Valsartan/hydroklortiazid "Jubilant" 160 mg+12,5 mg filmovertrukne tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

valsartan/hydroklortiazid "jubilant" 160 mg+12,5 mg filmovertrukne tabletter

jubilant pharmaceuticals nv - hydrochlorthiazid, valsartan - filmovertrukne tabletter - 160 mg+12,5 mg

Valsartan/hydrochlorthiazid "Fair-Med" 160 mg+12,5 mg filmovertrukne tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

valsartan/hydrochlorthiazid "fair-med" 160 mg+12,5 mg filmovertrukne tabletter

fair-med healthcare gmbh - hydrochlorthiazid, valsartan - filmovertrukne tabletter - 160 mg+12,5 mg

Valsartan/hydrochlorthiazid "Fair-Med" 320 mg+12,5 mg filmovertrukne tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

valsartan/hydrochlorthiazid "fair-med" 320 mg+12,5 mg filmovertrukne tabletter

fair-med healthcare gmbh - hydrochlorthiazid, valsartan - filmovertrukne tabletter - 320 mg+12,5 mg

Valsartan/hydrochlorthiazid "Fair-Med" 80 mg+12,5 mg filmovertrukne tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

valsartan/hydrochlorthiazid "fair-med" 80 mg+12,5 mg filmovertrukne tabletter

fair-med healthcare gmbh - hydrochlorthiazid, valsartan - filmovertrukne tabletter - 80 mg+12,5 mg

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

reconcile

forte healthcare limited - fluoxetin - psychoanaleptics - hunde - som hjælp til behandling af separationsrelaterede lidelser hos hunde manifesteret ved ødelæggelse og uhensigtsmæssig adfærd (vokalisering og uhensigtsmæssig afføring og / eller vandladning) og kun i kombination med adfærdsmæssige modifikationsteknikker.

Sapropterin Dipharma Den Europæiske Union - dansk - EMA (European Medicines Agency)

sapropterin dipharma

dipharma arzneimittel gmbh - sapropterin dihydrochlorid - phenylketonurias - andre alimentary tract and metabolism produkter, - sapropterin dipharma is indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with phenylketonuria (pku) who have been shown to be responsive to such treatment. sapropterin dipharma is also indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with tetrahydrobiopterin (bh4) deficiency who have been shown to be responsive to such treatment.

Cinacalcet Mylan Den Europæiske Union - dansk - EMA (European Medicines Agency)

cinacalcet mylan

mylan pharmaceuticals limited - cinacalcethydrochlorid - hyperparathyroidism, secondary; hypercalcemia - calciumhomeostase - behandling af sekundær hyperparathyroidisme (hpt) hos patienter med nyresygdom i sluttrinnet (esrd) ved vedligeholdelsesdialysebehandling. cinacalcet mylan kan bruges som en del af en terapeutiske regime inklusive fosfat bindemidler og/eller vitamin d steroler, som er relevant. reduktion af hypercalcaemia i patienter med:parathyroid carcinomaprimary hpt, for hvem parathyroidectomywould være angivet på grundlag af serum calcium-niveauer (som defineret i de relevante retningslinjer for behandling), men i hvem parathyroidectomy ikke er klinisk relevant, eller er kontraindiceret.

Clopidogrel Viatris (previously Clopidogrel Taw Pharma) Den Europæiske Union - dansk - EMA (European Medicines Agency)

clopidogrel viatris (previously clopidogrel taw pharma)

viatris limited - clopidogrel besilat - peripheral vascular diseases; stroke; myocardial infarction - antitrombotiske midler - secondary prevention of atherothrombotic events clopidogrel is indicated in:adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease. adult patients suffering from acute coronary syndrome. non-st segment elevation acute coronary syndrome (unstable angina or non-q-wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (asa). st-segment elevation akut myokardieinfarkt, i kombination med asa i medicinsk behandlede patienter, der er berettiget til trombolytisk terapi. in patients with moderate to high-risk transient ischaemic attack (tia) or minor ischaemic stroke (is) clopidogrel in combination with asa is indicated in:adult patients with moderate to high-risk tia (abcd2 score ≥4) or minor is (nihss ≤3) within 24 hours of either the tia or is event. prevention of atherothrombotic and thromboembolic events in atrial fibrillation:in adult patients with atrial fibrillation who have at least one risk factor for vascular events, are not suitable for treatment with vitamin k antagonists (vka) and who have a low bleeding risk, clopidogrel is indicated in combination with asa for the prevention of atherothrombotic and thromboembolic events, including stroke. for yderligere oplysninger henvises der til afsnit 5.