Oxyglobin Európai Unió - magyar - EMA (European Medicines Agency)

oxyglobin

opk biotech netherlands bv - hemoglobin glutamer-200 (szarvasmarha) - vÉr helyettesÍtŐ, perfÚziÓs megoldÁsok - kutyák - az oxigénglobin oxigén hordozóanyagot biztosít a kutyák számára, javítva a vérszegénység klinikai tüneteit legalább 24 órán keresztül, függetlenül az alapállapottól.

Ruconest Európai Unió - magyar - EMA (European Medicines Agency)

ruconest

pharming group n.v. - rekombináns humán c1-inhibitor - angioödéma, örökletes - drugs used in hereditary angioedema, other hematological agents - a ruconest az akut angioödémás rohamok kezelésére javallt az örökletes angioödéma (hae) felnőtteknél a c1-észteráz-inhibitor hiánya miatt.

Rivaroxaban Accord Európai Unió - magyar - EMA (European Medicines Agency)

rivaroxaban accord

accord healthcare s.l.u. - rivaroxaban - acute coronary syndrome; coronary artery disease; peripheral arterial disease; venous thromboembolism; stroke; atrial fibrillation; pulmonary embolism - antitrombotikus szerek - a vénás tromboembólia (vte) megelőzése felnőtt betegeknél, akik elektív csípő- vagy térdpótló műtéten mennek keresztül. kezelés a mélyvénás trombózis (dvt), mind a pulmonalis embolia (pe), illetve megelőzése, a visszatérő mvt, illetve pe felnőttek. (see section 4. 4 for haemodynamically unstable pe patients. kezelés a mélyvénás trombózis (dvt), mind a pulmonalis embolia (pe), illetve megelőzése, a visszatérő mvt, illetve pe felnőttek. (see section 4. 4 a hemodinamikailag instabil pe beteg). 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. kezelés a mélyvénás trombózis (dvt), mind a pulmonalis embolia (pe), illetve megelőzése, a visszatérő mvt, illetve pe felnőttek. (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 és 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. kezelés a mélyvénás trombózis (dvt), mind a pulmonalis embolia (pe), illetve megelőzése, a visszatérő mvt, illetve pe felnőttek. (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.

Phesgo Európai Unió - magyar - EMA (European Medicines Agency)

phesgo

roche registration gmbh - pertuzumab, trastuzumab - mellnövekedés - daganatellenes szerek - early breast cancer (ebc)phesgo is indicated for use in combination with chemotherapy in:the neoadjuvant treatment of adult patients with her2-positive, locally advanced, inflammatory, or early stage breast cancer at high risk of recurrencethe adjuvant treatment of adult patients with her2-positive early breast cancer at high risk of recurrencemetastatic breast cancer (mbc)phesgo is indicated for use in combination with docetaxel in adult patients with her2-positive metastatic or locally recurrent unresectable breast cancer, who have not received previous anti-her2 therapy or chemotherapy for their metastatic disease.

Xolair Európai Unió - magyar - EMA (European Medicines Agency)

xolair

novartis europharm limited - omalizumab - asthma; urticaria - gyógyszerek obstruktív légúti betegségek, - allergiás asthmaxolair jelzi a felnőttek, kamaszok, a gyerekek (6.