Simvastatin Accord Lituania - Lituavi - SMCA (Valstybinė vaistų kontrolės tarnyba)

simvastatin accord

accord healthcare b.v. - simvastatinas - plėvele dengtos tabletės - 40 mg; 20 mg; 10 mg - simvastatin

Cabazitaxel Accord Uni Eropa - Lituavi - EMA (European Medicines Agency)

cabazitaxel accord

accord healthcare s.l.u. - kabazitakselis - prostatos navikai, kastracija-atsparus - antinavikiniai vaistai - treatment of patients with hormone refractory metastatic prostate cancer previously treated with a docetaxel-containing regimen.

Sorafenib Accord Uni Eropa - Lituavi - EMA (European Medicines Agency)

sorafenib accord

accord healthcare s.l.u. - sorafenib tosilate - carcinoma, hepatocellular; carcinoma, renal cell - antinavikiniai vaistai - hepatocellular carcinomasorafenib accord is indicated for the treatment of hepatocellular carcinoma (see section 5. renal cell carcinomasorafenib accord is indicated for the treatment of patients with advanced renal cell carcinoma who have failed prior interferon-alpha or interleukin-2 based therapy or are considered unsuitable for such therapy.

Teriflunomide Accord Uni Eropa - Lituavi - EMA (European Medicines Agency)

teriflunomide accord

accord healthcare s.l.u. - teriflunomide - išsėtinė sklerozė, grįžtamoji-pervedimo - imunosupresantais, pasirinktinio imunosupresantais - teriflunomide accord is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

Palonosetron Accord Uni Eropa - Lituavi - EMA (European Medicines Agency)

palonosetron accord

accord healthcare s.l.u. - palonosetron - vomiting; nausea; cancer - vėmimą slopinančiais vaistais ir antinauseants, - palonosetron accord yra nurodyta suaugusiems:prevencijos ūmus pykinimas ir vėmimas, susijęs su labai emetogenic vėžio chemoterapija,prevencija, pykinimas ir vėmimas, susijęs su šiek tiek emetogenic vėžio chemoterapija. palonosetron accord yra nurodyta pediatrinių pacientų 1 mėnesio amžiaus ir vyresni:prevencijos ūmus pykinimas ir vėmimas, susijęs su labai emetogenic vėžio chemoterapija ir prevencijos pykinimas ir vėmimas, susijęs su šiek tiek emetogenic vėžio chemoterapija.

Zoledronic Acid Accord Uni Eropa - Lituavi - EMA (European Medicines Agency)

zoledronic acid accord

accord healthcare s.l.u. - zoledrono rūgšties monohidratas - hypercalcemia; fractures, bone; cancer - bisfosfonatai - skeleto pažeidimų susijusių reiškinių (patologinių lūžių, stuburo spaudimo, radiacija ar chirurginis arba naviko sukeltai hiperkalcemijai) suaugusiems pacientams su kaulus piktybinis procesas. gydymo suaugusių pacientų su naviko sukelta hypercalcaemia (tih).

OTC 50 FRANVET 500 mg/g, geriamieji milteliai Lituania - Lituavi - SMCA (Valstybinė vaistų kontrolės tarnyba)

otc 50 franvet 500 mg/g, geriamieji milteliai

huvepharma sa (prancūzija) - geriamieji milteliai - 1 g yra: oksitetraciklino (hidrochlorido) - 500 mg. - veršeliams, ėriukams, kiaulėms, triušiams ir naminiams paukščiams gydyti, sergant oksitetraciklinui jautrių mikroorganizmų sukeltomis kvėpavimo takų ir virškinimo trakto infekcinėmis ligomis.

Sunitinib Accord Uni Eropa - Lituavi - EMA (European Medicines Agency)

sunitinib accord

accord healthcare s.l.u. - sunitinibas - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - antinavikiniai vaistai - gastrointestinal stromal tumour (gist)sunitinib accord is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (gist) in adults after failure of imatinib treatment due to resistance or intolerance. metastatic renal cell carcinoma (mrcc)sunitinib accord is indicated for the treatment of advanced/metastatic renal cell carcinoma (mrcc) in adults. pancreatic neuroendocrine tumours (pnet)sunitinib accord is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours (pnet) with disease progression in adults.

Imfinzi Uni Eropa - Lituavi - EMA (European Medicines Agency)

imfinzi

astrazeneca ab - durvalumab - karcinoma, nesmulkiųjų ląstelių skausmas - antinavikiniai vaistai - non-small cell lung cancer (nsclc)imfinzi as monotherapy is indicated for the treatment of locally advanced, unresectable non small cell lung cancer (nsclc) in adults whose tumours express pd-l1 on ≥ 1% of tumour cells and whose disease has not progressed following platinum based chemoradiation therapy (see section 5. imfinzi in combination with tremelimumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic nsclc with no sensitising egfr mutations or alk positive mutations. small cell lung cancer (sclc)imfinzi in combination with etoposide and either carboplatin or cisplatin is indicated for the first-line treatment of adults with extensive-stage small cell lung cancer (es-sclc). biliary tract cancer (btc)imfinzi in combination with gemcitabine and cisplatin is indicated for the first line treatment of adults with unresectable or metastatic biliary tract cancer (btc). hepatocellular carcinoma (hcc)imfinzi in combination with tremelimumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (hcc).

Rozlytrek Uni Eropa - Lituavi - EMA (European Medicines Agency)

rozlytrek

roche registration gmbh  - entrectinib - cancer; carcinoma, non-small-cell lung - antinavikiniai vaistai - rozlytrek as monotherapy is indicated for the treatment of adult and paediatric patients 12 years of age and older with solid tumours expressing a neurotrophic tyrosine receptor kinase (ntrk) gene fusion,who have a disease that is locally advanced, metastatic or where surgical resection is likely to result in severe morbidity, andwho have not received a prior ntrk inhibitorwho have no satisfactory treatment options. rozlytrek as monotherapy is indicated for the treatment of adult patients with ros1 positive, advanced non small cell lung cancer (nsclc) not previously treated with ros1 inhibitors.