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

improvac

zoetis belgium sa - synthetic peptide analogue of gnrf conjugated to diptheria toxoid - sigalaste immunoloogilised omadused - male pigs (from 8 weeks of age); female pigs (from 14 weeks of age) - male pigs:induction of antibodies against gnrf to produce a temporary immunological suppression of testicular function. for use as an alternative to physical castration for the reduction of boar taint caused by the key boar taint compound androstenone, in entire male pigs following the onset of puberty. kahjuritõrjemeetodi, vitoolooli teise olulise osakaalu võib ka vähendada kui kaudset mõju. samuti vähenevad agressiivsed ja seksuaalsed (paigaldus) käitumised. female pigs:induction of antibodies against gnrf to produce a temporary immunological suppression of ovarian function (suppression of oestrus) in order to reduce the incidence of unwanted pregnancies in gilts intended for slaughter, and to reduce the associated sexual behaviour (standing oestrus).

Atectura Breezhaler Euroopa Liit - eesti - EMA (European Medicines Agency)

atectura breezhaler

novartis europharm limited  - indacaterol acetate, mometasone furoate - astma - ravimid hingamisteede obstruktiivsete haiguste, - atectura breezhaler is indicated as a maintenance treatment of asthma in adults and adolescents 12 years of age and older not adequately controlled with inhaled corticosteroids and inhaled short acting beta2-agonists.

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

olumiant

eli lilly nederland b.v. - baricitinib - artriit, reumatoidartriit - immunosupressandid - rheumatoid arthritisbaricitinib is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease modifying anti rheumatic drugs (dmards). olumiant võib kasutada monoteraapiana või kombinatsioonis metotreksaadiga. atopic dermatitisolumiant is indicated for the treatment of moderate to severe atopic dermatitis in adult and paediatric patients 2 years of age and older who are candidates for systemic therapy. alopecia areatabaricitinib is indicated for the treatment of severe alopecia areata in adult patients (see section 5. juvenile idiopathic arthritisbaricitinib is indicated for the treatment of active juvenile idiopathic arthritis in patients 2 years of age and older who have had an inadequate response or intolerance to one or more prior conventional synthetic or biologic dmards:- polyarticular juvenile idiopathic arthritis (polyarticular rheumatoid factor positive [rf+] or negative [rf-], extended oligoarticular),- enthesitis related arthritis, and- juvenile psoriatic arthritis. baricitinib may be used as monotherapy or in combination with methotrexate.

Enerzair Breezhaler Euroopa Liit - eesti - EMA (European Medicines Agency)

enerzair breezhaler

novartis europharm limited - indacaterol, glycopyrronium bromide, mometasone - astma - ravimid hingamisteede obstruktiivsete haiguste, - enerzair breezhaler is indicated as a maintenance treatment of asthma in adult patients not adequately controlled with a maintenance combination of a long acting beta2 agonist and a high dose of an inhaled corticosteroid who experienced one or more asthma exacerbations in the previous year.

Bemrist Breezhaler Euroopa Liit - eesti - EMA (European Medicines Agency)

bemrist breezhaler

novartis europharm limited  - indacaterol, mometasone furoate - astma - ravimid hingamisteede obstruktiivsete haiguste, - bemrist breezhaler is indicated as a maintenance   treatment of asthma in adults and adolescents 12 years of age and older not adequately controlled with inhaled corticosteroids and inhaled short acting beta2-agonists.

Zimbus Breezhaler Euroopa Liit - eesti - EMA (European Medicines Agency)

zimbus breezhaler

novartis europharm limited - glycopyrronium bromide, indacaterol (acetate), mometasone furoate - astma - ravimid hingamisteede obstruktiivsete haiguste, - maintenance treatment of asthma in adults whose disease is not adequately controlled.

NOREPINEPHRINE SINTETICA infusioonilahuse kontsentraat Eesti - eesti - Ravimiamet

norepinephrine sintetica infusioonilahuse kontsentraat

sintetica gmbh - norepinefriin (noradrenaliin) - infusioonilahuse kontsentraat - 1mg 1ml 1ml 10tk; 1mg 1ml 5ml 10tk; 1mg 1ml 10ml 10tk

BACLOFEN SINTETICA infusioonilahus Eesti - eesti - Ravimiamet

baclofen sintetica infusioonilahus

sintetica gmbh - baklofeen - infusioonilahus - 2mg 1ml 5ml 1tk; 2mg 1ml 20ml 1tk; 2mg 1ml 5ml 5tk

NOREPINEPHRINE SINTETICA infusioonilahus Eesti - eesti - Ravimiamet

norepinephrine sintetica infusioonilahus

sintetica gmbh - norepinefriin (noradrenaliin) - infusioonilahus - 0,1mg 1ml 50ml 1tk

BACLOFEN SINTETICA süstelahus Eesti - eesti - Ravimiamet

baclofen sintetica süstelahus

sintetica gmbh - baklofeen - süstelahus - 0,05mg 1ml 1ml 5tk