Eesti - eesti - Ravimiamet

agfa healthcare imaging agents gmbh - gadoteerhape - süstelahus - 279,32mg 1ml 5ml 1tk; 279,32mg 1ml 10ml 10tk; 279,32mg 1ml 60ml 10tk; 279,32mg 1ml 15ml 1tk; 279,32mg 1ml 20ml 10tk; 279,32mg 1ml 60ml 1tk

Eesti - eesti - Ravimiamet

bioveta a.s. - pöögitõrv - nahasprei, lahus - 200mg 1g 80g 1tk

Eesti - eesti - Ravimiamet

mundipharma ges.m.b.h. - buprenorfiin - transdermaalne plaaster - 20mcg 1h 5tk; 20mcg 1h 4tk; 20mcg 1h 12tk; 20mcg 1h 2tk; 20mcg 1h 3tk; 20mcg 1h 1tk

Eesti - eesti - Ravimiamet

mundipharma ges.m.b.h. - buprenorfiin - transdermaalne plaaster - 10mcg 1h 8tk; 10mcg 1h 12tk; 10mcg 1h 4tk; 10mcg 1h 10tk; 10mcg 1h 1tk; 10mcg 1h 2tk; 10mcg 1h 5tk

Eesti - eesti - Ravimiamet

mundipharma ges.m.b.h. - buprenorfiin - transdermaalne plaaster - 5mcg 1h 3tk; 5mcg 1h 8tk; 5mcg 1h 10tk; 5mcg 1h 1tk; 5mcg 1h 4tk; 5mcg 1h 5tk; 5mcg 1h 12tk

Euroopa Liit - eesti - EMA (European Medicines Agency)

pfizer europe ma eeig - tofacitinib - artriit, reumatoidartriit - immunosupressandid - rheumatoid arthritistofacitinib in combination with methotrexate (mtx) is indicated for the treatment of moderate to severe active rheumatoid arthritis (ra) in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying antirheumatic drugs (dmards) (see section 5. tofacitinib can be given as monotherapy in case of intolerance to mtx or when treatment with mtx is inappropriate (see sections 4. 4 ja 4. psoriatic arthritistofacitinib in combination with mtx is indicated for the treatment of active psoriatic arthritis (psa) in adult patients who have had an inadequate response or who have been intolerant to a prior disease modifying antirheumatic drug (dmard) therapy (see section 5. ulcerative colitistofacitinib is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (uc) who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent (see section 5. tofacitinib is indicated for the treatment of active polyarticular juvenile idiopathic arthritis (rheumatoid factor positive [rf+] or negative [rf-] polyarthritis and extended oligoarthritis), and juvenile psoriatic arthritis (psa) in patients 2 years of age and older, who have responded inadequately to previous therapy with disease modifying antirheumatic drugs (dmards). tofacitinib can be given in combination with methotrexate (mtx) or as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. ankylosing spondylitistofacitinib is indicated for the treatment of adult patients with active ankylosing spondylitis (as) who have responded inadequately to conventional therapy.

Euroopa Liit - eesti - EMA (European Medicines Agency)

pfizer limited - tofacitinib - artriit, reumatoidartriit - immunosupressandid - reumatoidartriidi ravis.

Euroopa Liit - eesti - EMA (European Medicines Agency)

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - dermatiidi ained, välja arvatud kortikosteroidid - atopic dermatitisadults and adolescentsdupixent is indicated for the treatment of moderate-to-severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. children 6 months to 11 years of agedupixent is indicated for the treatment of severe atopic dermatitis in children 6 months to 11 years old who are candidates for systemic therapy. asthmaadults and adolescentsdupixent is indicated in adults and adolescents 12 years and older as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), see section 5. 1, who are inadequately controlled with high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. children 6 to 11 years of agedupixent is indicated in children 6 to 11 years old as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), who are inadequately controlled with medium to high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. chronic rhinosinusitis with nasal polyposis (crswnp)dupixent is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adults with severe crswnp for whom therapy with systemic corticosteroids and/or surgery do not provide adequate disease control. prurigo nodularis (pn)dupixent is indicated for the treatment of adults with moderate-to-severe prurigo nodularis (pn) who are candidates for systemic therapy. eosinophilic esophagitis (eoe)dupixent is indicated for the treatment of eosinophilic esophagitis in adults and adolescents 12 years and older, weighing at least 40 kg, who are inadequately controlled by, are intolerant to, or who are not candidates for conventional medicinal therapy.

Euroopa Liit - eesti - EMA (European Medicines Agency)

ferrer internacional s.a. - loksapiin - schizophrenia; bipolar disorder - närvisüsteem - adasuve on näidustatud kiire kontrolli kerge kuni mõõduka agitatsioon täiskasvanud patsientidel skisofreenia või bipolaarne häire. patsiendid peavad saama regulaarse ravi kohe pärast ägeda agitatsiooni sümptomite kontrollimist.

Euroopa Liit - eesti - EMA (European Medicines Agency)

orphelia pharma sas - vigabatrin - spasms, infantile; epilepsies, partial - antiepileptics, - kigabeq on märgitud imikutel ja lastel alates 1 kuu vähem kui 7 aastased:ravi monotherapy infantiilse spasmid (lääne-sündroom). ravi kombinatsioonis teiste antiepileptilised ravimid patsientidel, kellel on vastupidav osaline epilepsia (fookuskaugus algusega krambid) koos või ilma sekundaarse teha üldistusi, et on koht, kus kõik muu sobiva ravimi kombinatsiooni on osutunud ebapiisavaks või ei ole talutav.