Altaxon 2 g prašek za raztopino za injiciranje/infundiranje Eslovènia - eslovè - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

altaxon 2 g prašek za raztopino za injiciranje/infundiranje

panpharma sa - ceftriakson - prašek za raztopino za injiciranje/infundiranje - ceftriakson 2 g / 1 viala - ceftriakson

Altaxon 1 g prašek za raztopino za injiciranje/infundiranje Eslovènia - eslovè - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

altaxon 1 g prašek za raztopino za injiciranje/infundiranje

panpharma sa - ceftriakson - prašek za raztopino za injiciranje/infundiranje - ceftriakson 1 g / 1 viala - ceftriakson

Entresto Unió Europea - eslovè - EMA (European Medicines Agency)

entresto

novartis europharm limited - sacubitril, valsartan - odpoved srca - angiotensin ii antagonisti, druge kombinacije, agente, ki delujejo na renin-angiotensin sistem - paediatric heart failureentresto is indicated in children and adolescents aged one year or older for treatment of symptomatic chronic heart failure with left ventricular systolic dysfunction. adult heart failureentresto is indicated in adult patients for treatment of symptomatic chronic heart failure with reduced ejection fraction.

Neparvis Unió Europea - eslovè - EMA (European Medicines Agency)

neparvis

novartis europharm limited - sacubitril, valsartan - odpoved srca - sredstva, ki delujejo na sistem renin-angiotenzin - paediatric heart failureneparvis is indicated in children and adolescents aged one year or older for treatment of symptomatic chronic heart failure with left ventricular systolic dysfunction (see section 5. adult heart failureneparvis is indicated in adult patients for treatment of symptomatic chronic heart failure with reduced ejection fraction (see section 5.

Zaditen 0,25 mg/ml kapljice za oko, raztopina Eslovènia - eslovè - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

zaditen 0,25 mg/ml kapljice za oko, raztopina

laboratoires thea - ketotifen - kapljice za oko, raztopina - ketotifen 0,25 mg / 1 ml - ketotifen

Hexyon Unió Europea - eslovè - EMA (European Medicines Agency)

hexyon

sanofi pasteur europe - filamentous haemagglutinin, haemophilus influenzae type b polysaccharide (polyribosylribitol phosphate), hepatitis b surface antigen, pertussis toxoid, poliovirus (inactivated) type 1 (mahoney strain) produced on vero cells, poliovirus (inactivated) type 2 (mef-1 strain) produced on vero cells, poliovirus (inactivated) type 3 (saukett strain) produced on vero cells, tetanus protein, tetanus toxoid adsorbed on aluminium hydroxide, hydrated, diphtheria toxoid - hepatitis b; tetanus; immunization; meningitis, haemophilus; whooping cough; poliomyelitis; diphtheria - cepiva - hexyon (dtap-ipv-hb-hib) je indicirano za osnovno in obnovitveno cepljenje dojenčkov in malčkov iz šestih tednih starosti proti davici, tetanus, oslovski kašelj, hepatitis b, otroški ohromelosti in invazivnih bolezni, ki povzroča haemophilus influenzae tipa b (hib). uporaba tega cepiva mora biti v skladu z uradnimi priporočili.