Roximstad 150 mg filmovertrukne tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

roximstad 150 mg filmovertrukne tabletter

stada arzneimittel ag - roxithromycin - filmovertrukne tabletter - 150 mg

Vabysmo Den Europæiske Union - dansk - EMA (European Medicines Agency)

vabysmo

roche registration gmbh - faricimab - wet macular degeneration; macular edema; diabetes complications - oftalmologiske - vabysmo is indicated for the treatment of adult patients with:neovascular (wet) age-related macular degeneration (namd),visual impairment due to diabetic macular oedema (dme).

Efastad 150 mg depotkapsler, hårde Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

efastad 150 mg depotkapsler, hårde

stada arzneimittel ag - venlafaxinhydrochlorid - depotkapsler, hårde - 150 mg

Efastad 75 mg depotkapsler, hårde Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

efastad 75 mg depotkapsler, hårde

stada arzneimittel ag - venlafaxinhydrochlorid - depotkapsler, hårde - 75 mg

Pramipexol "Stada" 0,18 mg tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

pramipexol "stada" 0,18 mg tabletter

stada arzneimittel ag - pramipexoldihydrochloridmonohydrat - tabletter - 0,18 mg

Pramipexol "Stada" 0,7 mg tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

pramipexol "stada" 0,7 mg tabletter

stada arzneimittel ag - pramipexoldihydrochloridmonohydrat - tabletter - 0,7 mg

Venlafaxin "Stada" 150 mg depotkapsler, hårde Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

venlafaxin "stada" 150 mg depotkapsler, hårde

stada arzneimittel ag - venlafaxinhydrochlorid - depotkapsler, hårde - 150 mg

Venlafaxin "Stada" 37,5 mg depotkapsler, hårde Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

venlafaxin "stada" 37,5 mg depotkapsler, hårde

stada arzneimittel ag - venlafaxinhydrochlorid - depotkapsler, hårde - 37,5 mg

Venlafaxin "Stada" 75 mg depotkapsler, hårde Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

venlafaxin "stada" 75 mg depotkapsler, hårde

stada arzneimittel ag - venlafaxinhydrochlorid - depotkapsler, hårde - 75 mg

Xarelto Den Europæiske Union - dansk - EMA (European Medicines Agency)

xarelto

bayer ag - rivaroxaban - arthroplasty, replacement; venous thromboembolism - antitrombotiske midler - xarelto, co-gives sammen med acetylsalicylsyre (asa) alene eller sammen med asa plus clopidogrel eller ticlopidin, der er indiceret til forebyggelse af atherothrombotic hændelser hos voksne patienter efter en akut koronar syndrom (acs) med forhøjet kardiale biomarkører. xarelto, 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. forebyggelse af venøs tromboembolisme (vte) hos voksne patienter, der gennemgår valgfri hofte- eller knæskifteoperation. behandling af dyb venøs trombose (dvt) og lungeemboli (pe), og forebyggelse af recidiverende dvt og pe i voksne. 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. paediatric population treatment 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. paediatric population treatment 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.