Gefrorenes pathogenreduziertes Apheresefrischplasma Th-J Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

gefrorenes pathogenreduziertes apheresefrischplasma th-j

institut für klinische transfusionsmedizin jena ggmbh (4608098) - gerinnungsaktives plasma vom menschen - infusionslösung - teil 1 - infusionslösung; gerinnungsaktives plasma vom menschen (10676) 0,88 milliliter

Gefrorenes Human-Frischplasma CPD AL BSD/BRK Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

gefrorenes human-frischplasma cpd al bsd/brk

blutspendedienst des bayerischen roten kreuzes, ggmbh (3138466) - gerinnungsaktives plasma vom menschen - infusionslösung - teil 1 - infusionslösung; gerinnungsaktives plasma vom menschen (10676) 0,82 milliliter

Gefrorenes Human-Frischplasma CPD L BSD/BRK Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

gefrorenes human-frischplasma cpd l bsd/brk

blutspendedienst des bayerischen roten kreuzes, ggmbh (3138466) - gerinnungsaktives plasma vom menschen - infusionslösung - teil 1 - infusionslösung; gerinnungsaktives plasma vom menschen (10676) 0,74 milliliter

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

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. , , ,.

Clopidogrel TAD Europäische Union - Deutsch - EMA (European Medicines Agency)

clopidogrel tad

tad pharma gmbh - clopidogrel (as hydrochloride) - peripheral vascular diseases; stroke; myocardial infarction - antithrombotische mittel - clopidogrel is indicated in adults for the prevention of atherothrombotic events in: , 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.

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

plavix

sanofi winthrop industrie - clopidogrel-hydrogensulfat - stroke; peripheral vascular diseases; atrial fibrillation; myocardial infarction; acute coronary syndrome - antithrombotische mittel - secondary prevention of atherothrombotic eventsclopidogrel is indicated in:adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from seven days until less than six 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 patients undergoing percutaneous coronary intervention (including patients undergoing a stent replacement) or medically treated patients eligible for thrombolytic/fibrinolytic therapy. in patients with moderate to high-risk transient ischemic attack (tia) or minor ischemic 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. prävention von atherothrombotischen und thromboembolischer ereignisse bei vorhofflimmern fibrillationin erwachsenen patienten mit vorhofflimmern, die mindestens einen risikofaktor für vaskuläre ereignisse, sind nicht geeignet für die behandlung mit vitamin-k-antagonisten und haben ein geringes blutungsrisiko, clopidogrel ist indiziert in kombination mit ass für die prävention von atherothrombotischen und thromboembolischer ereignisse, einschließlich schlaganfall.

Azathioprin AqVida 25 mg Filmtabletten Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

azathioprin aqvida 25 mg filmtabletten

aqvida gmbh (8135745) - azathioprin - filmtablette - teil 1 - filmtablette; azathioprin (04347) 25 milligramm