Zydelig Europeiska unionen - polska - EMA (European Medicines Agency)

zydelig

gilead sciences ireland uc - idelalisib - lymphoma, non-hodgkin; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, other antineoplastic agents - zydelig is indicated in combination with an anti‑cd20 monoclonal antibody (rituximab or ofatumumab) for the treatment of adult patients with chronic lymphocytic leukaemia (cll):who have received at least one prior therapy, oras first line treatment in the presence of 17p deletion or tp53 mutation in patients who are not eligible for any other therapies. zydelig is indicated as monotherapy for the treatment of adult patients with follicular lymphoma (fl) that is refractory to two prior lines of treatment.

Vipdomet Europeiska unionen - polska - EMA (European Medicines Agency)

vipdomet

takeda pharma a/s - alogliptin, benzoesan sodu, chlorowodorek metforminy - diabetes mellitus, type 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. potrójna terapia) jako uzupełnienie diety i ćwiczeń fizycznych w celu poprawy kontroli glikemii u pacjentów, gdy insuliny w stabilnej dawce i metformina sam nie zapewniają odpowiedniej kontroli glikemii.

Triumeq Europeiska unionen - polska - EMA (European Medicines Agency)

triumeq

viiv healthcare b.v. - dolutegravir sodium, lamivudine, abacavir (as sulfate) - infekcje hiv - Środki przeciwwirusowe do użytku ogólnoustrojowego - triumeq is indicated for the treatment of human immunodeficiency virus (hiv) infected adults,  adolescents and children  weighing at least 25 kg who are antiretroviral treatment-naïve or are infected with hiv without documented or clinically suspected resistance to any of the three antiretroviral agents in triumeq.

Tybost Europeiska unionen - polska - EMA (European Medicines Agency)

tybost

gilead sciences ireland uc - cobicistat - infekcje hiv - Środki przeciwwirusowe do użytku ogólnoustrojowego - tybost is indicated as a pharmacokinetic enhancer of atazanavir 300 mg once daily or darunavir 800 mg once daily as part of antiretroviral combination therapy in human immunodeficiency virus-1 (hiv-1) infected adults and adolescents aged 12 years and older:weighing at least 35 kg co‑administered with atazanavir orweighing at least 40 kg co‑administered with darunavir.

Xarelto Europeiska unionen - polska - EMA (European Medicines Agency)

xarelto

bayer ag - rywaroksaban - arthroplasty, replacement; venous thromboembolism - Środki przeciwzakrzepowe - xarelto, wprowadzone w połączeniu z kwas acetylosalicylowy (asa) w sam lub z ask plus lub tiklopidyna, klopidogrel, jest pokazana w celu zapobiegania aterotrombotičeskih zdarzeń u dorosłych pacjentów po ostrym zespołem wieńcowym (acs) z podwyższonym poziomem кардиальных biomarkerów. xarelto, 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. profilaktyka żylnej choroby zakrzepowo-zatorowej (Żchzz) u dorosłych pacjentów poddawanych planowej operacji wymiany stawu biodrowego lub kolanowego. leczenie zakrzepicy żył głębokich (dvt) i zatorowości płucnej (ТЭЛА) i zapobiegania nawrotom zakrzepicy żył głębokich i ТЭЛА u dorosłych. 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. paediatric population treatment 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. paediatric population treatment 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.