Italia - Italia - Ministero della Salute

nayamed international sàrl - pace maker bicamerali con sensore (dr)

Italia - Italia - AIFA (Agenzia Italiana del Farmaco)

janssen cilag s.p.a. - estradiolo - estradiolo

Uni Eropa - Italia - EMA (European Medicines Agency)

teva b.v. - salmeterol xinafoate, fluticasone propionato - pulmonary disease, chronic obstructive; asthma - farmaci per le malattie respiratorie ostruttive, - aerivio spiromax è indicato per l'uso negli adulti dai 18 anni in su. asthmaaerivio spiromax è indicato per il trattamento regolare di pazienti con asma grave in cui l'uso di un prodotto di combinazione (corticosteroidi inalatori e long-acting β2 agonista) è appropriato:in pazienti non adeguatamente controllati con minore forza di corticosteroidi prodotto di combinazione orpatients già controllata con alte dosi di corticosteroidi inalatori e long-acting β2 agonista. malattia polmonare ostruttiva cronica (bpco)aerivio spiromax è indicato per il trattamento sintomatico di pazienti con bpco con fev1.

Uni Eropa - Italia - EMA (European Medicines Agency)

teva b.v. - salmeterol fluticasone propionato - pulmonary disease, chronic obstructive; asthma - farmaci per le malattie respiratorie ostruttive, - airexar spiromax è indicato per l'uso negli adulti dai 18 anni in su. asthmaairexar spiromax is indicated for the regular treatment of patients with severe asthma where use of a combination product (inhaled corticosteroid and long-acting β2 agonist) is appropriate:- patients not adequately controlled on a lower strength corticosteroid combination productor- patients already controlled on a high dose inhaled corticosteroid and long-acting β2 agonist. malattia polmonare ostruttiva cronica (bpco)airexar spiromax è indicato per il trattamento sintomatico di pazienti con bpco con fev1.

Uni Eropa - Italia - EMA (European Medicines Agency)

teva pharma b.v. - budesonide, formoterol fumarate dihydrate - pulmonary disease, chronic obstructive; asthma - farmaci per le malattie respiratorie ostruttive, - asthma biresp spiromax is indicated in adults and adolescents (12 years and older) for the regular treatment of asthma, where use of a combination (inhaled corticosteroid and long-acting β₂ adrenoceptor agonist) is appropriate:in patients not adequately controlled with inhaled corticosteroids and “as needed” inhaled short-acting β₂ adrenoceptor agonists. orin patients already adequately controlled on both inhaled corticosteroids and long-acting β₂ adrenoceptor agonists. copdbiresp spiromax is indicated in adults, aged 18 years and older, for the symptomatic treatment of patients with copd with forced expiratory volume in 1 second (fev₁).

Uni Eropa - Italia - EMA (European Medicines Agency)

teva pharma b.v. - budesonide, formoterol fumarate dihydrate - pulmonary disease, chronic obstructive; asthma - farmaci per le malattie respiratorie ostruttive, - asthma duoresp spiromax is indicated in adults and adolescents (12 years and older) for the regular treatment of asthma, where use of a combination (inhaled corticosteroid and long-acting β₂ adrenoceptor agonist) is appropriate:in patients not adequately controlled with inhaled corticosteroids and “as needed” inhaled short-acting β₂ adrenoceptor agonists. orin patients already adequately controlled on both inhaled corticosteroids and long-acting β₂ adrenoceptor agonists. copdduoresp spiromax is indicated in adults, aged 18 years and older for the symptomatic treatment of patients with copd with forced expiratory volume in 1 second (fev₁).

Swiss - Italia - Swissmedic (Swiss Agency for Therapeutic Products)

novo nordisk pharma ag - eptacogum alfa (activatum) - raumtemperaturstabiles injektionspräparat - praeparatio cryodesiccata: eptacogum alfa (activatum) 1 mg, natrii chloridum, calcii chloridum dihydricum, glycyl-glycinum, polysorbatum 80, saccharum, mannitolum, antiox.: methioninum 0.5 mg, pro vitro. solvens: histidinum, aqua ad iniectabile q.s. ad solutionem pro 1.12 ml. solutio reconstituta: eptacogum alfa (activatum) 1 mg, saccharum, aqua ad iniectabile q.s. ad solutionem pro 1 ml. - hemmkörperhämophilie; schwere postpartale blutungen. - biotechnologika

Swiss - Italia - Swissmedic (Swiss Agency for Therapeutic Products)

novo nordisk pharma ag - eptacogum alfa (activatum) - raumtemperaturstabiles injektionspräparat - praeparatio cryodesiccata: eptacogum alfa (activatum) 2 mg, natrii chloridum, calcii chloridum dihydricum, glycyl-glycinum, polysorbatum 80, saccharum, mannitolum, antiox.: methioninum 1 mg, pro vitro. solvens: histidinum, aqua ad iniectabile q.s. ad solutionem pro 2.1 ml. solutio reconstituta: eptacogum alfa (activatum) 2 mg, saccharum, aqua ad iniectabile q.s. ad solutionem pro 2 ml. - hemmkörperhämophilie; schwere postpartale blutungen. - biotechnologika

Swiss - Italia - Swissmedic (Swiss Agency for Therapeutic Products)

novo nordisk pharma ag - eptacogum alfa (activatum) - raumtemperaturstabiles injektionspräparat - praeparatio cryodesiccata: eptacogum alfa (activatum) 5 mg, natrii chloridum, calcii chloridum dihydricum, glycyl-glycinum, polysorbatum 80, saccharum, mannitolum, antiox.: methioninum 2.5 mg, pro vitro. solvens: histidinum, aqua ad iniectabile q.s. ad solutionem pro 5.17 ml. solutio reconstituta: eptacogum alfa (activatum) 5 mg, saccharum, aqua ad iniectabile q.s. ad solutionem pro 5 ml. - hemmkörperhämophilie; schwere postpartale blutungen. - biotechnologika

Swiss - Italia - Swissmedic (Swiss Agency for Therapeutic Products)

novo nordisk pharma ag - eptacogum alfa (activatum) - raumtemperaturstabiles injektionspräparat - praeparatio cryodesiccata: eptacogum alfa (activatum) 8 mg, natrii chloridum, calcii chloridum dihydricum, glycyl-glycinum, polysorbatum 80, saccharum, mannitolum, antiox.: methioninum 4 mg, pro vitro. solvens: histidinum, aqua ad iniectabile q.s. ad solutionem pro 8.3 ml. solutio reconstituta: eptacogum alfa (activatum) 8 mg, saccharum, aqua ad iniectabile q.s. ad solutionem pro 8 ml. - hemmkörperhämophilie; schwere postpartale blutungen. - biotechnologika