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

rybrevant

janssen-cilag international n.v.    - amivantamab - kartsinoom, mitteväikerakk-kopsu - antineoplastilised ained - rybrevant as monotherapy is indicated for treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with activating epidermal growth factor receptor (egfr) exon 20 insertion mutations, after failure of platinum-based chemotherapy.

XANAX tablett Eesti - eesti - Ravimiamet

xanax tablett

first pharma oÜ - alprasolaam - tablett - 1mg 30tk

ATROVENT nebuliseeritav lahus Eesti - eesti - Ravimiamet

atrovent nebuliseeritav lahus

boehringer ingelheim international gmbh - ipratroopiumbromiid - nebuliseeritav lahus - 0,25mg 1ml 20ml 1tk

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

padcev

astellas pharma europe b.v. - enfortumab vedotin - carcinoma, transitional cell; urologic neoplasms - antineoplastilised ained - padcev as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial cancer who have previously received a platinum-containing chemotherapy and a programmed death receptor 1 or programmed death ligand 1 inhibitor.

MEDROL tablett Eesti - eesti - Ravimiamet

medrol tablett

lex ano uab - metüülprednisoloon - tablett - 4mg 100tk

XANAX tablett Eesti - eesti - Ravimiamet

xanax tablett

lex ano uab - alprasolaam - tablett - 0,5mg 100tk

MEDROL tablett Eesti - eesti - Ravimiamet

medrol tablett

lex ano uab - metüülprednisoloon - tablett - 16mg 50tk

XANAX tablett Eesti - eesti - Ravimiamet

xanax tablett

lex ano uab - alprasolaam - tablett - 1mg 30tk

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

pedmarqsi

fennec pharmaceuticals (eu) limited - sodium thiosulfate - ear diseases; ototoxicity - kõik muud ravitoimingud - pedmarqsi is indicated for the prevention of ototoxicity induced by cisplatin chemotherapy in patients 1 month to < 18 years of age with localised, non-metastatic, solid tumours.

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

tibsovo

les laboratoires servier - ivosidenib - leukemia, myeloid, acute; cholangiocarcinoma - antineoplastilised ained - tibsovo in combination with azacitidine is indicated for the treatment of adult patients with newly diagnosed acute myeloid leukaemia (aml) with an isocitrate dehydrogenase-1 (idh1) r132 mutation who are not eligible to receive standard induction chemotherapy (see section 5. tibsovo monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic cholangiocarcinoma with an idh1 r132 mutation who were previously treated by at least one prior line of systemic therapy.