Fostair NEXThaler 100micrograms/dose / 6micrograms/dose dry powder inhaler Didžioji Britanija - anglų - MHRA (Medicines & Healthcare Products Regulatory Agency)

fostair nexthaler 100micrograms/dose / 6micrograms/dose dry powder inhaler

chiesi ltd - beclometasone dipropionate; formoterol fumarate dihydrate - inhalation powder - 100microgram/1dose ; 6microgram/1dose

Fostair NEXThaler 200micrograms/dose / 6micrograms/dose dry powder inhaler Didžioji Britanija - anglų - MHRA (Medicines & Healthcare Products Regulatory Agency)

fostair nexthaler 200micrograms/dose / 6micrograms/dose dry powder inhaler

chiesi ltd - formoterol fumarate dihydrate; beclometasone dipropionate - inhalation powder - 6microgram/1dose ; 200microgram/1dose

FOSTER NEXTHALER INHALATION POWDER 100 MCG6 MCG PER DOSE Singapūras - anglų - HSA (Health Sciences Authority)

foster nexthaler inhalation powder 100 mcg6 mcg per dose

orient europharma pte ltd - beclometasone dipropionate anhydrous (micronized); formoterol fumarate dihydrate (micronized) - powder, metered - beclometasone dipropionate anhydrous (micronized) 100mcg/dose; formoterol fumarate dihydrate (micronized) 6mcg/dose

Fostair Nexthaler 200 micrograms/12 micrograms per metered dose inhalation powder Airija - anglų - HPRA (Health Products Regulatory Authority)

fostair nexthaler 200 micrograms/12 micrograms per metered dose inhalation powder

chiesi farmaceutici s.p.a. - beclometasone dipropionate; formoterol fumarate dihydrate - inhalation powder - 200 micrograms/ 12 microgram(s) - formoterol and beclometasone

Budesonide/Formoterol Teva Europos Sąjunga - anglų - EMA (European Medicines Agency)

budesonide/formoterol teva

teva pharma b.v. - budesonide, formoterol fumarate dihydrate - pulmonary disease, chronic obstructive; asthma - drugs for obstructive airway diseases, - budesonide/formoterol teva is indicated in adults 18 years of age and older only.asthmabudesonide/formoterol teva is indicated in 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.copdsymptomatic treatment of patients with severe copd (fev1 < 50% predicted normal) and a history of repeated exacerbations, who have significant symptoms despite regular therapy with long-acting bronchodilators.

Budesonide/Formoterol Teva Pharma B.V. Europos Sąjunga - anglų - EMA (European Medicines Agency)

budesonide/formoterol teva pharma b.v.

teva pharma b.v. - budesonide, formoterol - asthma - drugs for obstructive airway diseases, - budesonide/formoterol teva pharma b.v. is indicated in adults 18 years of age and older only.asthmabudesonide/formoterol teva pharma b.v. is indicated in the regular treatment of asthma, where use of a combination (inhaled corticosteroid and long-acting β2 adrenoceptor agonist) is appropriate: orin patients not adequately controlled with inhaled corticosteroids and “as needed” inhaled short-acting β2 adrenoceptor agonists.in patients already adequately controlled on both inhaled corticosteroids and long-acting β2 adrenoceptor agonists. 

Vylaer Spiromax Europos Sąjunga - anglų - EMA (European Medicines Agency)

vylaer spiromax

teva pharma b.v. - budesonide, formoterol fumarate dihydrate - pulmonary disease, chronic obstructive; asthma - drugs for obstructive airway diseases, - vylaer spiromax is indicated in adults 18 years of age and older only.asthmavylaer spiromax is indicated in 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.copdsymptomatic treatment of patients with severe copd (fev1 < 50% predicted normal) and a history of repeated exacerbations, who have significant symptoms despite regular therapy with long-acting bronchodilators.