Tolvaptan Accord यूरोपीय संघ - लिथुआनियाई - EMA (European Medicines Agency)

tolvaptan accord

accord healthcare s.l.u. - tolvaptan - netinkamas adh sindromas - diuretikai, - tolvaptan is indicated in adults for the treatment of hyponatremia secondary to the syndrome of inappropriate antidiuretic hormone secretion (siadh).

Imatinib Accord यूरोपीय संघ - लिथुआनियाई - EMA (European Medicines Agency)

imatinib accord

accord healthcare s.l.u. - imatinibas - precursor cell lymphoblastic leukemia-lymphoma; dermatofibrosarcoma; myelodysplastic-myeloproliferative diseases; leukemia, myelogenous, chronic, bcr-abl positive; hypereosinophilic syndrome - imatinibas - imatinib accord is indicated for the treatment of- adult 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. - adult patients with unresectable dermatofibrosarcoma protuberans (dfsp) and adult patients with recurrent and/or metastatic dfsp who are not eligible for surgery. - the 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. patients who have a low or very low risk of recurrence should not receive adjuvant treatmentthe effect of imatinib on the outcome of bone marrow transplantation has not been determined. 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 dfsp. the experience with imatinib in patients with mds/mpd associated with pdgfr gene re-arrangements is very limited (see section 5. išskyrus naujai diagnozuota lėtinė fazė lml, nėra kontroliuojamų tyrimų rodo, klinikinės naudos ar padidėjo išgyvenamumas šių ligų. .

Atorvastatin Accord लिथुआनिया - लिथुआनियाई - SMCA (Valstybinė vaistų kontrolės tarnyba)

atorvastatin accord

accord healthcare b.v. - atorvastatinas - plėvele dengtos tabletės - 40 mg; 10 mg; 20 mg - atorvastatin

Bosentan Accord लिथुआनिया - लिथुआनियाई - SMCA (Valstybinė vaistų kontrolės tarnyba)

bosentan accord

accord healthcare b.v. - bozentanas - plėvele dengtos tabletės - 125 mg; 62,5 mg - bosentan

Azacitidine Accord यूरोपीय संघ - लिथुआनियाई - EMA (European Medicines Agency)

azacitidine accord

accord healthcare s.l.u. - azacitidinas - myelodysplastic syndromes; leukemia, myelomonocytic, chronic; leukemia, myeloid, acute - antinavikiniai vaistai - azacitidine sutarimu skiriamas gydymas suaugusiems pacientams, kurie negali gauti kraujodaros kamieninių ląstelių transplantacijos (hsct) su:- tarpinės-2 ir didelės rizikos mielodisplazinio sindromai (vni) pagal tarptautinių prognostinė balų sistemą (ipss),- lėtinis myelomonocytic leukemija (cmml) su 10-29 % čiulpuose blastų be myeloproliferative sutrikimas,- ūminės mieloidinės leukemijos (ppp) su 20-30 % blastų ir multi-lineage dysplasia, pagal pasaulio sveikatos organizacijos (pso) klasifikavimo,- ppp su >30% čiulpuose blastų pagal pso klasifikaciją.

Savene यूरोपीय संघ - लिथुआनियाई - EMA (European Medicines Agency)

savene

clinigen healthcare b.v. - deksrazoksano hidrochlorido - diagnostikos ir terapinių medžiagų ekstravazacija - visi kiti gydomieji produktai - savene skirtas antraciklino ekstravazacijos gydymui.

Epirubicin Accord लिथुआनिया - लिथुआनियाई - SMCA (Valstybinė vaistų kontrolės tarnyba)

epirubicin accord

accord healthcare b.v. - epirubicino hidrochloridas - injekcinis ar infuzinis tirpalas - 2 mg/ml - epirubicin

Vinorelbine Accord लिथुआनिया - लिथुआनियाई - SMCA (Valstybinė vaistų kontrolės tarnyba)

vinorelbine accord

accord healthcare b.v. - vinorelbinas - koncentratas infuziniam tirpalui - 10 mg/ml - vinorelbine