Europäische Union - Deutsch - EMA (European Medicines Agency)

viatris limited - clopidogrel besilate - peripheral vascular diseases; stroke; myocardial infarction - antithrombotische mittel - 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 acute myocardial infarction, in kombination mit ass bei medizinisch behandelten patienten, für die eine thrombolytische therapie. 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. weitere informationen finden sie in abschnitt 5.

Europäische Union - Deutsch - EMA (European Medicines Agency)

viatris limited - pirfenidone - idiopathic pulmonary fibrosis; lung diseases; respiratory tract diseases - immunsuppressiva - pirfenidone viatris is indicated in adults for the treatment of mild to moderate idiopathic pulmonary fibrosis (ipf).

Europäische Union - Deutsch - EMA (European Medicines Agency)

viatris limited - dapagliflozin - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - drogen bei diabetes verwendet - type 2 diabetes mellitusdapagliflozin viatris is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise- as monotherapy when metformin is considered inappropriate due to intolerance. - in addition to other medicinal products for the treatment of type 2 diabetes. for study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 und 5. heart failuredapagliflozin viatris is indicated in adults for the treatment of symptomatic chronic heart failure with reduced ejection fraction. chronic kidney diseasedapagliflozin viatris is indicated in adults for the treatment of chronic kidney disease.

Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

viatris pharma gmbh (8183833) - gabapentin - hartkapsel - teil 1 - hartkapsel; gabapentin (22308) 400 milligramm

Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

viatris pharma gmbh (8183833) - gabapentin - hartkapsel - teil 1 - hartkapsel; gabapentin (22308) 300 milligramm

Europäische Union - Deutsch - EMA (European Medicines Agency)

teva pharma b.v. - budesonide, formoterol - asthma - medikamente für obstruktive atemwegserkrankungen, - budesonid / formoterol teva pharma b. ist nur bei erwachsenen ab 18 jahren angezeigt. asthmabudesonide/formoterol teva pharma b. is indicated in the regular treatment of asthma, where use of a combination (inhaled corticosteroid and long-acting β2 adrenoceptor agonist) is appropriate: orin patients not adequately controlled with inhaled corticosteroids and “as needed” inhaled short-acting β2 adrenoceptor agonists. in patients already adequately controlled on both inhaled corticosteroids and long-acting β2 adrenoceptor agonists.

Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

schuck gmbh (3067418) - ouabainum (pot.-angaben) - mischung - teil 1 - mischung; ouabainum (pot.-angaben) (15069) 0,5 gramm

Europäische Union - Deutsch - EMA (European Medicines Agency)

upjohn eesv - sildenafil - erektile dysfunktion - urologische - behandlung von männern mit erektiler dysfunktion, bei der es sich nicht um eine für eine befriedigende sexuelle leistung ausreichende peniserektion handelt. um für viagra wirksam zu sein, ist eine sexuelle stimulation erforderlich.

Österreich - Deutsch - AGES (Agentur für Gesundheit und Ernährungssicherheit)

+pharma arzneimittel gmbh - sitagliptin hydrochlorid monohydrat -

Österreich - Deutsch - AGES (Agentur für Gesundheit und Ernährungssicherheit)

+pharma arzneimittel gmbh - sitagliptin hydrochlorid monohydrat -