Suïssa - italià - Swissmedic (Swiss Agency for Therapeutic Products)

viatris pharma gmbh - azelastini hydrochloridum, fluticasoni propionas - sospensione - azelastini hydrochloridum 0.137 mg, fluticasoni propionas 0.05 mg, dinatrii edetas, glycerolum, cellulosum microcristallinum e carmellosum natricum, polysorbatum 80, benzalkonii chloridum 0,014 mg, alcol phenylethylicus, acqua purificata, alla sospensione per dosi. - saisonaler und perennialer allergischer schnupfen - synthetika

Suïssa - italià - Swissmedic (Swiss Agency for Therapeutic Products)

sanofi-aventis (suisse) sa - virus poliomyelitis typus 1 inactivatus, virus poliomyelitis typus 2 inactivatus, virus poliomyelitis typus 3 inactivatus, toxoidum diphtheriae, toxoidum tetani, bordetellae pertussis antigenum - sospensione iniettabile - virus poliomyelitis typus 1 inactivatus 40 u., virus poliomyelitis typus 2 inactivatus 8 u., virus poliomyelitis typus 3 inactivatus 32 u., toxoidum diphtheriae 20 u.i., toxoidum tetani 40 u.i., bordetellae pertussis antigenum: toxoidum pertussis 25 µg et haemagglutininum filamentosum 25 µg, aluminium 0.3 mg ut aluminii hydroxidum hydricum ad adsorptionem, formaldehydum, medium 199 cum phenylalaninum 12.5 µg, ethanolum 2 mg, phenoxyethanolum, acidum aceticum glaciale q.s. ad ph, natrii hydroxidum q.s. ad ph, aqua ad iniectabile q.s. ad suspensionem pro 0.5 ml, residui: glutaralum, neomycinum, streptomycinum, polymyxinum b. - immunizzazione attiva contro difterite, tetano, pertosse e poliomielite nei bambini dai 2 mesi fino ai 7 anni di età - vaccini

Suïssa - italià - Swissmedic (Swiss Agency for Therapeutic Products)

sanofi-aventis (suisse) sa - toxoidum diphtheriae, toxoidum tetani, bordetellae pertussis antigenum, virus poliomyelitis typus 1 inactivatus (d-antigène), virus poliomyelitis typus 2 inactivatus (d-antigène), virus poliomyelitis typus 3 inactivatus (d-antigène), polysaccharida haemophili influenzae typus b 1482 conjugata cum toxoido tetani - sospensione iniettabile et lyophilisat - i) composant dpta-ipv (suspension): toxoidum diphtheriae min. 20 u.i., toxoidum tetani min. 40 u.i., bordetellae pertussis antigenum: toxoidum pertussis 25 µg et haemagglutininum filamentosum 25 µg, virus poliomyelitis typus 1 inactivatus (d-antigène) 40 u., virus poliomyelitis typus 2 inactivatus (d-antigène) 8 u., virus poliomyelitis typus 3 inactivatus (d-antigène) 32 u., aluminium 0.3 mg ut aluminii hydroxidum hydricum ad adsorptionem, formaldehydum, medium 199 cum phenylalaninum 12.5 µg, acidum aceticum glaciale q.s. ad ph, natrii hydroxidum q.s. ad ph, phenoxyethanolum, ethanolum anhydricum 2 mg, aqua ad iniectabile q.s. ad suspensionem pro 0.5 ml, residui: neomycinum, streptomycinum, polymyxini b sulfas. ii) composant hib (poudre): polysaccharida haemophili influenzae typus b 1482 conjugata cum toxoido tetani 10 µg, trometamolum, saccharum, acidum hydrochloridum q.s. ad ph, pro praeparatione. - non appena il 2 ° mese fino al 24 ° mese è andato, per l'immunizzazione attiva contro difterite, tetano, pertosse, poliomielite, haemophilus influenzae di tipo b - vaccini

Suïssa - italià - Swissmedic (Swiss Agency for Therapeutic Products)

sanofi-aventis (suisse) sa - toxoidum tetani, toxoidum diphtheriae, virus e poliomielite di tipo 1 inactivatus, virus e poliomielite di tipo 2 inactivatus, virus e poliomielite di tipo 3 inactivatus - sospensione iniettabile - toxoidum tetani min. 20 u.i., toxoidum diphtheriae min. 2 u.i., virus poliomyelitis typus 1 inactivatus 40 u., virus poliomyelitis typus 2 inactivatus 8 u., virus poliomyelitis typus 3 inactivatus 32 u., aluminium 0.35 mg ut aluminii hydroxidum hydricum ad adsorptionem, formaldehydum, medium 199, phenoxyethanolum, ethanolum anhydricum 1.98 µg, aqua ad iniectabilia q.s. ad suspensionem pro 0.5 ml, residui: neomycinum, streptomycinum, polymyxinum b. - immunizzazione attiva, un richiamo dell'immunizzazione contro la difterite, il tetano, la poliomielite e il più presto 5 anni di età - vaccini

Suïssa - italià - Swissmedic (Swiss Agency for Therapeutic Products)

eisai pharma ag - perampanelum anhydricum - sospensione orale - perampanelum anhydricum 0.5 mg, sorbitolum liquidum cristallisabile 250 mg corresp. sorbitolum 175 mg, cellulosum microcristallinum, carmellosum natricum, poloxamerum 188, dimeticonum, polysorbatum 65, methylcellulosum, silica colloidalis hydrica, macrogoli 12 stearas, e 210 < 5 µg, e 200, acidum sulfuricum concentratum, acidum citricum, e 211 1.1 mg, aqua purificata q.s. ad suspensionem pro 1 ml corresp. natrium 0.418 mg. - antiepileptikum - synthetika

Suïssa - italià - Swissmedic (Swiss Agency for Therapeutic Products)

sanofi-aventis (suisse) sa - haemagglutininum influenzae a (h1n1) (virus souche a/guangdong-maonan/swl1536/2019 (h1n1)-pdm09: reassortant virus cnic-19 derived from a/guangdong-maonan/swl1536/2019), haemagglutininum influenzae a (h3n2) (virus souche a/hong kong/2671/2019 (h3n2)-like: reassortant virus ivr-208 derived from a/hong kong/2671/2019), haemagglutininum influenzae b (virus souche b/washington/02/2019 (victoria lineage)) - sospensione iniettabile in siringa pre-riempita - haemagglutininum influenzae a (h1n1) (virus souche a/guangdong-maonan/swl1536/2019 (h1n1)-pdm09: reassortant virus cnic-19 derived from a/guangdong-maonan/swl1536/2019) 15 µg, haemagglutininum influenzae a (h3n2) (virus souche a/hong kong/2671/2019 (h3n2)-like: reassortant virus ivr-208 derived from a/hong kong/2671/2019) 15 µg, haemagglutininum influenzae b (virus souche b/washington/02/2019 (victoria lineage)) 15 µg, haemagglutininum influenzae b (virus souche b/phuket/3073/2013 (yamagata lineage)) 15 µg, natrii chloridum, kalii chloridum, dinatrii phosphas dihydricus, kalii dihydrogenophosphas, aqua ad iniectabilia q.s. ad suspensionem pro 0.5 ml corresp. natrium 1.72 mg, kalium 0.08 mg, residui: formaldehydum, octoxinolum-9, neomycinum, ovalbuminum. - immunizzazione attiva contro l'influenza, come già nel 6 ° mese - vaccini

Suïssa - italià - Swissmedic (Swiss Agency for Therapeutic Products)

sanofi-aventis (suisse) sa - haemagglutininum influenzae a (h1n1) (virus souche a/victoria/2570/2019 (h1n1)-pdm09: reassortant virus ivr-215 derived from a/victoria/2570/2019), haemagglutininum influenzae a (h3n2) (virus souche a/cambodia/e0826360/2020 (h3n2)-like: reassortant virus ivr-221 derived from a/cambodia/e0826360/2020), haemagglutininum influenzae b (virus souche b/washington/02/2019 (victoria lineage)) - sospensione iniettabile in siringa pre-riempita - haemagglutininum influenzae a (h1n1) (virus souche a/victoria/2570/2019 (h1n1)-pdm09: reassortant virus ivr-215 derived from a/victoria/2570/2019) 15 µg, haemagglutininum influenzae a (h3n2) (virus souche a/cambodia/e0826360/2020 (h3n2)-like: reassortant virus ivr-221 derived from a/cambodia/e0826360/2020) 15 µg, haemagglutininum influenzae b (virus souche b/washington/02/2019 (victoria lineage)) 15 µg, haemagglutininum influenzae b (virus souche b/phuket/3073/2013 (yamagata lineage)) 15 µg, natrii chloridum, kalii chloridum, dinatrii phosphas dihydricus, kalii dihydrogenophosphas, aqua ad iniectabile q.s. ad suspensionem pro 0.5 ml corresp. natrium 1.72 mg, kalium 0.08 mg, residui: formaldehydum, octoxinolum-9, neomycinum, ovalbuminum. - immunizzazione attiva contro l'influenza, come già nel 6 ° mese - vaccini

Suïssa - italià - Swissmedic (Swiss Agency for Therapeutic Products)

sanofi-aventis (suisse) sa - haemagglutininum influenzae a (h1n1) (virus souche a/victoria/2570/2019 (h1n1)pdm09-like: reassortant virus ivr-215 derived from a/victoria/2570/2019), haemagglutininum influenzae a (h3n2) (virus souche a/darwin/9/2021 (h3n2)-like: reassortant virus ivr-228 derived from a/darwin/9/2021), haemagglutininum influenzae b (virus souche b/austria/1359417/2021-like: b/michigan/01/2021, wilde type (victoria lineage)) - sospensione iniettabile in siringa pre-riempita - haemagglutininum influenzae a (h1n1) (virus souche a/victoria/2570/2019 (h1n1)pdm09-like: reassortant virus ivr-215 derived from a/victoria/2570/2019) 15 µg, haemagglutininum influenzae a (h3n2) (virus souche a/darwin/9/2021 (h3n2)-like: reassortant virus ivr-228 derived from a/darwin/9/2021) 15 µg, haemagglutininum influenzae b (virus souche b/austria/1359417/2021-like: b/michigan/01/2021, wilde type (victoria lineage)) 15 µg, haemagglutininum influenzae b (virus souche b/phuket/3073/2013-like: b/phuket/3073/2013, wilde type (yamagata lineage)) 15 µg, natrii chloridum, kalii chloridum, dinatrii phosphas dihydricus, kalii dihydrogenophosphas, aqua ad iniectabile q.s. ad suspensionem pro 0.5 ml corresp. natrium 1.72 mg, kalium 0.08 mg, residui: formaldehydum, octoxinolum-9, neomycinum, ovalbuminum. - immunizzazione attiva contro l'influenza, come già nel 6 ° mese - vaccini

Suïssa - italià - Swissmedic (Swiss Agency for Therapeutic Products)

nobel pharma schweiz ag - nitisinonum - sospensione - nitisinonum 4.00 mg, hypromellosum, glycerolum 500 mg, polysorbatum 80, e 211 1.00 mg, acidum tartaricum, aromatica (erdbeeren) cum propylenglycolum, aqua purificata ad solutionem pro 1 ml corresp. natrium 0.1595 mg. - hereditäre tyrosinämie typ 1 (ht-1) - synthetika

Suïssa - italià - OFAG-BLW (Bundesamt für Landwirtschaft)

realchemie nederland b.v. - mesosulfuron-metil; iodosulfuron-metile-sodio - gp 005938-00/001 - germania - erbicida ;