Evropska unija - slovenščina - EMA (European Medicines Agency)

chiesi farmaceutici s.p.a. - beclometasone dipropionate, formoterol fumarate dihidrat, glycopyrronium bromid - pljučna bolezen, kronična obstruktivna bolezen - zdravila za obstruktivne pljučne bolezni, - 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.

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

chiesi farmaceutici s.p.a. - formoterolfumarat dihidrat, beklometazondipropionat, glikopironij - inhalacijska raztopina pod tlakom - formoterolfumarat dihidrat 5 µg / 1 odmerek; beklometazondipropionat 87 µg / 1 odmerek; glikopironij 9 µg / 1 odmerek - formoterol, glikopironijev bromid in beklometazon

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

chiesi farmaceutici s.p.a. - formoterolfumarat dihidrat, beklometazondipropionat, glikopironij - inhalacijska raztopina pod tlakom - formoterolfumarat dihidrat 5 µg / 1 odmerek; beklometazondipropionat 87 µg / 1 odmerek; glikopironij 9 µg / 1 odmerek - formoterol, glikopironijev bromid in beklometazon

Evropska unija - slovenščina - EMA (European Medicines Agency)

chiesi farmaceutici s.p.a. - formoterol fumarate dihydrate, glycopyrronium, beclometasone dipropionate - pljučna bolezen, kronična obstruktivna bolezen - zdravila za obstruktivne pljučne bolezni, - vzdrževalnega zdravljenja pri odraslih bolnikih z zmerno do hudo kronična obstruktivna pljučna bolezen (kopb), ki ni primerno obravnavana kombinacija inhalacijski kortikosteroidi in dolgotrajnim delovanjem beta2-agonist (učinkov na simptomi nadzor in preprečevanje poslabšanj glej oddelek 5.

Evropska unija - slovenščina - EMA (European Medicines Agency)

chiesi farmaceutici s.p.a. - beclometasone dipropionate, formoterol fumarate dihidrat, glycopyrronium - pljučna bolezen, kronična obstruktivna bolezen - zdravila za obstruktivne pljučne bolezni, - vzdrževalnega zdravljenja pri odraslih bolnikih z zmerno do hudo kronična obstruktivna pljučna bolezen (kopb), ki ni primerno obravnavana kombinacija inhalacijski kortikosteroidi in dolgotrajnim delovanjem beta2-agonist (učinkov na simptomi nadzor in preprečevanje poslabšanj glej oddelek 5.

Evropska unija - slovenščina - EMA (European Medicines Agency)

linde healthcare ab - dušikov oksid - hypertension, pulmonary; respiratory insufficiency - drugi proizvodi dihal - inomax, v povezavi s podporo pri dihanju in druge ustrezne aktivne snovi, je navedeno:za zdravljenje novorojenih dojenčkov ≥34 tedna nosečnosti z hypoxic respiratorna odpoved, povezanih z izvedenim ali echocardiographic dokazov, pljučna hipertenzija, da se izboljša oksigenacijo in da se zmanjša potreba po extracorporeal membrane oksigenacijo;kot del zdravljenja za obporodne - in post-operativni pljučne hipertenzije pri odraslih in novorojenih dojenčkov, dojenčkih in malčkih, otrocih in mladostnikih, starosti 0-17 years v povezavi z operacijo srca, da bi selektivno zmanjšanje pljučni arterijski tlak in izboljša desnega prekata funkcijo in oksigenacijo.

Evropska unija - slovenščina - EMA (European Medicines Agency)

swedish orphan biovitrum ab (publ) - avatrombopag maleate - trombocitopenija - antihemoragije - doptelet je primerna za zdravljenje hude trombocitopenije pri odraslih bolnikih s kronično bolezen jeter, ki so načrtovani, da opravijo invaziven postopek. doptelet is indicated for the treatment of primary chronic immune thrombocytopenia (itp) in adult patients who are refractory to other treatments (e. kortikosteroidi, imunoglobulini).

Evropska unija - slovenščina - EMA (European Medicines Agency)

mylan ire healthcare limited - fondaparinuks natrij - venous thrombosis; pulmonary embolism; myocardial infarction; angina, unstable - antitrombotična sredstva - 5 mg / 0. 3 ml in 2. 5 mg / 0. 5-ml solution for injectionprevention of venous thromboembolic events (vte) in adults undergoing major orthopaedic surgery of the lower limbs such as hip fracture, major knee surgery or hip-replacement surgery. preprečevanje vte pri odraslih, ki opravljajo abdominalno kirurgijo, ki so presodilo, da je velika verjetnost, thromboembolic zapletov, kot bolnikov, ki abdominalno operacijo raka. preprečevanje vte pri odraslih bolnike, ki so presodilo, da je na visoko tveganje za vte in ki so immobilised zaradi akutne bolezni, kot so srčno insuficienco in / ali akutne dihalne motnje in / ali akutne nalezljive ali vnetnih bolezni. zdravljenje odraslih z akutno simptomatsko spontano površno-venska tromboza spodnjih okončin brez sočasnega globoko vensko trombozo. 5 mg / 0. 5-ml solution for injectiontreatment of unstable angina or non-st-segment-elevation myocardial infarction (ua/nstemi) in adult patients for whom urgent (< 120 mins) invasive management (pci) is not indicated. infarkt (stemi) pri odraslih bolnikih, ki se upravljajo z thrombolytics ali ki sprva so prejeli nobena druga oblika reperfusion terapija. 5 mg / 0. 4-ml, 7. 5 mg / 0. 6-ml in 10 mg/0. 8-ml solution for injectiontreatment of adults with acute deep-vein thrombosis (dvt) and treatment of acute pulmonary embolism (pe), except in haemodynamically unstable patients or patients who require thrombolysis or pulmonary embolectomy.

Evropska unija - slovenščina - EMA (European Medicines Agency)

accord healthcare s.l.u. - rivaroksaban - acute coronary syndrome; coronary artery disease; peripheral arterial disease; venous thromboembolism; stroke; atrial fibrillation; pulmonary embolism - antitrombotična sredstva - preprečevanje venska trombembolija (vte) pri odraslih bolnikih, ki so v postopku izbirni kirurški zamenjavi kolka ali kolena. zdravljenje globoke venske tromboze (dvt) in pljučna embolija (pe), in preprečevanje ponavljajočih se dvt in pe pri odraslih. (see section 4. 4 for haemodynamically unstable pe patients. zdravljenje globoke venske tromboze (dvt) in pljučna embolija (pe), in preprečevanje ponavljajočih se dvt in pe pri odraslih. (see section 4. 4 za haemodynamically nestabilno pe bolnikov). adultsprevention of stroke and systemic embolism in adult patients with non valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. zdravljenje globoke venske tromboze (dvt) in pljučna embolija (pe), in preprečevanje ponavljajočih se dvt in pe pri odraslih. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing from 30 kg to 50 kg after at least 5 days of initial parenteral anticoagulation treatment. rivaroxaban accord, co administered with acetylsalicylic acid (asa) alone or with asa plus ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers (see sections 4. 3, 4. 4 in 5. rivaroxaban accord, co administered with acetylsalicylic acid (asa), is indicated for the prevention of atherothrombotic events in adult patients with coronary artery disease (cad) or symptomatic peripheral artery disease (pad) at high risk of ischaemic events. adultsprevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. zdravljenje globoke venske tromboze (dvt) in pljučna embolija (pe), in preprečevanje ponavljajočih se dvt in pe pri odraslih. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing more than 50 kg after at least 5 days of initial parenteral anticoagulation treatment.

Evropska unija - slovenščina - EMA (European Medicines Agency)

astrazeneca ab - chadox1-sars-cov-2 - covid-19 virus infection - cepiva - vaxzevria is indicated for active immunisation to prevent covid 19 caused by sars cov 2, in individuals 18 years of age and older. uporaba tega cepiva mora biti v skladu z uradnimi priporočili.