Efient Euroopa Liit - eesti - EMA (European Medicines Agency)

efient

substipharm - prasugreel - acute coronary syndrome; angina, unstable; myocardial infarction - antitrombootilised ained - efient, mida manustatakse koos atsetüülsalitsüülhappega (asa), on näidustatud aterotrombootiliste sündmuste ennetamiseks ägeda koronaarsündroomi (i. ebastabiilse stenokardia, mitte-st-segmendi-elevatsiooniga müokardiinfarkt [ua / nstemi] või st-segmendi elevatsiooniga müokardiinfarkt [stemi]) kellele tehakse primaarne või hilisemat perkutaanse koronaarse interventsiooni (pci).

Vipdomet Euroopa Liit - eesti - EMA (European Medicines Agency)

vipdomet

takeda pharma a/s - alogliptin bensoaat, metformiin vesinikkloriid - suhkurtõbi, tüüp 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - vipdomet is indicated in the treatment of adult patients aged 18 years and older with type-2 diabetes mellitus:as an adjunct to diet and exercise to improve glycaemic control in adult patients, inadequately controlled on their maximal tolerated dose of metformin alone, or those already being treated with the combination of alogliptin and metformin;in combination with pioglitazone (i. triple combination therapy) as an adjunct to diet and exercise in adult patients inadequately controlled on their maximal tolerated dose of metformin and pioglitazone;in combination with insulin (i. kolmekordne kombineeritud ravi) lisandina toitumise ja treeningu parandamiseks glycaemic kontrolli patsientidel, kui insuliini kell stabiilne annus ja metformiin üksi ei taga piisavat kontrolli glycaemic.

Nexpovio Euroopa Liit - eesti - EMA (European Medicines Agency)

nexpovio

stemline therapeutics b.v. - selinexor - mitu müeloomit - antineoplastilised ained - nexpovio is indicatedin combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy. in combination with dexamethasone for the treatment of multiple myeloma in adult patients who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, two immunomodulatory agents and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.

Orserdu Euroopa Liit - eesti - EMA (European Medicines Agency)

orserdu

stemline therapeutics b.v. - elacestrant - rinnanäärmed - endokriinset ravi - orserdu monotherapy is indicated for the treatment of postmenopausal women, and men, with estrogen receptor (er) positive, her2-negative, locally advanced or metastatic breast cancer with an activating esr1 mutation who have disease progression following at least one line of endocrine therapy including a cdk 4/6 inhibitor.

Anoro Ellipta (previously Anoro) Euroopa Liit - eesti - EMA (European Medicines Agency)

anoro ellipta (previously anoro)

glaxosmithkline (ireland) limited - umeclidinium bromiid, vilanterol trifenatate - kopsuhaigus, krooniline obstruktiivne - ravimid hingamisteede obstruktiivsete haiguste, - anoro ellipta on näidustatud hooldus bronchodilator ravi, et leevendada sümptomeid täiskasvanud patsientidel, kellel on krooniline obstruktiivne kopsuhaigus (copd).

Bretaris Genuair Euroopa Liit - eesti - EMA (European Medicines Agency)

bretaris genuair

covis pharma europe b.v. - aclidinium bromide - kopsuhaigus, krooniline obstruktiivne - ravimid hingamisteede obstruktiivsete haiguste, - bretaris genuair on näidustatud kroonilise obstruktiivse kopsuhaiguse (kok) täiskasvanud patsientide sümptomite leevendamiseks bronhodilataatorite hoolduseks.

Brimica Genuair Euroopa Liit - eesti - EMA (European Medicines Agency)

brimica genuair

covis pharma europe b.v. - formoterol fumarate dihydrate, aclidinium bromide - kopsuhaigus, krooniline obstruktiivne - ravimid hingamisteede obstruktiivsete haiguste, - brimica genuair on näidustatud kroonilise obstruktiivse kopsuhaiguse (kok) raviks täiskasvanud patsientidel, kes hoiavad bronhodilataatorit õhuvoolu takistamiseks ja sümptomite leevendamiseks..

Incruse Ellipta (previously Incruse) Euroopa Liit - eesti - EMA (European Medicines Agency)

incruse ellipta (previously incruse)

glaxosmithkline (ireland) limited - umeklidiiniumbromiid - kopsuhaigus, krooniline obstruktiivne - ravimid hingamisteede obstruktiivsete haiguste, - kroonilise obstruktiivse kopsuhaiguse (kok) täiskasvanud patsientide sümptomite leevendamiseks on näidustatud bronhodilataatori hooldus.

Laventair Ellipta (previously Laventair) Euroopa Liit - eesti - EMA (European Medicines Agency)

laventair ellipta (previously laventair)

glaxosmithkline (ireland) limited - umeclidinium bromiid, vilanterol - kopsuhaigus, krooniline obstruktiivne - ravimid hingamisteede obstruktiivsete haiguste, - laventair ellipta on näidustatud hooldus bronchodilator ravi, et leevendada sümptomeid täiskasvanud patsientidel, kellel on krooniline obstruktiivne kopsuhaigus (copd).

Nucala Euroopa Liit - eesti - EMA (European Medicines Agency)

nucala

glaxosmithkline trading services - mepolizumab - astma - ravimid hingamisteede obstruktiivsete haiguste, - severe eosinophilic asthmanucala is indicated as an add-on treatment for severe refractory eosinophilic asthma in adults, adolescents and children aged 6 years and older. chronic rhinosinusitis with nasal polyps (crswnp)nucala is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adult patients with severe crswnp for whom therapy with systemic corticosteroids and/or surgery do not provide adequate control. eosinophilic granulomatosis with polyangiitis (egpa)nucala is indicated as an add-on treatment for patients aged 6 years and older with relapsing-remitting or refractory eosinophilic granulomatosis with polyangiitis (egpa). hypereosinophilic syndrome (hes)nucala is indicated as an add-on treatment for adult patients with inadequately controlled hypereosinophilic syndrome without an identifiable non-haematologic secondary cause.