Lartruvo Európska únia - slovenčina - EMA (European Medicines Agency)

lartruvo

eli lilly nederland b.v. - olaratumab - sarkóm - antineoplastické činidlá - lartruvo je indikovaný v kombinácii s doxorubicínom na liečbu dospelých pacientov s pokročilým sarkómom mäkkého tkaniva, ktorí nie sú ochotná rcinóm operácii alebo rádioterapii a ktorí neboli predtým liečení s doxorubicínom (pozri oddiel 5.

Novalgin 500 mg/ml Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

novalgin 500 mg/ml

opella healthcare slovakia s.r.o., slovensko - metamizol, sodná soľ - 07 - analgetica, antipyretica

Novalgin 500 mg Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

novalgin 500 mg

opella healthcare slovakia s.r.o., slovensko - metamizol, sodná soľ - 07 - analgetica, antipyretica

Comirnaty Európska únia - slovenčina - EMA (European Medicines Agency)

comirnaty

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - vakcíny - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. použitie tejto vakcíny by mali byť v súlade s oficiálne odporúčania.

Litfulo Európska únia - slovenčina - EMA (European Medicines Agency)

litfulo

pfizer europe ma eeig - ritlecitinib tosilate - alopecia areata - imunosupresíva - litfulo is indicated for the treatment of severe alopecia areata in adults and adolescents 12 years of age and older.

Ibaflin Európska únia - slovenčina - EMA (European Medicines Agency)

ibaflin

intervet international bv - ibafloxacín - antibakteriálne látky na systémové použitie - dogs; cats - psy:ibaflin je indikovaný na liečbu nasledujúcich podmienok v psov:kožné infekcie (pyoderma - povrchné a hlboké, rany, abscesy) spôsobené citlivé kmene staphylococci, escherichia coli a proteus mirabilis;akútna, nekomplikované infekcie močových-traktu, infekcie, spôsobené citlivé kmene staphylococci, proteus druhov, projekt spp. , e. coli a klebsiella spp. ;dýchacích ciest-ciest (infekcie horných ciest) spôsobené citlivé kmene staphylococci, e. coli a klebsiella spp. ibaflin gél je uvedené v psov na liečbu nasledujúcich podmienok:kožné infekcie (pyoderma - povrchné a hlboké, rany, abscesy) spôsobené náchylné patogénov ako je staphylococcus spp. , e. coli a p. mirabilis. mačky:ibaflin gél je uvedené v mačky na liečbu nasledujúcich podmienok:kožné infekcie (soft-tissue infekcie - rany, abscesy) spôsobené náchylné patogénov ako je staphylococcus spp. , e. coli, proteus spp. a pasteurella spp. ;horných dýchacích ciest-traktu, infekcie spôsobené náchylné patogénov ako je staphylococcus spp. , e. coli, klebsiella spp. a pasteurella spp.

Nobilis OR Inac Európska únia - slovenčina - EMA (European Medicines Agency)

nobilis or inac

intervet international bv - inaktivovaná celobunková suspenzia sérotypu a ornithobacterium rhinotracheale, kmeň b3263 / 91 - imunologická liečba - kura - na pasívnu imunizáciu brojlerov vyvolanú aktívnou imunizáciou chovných brojlerov chovaných na zníženie infekcie sérotypom ornithobacterium rhinotracheale, keď je tento činiteľ zahrnutý. v poľných podmienkach pasívna imunita je prevedené počas ležal na 43 týždňov po poslednom očkovaní brojlerov chovateľov, čo v trvaní pasívnu imunitu v brojlery najmenej 14 dní po vyliahnutí.

Pruban Európska únia - slovenčina - EMA (European Medicines Agency)

pruban

intervet international bv - resokortol butyrát - kortikosteroidy, dermatologické prípravky - psy - liečba akútnej lokalizovanej vlhkej dermatitídy.