LITHIUM CARBONICUM SLOVAKOFARMA tablett Eesti - eesti - Ravimiamet

lithium carbonicum slovakofarma tablett

saneca pharmaceuticals a.s. - liitium - tablett - 300mg 100tk

Ryeqo Euroopa Liit - eesti - EMA (European Medicines Agency)

ryeqo

gedeon richter plc. - relugolix, norethisterone acetate, estradiol hemihydrate - leiomüoom - hüpofüüsi ja hüpotaalamuse hormoonid ja analoogid - ryeqo is indicated in adult women of reproductive age for:- treatment of moderate to severe symptoms of uterine fibroids,- symptomatic treatment of endometriosis in women with a history of previous medical or surgical treatment for their endometriosis.

Litak Euroopa Liit - eesti - EMA (European Medicines Agency)

litak

lipomed gmbh - cladribine - leukeemia, karvane rakk - antineoplastilised ained - litak on näidustatud karvrakulise leukeemia raviks.

Teslascan Euroopa Liit - eesti - EMA (European Medicines Agency)

teslascan

ge healthcare as - mangafodipiini trinaatrium - magnetresonantstomograafia - kontrastsusmeedium - see ravim on mõeldud ainult diagnostiliseks kasutamiseks. seevastu keskmise diagnostika magnetresonantstomograafia (mri) avastamiseks kahjustused maksa kahtlus, et need võivad olla tingitud metastaatilise haiguse või hepatotsellulaarne kartsinoomide. lisandina, et mri abi uurimise keskuse pankrease kahjustused.

AMSALYO infusioonilahuse pulber Eesti - eesti - Ravimiamet

amsalyo infusioonilahuse pulber

thissen laboratories - amsakriin - infusioonilahuse pulber - 75mg 5tk

Mekinist Euroopa Liit - eesti - EMA (European Medicines Agency)

mekinist

novartis europharm limited - trametiniib - melanoom - antineoplastilised ained - melanomatrametinib as monotherapy or in combination with dabrafenib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a braf v600 mutation (see sections 4. 4 ja 5. trametinib monotherapy has not demonstrated clinical activity in patients who have progressed on a prior braf inhibitor therapy (see section 5. adjuvant treatment of melanomatrametinib in combination with dabrafenib is indicated for the adjuvant treatment of adult patients with stage iii melanoma with a braf v600 mutation, following complete resection. mitteväikerakk-kopsuvähk (mitteväikerakk-kopsuvähi)trametinib koos dabrafenib on näidustatud ravi täiskasvanud patsientidel, kaugelearenenud mitteväikerakk-kopsuvähi, mille braf v600 mutatsioon.

XYLOCAINE 2% WITH ADRENALINE süstelahus Eesti - eesti - Ravimiamet

xylocaine 2% with adrenaline süstelahus

recipharm monts - lidokaiin+epinefriin (adrenaliin) - süstelahus - 20mg+5mcg 1ml 20ml 5tk

Tecartus Euroopa Liit - eesti - EMA (European Medicines Agency)

tecartus

kite pharma eu b.v. - autologous peripheral blood t cells cd4 and cd8 selected and cd3 and cd28 activated transduced with retroviral vector expressing anti-cd19 cd28/cd3-zeta chimeric antigen receptor and cultured (brexucabtagene autoleucel) - lümfoom, mantle-cell - antineoplastilised ained - mantle cell lymphomatecartus is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (mcl) after two or more lines of systemic therapy including a bruton’s tyrosine kinase (btk) inhibitor. acute lymphoblastic leukaemiatecartus is indicated for the treatment of adult patients 26 years of age and above with relapsed or refractory b-cell precursor acute lymphoblastic leukaemia (all).

Oxbryta Euroopa Liit - eesti - EMA (European Medicines Agency)

oxbryta

pfizer europe ma eeig  - voxelotor - anemia; anemia, hemolytic; anemia, sickle cell - other hematological agents - oxbryta is indicated for the treatment of haemolytic anaemia due to sickle cell disease (scd) in adults and paediatric patients 12 years of age and older as monotherapy or in combination with hydroxycarbamide.

P3-GAMO GR Eesti - eesti - Ecolab

p3-gamo gr

ecolab deutschland gmbh -