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sanofi-aventis estonia oÜ - oksaliplatiin - infusioonilahuse kontsentraat - 5mg 1ml 20ml 1tk; 5mg 1ml 40ml 1tk

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accord healthcare b.v. - paklitakseel - infusioonilahuse kontsentraat - 6mg 1ml 25ml 1tk; 6mg 1ml 5ml 1tk; 6mg 1ml 16.7ml 1tk

Euroopa Liit - eesti - EMA (European Medicines Agency)

pfizer europe ma eeig - pemetrexed disodium, pemetrexed disodium hemipentahydrate - carcinoma, non-small-cell lung; mesothelioma - antineoplastilised ained - malignant pleural mesotheliomapemetrexed pfizer in combination with cisplatin is indicated for the treatment of chemotherapy naïve patients with unresectable malignant pleural mesothelioma. non-small cell lung cancerpemetrexed pfizer in combination with cisplatin is indicated for the first-line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology. pemetrexed pfizer is indicated as monotherapy for the maintenance treatment of locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology in patients whose disease has not progressed immediately following platinum-based chemotherapy. pemetrexed pfizer is indicated as monotherapy for the second-line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology.

Euroopa Liit - eesti - EMA (European Medicines Agency)

roche registration gmbh - atezolüsumab - carcinoma, transitional cell; carcinoma, non-small-cell lung; urologic neoplasms; breast neoplasms; small cell lung carcinoma - antineoplastilised ained - urothelial carcinomatecentriq as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc):- after prior platinum containing chemotherapy, or - who are considered cisplatin ineligible, and whose tumours have a pd-l1 expression ≥ 5% (see section 5. non-small cell lung cancer tecentriq, in combination with bevacizumab, paclitaxel and carboplatin, is indicated for the first-line treatment of adult patients with metastatic non-squamous non small cell lung cancer (nsclc). in patients with egfr mutant or alk-positive nsclc, tecentriq, in combination with bevacizumab, paclitaxel and carboplatin, is indicated only after failure of appropriate targeted therapies (see section 5. tecentriq, in combination with nab paclitaxel and carboplatin, is indicated for the first line treatment of adult patients with metastatic non-squamous nsclc who do not have egfr mutant or alk positive nsclc (see section 5. tecentriq as monotherapy is indicated for the first-line treatment of adult patients with metastatic non-small cell lung cancer (nsclc) whose tumours have a pd-l1 expression ≥ 50% tumour cells (tc) or ≥ 10% tumour-infiltrating immune cells (ic) and who do not have egfr mutant or alk-positive nsclc (see section 5. tecentriq nagu monotherapy on näidustatud ravi täiskasvanud patsientidel, kellel on lokaalselt kaugelearenenud või metastaatilise mitteväikerakk-kopsuvähi pärast eelnevat keemiaravi. patients with egfr mutant or alk positive nsclc should also have received targeted therapies before receiving tecentriq (see section 5. small cell lung cancertecentriq, in combination with carboplatin and etoposide, is indicated for the first-line treatment of adult patients with extensive-stage small cell lung cancer (es-sclc) (see section 5. hepatocellular carcinomatecentriq, in combination with bevacizumab, is indicated for the treatment of adult patients with advanced or unresectable hepatocellular carcinoma (hcc) who have not received prior systemic therapy (see section 5. urothelial carcinomatecentriq as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc):- after prior platinum containing chemotherapy, or- who are considered cisplatin ineligible, and whose tumours have a pd-l1 expression ≥ 5% (see section 5. non-small cell lung cancertecentriq as monotherapy is indicated for the first-line treatment of adult patients with metastatic non-small cell lung cancer (nsclc) whose tumours have a pd-l1 expression ≥ 50% tumour cells (tc) or ≥ 10% tumour-infiltrating immune cells (ic) and who do not have egfr mutant or alk-positive nsclc (see section 5. tecentriq nagu monotherapy on näidustatud ravi täiskasvanud patsientidel, kellel on lokaalselt kaugelearenenud või metastaatilise mitteväikerakk-kopsuvähi pärast eelnevat keemiaravi. patients with egfr mutant or alk positive nsclc should also have received targeted therapies before receiving tecentriq (see section 5. triple-negative breast cancertecentriq in combination with nab-paclitaxel is indicated for the treatment of adult patients with unresectable locally advanced or metastatic triple-negative breast cancer (tnbc) whose tumours have pd-l1 expression ≥ 1% and who have not received prior chemotherapy for metastatic disease.

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sandoz pharmaceuticals d.d. - paklitakseel - infusioonilahuse kontsentraat - 6mg 1ml 5ml 20tk; 6mg 1ml 16.7ml 20tk; 6mg 1ml 50ml 1tk; 6mg 1ml 5ml 10tk; 6mg 1ml 100ml 20tk; 6mg 1ml 25ml 5tk; 6mg 1ml 25ml 20tk; 6mg 1ml 16.7ml 10tk; 6mg 1ml 5ml 1tk; 6mg 1ml 25ml 1tk; 6mg 1ml 100ml 10tk; 6mg 1ml 25ml 10tk; 6mg 1ml 100ml 1tk; 6mg 1ml 50ml 5tk; 6mg 1ml 5ml 5tk; 6mg 1ml 100ml 5tk; 6mg 1ml 50ml 10tk; 6mg 1ml 50ml 20tk

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actavis group ptc ehf. - oksaliplatiin - infusioonilahuse kontsentraat - 5mg 1ml 20ml 1tk; 5mg 1ml 40ml 1tk; 5mg 1ml 10ml 1tk

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hospira uk limited - oksaliplatiin - infusioonilahuse pulber - 5mg 1ml 100mg 1tk

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sandoz pharmaceuticals d.d. - paklitakseel - infusioonilahuse kontsentraat - 6mg 1ml 16.7ml 1tk; 6mg 1ml 25ml 1tk; 6mg 1ml 50ml 1tk; 6mg 1ml 5ml 1tk

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mylan s.a.s. - oksaliplatiin - infusioonilahuse kontsentraat - 5mg 1ml 20ml 1tk; 5mg 1ml 10ml 1tk; 5mg 1ml 40ml 1tk

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fresenius kabi oncology plc - oksaliplatiin - infusioonilahuse pulber - 5mg 1ml 100mg 1tk; 5mg 1ml 50mg 1tk