Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

novartis europharm limited - inclisiran - hypercholesterolemia; dyslipidemias - lipidą keičiančios medžiagos - leqvio is indicated in adults with primary hypercholesterolaemia (heterozygous familial and non-familial) or mixed dyslipidaemia, as an adjunct to diet:in combination with a statin or statin with other lipid-lowering therapies in patients unable to reach ldl-c goals with the maximum tolerated dose of a statin, oralone or in combination with other lipid-lowering therapies in patients who are statin-intolerant, or for whom a statin is contraindicated.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

novartis europharm limited  - capmatinib dihydrochloride monohydrate - karcinoma, nesmulkiųjų ląstelių skausmas - antinavikiniai vaistai - tabrecta as monotherapy is indicated for the treatment of adult patients with advanced non small cell lung cancer (nsclc) harbouring alterations leading to mesenchymal epithelial transition factor gene exon 14 (metex14) skipping, who require systemic therapy following prior treatment with immunotherapy and/or platinum based chemotherapy.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

novartis europharm limited - travoprostas - ocular hypertension; glaucoma, open-angle - ophthalmologicals, antiglaucoma preparations and miotics - padidėjęs akispūdis suaugusiems pacientams, sergantiems akių hipertenzija ar atviros kameros glaukoma, sumažėja (žr. 5 skyrių). sumažėjimas, padidėjęs akispūdis, pediatrijos pacientų amžius nuo 3 metų iki < 18 metų su akių hipertenzija ar vaikų glaukoma.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

novartis europharm limited  - gozetotide - radionuklidų vaizdavimas - diagnostikos radiofarmaciniai preparatai - Šis vaistas yra skirtas tik diagnostikai. locametz, after radiolabelling with gallium 68, is indicated for the detection of prostate specific membrane antigen (psma) positive lesions with positron emission tomography (pet) in adults with prostate cancer (pca) in the following clinical settings:primary staging of patients with high risk pca prior to primary curative therapy,suspected pca recurrence in patients with increasing levels of serum prostate specific antigen (psa) after primary curative therapy,identification of patients with psma positive progressive metastatic castration resistant prostate cancer (mcrpc) for whom psma targeted therapy is indicated (see section 4.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

novartis europharm limited  - lutetium (177lu) vipivotide tetraxetan - prostatos navikai, kastracija-atsparus - terapiniai radiofarmaciniai preparatai - pluvicto in combination with androgen deprivation therapy (adt) with or without androgen receptor (ar) pathway inhibition is indicated for the treatment of adult patients with progressive prostate-specific membrane antigen (psma)-positive metastatic castration-resistant prostate cancer (mcrpc) who have been treated with ar pathway inhibition and taxane based chemotherapy.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

novartis europharm limited - tislelizumab - esophageal squamous cell carcinoma - antinavikiniai vaistai - oesophageal squamous cell carcinoma (oscc) tevimbra as monotherapy is indicated for the treatment of adult patients with unresectable, locally advanced or metastatic oesophageal squamous cell carcinoma after prior platinum-based chemotherapy.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

teva gmbh - dimetilfumaratas - multiple sclerosis, relapsing-remitting; multiple sclerosis - imunosupresantai - dimethyl fumarate teva is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

teva gmbh - apiksabanas - plėvele dengtos tabletės - 2,5 mg - apixaban

Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

teva gmbh - apiksabanas - plėvele dengtos tabletės - 5 mg - apixaban

Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

teva gmbh - fampridinas - pailginto atpalaidavimo tabletės - 10 mg - fampridine