Unione Europea - italiano - EMA (European Medicines Agency)

aimmune therapeutics ireland limited - defatted powder of arachis hypogaea l., semen (peanuts) - peanut hypersensitivity - allergens - palforzia is indicated for the treatment of patients aged 4 to 17 years with a confirmed diagnosis of peanut allergy. palforzia may be continued in patients 18 years of age and older. palforzia should be used in conjunction with a peanut-avoidant diet.

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

max zeller söhne ag - escherichia coli viva - tropfen zum einnehmen, suspension - escherichia coli viva 15 - 45 mio. u., natrii chloridum corresp. natrium 2.382 mg, magnesii sulfas heptahydricus, kalii chloridum, calcii chloridum dihydricum, magnesii chloridum hexahydricum, aqua purificata ad suspensionem pro 1 ml, corresp. 14 guttae. - bei reizdarm (colon irritabile) - batteri e hefepräparate

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

max zeller söhne ag - escherichia coli viva - tropfen zum einnehmen, suspension - escherichia coli viva 15 - 45 mio. u., natrii chloridum corresp. natrium 2.382 mg, magnesii sulfas heptahydricus, kalii chloridum, calcii chloridum dihydricum, magnesii chloridum hexahydricum, aqua purificata ad suspensionem pro 1 ml, corresp. 14 guttae. - bei reizdarm (colon irritabile) - batteri e hefepräparate

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

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

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

viatris pharma gmbh - clarithromycinum - granulato per la realizzazione di una kindersuspension orale - clarithromycinum 250 mg, arom.: vanillinum e altri, conserv.: e 202, excipiens annuncio granulatum corrisp. sospensione reconstituta 5 ml. - malattie infettive - synthetika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

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

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

mepha pharma ag - amoxicillinum anhydricum, acido clavulanicum - pulver zur herstellung einer suspension zum einneh - amoxicillinum anhydricum 250 mg ut amoxicillinum trihydricum, acidum clavulanicum 62.5 mg ut kalii clavulanas, silica colloidalis anhydrica, xanthani gummi, crospovidonum, carmellosum natricum, aspartamum 16.64 mg, aromatica (erdbeer) cum alcohol benzylicus et propylenglycolum, ad pulverem corresp. suspensio reconstituta 5 ml corresp. natrium max. 4.7 mg. - malattie infettive - synthetika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

glaxosmithkline ag - glycoproteini e viri varicellae zoster antigenum - pulver und suspension zur herstellung einer injektionssuspension - pulver: glycoproteini e viri varicellae zoster antigenum 50 µg, saccharum, polysorbatum 80, natrii dihydrogenophosphas dihydricus, dikalii phosphas anhydricus, pro praeparatione. solvens: adeps a 3-o-desacyl-4’-monophosphorylatus, quillajae saponariae molina saponinum purificatum, 1,2-dioleoyl-sn-glycero-3-phosphocholinum, cholesterolum, dinatrii phosphas, kalii dihydrogenophosphas, natrii chloridum, aqua ad iniectabile q.s. ad suspensionem pro 0.5 ml. suspensio reconstituta: glycoproteini e viri varicellae zoster antigenum 50 µg, saccharum, polysorbatum 80, adeps a 3-o-desacyl-4’-monophosphorylatus, quillajae saponariae molina saponinum purificatum, 1,2-dioleoyl-sn-glycero-3-phosphocholinum, cholesterolum, natrii chloridum, natrii dihydrogenophosphas anhydricus, dikalii phosphas anhydricus, dinatrii phosphas, kalii dihydrogenophosphas, aqua ad iniectabile q.s. ad suspensionem pro 0.5 ml corresp. natrium 1.77 mg, kalium 0.18 mg. - prävention von herpes zoster - vaccini

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

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)

glaxosmithkline ag - fluticasoni furoas - nasenspray, suspension - fluticasoni furoas 27.5 µg, glucosum, cellulosum dispergibile, polysorbatum 80, dinatrii edetas, benzalkonii chloridum 8.25 µg, aqua purificata, ad suspensionem pro dosi, doses pro vase 120. - la rinite - synthetika