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

regkirona

celltrion healthcare hungary kft. - regdanvimab - covid-19 virus infection - suguhormoonid ja immunoglobuliinid, - regdanvimab is indicated for the treatment of adults with coronavirus disease 2019 (covid-19) who do not require supplemental oxygen and who are at increased risk of progressing to severe covid-19.

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

evusheld

astrazeneca ab - tixagevimab, cilgavimab - covid-19 virus infection - prevention of covid-19.

Toxicol vet. süstesuspensioon Eesti - eesti - Ravimiamet

toxicol vet. süstesuspensioon

zoetis belgium - escherichia coli+clostridium - süstesuspensioon - 10annus 1tk; 20annus 1tk

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

xevudy

glaxosmithkline trading services limited - sotrovimab - covid-19 virus infection - suguhormoonid ja immunoglobuliinid, - xevudy is indicated for the treatment of adults and adolescents (aged 12 years and over and weighing at least 40 kg) with coronavirus disease 2019 (covid-19) who do not require oxygen supplementation and who are at increased risk of progressing to severe covid-19.

FLUDARABINE ACCORD 25 MG/ML süste-/infusioonilahuse kontsentraat Eesti - eesti - Ravimiamet

fludarabine accord 25 mg/ml süste-/infusioonilahuse kontsentraat

accord healthcare b.v. - fludarabiin - süste-/infusioonilahuse kontsentraat - 25mg 1ml 2ml 1tk; 25mg 1ml 2ml 10tk

FLUDARABINE EBEWE" 25MG/ML" süste-/infusioonilahuse kontsentraat Eesti - eesti - Ravimiamet

fludarabine ebewe" 25mg/ml" süste-/infusioonilahuse kontsentraat

sandoz pharmaceuticals d.d. - fludarabiin - süste-/infusioonilahuse kontsentraat - 25mg 1ml 2ml 1tk; 25mg 1ml 2ml 5tk; 25mg 1ml 2ml 10tk

FLUDARABINE ACTAVIS süste-/infusioonilahuse kontsentraat Eesti - eesti - Ravimiamet

fludarabine actavis süste-/infusioonilahuse kontsentraat

actavis group ptc ehf. - fludarabiin - süste-/infusioonilahuse kontsentraat - 25mg 1ml 2ml 5tk

Veklury Euroopa Liit - eesti - 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.

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

nuvaxovid

novavax cz, a.s. - sars cov-2 (original) recombinant spike protein, sars-cov-2 (omicron xbb.1.5) recombinant spike protein - covid-19 virus infection - covid-19 vaccines - nuvaxovid is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 12 years of age and older. kasutamist see vaktsiin peaks olema kooskõlas ametlike soovitustega. nuvaxovid xbb. 5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 12 years of age and older. kasutamist see vaktsiin peaks olema kooskõlas ametlike soovitustega.

Cegfila (previously Pegfilgrastim Mundipharma) Euroopa Liit - eesti - EMA (European Medicines Agency)

cegfila (previously pegfilgrastim mundipharma)

mundipharma corporation (ireland) limited - pegfilgrastim - neutropeenia - immunostimulants, - neutropeenia ja febriilse neutropeenia esinemissageduse vähendamine ravitud tsütotoksilise kemoteraapia pahaloomulise kasvaja (välja arvatud krooniline müeloidne leukeemia ja müelodüsplastilised sündroomid).