Denise 150+30 mikrogram tabletter Denemarken - Deens - Lægemiddelstyrelsen (Danish Medicines Agency)

denise 150+30 mikrogram tabletter

2care4 aps - desogestrel, ethinylestradiol - tabletter - 150+30 mikrogram

Steward 30 WG Pulver Denemarken - Deens - SEGES Landbrug & Fødevarer

steward 30 wg pulver

fmc agricultural solutions a/s (tidligere: cheminova a/s) - indoxacarb - pulver - 300 g/kg indoxacarb

Leverette 21 150+30 mikrogram filmovertrukne tabletter Denemarken - Deens - Lægemiddelstyrelsen (Danish Medicines Agency)

leverette 21 150+30 mikrogram filmovertrukne tabletter

exeltis healthcare s.l - ethinylestradiol, levonorgestrel - filmovertrukne tabletter - 150+30 mikrogram

Azacitidine Mylan Europese Unie - Deens - EMA (European Medicines Agency)

azacitidine mylan

mylan ireland limited - azacitidin - myelodysplastic syndromes; leukemia, myelomonocytic, chronic; leukemia, myeloid, acute - antineoplastiske midler - azacitidine mylan is indicated for the treatment of adult patients who are not eligible for haematopoietic stem cell transplantation (hsct) with:intermediate 2 and high risk myelodysplastic syndromes (mds) according to the international prognostic scoring system (ipss),chronic myelomonocytic leukaemia (cmml) with 10 29% marrow blasts without myeloproliferative disorder,acute myeloid leukaemia (aml) with 20 30% blasts and multi lineage dysplasia, according to world health organisation (who) classification,aml with > 30% marrow blasts according to the who classification.

Vidanix 75+30 mikrogram overtrukne tabletter Denemarken - Deens - Lægemiddelstyrelsen (Danish Medicines Agency)

vidanix 75+30 mikrogram overtrukne tabletter

2care4 aps - ethinylestradiol, gestoden - overtrukne tabletter - 75+30 mikrogram

Rivaroxaban Viatris (previously Rivaroxaban Mylan) Europese Unie - Deens - EMA (European Medicines Agency)

rivaroxaban viatris (previously rivaroxaban mylan)

mylan ireland limited - rivaroxaban - venous thromboembolism; pulmonary embolism; acute coronary syndrome; stroke; coronary artery disease; peripheral arterial disease; atrial fibrillation - antitrombotiske midler - rivaroxaban mylan co-administered with acetylsalicylic acid (asa) alone or with asa plus clopidogrel or ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers.  rivaroxaban mylan 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.  ------prevention of venous thromboembolism (vte) in adult patients undergoing elective hip or knee replacement surgery.  treatment of deep vein thrombosis (dvt) and pulmonary embolism (pe), and prevention of recurrent dvt and pe in adults. -------adults prevention 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.

Zometa Europese Unie - Deens - EMA (European Medicines Agency)

zometa

phoenix labs unlimited company - zoledronic syre, zoledronic citronsyre monohydrat - cancer; fractures, bone - narkotika til behandling af knoglesygdomme - forebyggelse af skelet-relaterede hændelser (patologiske frakturer, spinal kompression, strålebehandling eller operation for at knogle, eller tumor-induceret hypercalcaemia) hos patienter med fremskreden maligne sygdomme, der involverer knogle;behandling af tumor-induceret hypercalcaemia (tih);forebyggelse af skelet-relaterede hændelser (patologiske frakturer, spinal kompression, strålebehandling eller operation for at knogle, eller tumor-induceret hypercalcaemia) hos patienter med fremskreden maligne sygdomme, der involverer knogle;behandling af tumor-induceret hypercalcaemia (tih);forebyggelse af skelet-relaterede hændelser (patologiske frakturer, spinal kompression, strålebehandling eller kirurgi til knogle, eller tumor-induceret hypercalcaemia) hos voksne patienter med fremskredne lidelser, der involverer knogle;behandling af voksne patienter med tumor-induceret hypercalcaemia (tih).

Anoro Ellipta (previously Anoro) Europese Unie - Deens - EMA (European Medicines Agency)

anoro ellipta (previously anoro)

glaxosmithkline (ireland) limited - umeclidinium bromid, vilanterol trifenatate - pulmonal sygdom, kronisk obstruktiv - medicin for obstruktiv sygdomme, - anoro ellipta er anført som vedligeholdelse bronkodilaterende behandling til at lindre symptomer i voksne patienter med kronisk obstruktiv lungesygdom (kol).

Aripiprazole Mylan Pharma (previously Aripiprazole Pharmathen) Europese Unie - Deens - EMA (European Medicines Agency)

aripiprazole mylan pharma (previously aripiprazole pharmathen)

mylan pharmaceuticals limited - aripiprazol - schizophrenia; bipolar disorder - psykoleptika - aripiprazol mylan pharma er indiceret til behandling af skizofreni hos voksne og hos unge i alderen 15 år og ældre. aripiprazol mylan pharma er indiceret til behandling af moderate til svære maniske episoder i bipolar lidelse og til forebyggelse af nye maniske episode i voksne, der har oplevet overvejende maniske episoder og hvis maniske episoder svarede, at aripiprazol-behandling. aripiprazol mylan pharma er indiceret til behandling i op til 12 uger af moderate til svære maniske episoder i bipolar jeg uorden i unge i alderen 13 år og ældre.