XIMARACT Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

ximaract

bausch & lomb-iom s.p.a. - cefuroxime - cefuroxime

Kymriah Zellsuspension zur Infusione Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

kymriah zellsuspension zur infusione

novartis pharma schweiz ag - tisagenlecleucelum car positive e vitali t-cellule. contiene cellule geneticamente modificate - zellsuspension zur infusione - beutel: tisagenlecleucelum car-positive lebensfähige t-zellen. enthält genetisch veränderte zellen 1,2x10e6–6,0x10e8 pro dosi, natrium, chloridum, magnesium, acetas, gluconas, glucosum, 5-hydroxymethylfurfuralum, albuminum, n-acetyltryptophanum natricum, caprylas, aluminium, dextranum 40, dimethylis sulfoxidum, dimethylis sulfonum, q.s. pro 50 ml. - 1) die behandlung von pädiatrischen und jungen erwachsenen patienten im alter bis zu 25 jahren mit akuter lymphatischer b-zell-leukämie (b-zell-all), die refraktär ist, nach einer transplantation rezidiviert ist oder nach zwei therapielinien oder später rezidiviert ist. 2) die behandlung erwachsener patienten mit rezidiviertem oder refraktärem diffus grosszelligem b-zell-lymphom (dlbcl) nach zwei oder mehr linien einer systemischen therapie. 3) behandlung erwachsener patienten mit rezidiviertem oder refraktärem follikulärem lymphom (fl) nach drei oder mehr linien einer systemischen therapie, - trapianto: gentherapieprodukt

Adacel-Polio 0.5 ml suspension injectable en seringue préremplie Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

adacel-polio 0.5 ml suspension injectable en seringue préremplie

sanofi-aventis (suisse) sa - toxoidum diphtheriae, toxoidum tetani, toxoidum pertussis, haemagglutininum filamentosum, pertactinum, fimbriae types 2 et 3, virus poliomyelitis typus 1 inactivatus, virus poliomyelitis typus 2 inactivatus, virus poliomyelitis typus 3 inactivatus - suspension injectable en seringue préremplie - toxoidum diphtheriae min. 2 u.i., toxoidum tetani min. 20 u.i., toxoidum pertussis 2.5 µg, haemagglutininum filamentosum 5 µg, pertactinum 3 µg, fimbriae types 2 et 3 5 µg, virus poliomyelitis typus 1 inactivatus 29 u., virus poliomyelitis typus 2 inactivatus 7 u., virus poliomyelitis typus 3 inactivatus 26 u., aluminii phosphas corresp. aluminium 0.33 mg, phenoxyethanolum, ethanolum 1.01 mg, polysorbatum 80, aqua ad iniectabile, ad suspensionem pro 0.5 ml corresp. ethanolum 0.3 % v/v, residui: formaldehydum, glutaralum, streptomycinum, neomycinum, polymyxinum b, albuminum seri bovis. - vaccination de rappel contre la diphtérie, le tétanos, la coqueluche et la poliomyélite chez les personnes à partir du 4ème anniversaire - vaccini

Adacel 0.5 ml suspension injectable en seringue préremplie Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

adacel 0.5 ml suspension injectable en seringue préremplie

sanofi-aventis (suisse) sa - toxoidum diphtheriae, toxoidum tetani, toxoidum pertussis, haemagglutininum filamentosum, pertactinum, fimbriae types 2 et 3 - suspension injectable en seringue préremplie - toxoidum diphtheriae min. 2 u.i., toxoidum tetani min. 20 u.i., toxoidum pertussis 2.5 µg, haemagglutininum filamentosum 5 µg, pertactinum 3 µg, fimbriae types 2 et 3 5 µg, aluminii phosphas corresp. aluminium 0.33 mg, phenoxyethanolum, aqua ad iniectabile, ad suspensionem pro 0.5 ml, residui: formaldehydum, glutaralum. - vaccination de rappel contre la diphtérie, le tétanos et la coqueluche chez les personnes à partir du 4ème anniversaire - vaccini

Efluelda 0.7 ml suspension injectable en seringue préremplie Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

efluelda 0.7 ml suspension injectable en seringue préremplie

sanofi-aventis (suisse) sa - haemagglutininum influenzae a (h1n1) (virus souche a/michigan/45/2015 (h1n1)-like: reassortant virus nymc x-275 derived from a/michigan/45/2015), haemagglutininum influenzae a (h3n2) (virus souche a/singapore/infimh-16-0019/2016 (h3n2)-like: reassortant virus ivr-186 derived from a/singapore/infimh-16-0019/2016 ), haemagglutininum influenzae b (virus souche b/colorado/06/2017-like: reassortant virus nymc bx-69a derived from b/maryland/15/2016 (victoria lineage)) - suspension injectable en seringue préremplie - haemagglutininum influenzae a (h1n1) (virus souche a/michigan/45/2015 (h1n1)-like: reassortant virus nymc x-275 derived from a/michigan/45/2015) 60 µg, haemagglutininum influenzae a (h3n2) (virus souche a/singapore/infimh-16-0019/2016 (h3n2)-like: reassortant virus ivr-186 derived from a/singapore/infimh-16-0019/2016 ) 60 µg, haemagglutininum influenzae b (virus souche b/phuket/3073/2013 (yamagata lineage) (wild type)) 60 µg, haemagglutininum influenzae b (virus souche b/colorado/06/2017-like: reassortant virus nymc bx-69a derived from b/maryland/15/2016 (victoria lineage)) 60 µg, natrii chloridum, dinatrii phosphas, natrii dihydrogenophosphas anhydricus, octoxinolum-9, aqua ad iniectabile q.s. ad suspensionem pro 0.7 ml corresp. natrium 2.72 mg. - immunisation active contre l'influenza, dès 65 ans - vaccini

Efluelda 0.7 ml suspension injectable en seringue préremplie Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

efluelda 0.7 ml suspension injectable en seringue préremplie

sanofi-aventis (suisse) sa - haemagglutininum influenzae a (h1n1) (virus souche a/victoria/2570/2019 (h1n1)-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 san-010 derived from a/darwin/9/2021), haemagglutininum influenzae b (virus souche b/austria/1359417/2021-like: derived from b/michigan/01/2021 (victoria lineage)(wild type)) - suspension injectable en seringue préremplie - haemagglutininum influenzae a (h1n1) (virus souche a/victoria/2570/2019 (h1n1)-like: reassortant virus ivr-215 derived from a/victoria/2570/2019) 60 µg, haemagglutininum influenzae a (h3n2) (virus souche a/darwin/9/2021 (h3n2)-like: reassortant virus san-010 derived from a/darwin/9/2021) 60 µg, haemagglutininum influenzae b (virus souche b/austria/1359417/2021-like: derived from b/michigan/01/2021 (victoria lineage)(wild type)) 60 µg, haemagglutininum influenzae b (virus souche b/phuket/3073/2013 (yamagata lineage) (wild type)) 60 µg, natrii chloridum, dinatrii phosphas, natrii dihydrogenophosphas anhydricus, octoxinolum-9, aqua ad iniectabile q.s. ad suspensionem pro 0.7 ml corresp. natrium 2.72 mg. - immunisation active contre l'influenza, dès 65 ans - vaccini

Zinat 250 mg Compresse rivestite con film Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

zinat 250 mg compresse rivestite con film

sandoz pharmaceuticals ag - cefuroximum - compresse rivestite con film - cefuroximum 250 mg ut cefuroximum axetili, carmellosum natricum conexum, oleum vegetabile hydrogenatum, conserv.: e 211, propylis parahydroxybenzoas, e 218, excipiens pro compresso obducto. - malattie infettive - synthetika

Zinat 500 mg Compresse rivestite con film Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

zinat 500 mg compresse rivestite con film

sandoz pharmaceuticals ag - cefuroximum - compresse rivestite con film - cefuroximum 500 mg ut cefuroximum axetili, carmellosum natricum conexum, oleum vegetabile hydrogenatum, conserv.: e 211, propylis parahydroxybenzoas, e 218, excipiens pro compresso obducto. - malattie infettive - synthetika

Zinat Polvere per Sospensione orale Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

zinat polvere per sospensione orale

sandoz pharmaceuticals ag - cefuroximum - polvere per sospensione orale - cefuroximum 125 mg ut cefuroximum axetili, arom.: vanillinum et alia, aspartamum, excipiens ad granulatum corresp. suspensio reconstituta 5 ml. - malattie infettive - synthetika