FLUARIX TETRA süstesuspensioon süstlis Eesti - eesti - Ravimiamet

fluarix tetra süstesuspensioon süstlis

glaxosmithkline biologicals - gripiviirus, inaktiveeritud, tükeldatud viirus või pinnaantigeen - süstesuspensioon süstlis - 1annus 0.5ml 0.5ml 10tk; 1annus 0.5ml 0.5ml 1tk

VITAMIN C SOPHARMA süste-/infusioonilahus Eesti - eesti - Ravimiamet

vitamin c sopharma süste-/infusioonilahus

sopharma ad - askorbiinhape - süste-/infusioonilahus - 100mg 1ml 2ml 10tk; 100mg 1ml 5ml 10tk

Spikevax (previously COVID-19 Vaccine Moderna) Euroopa Liit - eesti - EMA (European Medicines Agency)

spikevax (previously covid-19 vaccine moderna)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) 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 - vaktsiinid - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

Vaxneuvance Euroopa Liit - eesti - EMA (European Medicines Agency)

vaxneuvance

merck sharp & dohme b.v.  - pneumococcal polysaccharide conjugate vaccine (adsorbed) - pneumokoki infektsioonid - pneumococcus, purified polysaccharides antigen conjugated - vaxneuvance is indicated for active immunisation for the prevention of invasive disease, pneumonia and acute otitis media caused by streptococcus pneumoniae in infants, children and adolescents from 6 weeks to less than 18 years of age. vaxneuvance is indicated for active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. vt lõigud 4. 4 ja 5. 1, mis käsitleb kaitset spetsiifiliste pneumokokkide serotüüpide eest. the use of vaxneuvance should be in accordance with official recommendations.

Tezspire Euroopa Liit - eesti - EMA (European Medicines Agency)

tezspire

astrazeneca ab - tezepelumab - astma - ravimid hingamisteede obstruktiivsete haiguste, - tezspire is indicated as an add-on maintenance treatment in adults and adolescents 12 years and older with severe asthma who are inadequately controlled despite high dose inhaled corticosteroids plus another medicinal product for maintenance treatment.

MAGROMAG toimeainet modifitseeritult vabastav kõvakapsel Eesti - eesti - Ravimiamet

magromag toimeainet modifitseeritult vabastav kõvakapsel

olainfarm as - nitrofurantoiin - toimeainet modifitseeritult vabastav kõvakapsel - 100mg 14tk

Arexvy Euroopa Liit - eesti - EMA (European Medicines Agency)

arexvy

glaxosmithkline biologicals s.a.  - respiratory syncytial virus recombinant glycoprotein f stabilised in the pre-fusion conformation (rsvpref3) produced in chinese hamster ovary (cho) cells by recombinant dna technology - respiratoorsed süntsüütilised viirusinfektsioonid - vaktsiinid - arexvy is indicated for active immunisation for the prevention of lower respiratory tract disease (lrtd) caused by respiratory syncytial virus in adults 60 years of age and older. kasutamist see vaktsiin peaks olema kooskõlas ametlike soovitustega.

Vanflyta Euroopa Liit - eesti - EMA (European Medicines Agency)

vanflyta

daiichi sankyo europe gmbh - quizartinib dihydrochloride - leukeemia, müeloid - antineoplastic agents, protein kinase inhibitors - vanflyta is indicated in combination with standard cytarabine and anthracycline induction and standard cytarabine consolidation chemotherapy, followed by vanflyta single-agent maintenance therapy for adult patients with newly diagnosed acute myeloid leukaemia (aml) that is flt3-itd positive.

Enrylaze Euroopa Liit - eesti - EMA (European Medicines Agency)

enrylaze

jazz pharmaceuticals ireland limited - crisantaspase - prekursorko-lümfoblastne leukeemia-lümfoom - antineoplastilised ained - enrylaze is indicated as a component of a multi-agent chemotherapeutic regimen for the treatment of acute lymphoblastic leukaemia (all) and lymphoblastic lymphoma (lbl) in adult and paediatric patients (1 month and older) who developed hypersensitivity or silent inactivation to e. coli-derived asparaginase.

Cubicin Euroopa Liit - eesti - EMA (European Medicines Agency)

cubicin

merck sharp & dohme b.v. - daptomütsiin - gram-positive bacterial infections; bacteremia; soft tissue infections; endocarditis, bacterial - antibacterials süsteemseks kasutamiseks, - cubicin on näidustatud järgmiste infektsioonide raviks. täiskasvanute ja laste (1-kuni 17-aastased) patsiendid, kellel on keerulised naha ja pehmete kudede infektsioonid (cssti). täiskasvanud patsientidel, kellel on õigus külgedega nakkuslik endokardiit (rie) tänu staphylococcus aureus. on soovitatav, et otsus kasutada daptomycin tuleks arvesse võtta antibakteriaalsete vastuvõtlikkus organismi ja peaks olema aluseks asjatundja nõu. täiskasvanute ja laste (1-kuni 17-aastased) patsiendid, kellel on staphylococcus aureus ' e bacteraemia (sab). täiskasvanutel kasutamiseks bacteraemia peaks olema seotud rie või cssti, kuigi pediaatrilised patsiendid kasutada bacteraemia peaks olema seotud cssti. daptomycin on aktiivne vastu gram-positiivsed bakterid ainult. kombineeritud infektsioonid, kus gram negatiivsed ja/või teatavate anaeroobsete bakterite kahtlustatakse, cubicin peaks olema, co-manustada koos asjakohaste antibakteriaalne agent(s). tuleks arvesse võtta ametlikke juhiseid sobiva kasutada antibakteriaalseid aineid.