Meropenem Fairmed Healthcare 1 g Pulver zur Herstellung einer Injektions-/Infusionslösung Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

meropenem fairmed healthcare 1 g pulver zur herstellung einer injektions-/infusionslösung

fairmed healthcare gmbh (8096063) - meropenem-trihydrat - pulver zur herstellung einer injektions-/infusionslösung - 1 g - teil 1 - pulver zur herstellung einer injektions-/infusionslösung; meropenem-trihydrat (27630) 1140,6 milligramm

Abiraterone Accord Europäische Union - Deutsch - EMA (European Medicines Agency)

abiraterone accord

accord healthcare s.l.u. - abirateronacetat - prostata-neoplasmen - endokrine therapie - abiraterone accord is indicated with prednisone or prednisolone for:the treatment of newly diagnosed high risk metastatic hormone sensitive prostate cancer (mhspc) in adult men in combination with androgen deprivation therapy (adt)the treatment of metastatic castration resistant prostate cancer (mcrpc) in adult men who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicatedthe treatment of mcrpc in adult men whose disease has progressed on or after a docetaxel based chemotherapy regimen.

CARDIOXANE 500 mg, Pulver zur Herstellung einer Infusionslösung Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

cardioxane 500 mg, pulver zur herstellung einer infusionslösung

clinigen healthcare b.v. (8181225) - dexrazoxan - pulver zur herstellung einer infusionslösung - teil 1 - pulver zur herstellung einer infusionslösung; dexrazoxan (26073) 500 milligramm

Exubera Europäische Union - Deutsch - EMA (European Medicines Agency)

exubera

pfizer limited - insulin human - diabetes mellitus - drogen bei diabetes verwendet - exubera ist indiziert für die behandlung von erwachsenen patienten mit typ-2-diabetes mellitus notadequately gesteuert mit oralen antidiabetika und erfordern insulin-therapie. exubera ist auch indiziert für die behandlung von erwachsenen patienten mit typ-1-diabetes mellitus, inaddition zu lang oder mittelfristige wirkendes subkutanes insulin, für wen sich die potenziellen vorteile ofadding inhalative insulin wiegen als die möglichen bedenken zur sicherheit vorliegen (siehe abschnitt 4.

Optalidon Zahnschmerz mit Diclofenac 25 mg Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

optalidon zahnschmerz mit diclofenac 25 mg

novartis consumer health gmbh (3003453) - diclofenac-kalium - überzogene tablette - teil 1 - überzogene tablette; diclofenac-kalium (11927) 25 milligramm

Hydrocortison NCH Creme 0,25 % Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

hydrocortison nch creme 0,25 %

novartis consumer health gmbh (3003453) - hydrocortison - creme - teil 1 - creme; hydrocortison (00758) 0,05 gramm

Azithromycin Spirig HC 250 Filmtabletten Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

azithromycin spirig hc 250 filmtabletten

spirig healthcare ag - azithromycinum - filmtabletten - azithromycinum 250 mg ut azithromycinum monohydricum, excipiens pro compresso obducto. - infektionskrankheiten - synthetika

Clopidogrel Viatris (previously Clopidogrel Taw Pharma) Europäische Union - Deutsch - EMA (European Medicines Agency)

clopidogrel viatris (previously clopidogrel taw pharma)

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.

Clopidogrel Taw Pharma (previously Clopidogrel Mylan) Europäische Union - Deutsch - EMA (European Medicines Agency)

clopidogrel taw pharma (previously clopidogrel mylan)

taw pharma (ireland) limited - clopidogrel-hydrochlorid - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - 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), ischaemic 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 combination with asa in medically treated patients eligible for thrombolytic therapy. , , 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 further information please refer to section 5. , , ,.