Eesti - eesti - Ravimiamet

krka d.d. novo mesto - kvetiapiin - õhukese polümeerikattega tablett - 300mg 10tk; 300mg 240tk; 300mg 120tk; 300mg 90tk; 300mg 60tk; 300mg 180tk; 300mg 50tk; 300mg 100tk

Eesti - eesti - Ravimiamet

krka d.d. novo mesto - kvetiapiin - õhukese polümeerikattega tablett - 100mg 250tk; 100mg 100tk; 100mg 50tk; 100mg 10tk; 100mg 30tk; 100mg 60tk; 100mg 20tk

Eesti - eesti - Ravimiamet

krka d.d. novo mesto - kvetiapiin - õhukese polümeerikattega tablett - 25mg 60tk; 25mg 30tk; 25mg 100tk; 25mg 10tk; 25mg 6tk; 25mg 20tk

Eesti - eesti - Ravimiamet

krka d.d. novo mesto - kvetiapiin - õhukese polümeerikattega tablett - 200mg 30tk; 200mg 100tk; 200mg 90tk; 200mg 20tk; 200mg 60tk; 200mg 98tk; 200mg 10tk; 200mg 250tk

Euroopa Liit - eesti - EMA (European Medicines Agency)

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 - vaktsiinid - 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. kasutamist see vaktsiin peaks olema kooskõlas ametlike soovitustega.

Euroopa Liit - eesti - EMA (European Medicines Agency)

janssen-cilag international n.v.   - paliperidoonpalmitaat - skisofreenia - psühhoeptikumid - byannli (previously paliperidone janssen-cilag international) a 6 monthly injection, is indicated for the maintenance treatment of schizophrenia in adult patients who are clinically stable on 1 monthly or 3 monthly paliperidone palmitate injectable products (see section 5.

Euroopa Liit - eesti - EMA (European Medicines Agency)

novartis europharm ltd. - aliskireen - hüpertensioon - reniini-angiotensiini süsteemi toimivad ained - essentsiaalse hüpertensiooni ravi.

Euroopa Liit - eesti - EMA (European Medicines Agency)

cis bio international - ioflupaan (123l) - radionuclide imaging; dementia; movement disorders - diagnostilised radiofarmatseutilised ühendid - see ravim on mõeldud ainult diagnostiliseks kasutamiseks. striascan on näidustatud avastada kaotus funktsionaalne dopaminergic neuron terminalide striatum:täiskasvanud patsientidel, kellel on kliiniliselt ebakindel parkinsonian sündroomid, näiteks need, kellel on varajased sümptomid, et aidata eristada oluline värin alates parkinsonian sündroomid, mis on seotud idiopaatiline parkinsoni tõbi, sclerosis süsteemi atroofia ja progressiivne supranuclear halvatus. striascan ei suuda teha vahet parkinsoni tõbi, sclerosis süsteemi atroofia ja progressiivne supranuclear halvatus. täiskasvanud patsientidel, et aidata eristada arvatav dementsus koos lewy kehad alzheimeri tõbi. striascan ei suuda teha vahet dementsus koos lewy kehad ja parkinsoni tõbi, dementsus.

Eesti - eesti - Ravimiamet

laboratorios liconsa s.a. - losartaan - õhukese polümeerikattega tablett - 50mg 10tk; 50mg 7tk; 50mg 21tk; 50mg 105tk; 50mg 210tk

Eesti - eesti - Ravimiamet

laboratorios liconsa s.a. - losartaan - õhukese polümeerikattega tablett - 12,5mg 7tk; 12,5mg 105tk; 12,5mg 21tk; 12,5mg 100tk; 12,5mg 112tk; 12,5mg 14tk; 12,5mg 110tk; 12,5mg 280tk