -
italiano -
Swissmedic (Swiss Agency for Therapeutic Products)
influvac tetra 0.5 ml sospensione iniettabile
mylan pharma gmbh - haemagglutininum influenzae a (h1n1) (virus-stamm a/victoria/2570/2019 (h1n1)-pdm09: reassortant virus ivr-215 derived from a/victoria/2570/2019), haemagglutininum influenzae a (h3n2) (virus-stamm a/cambodia/e0826360/2020 (h3n2)-like: reassortant virus ivr-224 derived from a/cambodia/e0826360/2020), haemagglutininum influenzae b (virus-stamm b/washington/02/2019 (victoria lineage)) - sospensione iniettabile - haemagglutininum influenzae a (h1n1) (virus-stamm a/victoria/2570/2019 (h1n1)-pdm09: reassortant virus ivr-215 derived from a/victoria/2570/2019) 15 µg, haemagglutininum influenzae a (h3n2) (virus-stamm a/cambodia/e0826360/2020 (h3n2)-like: reassortant virus ivr-224 derived from a/cambodia/e0826360/2020) 15 µg, haemagglutininum influenzae b (virus-stamm b/washington/02/2019 (victoria lineage)) 15 µg, haemagglutininum influenzae b (virus-stamm b/phuket/3073/2013 (yamagata lineage)) 15 µg, kalii chloridum, kalii dihydrogenophosphas, dinatrii phosphas dihydricus, natrii chloridum, calcii chloridum dihydricum, magnesii chloridum hexahydricum, aqua ad iniectabile q.s. ad suspensionem pro 0.5 ml corresp. natrium 2.0 mg, kalium 0.1 mg, residui: cetrimidum, formaldehydum, gentamicini sulfas, polysorbatum 80, ovalbuminum. - aktive immunisierung gegen influenza, ab 6 monaten - vaccini
Svizzera -
italiano -
Swissmedic (Swiss Agency for Therapeutic Products)
influvac tetra 0.5 ml sospensione iniettabile
viatris pharma gmbh - haemagglutininum influenzae a (h1n1) (virus-stamm a/victoria/2570/2019 (h1n1)-pdm09: reassortant virus ivr-215 derived from a/victoria/2570/2019), haemagglutininum influenzae a (h3n2) (virus-stamm a/darwin/9/2021 (h3n2)-like: reassortant virus derived from a/darwin/9/2021, san-010), haemagglutininum influenzae b (virus-stamm b/austria/1359417/2021 -like: reassortant virus bvr-26 derived from b/austria/1359417/2021 (victoria lineage)) - sospensione iniettabile - haemagglutininum influenzae a (h1n1) (virus-stamm a/victoria/2570/2019 (h1n1)-pdm09: reassortant virus ivr-215 derived from a/victoria/2570/2019) 15 µg, haemagglutininum influenzae a (h3n2) (virus-stamm a/darwin/9/2021 (h3n2)-like: reassortant virus derived from a/darwin/9/2021, san-010) 15 µg, haemagglutininum influenzae b (virus-stamm b/austria/1359417/2021 -like: reassortant virus bvr-26 derived from b/austria/1359417/2021 (victoria lineage)) 15 µg, haemagglutininum influenzae b (virus-stamm b/phuket/3073/2013 (yamagata lineage)) 15 µg, kalii chloridum, kalii dihydrogenophosphas, dinatrii phosphas dihydricus, natrii chloridum, calcii chloridum dihydricum, magnesii chloridum hexahydricum, aqua ad iniectabile q.s. ad suspensionem pro 0.5 ml corresp. natrium 2.0 mg, kalium 0.1 mg, residui: cetrimidum, formaldehydum, gentamicini sulfas, polysorbatum 80, ovalbuminum. - aktive immunisierung gegen influenza, ab 6 monaten - vaccini
Italia -
italiano -
Adama
merpan® 80 wdg
adama - granuli idrodispersibili - captano 80% (800g/kg) - fungicidi
Svizzera -
italiano -
Swissmedic (Swiss Agency for Therapeutic Products)
infanrix dtpa-ipv+hib pulver und suspension zur herstellung einer injektionssuspension
glaxosmithkline ag - toxoidum diphtheriae, toxoidum tetani, toxoidum pertosse, haemagglutininum filamentosum (b. pertussis, pertactinum (b. pertussis, il virus della poliomielite di tipo 1 inactivatus (stamm mahoney), virus e poliomielite di tipo 2 inactivatus (stamm mef-1), un virus e la poliomielite di tipo 3 inactivatus (stamm saukett), polysaccharida haemophili influenzae di tipo b 20752 conjugata con toxoido tetani - pulver und suspension zur herstellung einer injektionssuspension - i) dtpa-ipv: toxoidum diphtheriae min. 30 u.i., toxoidum tetani min. 40 u.i., toxoidum pertussis 25 µg, haemagglutininum filamentosum (b. pertussis) 25 µg, pertactinum (b. pertussis) 8 µg, virus poliomyelitis typus 1 inactivatus (stamm mahoney) 40 u., virus poliomyelitis typus 2 inactivatus (stamm mef-1) 8 u., virus poliomyelitis typus 3 inactivatus (stamm saukett) 32 u., aluminium 0.5 mg ut aluminii hydroxidum hydricum ad adsorptionem, natrii chloridum corresp. natrium 1.8 mg, medium 199, aqua ad iniectabile ad suspensionem pro 0.5 ml, residui: neomycini sulfas, polymyxini b sulfas, polysorbatum 80, formaldehydum. ii) hib: polysaccharida haemophili influenzae typus b 20752 conjugata cum toxoido tetani 10 µg, lactosum, pro praeparatione. i) et ii) corresp. dtpa-ipv + hib: toxoidum diphtheriae min. 30 u.i., toxoidum tetani min. 40 u.i., toxoidum pertussis 25 µg, haemagglutininum filamentosum (b. pertussis) 25 µg, pertactinum (b. pertussis) 8 µg, virus poliomyelitis typus 1 inactivatus (stamm mahoney) 40 u., virus poliomyelitis typus 2 inactivatus (stamm mef-1) 8 u., virus poliomyelitis typus 3 inactivatus (stamm saukett) 32 u., polysaccharida haemophili influenzae typus b 20752 conjugata cum toxoido tetani 10 µg, aluminium 0.5 mg ut aluminii hydroxidum hydricum ad adsorptionem, natrii chloridum corresp. natrium 1.8 mg, medium 199, lactosum, aqua ad iniectabile ad suspensionem pro 0.5 ml, residui: neomycini sulfas, polymyxini b sulfas, polysorbatum 80, formaldehydum. - aktive immunisierung gegen diphtherie, tetanus, pertussis, poliomyelitis und haemophilus influenzae typ b, ab dem vollendeten 2. lebensmonat, auffrischimpfung (4. dosis), ab dem vollendeten 12. lebensmonat - vaccini
Svizzera -
italiano -
Swissmedic (Swiss Agency for Therapeutic Products)
infanrix hexa pulver und suspension zur herstellung einer injektionssuspension
glaxosmithkline ag - toxoidum diphtheriae, toxoidum tetani, toxoidum pertussis, haemagglutininum filamentosum (b. pertussis), pertactinum (b. pertussis), virus poliomyelitis typus 1 inactivatus (stamm mahoney), virus poliomyelitis typus 2 inactivatus (stamm mef-1), virus poliomyelitis typus 3 inactivatus (stamm saukett), hepatitidis b viri antigenum adnr, polysaccharida haemophili influenzae typus b 20752 conjugata cum toxoido tetani - pulver und suspension zur herstellung einer injektionssuspension - i) dtpa-hepb-ipv: toxoidum diphtheriae min. 30 u.i., toxoidum tetani min. 40 u.i., toxoidum pertussis 25 µg, haemagglutininum filamentosum (b. pertussis) 25 µg, pertactinum (b. pertussis) 8 µg, virus poliomyelitis typus 1 inactivatus (stamm mahoney) 40 u.i., virus poliomyelitis typus 2 inactivatus (stamm mef-1) 8 u.i., virus poliomyelitis typus 3 inactivatus (stamm saukett) 32 u.i., hepatitidis b viri antigenum adnr 10 µg, aluminium 0.5 mg ut aluminii hydroxidum hydricum ad adsorptionem, aluminium 0.2 mg ut aluminii phosphas, natrii chloridum corresp. natrium 1.8 mg, medium 199, aqua ad iniectabile ad suspensionem pro 0.5 ml, residui: neomycini sulfas, polymyxini b sulfas, formaldehydum, polysorbatum 20, polysorbatum 80. ii) hib: polysaccharida haemophili influenzae typus b 20752 conjugata cum toxoido tetani 10 µg, lactosum, aluminium 0.12 mg ut aluminii phosphas, pro praeparatione. i) et ii) corresp. dtpa-hepb-ipv + hib: toxoidum diphtheriae min. 30 u.i., toxoidum tetani min. 40 u.i., toxoidum pertussis 25 µg, haemagglutininum filamentosum (b. pertussis) 25 µg, pertactinum (b. pertussis) 8 µg, virus poliomyelitis typus 1 inactivatus (stamm mahoney) 40 u.i., virus poliomyelitis typus 2 inactivatus (stamm mef-1) 8 u.i., virus poliomyelitis typus 3 inactivatus (stamm saukett) 32 u.i., hepatitidis b viri antigenum adnr 10 µg, polysaccharida haemophili influenzae typus b 20752 conjugata cum toxoido tetani 10 µg, aluminium 0.5 mg ut aluminii hydroxidum hydricum ad adsorptionem, aluminium 0.32 mg ut aluminii phosphas, natrii chloridum corresp. natrium 1.8 mg, medium 199, lactosum, aqua ad iniectabile ad suspensionem pro 0.5 ml, residui: neomycini sulfas, polymyxini b sulfas, formaldehydum, polysorbatum 20, polysorbatum 80. - vaccinazione primaria e di richiamo, contro difterite, tetano, pertosse, epatite b, poliomielite e haemophilus influenzae di tipo b, a partire dal compimento del 6. settimana di vita - vaccini