Dinolytic süstelahus Eesti - eesti - Ravimiamet

dinolytic süstelahus

zoetis belgium - dinoprost - süstelahus - 12,5mg 1ml 100ml 1tk; 12,5mg 1ml 10ml 1tk

Enzaprost Bovis süstelahus Eesti - eesti - Ravimiamet

enzaprost bovis süstelahus

ceva sante animale - dinoprost - süstelahus - 12,5mg 1ml 2ml 10tk; 12,5mg 1ml 2ml 1tk; 12,5mg 1ml 50ml 1tk; 12,5mg 1ml 10ml 1tk; 12,5mg 1ml 20ml 1tk; 12,5mg 1ml 100ml 1tk

Enzaprost süstelahus Eesti - eesti - Ravimiamet

enzaprost süstelahus

ceva sante animale - dinoprost - süstelahus - 5mg 1ml 30ml 1tk; 5mg 1ml 50ml 1tk; 5mg 1ml 5ml 10tk; 5mg 1ml 10ml 5tk

Dinolytic süstelahus Eesti - eesti - Ravimiamet

dinolytic süstelahus

zoetis belgium - dinoprost - süstelahus - 5mg 1ml 10ml 5tk; 5mg 1ml 10ml 25tk; 5mg 1ml 10ml 1tk

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

tyenne

fresenius kabi deutschland gmbh - totsilizumab - arthritis, rheumatoid; cytokine release syndrome; arthritis, juvenile rheumatoid; covid-19 virus infection; giant cell arteritis - immunosupressandid - tyenne, in combination with methotrexate (mtx), is indicated for- the treatment of severe, active and progressive rheumatoid arthritis (ra) in adults not previously treated with mtx. - the treatment of moderate to severe active ra in adult patients who have either responded inadequately to, or who were intolerant to, previous therapy with one or more disease-modifying anti-rheumatic drugs (dmards) or tumour necrosis factor (tnf) antagonists. in these patients, tyenne can be given as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. tocilizumab has been shown to reduce the rate of progression of joint damage as measured by x-ray and to improve physical function when given in combination with methotrexate. tyenne is indicated for the treatment of coronavirus disease 2019 (covid-19) in adults who are receiving systemic corticosteroids and require supplemental oxygen or mechanical ventilation. tyenne is indicated for the treatment of active systemic juvenile idiopathic arthritis (sjia) in patients 1 year of age and older, who have responded inadequately to previous therapy with nsaids and systemic corticosteroids. tyenne can be given as monotherapy (in case of intolerance to mtx or where treatment with mtx is inappropriate) or in combination with mtx. tyenne in combination with methotrexate (mtx) is indicated for the treatment of juvenile idiopathic polyarthritis (pjia; rheumatoid factor positive or negative and extended oligoarthritis) in patients 2 years of age and older, who have responded inadequately to previous therapy with mtx. tyenne can be given as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. tyenne is indicated for the treatment of chimeric antigen receptor (car) t cell-induced severe or life-threatening cytokine release syndrome (crs) in adults and paediatric patients 2 years of age and older. tyenne is indicated for the treatment of giant cell arteritis (gca) in adult patients.

Airexar Spiromax Euroopa Liit - eesti - EMA (European Medicines Agency)

airexar spiromax

teva b.v. - salmeterol, fluticasone propionaat - pulmonary disease, chronic obstructive; asthma - ravimid hingamisteede obstruktiivsete haiguste, - airexar spiromax on näidustatud kasutamiseks täiskasvanutel vanuses 18 aastat ja vanemad ainult. asthmaairexar spiromax is indicated for the regular treatment of patients with severe asthma where use of a combination product (inhaled corticosteroid and long-acting β2 agonist) is appropriate:- patients not adequately controlled on a lower strength corticosteroid combination productor- patients already controlled on a high dose inhaled corticosteroid and long-acting β2 agonist. krooniline obstruktiivne kopsuhaigus (copd)airexar spiromax on näidustatud sümptomaatiline ravi patsientidel, kellel copd), koos fev1.