Den Europæiske Union - estisk - EMA (European Medicines Agency)

sun pharmaceutical industries (europe) b.v. - ertapiin-naatrium - bakteriaalsed infektsioonid - ertapenem - treatmentertapenem sun is indicated in paediatric patients (3 months to 17 years of age) and in adults for the treatment of the following infections when caused by bacteria known or very likely to be susceptible to ertapenem and when parenteral therapy is required (see sections 4. 4 ja 5. 1):- intra-abdominal infections- community acquired pneumonia- acute gynaecological infections- diabetic foot infections of the skin and soft tissue (see section 4. 4)preventionertapenem sun is indicated in adults for the prophylaxis of surgical site infection following elective colorectal surgery (see section 4. tuleks arvesse võtta ametlikke juhiseid sobiva kasutada antibakteriaalseid aineid.

Estland - estisk - Ravimiamet

icg farma uab - asatsitidiin - süstesuspensiooni pulber - 25mg 1ml 6ml 1tk; 25mg 1ml 4ml 1tk

Den Europæiske Union - estisk - EMA (European Medicines Agency)

accord healthcare s.l.u. - imatiniib - precursor cell lymphoblastic leukemia-lymphoma; dermatofibrosarcoma; myelodysplastic-myeloproliferative diseases; leukemia, myelogenous, chronic, bcr-abl positive; hypereosinophilic syndrome - imatiniib - 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. välja arvatud äsja diagnoositud kroonilise faasi cml, ei ole kontrollitud uuringud, mis näitab kliiniline kasu või suurenenud ellujäämise eest need haigused. .

Den Europæiske Union - estisk - EMA (European Medicines Agency)

les laboratoires servier - piksantrooni dimaleaat - lümfoom, mitte-hodgkini - antineoplastilised ained - pixuvri on näidustatud monoteraapiana täiskasvanud patsientidel, kellel on retsidiveerunud või refraktaarseid agressiivseid mitte-hodgkini b-rakulisi lümfoomi (nhl). pixantrone ravi ei ole tõestatud patsientidel, kellel viimase ravile viienda rea või rohkem keemiaravi kasutamisel.

Estland - estisk - Ravimiamet

takeda pharmaceuticals international ag ireland branch - lantaan - närimistablett - 1000mg 90tk; 1000mg 50tk; 1000mg 100tk; 1000mg 15tk; 1000mg 30tk; 1000mg 10tk

Estland - estisk - Ravimiamet

takeda pharmaceuticals international ag ireland branch - lantaan - suukaudne pulber - 1000mg 90tk

Estland - estisk - Ravimiamet

shire pharmaceutical contracts limited - lantaan - närimistablett - 250mg 200tk; 250mg 40tk; 250mg 90tk; 250mg 400tk

Estland - estisk - Ravimiamet

takeda pharmaceuticals international ag ireland branch - lantaan - närimistablett - 750mg 90tk; 750mg 30tk; 750mg 45tk; 750mg 75tk

Estland - estisk - Ravimiamet

takeda pharmaceuticals international ag ireland branch - lantaan - närimistablett - 500mg 45tk; 500mg 200tk; 500mg 100tk; 500mg 20tk; 500mg 90tk

Estland - estisk - Ravimiamet

krka, d.d., novo mesto - butafosfaan+tsüanokobalamiin - süstelahus - 100mg+0,05mg 1ml 250ml 1tk; 100mg+0,05mg 1ml 100ml 1tk