Airexar Spiromax Unjoni Ewropea - Malti - EMA (European Medicines Agency)

airexar spiromax

teva b.v. - salmeterol, fluticasone propionate - pulmonary disease, chronic obstructive; asthma - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - airexar spiromax huwa indikat għall-użu fl-adulti li għandhom 18-il sena 'l fuq biss. 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. mard pulmonari ostruttiv kroniku (copd)airexar spiromax huwa indikat għall-kura sintomatika ta ' pazjenti b'copd, bil-fev1.

Avamys Unjoni Ewropea - Malti - EMA (European Medicines Agency)

avamys

glaxosmithkline (ireland) limited - fluticasone furoate - rhinitis, allergic, seasonal; rhinitis, allergic, perennial - fl-imnieħer preparazzjonijiet, kortikosterojdi - adulti, adoloxxenti (12-il sena jew aktar) u tfal (6-11-il sena). avamys huwa indikat għat-trattament tas-sintomi ta 'rinite allerġika.

BiResp Spiromax Unjoni Ewropea - Malti - EMA (European Medicines Agency)

biresp spiromax

teva pharma b.v. - budesonide, formoterol fumarate dihydrate - pulmonary disease, chronic obstructive; asthma - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - 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).

DuoResp Spiromax Unjoni Ewropea - Malti - EMA (European Medicines Agency)

duoresp spiromax

teva pharma b.v. - budesonide, formoterol fumarate dihydrate - pulmonary disease, chronic obstructive; asthma - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - 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).

Relvar Ellipta Unjoni Ewropea - Malti - EMA (European Medicines Agency)

relvar ellipta

glaxosmithkline (ireland) limited - fluticasone furoate, vilanterol - mard tal-pulmun, obstructive kronika - adrenerġiji u mediċini oħra għal mard ta 'l-arja li torbot - l-ażżma-indikazzjoni:relvar ellipta huwa indikat fit-trattament regolari ta ' l-ażżma fl-adulti u adolexxenti minn 12-il sena u akbar, meta l-użu tat-taħlita tal-prodott (li jaġixxu fit-tul beta2-agonist u kortikosterojdi meħuda man-nifs) huwa xieraq:pazjenti li mhumiex adegwatament ikkontrollati bil-kortikosterojdi meħuda man-nifs u l - "kif meħtieġ" man-nifs qasir waqt li jaġixxi beta2-agonisti. pazjenti li diġà ikkontrollati adegwatament fuq iż-żewġ kortikosterojdi meħuda man-nifs u li jaħdem fit-tul beta2-agonist. copd l-indikazzjoni:relvar ellipta huwa indikat għall-kura sintomatika ta ' adulti b'copd bil-fev1.

Revinty Ellipta Unjoni Ewropea - Malti - EMA (European Medicines Agency)

revinty ellipta

glaxosmithkline (ireland) limited - fluticasone furoate, vilanterol trifenatate - ażma - adrenerġiji u mediċini oħra għal mard ta 'l-arja li torbot - l-ażżma indicationrevinty ellipta huwa indikat fit-trattament regolari ta ' l-ażżma fl-adulti u adolexxenti minn 12-il sena u akbar, meta l-użu tat-taħlita tal-prodott (li jaġixxu fit-tul beta2-agonist u kortikosterojdi meħuda man-nifs) huwa xieraq:pazjenti li mhumiex adegwatament ikkontrollati bil-kortikosterojdi meħuda man-nifs u l - "kif meħtieġ" man-nifs qasir waqt li jaġixxi beta2-agonisti. copd indicationrevinty ellipta huwa indikat għall-kura sintomatika ta ' adulti b'copd bil-fev1.

Natpar Unjoni Ewropea - Malti - EMA (European Medicines Agency)

natpar

takeda pharmaceuticals international ag ireland branch - ormon tal-paratirojde - ipoparatirojdiżmu - homeostasi tal-kalċju - natpar huwa indikat bħala trattament aġġuntiv ta 'pazjenti adulti b'ipoparatirojdiżmu kroniku li ma jistgħux jiġu kkontrollati b'mod adegwat b'terapija standard waħidha.

Ozurdex Unjoni Ewropea - Malti - EMA (European Medicines Agency)

ozurdex

abbvie deutschland gmbh & co. kg - dexamethasone - macular edema; uveitis - ophthalmologicals, other ophthalmologicals - ozurdex huwa indikat għall-kura ta ' pazjenti adulti b'edema makulari tad-dijabete li ġejjin jew fergħa tar-retina-okklużjoni tal-vina (brvo) jew ċentrali tar-retina-okklużjoni tal-vina (crvo). ozurdex huwa indikat għall-kura ta 'pazjenti adulti b'infjammazzjoni ta' l-segment posterjuri ta ' l-għajn l-preżentazzjoni kif noninfectious uveite. ozurdex huwa indikat għall-kura ta 'pazjenti adulti b'indeboliment tal-vista minħabba ta' edima makulari dijabetika (dme) li huma pazjenti psewdoafakiċi jew li huma kkunsidrati bħala mhux biżżejjed li jirrispondu għal, jew li mhux tajbin għall-non-terapija tal-kortikosterojdi.

Trimbow Unjoni Ewropea - Malti - EMA (European Medicines Agency)

trimbow

chiesi farmaceutici s.p.a. - beclometasone dipropionate, formoterol fumarate dihydrate, glycopyrronium bromide - mard tal-pulmun, obstructive kronika - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - maintenance treatment of asthma, in adults not adequately controlled with a maintenance combination of a long-acting beta2-agonist and high dose of inhaled corticosteroid, and who experienced one or more asthma exacerbations in the previous year. copdmaintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (copd) who are not adequately treated by a combination of an inhaled corticosteroid and a long-acting beta2-agonist or a combination of a long-acting beta2-agonist and a long-acting muscarinic antagonist (for effects on symptoms control and prevention of exacerbations see section 5. asthmamaintenance treatment of asthma, in adults not adequately controlled with a maintenance combination of a long-acting beta2-agonist and medium dose of inhaled corticosteroid, and who experienced one or more asthma exacerbations in the previous year.

Elebrato Ellipta Unjoni Ewropea - Malti - EMA (European Medicines Agency)

elebrato ellipta

glaxosmithkline trading services limited - fluticasone furoate, bromur tal-umeclidinium, trifenatate tal-vilanterol - mard tal-pulmun, obstructive kronika - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - elebrato ellipta hija indikata bħala trattament manutenzjoni fil-pazjenti adulti ma moderat severi kronika eliminat pulmonari marda (copd) li m'humiex ittrattati adegwatament mill-għaqda tal-corticosteroid bin-nifs u a twila u jaġixxu β2-agonist.