ACTIKERALL nahalahus Estland - estniska - Ravimiamet

actikerall nahalahus

almirall hermal gmbh - fluorouratsiil+salitsüülhape - nahalahus - 5mg+100mg 1g 25ml 1tk

TRAMADOL LANNACHER 200 MG toimeainet prolongeeritult vabastav tablett Estland - estniska - Ravimiamet

tramadol lannacher 200 mg toimeainet prolongeeritult vabastav tablett

g.l. pharma gmbh - tramadool - toimeainet prolongeeritult vabastav tablett - 200mg 30tk

Foresto ravimkaelarihm Estland - estniska - Ravimiamet

foresto ravimkaelarihm

bayer animal health gmbh - flumetriin+imidaklopriid - ravimkaelarihm - 2,03g+4,5g 45g 45g 2tk; 2,03g+4,5g 45g 45g 12tk

Foresto ravimkaelarihm Estland - estniska - Ravimiamet

foresto ravimkaelarihm

bayer animal health gmbh - flumetriin+imidaklopriid - ravimkaelarihm - 45mg+100mg 1g 12.5g 1tk

Comirnaty Europeiska unionen - estniska - 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 - 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.

MicardisPlus Europeiska unionen - estniska - EMA (European Medicines Agency)

micardisplus

boehringer ingelheim international gmbh - telmisartan, hydrochlorothiazide - hüpertensioon - reniini-angiotensiini süsteemi toimivad ained - essentsiaalse hüpertensiooni ravi. micardisplus fikseeritud annuse kombinatsioon (40 mg telmisartan / 12. 5 mg hydrochlorothiazide, 80 mg telmisartan / 12. 5 mg hydrochlorothiazide) on näidustatud patsientidele, kelle vererõhk ei ole adekvaatselt kontrollitav kohta telmisartan üksi. micardisplus fikseeritud annuse kombinatsioon (80 mg telmisartan / 25 mg hydrochlorothiazide) on näidustatud patsientidele, kelle vererõhk ei ole adekvaatselt kontrollitav kohta micardisplus (80 mg telmisartan / 12. 5 mg hydrochlorothiazide) või patsientidel, kes on eelnevalt stabiliseeritud kohta telmisartan ja hydrochlorothiazide antud eraldi.

VarroMed Europeiska unionen - estniska - EMA (European Medicines Agency)

varromed

beevital gmbh - oksaalhape dihüdraat, sipelghape - nahaparasiidi paikseks kasutamiseks, sh. insektitsiidid - mesilased - varrooosi (varroa destructor) ravi mesilastekolooniatega koos poorega või ilma.

Privigen Europeiska unionen - estniska - EMA (European Medicines Agency)

privigen

csl behring gmbh - inimese normaalne immunoglobuliin (ivig) - purpura, thrombocytopenic, idiopathic; bone marrow transplantation; immunologic deficiency syndromes; guillain-barre syndrome; mucocutaneous lymph node syndrome - suguhormoonid ja immunoglobuliinid, - asendamine ravi täiskasvanutel, lastel ja noorukitel (0-18 aastat): primaarsed immuunpuudulikkuse (pid) sündroomid häirega antikehade tootmist;hypogammaglobulinaemia ja korduvate bakteriaalsete nakkuste raviks patsientidel, kellel on krooniline lümfoidne leukeemia, kellest profülaktika antibiootikumidega on ebaõnnestunud;hypogammaglobulinaemia ja korduvate bakteriaalsete infektsioonide platoo-etapp-mitu-myeloma patsientidel, kes on allunud pneumokoki vaktsineerimist;hypogammaglobulinaemia patsientidel pärast allogeensete vereloome-tüvirakkude siirdamine (hsct);kaasasündinud aids korduvate bakteriaalsete infektsioonide. immunomodulation täiskasvanutel, lastel ja noorukitel (0-18 aastat): esmane trombotsütopeenia immuunsüsteemi (itp) patsientidel on suur risk verejooksu või enne operatsiooni, et parandada trombotsüütide arv;guillain-barré sündroom;kawasaki haigus;krooniline põletikuline demüeliniseerivate polüneuropaatia (cidp). ainult piiratud kogemused on saadaval kasutamise intravenoosse immunoglobuliinid lastel cidp.

PROPOFOL FRESENIUS 10 MG/ML süste-/infusiooniemulsioon Estland - estniska - Ravimiamet

propofol fresenius 10 mg/ml süste-/infusiooniemulsioon

fresenius kabi deutschland gmbh - propofool - süste-/infusiooniemulsioon - 10mg 1ml 100ml 1tk; 10mg 1ml 50ml 10tk; 10mg 1ml 50ml 1tk; 10mg 1ml 20ml 5tk; 10mg 1ml 20ml 10tk; 10mg 1ml 100ml 10tk

PROPOVEN 1% süste-/infusiooniemulsioon Estland - estniska - Ravimiamet

propoven 1% süste-/infusiooniemulsioon

fresenius kabi deutschland gmbh - propofool - süste-/infusiooniemulsioon - 10mg 1ml 20ml 10tk; 10mg 1ml 50ml 1tk; 10mg 1ml 20ml 5tk