Linatera 0,02 mg/3 mg filmsko obložene tablete স্লোভানিয়া - স্লোভেনীয় - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

linatera 0,02 mg/3 mg filmsko obložene tablete

bayer d.o.o. - drospirenon; etinilestradiol - filmsko obložena tableta - drospirenon 3 mg / 1 tableta  etinilestradiol0,02 mg / 1 tableta; etinilestradiol 0,02 mg / 1 tableta - drospirenon in etinilestradiol

Yasminelle 0,02 mg/3 mg filmsko obložene tablete স্লোভানিয়া - স্লোভেনীয় - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

yasminelle 0,02 mg/3 mg filmsko obložene tablete

bayer d.o.o. - drospirenon; etinilestradiol - filmsko obložena tableta - drospirenon 3 mg / 1 tableta  etinilestradiol0,02 mg / 1 tableta; etinilestradiol 0,02 mg / 1 tableta - drospirenon in etinilestradiol

YAZ 0,02 mg/3 mg filmsko obložene tablete স্লোভানিয়া - স্লোভেনীয় - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

yaz 0,02 mg/3 mg filmsko obložene tablete

bayer d.o.o. - drospirenon; etinilestradiol - filmsko obložena tableta - drospirenon 3 mg / 1 tableta  etinilestradiol0,02 mg / 1 tableta; etinilestradiol 0,02 mg / 1 tableta - drospirenon in etinilestradiol

Veklury ইউরোপীয় ইউনিয়ন - স্লোভেনীয় - EMA (European Medicines Agency)

veklury

gilead sciences ireland uc - remdesivir - covid-19 virus infection - veklury is indicated for the treatment of coronavirus disease 2019 (covid 19) in:adults and paediatric patients (at least 4 weeks of age and weighing at least 3 kg) with pneumonia requiring supplemental oxygen (low- or high-flow oxygen or other non-invasive ventilation at start of treatment)adults and paediatric patients (weighing at least 40 kg) who do not require supplemental oxygen and who are at increased risk of progressing to severe covid-19.

Mavenclad ইউরোপীয় ইউনিয়ন - স্লোভেনীয় - EMA (European Medicines Agency)

mavenclad

merck europe b.v. - cladribine - multiple skleroza - imunosupresivi - zdravljenje odraslih bolnikov z zelo aktivno ponavljajočo multiplo sklerozo (ms), opredeljeni v kliničnih ali slikanje funkcije.

Extavia ইউরোপীয় ইউনিয়ন - স্লোভেনীয় - EMA (European Medicines Agency)

extavia

novartis europharm limited - interferon beta-1b - multiple skleroza - immunostimulants, - extavia je primerna za zdravljenje:pri bolnikih z eno demielinizirajoče dogodek z aktivno vnetni proces, če je dovolj resen, da bi lahko jamčili zdravljenje z intravensko kortikosteroidi, če alternativne diagnoze so bile izključene, če so odločeni, da se na visoko tveganje za razvoj klinično dokončne multiple sclerosis;pri bolnikih z recidivno-nakazila multiplo sklerozo in dva ali več zagonov v zadnjih dveh letih;pri bolnikih s sekundarno progresivno multiplo sklerozo, ki imajo aktivno bolezen, dokazuje zagonov.

MenQuadfi ইউরোপীয় ইউনিয়ন - স্লোভেনীয় - EMA (European Medicines Agency)

menquadfi

sanofi pasteur - neisseria meningitidis group c polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group a polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group y polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group w-135 polysaccharide conjugated to tetanus toxoid - meningitis, meningokokni - cepiva - menquadfi is indicated for active immunisation of individuals from the age of 12 months and older against invasive meningococcal disease caused by neisseria meningitidis serogroups a, c, w, and y. the use of this vaccine should be in accordance with available official recommendations.