Suomi - suomi - Fimea (Suomen lääkevirasto)

dechra regulatory b.v. - potassium bromide - tabletti - 325 mg - bromidit

Suomi - suomi - Fimea (Suomen lääkevirasto)

domes pharma - potassium bromide - tabletti - 600 mg

Suomi - suomi - Fimea (Suomen lääkevirasto)

boehringer ingelheim international gmbh - fenoterol hydrobromide, ipratropium bromide monohydrate - sumutinliuos - fenoteroli ja ipratropiumbromidi

Suomi - suomi - Fimea (Suomen lääkevirasto)

boehringer ingelheim international gmbh - fenoterol hydrobromide, ipratropium bromide monohydrate - inhalaatiosumute, liuos - 20 / 50 mikrog / annos - fenoteroli ja ipratropiumbromidi

Suomi - suomi - Fimea (Suomen lääkevirasto)

ratiopharm gmbh - dextromethorphan hydrobromide - oraaliliuos - 2 mg/ml - dekstrometorfaani

Euroopan unioni - suomi - EMA (European Medicines Agency)

accord healthcare s.l.u. - rivaroksabaani - acute coronary syndrome; coronary artery disease; peripheral arterial disease; venous thromboembolism; stroke; atrial fibrillation; pulmonary embolism - antitromboottiset aineet - laskimotromboembolian (vte) ehkäisy aikuisilla potilailla, jotka saavat elektiivisen lonkan tai polven korvaavan leikkauksen. hoito syvä laskimotukos (dvt) ja keuhkoembolian (pe), ja toistuvien dvt ja pe aikuisilla. (see section 4. 4 for haemodynamically unstable pe patients. hoito syvä laskimotukos (dvt) ja keuhkoembolian (pe), ja toistuvien dvt ja pe aikuisilla. (see section 4. 4 hemodynaamisesti epävakaa pe potilaat). adultsprevention of stroke and systemic embolism in adult patients with non valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. hoito syvä laskimotukos (dvt) ja keuhkoembolian (pe), ja toistuvien dvt ja pe aikuisilla. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing from 30 kg to 50 kg after at least 5 days of initial parenteral anticoagulation treatment. rivaroxaban accord, co administered with acetylsalicylic acid (asa) alone or with asa plus ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers (see sections 4. 3, 4. 4 ja 5. rivaroxaban accord, co administered with acetylsalicylic acid (asa), is indicated for the prevention of atherothrombotic events in adult patients with coronary artery disease (cad) or symptomatic peripheral artery disease (pad) at high risk of ischaemic events. adultsprevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. hoito syvä laskimotukos (dvt) ja keuhkoembolian (pe), ja toistuvien dvt ja pe aikuisilla. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing more than 50 kg after at least 5 days of initial parenteral anticoagulation treatment.

Euroopan unioni - suomi - EMA (European Medicines Agency)

shionogi b.v. - lusutrombopag - trombosytopenia - hemostaatit - mulpleo on tarkoitettu hoitoon vaikea trombosytopenia aikuisilla potilailla, joilla on krooninen maksasairaus, joille tehdään invasiivisia toimenpiteitä.

Euroopan unioni - suomi - EMA (European Medicines Agency)

swedish orphan biovitrum ab (publ) - avatrombopag maleate - trombosytopenia - hemostaatit - doptelet on tarkoitettu hoitoon vaikea trombosytopenia aikuisilla potilailla, joilla on krooninen maksasairaus, joka on määrä suorittaa invasiivisia menettely. doptelet is indicated for the treatment of primary chronic immune thrombocytopenia (itp) in adult patients who are refractory to other treatments (e. kortikosteroidit, immunoglobuliinit).

Suomi - suomi - Fimea (Suomen lääkevirasto)

hameln pharma gmbh - rocuronium bromide - injektio-/infuusioneste, liuos - 10 mg/ml - rokuroniumbromidi

Suomi - suomi - Fimea (Suomen lääkevirasto)

b. braun melsungen ag - rocuronium bromide - injektio-/infuusioneste, liuos - 10 mg/ml - rokuroniumbromidi