Adempas Uniunea Europeană - română - EMA (European Medicines Agency)

adempas

bayer ag - riociguat - hipertensiune arterială, pulmonară - antihipertensive pentru hipertensiunea arterială pulmonară - chronic thromboembolic pulmonary hypertension (cteph)adempas is indicated for the treatment of adult patients with who functional class (fc) ii to iii withinoperable cteph,persistent or recurrent cteph after surgical treatment,to improve exercise capacity. pulmonary arterial hypertension (pah)adultsadempas, as monotherapy or in combination with endothelin receptor antagonists, is indicated for the treatment of adult patients with pulmonary arterial hypertension (pah) with who functional class (fc) ii to iii to improve exercise capacity. eficacitatea a fost demonstrată într-un hap populației, inclusiv etiologii ale idiopatică sau ereditară pah sau htap asociată bolilor de țesut conjunctiv. paediatricsadempas is indicated for the treatment of pah in paediatric patients aged less than 18 years of age and body weight ≥ 50 kg with who functional class (fc) ii to iii in combination with endothelin receptor antagonists.

Descovy Uniunea Europeană - română - EMA (European Medicines Agency)

descovy

gilead sciences ireland uc - emtricitabină, tenofovir alafenamide - infecții cu hiv - antivirale pentru uz sistemic - descovy is indicated in combination with other antiretroviral agents for the treatment of adults and adolescents (aged 12 years and older with body weight at least 35 kg) infected with human immunodeficiency virus type 1 (hiv-1).

Odefsey Uniunea Europeană - română - EMA (European Medicines Agency)

odefsey

gilead sciences ireland uc - emtricitabina, clorhidrat de rilpivirină, tenofovir alafenamide - infecții cu hiv - antivirale pentru uz sistemic - tratament de adulţi şi adolescenţi (cu vârsta de 12 ani şi mai în vârstă cu corp greutate cel puţin 35 kg) infectate cu virusul imunodeficienţei umane 1 (hiv 1), fără mutaţii cunoscute asociate cu rezistenta la non-nucleozidici inhibitor de revers transcriptazei (nnrti) clasa, tenofovir sau emtricitabine şi cu un viral load ≤ hiv 1 arn 100.000 copii/ml.

Lorviqua Uniunea Europeană - română - EMA (European Medicines Agency)

lorviqua

pfizer europe ma eeig - lorlatinib - carcinom, pulmonar non-celulă mică - antineoplastic agents, protein kinase inhibitors - lorviqua as monotherapy is indicated for the treatment of adult patients with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc) previously not treated with an alk inhibitor. lorviqua as monotherapy is indicated for the treatment of adult patients with alk‑positive advanced nsclc whose disease has progressed after:alectinib or ceritinib as the first alk tyrosine kinase inhibitor (tki) therapy; orcrizotinib and at least one other alk tki.

Twinvir™ 90 mg + 400 mg comprimate filmate Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

twinvir™ 90 mg + 400 mg comprimate filmate

incepta pharmaceuticals ltd. - ledipasvirum + sofosbuvirum - comprimate filmate - 90 mg + 400 mg

Epclusa Uniunea Europeană - română - EMA (European Medicines Agency)

epclusa

gilead sciences ireland uc - sofosbuvir, velpatasvir - hepatita c, cronică - antivirale pentru uz sistemic - epclusa is indicated for the treatment of chronic hepatitis c virus (hcv) infection in patients 3 years of age and older (see sections 4. 2, 4. 4 și 5.

Harvoni Uniunea Europeană - română - EMA (European Medicines Agency)

harvoni

gilead sciences ireland uc - ledipasvir, sofosbuvir - hepatita c, cronică - antivirale pentru uz sistemic - harvoni is indicated for the treatment of chronic hepatitis c (chc) in adult and paediatric patients aged 3 years and above (see sections 4. 2, 4. 4 și 5. pentru virusul hepatitei c (vhc) genotip-activitatea specifică a se vedea secțiunile 4. 4 și 5.