holoxan 1 g pulveris infūziju šķīduma pagatavošanai
baxter latvia, sia, latvia - ifosfamīds - pulveris infūziju šķīduma pagatavošanai - 1 g
palonosetron hospira
pfizer europe ma eeig - palonosetron hydrochloride - nausea; vomiting; cancer - pretvemšanas un antinauseants, - palonosetron hospira ir norādīts pieaugušajiem:novērst akūtas slikta dūša un vemšana, kas saistīta ar ļoti emetogenic vēža ķīmijterapija;novēršanu, slikta dūša un vemšana, kas saistīta ar mēreni emetogenic vēža ķīmijterapija. palonosetron hospira ir norādīts pediatrijas pacientiem no 1 mēneša vecuma un vecākiem:novērst akūtas slikta dūša un vemšana, kas saistīta ar ļoti emetogenic vēža ķīmijterapija un novēršanu, slikta dūša un vemšana, kas saistīta ar mēreni emetogenic vēža ķīmijterapija.
docetaxel hospira 10 mg/ml koncentrāts infūziju šķīduma pagatavošanai
hospira uk limited, united kingdom - docetaksels - koncentrāts infūziju šķīduma pagatavošanai - 10 mg/ml
gemcitabine accord 100 mg/ml koncentrāts infūziju šķīduma pagatavošanai
accord healthcare b.v., netherlands - gemcitabīns - koncentrāts infūziju šķīduma pagatavošanai - 100 mg/ml
gemcit 38 mg/ml pulveris infūziju šķīduma pagatavošanai
fresenius kabi polska sp.z o.o., poland - gemcitabīns - pulveris infūziju šķīduma pagatavošanai - 38 mg/ml
gemcitabine kabi 38 mg/ml koncentrāts infūziju šķīduma pagatavošanai
fresenius kabi polska sp.z o.o., poland - gemcitabīns - koncentrāts infūziju šķīduma pagatavošanai - 38 mg/ml
amikacin b.braun 5 mg/ml šķīdums infūzijām
b.braun melsungen ag, germany - amikacīns - Šķīdums infūzijām - 5 mg/ml
amikacin b.braun 10 mg/ml šķīdums infūzijām
b.braun melsungen ag, germany - amikacīns - Šķīdums infūzijām - 10 mg/ml
ondansetron kalceks 2 mg/ml šķīdums injekcijām/infūzijām
kalceks, a/s, latvia - ondansetrons - Šķīdums injekcijām/infūzijām - 2 mg/ml
tecentriq
roche registration gmbh - atezolizumabs - carcinoma, transitional cell; carcinoma, non-small-cell lung; urologic neoplasms; breast neoplasms; small cell lung carcinoma - antineoplastiski līdzekļi - 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 kā monotherapy ir norādīts ārstēšanai pieaugušiem pacientiem ar lokāli papildu vai metastātiska nsclc pēc iepriekšējas ķīmijterapijas. 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 kā monotherapy ir norādīts ārstēšanai pieaugušiem pacientiem ar lokāli papildu vai metastātiska nsclc pēc iepriekšējas ķīmijterapijas. 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.