Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

egis pharmaceuticals plc - nitroglycerinum - spray sublingual - 0,4 mg/doza

Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

bayer pharma ag - comprimate filmate - 10 mg

Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

bayer pharma ag - comprimate filmate - 20 mg

Uniunea Europeană - română - EMA (European Medicines Agency)

actavis group ptc ehf - imatinib - leukemia, myelogenous, chronic, bcr-abl positive; precursor cell lymphoblastic leukemia-lymphoma; myelodysplastic-myeloproliferative diseases; hypereosinophilic syndrome; dermatofibrosarcoma - protein kinase inhibitors, antineoplastic agents - imatinib actavis is indicated for the treatment of: , 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;, paediatric patients with ph+ cml in chronic phase after failure of interferon-alpha therapy, or in accelerated phase or blast crisis;, adult patients with ph+ cml in blast crisis;, adult 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-pdgfr rearrangement;, 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. , efectul de imatinib pe rezultatul de transplantul de măduvă osoasă nu a fost determinată. imatinib actavis is indicated for: , 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. experiența cu imatinib la pacienții cu mds/mpd asociate cu genei fcdp-re-aranjamente este foarte limitat. nu există studii controlate care să demonstreze un beneficiu clinic sau a crescut de supraviețuire pentru aceste boli.

România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

octapharma (ip) ltd. - imunoglobulina normala pt. adm. intravasculara - sol. perf. - 50mg/ml - imunoglobuline imunoglobulina umana normala

România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

octapharma (ip) ltd. - albuminum humanum - sol. perf. - 200g/l - sange si substituenti de sange substituenti de sange si fractiuni proteice plasmatice

România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

octapharma (ip) ltd. - albuminum humanum - sol. perf. - 50g/l - sange si substituenti de sange substituenti de sange si fractiuni proteice plasmatice

România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

octapharma (ip) ltd. - combinatii (factori de coagulare) - pulb+solv. pt. sol. perf. - 500ui - vitamina k si alte hemostatice factori ai coagularii sanguine

România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

octapharma (ip) ltd. - factor ix de coagulare - pulb. + solv. pt. sol. perf. - 500 ui - vitamina k si alte hemostatice factori ai coagularii sanguine

România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

octapharma (ip) ltd. - factor ix de coagulare - pulb. + solv. pt. sol. perf. - 1000ui - vitamina k si alte hemostatice factori ai coagularii sanguine