SOLIDON kaetud tablett Eesti - eesti - Ravimiamet

solidon kaetud tablett

adelco - chromatourgia athinon e.colocotronis bros s.a. - kloorpromasiin - kaetud tablett - 100mg 50tk

DELCO SPRAY Eesti - eesti - Ecolab

delco spray

ecolab deutschland gmbh -

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.

VidPrevtyn Beta Euroopa Liit - eesti - EMA (European Medicines Agency)

vidprevtyn beta

sanofi pasteur - sars-cov-2 prefusion spike delta tm protein, recombinant (b.1.351 strain) - covid-19 virus infection - vaktsiinid - vidprevtyn beta is indicated as a booster for active immunisation to prevent covid-19 in adults who have previously received an mrna or adenoviral vector covid-19 vaccine (see sections 4. 2 ja 5. 1 in product information document). kasutamist see vaktsiin peaks olema kooskõlas ametlike soovitustega.

Nobilis RT+IBmulti+ND+EDS süsteemulsioon Eesti - eesti - Ravimiamet

nobilis rt+ibmulti+nd+eds süsteemulsioon

intervet international b.v. - newcastle'i tõve viirus-/paramüksoviirusvaktsiin+lindude nakkava bronhiidi viirusvaktsiin+lindude adenoviirusvaktsiin+lindude rinotrahheiidi viirusvaktsiin - süsteemulsioon - 1annus 500annus 1tk

Jcovden (previously COVID-19 Vaccine Janssen) Euroopa Liit - eesti - EMA (European Medicines Agency)

jcovden (previously covid-19 vaccine janssen)

janssen-cilag international nv - adenovirus type 26 encoding the sars-cov-2 spike glycoprotein (ad26.cov2-s) - covid-19 virus infection - vaktsiinid - jcovden is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 18 years of age and older. kasutamist see vaktsiin peaks olema kooskõlas ametlike soovitustega.

COVID-19 Vaccine (inactivated, adjuvanted) Valneva Euroopa Liit - eesti - EMA (European Medicines Agency)

covid-19 vaccine (inactivated, adjuvanted) valneva

valneva austria gmbh - covid-19 vaccine (inactivated, adjuvanted, adsorbed) - covid-19 virus infection - vaktsiinid - covid-19 vaccine (inactivated, adjuvanted) valneva is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 18 to 50 years of age.  the use of this vaccine should be in accordance with official recommendations.

Ornivac ND+IB2+EDS süsteemulsioon Eesti - eesti - Ravimiamet

ornivac nd+ib2+eds süsteemulsioon

bioveta a.s. - newcastle'i tõve viirus-/paramüksoviirusvaktsiin+lindude nakkava bronhiidi viirusvaktsiin+lindude adenoviirusvaktsiin - süsteemulsioon - 0,5ml+0,5ml+0,5ml 1annus 250ml 1tk; 0,5ml+0,5ml+0,5ml 1annus 250ml 10tk

Nobilis IB+ND+EDS süsteemulsioon Eesti - eesti - Ravimiamet

nobilis ib+nd+eds süsteemulsioon

intervet international b.v. - newcastle'i tõve viirus-/paramüksoviirusvaktsiin+lindude nakkava bronhiidi viirusvaktsiin+lindude adenoviirusvaktsiin - süsteemulsioon - 1annus+1annus+1annus 0.5ml 500ml 1tk

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

zinbryta

biogen idec ltd - daklüsumab - hulgiskleroos - immunosupressandid - zinbryta on näidustatud täiskasvanud patsientidel hulgiskleroosi retsidiivsete vormide (rms).