FUROSEMID HAMELN 10 mg/ml Romania - rumeno - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

furosemid hameln 10 mg/ml

siegfried hameln gmbh - germania - furosemidum - sol inj. - 10mg/ml - diuretice cu efect puternic ( de ansa) sulfonamide

Clopidogrel Acino Pharma GmbH Unione Europea - rumeno - EMA (European Medicines Agency)

clopidogrel acino pharma gmbh

acino pharma gmbh - clopidogrel - peripheral vascular diseases; stroke; myocardial infarction - agenți antitrombotici - clopidogrelul este indicat la adulți pentru prevenirea evenimentelor aterotrombotice la:pacienții care suferă de infarct miocardic (de la câteva zile până la mai puțin de 35 zile), accident vascular cerebral ischemic (mai vechi de 7 zile până la mai puțin de 6 luni) sau boală arterială periferică dovedită. pentru informații suplimentare vă rugăm să consultați secțiunea 5.

Imatinib Koanaa Unione Europea - rumeno - EMA (European Medicines Agency)

imatinib koanaa

koanaa healthcare gmbh - imatinib mesilat - leukemia, myelogenous, chronic, bcr-abl positive; precursor cell lymphoblastic leukemia-lymphoma; myelodysplastic-myeloproliferative diseases; hypereosinophilic syndrome; dermatofibrosarcoma; gastrointestinal stromal tumors - agenți antineoplazici - imatinib koanaa is indicated for the treatment ofadult and paediatric patients with newly diagnosed philadelphia chromosome (bcr-abl) positive (ph+) chronic myeloid leukaemia (cml) for whom bone marrow transplantation is not considered as the first line of treatment. adult and paediatric patients with ph+ cml in chronic phase after failure of interferon-alpha therapy, or in accelerated phase or blast crisis. adult and paediatric patients with newly diagnosed philadelphia chromosome positive acute lymphoblastic leukaemia (ph+ all) integrated with chemotherapy. adult patients with relapsed or refractory ph+ all as monotherapy. adult patients with myelodysplastic/myeloproliferative diseases (mds/mpd) associated with platelet-derived growth factor receptor (pdgfr) gene re-arrangements. adult patients with advanced hypereosinophilic syndrome (hes) and/or chronic eosinophilic leukaemia (cel) with fip1l1-pdgfrα rearrangement. the effect of imatinib on the outcome of bone marrow transplantation has not been determined. imatinib koanaa is indicated forthe treatment of adult patients with kit (cd 117) positive unresectable and/or metastatic malignant gastrointestinal stromal tumours (gist). the adjuvant treatment of adult patients who are at significant risk of relapse following resection of kit (cd117)-positive gist. pacienții care au un risc scăzut sau foarte scăzut de recidivă nu trebuie să primească tratament adjuvant. the treatment of adult patients with unresectable dermatofibrosarcoma protuberans (dfsp) and adult patients with recurrent and/or metastatic dfsp who are not eligible for surgery. in adult and paediatric patients, the effectiveness of imatinib is based on overall haematological and cytogenetic response rates and progression-free survival in cml, on haematological and cytogenetic response rates in ph+ all, mds/mpd, on haematological response rates in hes/cel and on objective response rates in adult patients with unresectable and/or metastatic gist and dfsp and on recurrence-free survival in adjuvant gist. the experience with imatinib in patients with mds/mpd associated with pdgfr gene re-arrangements is very limited (see section 5. cu excepția nou diagnosticate în faza cronică a lgc, nu există studii controlate care să demonstreze un beneficiu clinic sau a crescut de supraviețuire pentru aceste boli.

Acesol-Jurabek solutie perfuzabila 2,0 g + 5,0 g + 1,0 g Moldavia - rumeno - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

acesol-jurabek solutie perfuzabila 2,0 g + 5,0 g + 1,0 g

jurabek laboratories im srl - natrii acetas+natrii chloridum+amoxicillinum chloridum - solutie perfuzabila - 2,0 g + 5,0 g + 1,0 g

Disol-Jurabek solutie perfuzabila 2,0 g + 6,0 g Moldavia - rumeno - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

disol-jurabek solutie perfuzabila 2,0 g + 6,0 g

jurabek laboratories im srl - natrii acetas+natrii chloridum - solutie perfuzabila - 2,0 g + 6,0 g

ENCEPUR ADULTI 1,5 µg/0,5 ml Romania - rumeno - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

encepur adulti 1,5 µg/0,5 ml

gsk vaccines gmbh - germania - vaccin impotriva encefalitei de capuse - susp. inj. in seringa preumpluta - 1,5µg/0,5ml - vaccinuri virale vaccinuri contra encefalitei

Betmiga Unione Europea - rumeno - EMA (European Medicines Agency)

betmiga

astellas pharma europe b.v. - mirabegron - vezica urinară, hiperactivă - urologicals - tratamentul simptomatic al urgenței. creșterea frecvenței micțiunilor și / sau incontinență imperioasă ca pot să apară la pacienții adulți cu hiperactivă-sindrom de vezică.