Clopidogrel Taw Pharma (previously Clopidogrel Mylan) Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

clopidogrel taw pharma (previously clopidogrel mylan)

taw pharma (ireland) limited - υδροχλωρική κλοπιδογρέλη - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - Αντιθρομβωτικοί παράγοντες - , , , , 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 Viatris (previously Clopidogrel Taw Pharma) Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

clopidogrel viatris (previously clopidogrel taw pharma)

viatris limited - κλοπιδογρέλη besilate - peripheral vascular diseases; stroke; myocardial infarction - Αντιθρομβωτικοί παράγοντες - 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). Υψόμετρο τμήμα του st οξύ έμφραγμα του μυοκαρδίου, σε συνδυασμό με ΑΣΟ σε ιατρικά ασθενών επιλέξιμων για θρομβολυτική θεραπεία. 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. Για περαιτέρω πληροφορίες ανατρέξτε στην παράγραφο 5.

Teriflunomide Mylan Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

teriflunomide mylan

mylan pharmaceuticals limited - teriflunomide - Η Σκλήρυνση Κατά Πλάκας, Υποτροπιάζουσα-Διαλείπουσα - Ανοσοκατασταλτικά - teriflunomide mylan is indicated for the treatment of adult patients and paediatric patients aged 10 years and older (body weight > 40 kg) with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 of the smpc for important information on the population for which efficacy has been established).

Aubagio Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

aubagio

sanofi winthrop industrie - teriflunomide - Πολλαπλή σκλήρυνση - Επιλεκτικά ανοσοκατασταλτικά - aubagio is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

Plavix Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

plavix

sanofi winthrop industrie - κλοπιδογρέλης - stroke; peripheral vascular diseases; atrial fibrillation; myocardial infarction; acute coronary syndrome - Αντιθρομβωτικοί παράγοντες - 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. Πρόληψη της αθηροθρομβωτικά και θρομβοεμβολικών επεισοδίων σε κολπική fibrillationin ενήλικες ασθενείς με κολπική μαρμαρυγή που έχουν τουλάχιστον έναν παράγοντα κινδύνου για αγγειακά συμβάματα, δεν είναι κατάλληλοι για θεραπεία με βιταμίνη Κ ανταγωνιστές και οι οποίοι έχουν χαμηλό κίνδυνο αιμορραγίας, η κλοπιδογρέλη ενδείκνυται σε συνδυασμό με ΑΣΟ για την πρόληψη της αθηροθρομβωτικά και θρομβοεμβολικών επεισοδίων, συμπεριλαμβανομένων εγκεφαλικό επεισόδιο.

VINCRISTINE SULPHATE 1MG/ML SOLUTION FOR INJECTION OR INFUSION Κύπρος - Ελληνικά - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

vincristine sulphate 1mg/ml solution for injection or infusion

pfizer hellas ae (0000003442) 243 messoghion avenue, neo psychiko, athens, 15451 - vincristine sulfate - solution for injection or infusion - 1mg/ml - vincristine sulfate (0000207863) 1mg - vincristine

MYCORIL 1% W/W CREAM Κύπρος - Ελληνικά - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

mycoril 1% w/w cream

remedica ltd (0000003171) aharnon str., lemesos, 3056 - clotrimazole - cream - 1% w/w - clotrimazole (0023593751) 1g - clotrimazole

CISPLATIN 1MG/ML CONCENTRATE FOR SOLUTION FOR INFUSION Κύπρος - Ελληνικά - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

cisplatin 1mg/ml concentrate for solution for infusion

pfizer hellas ae (0000003442) 243 messoghion avenue, neo psychiko, athens, 15451 - cisplatin - concentrate for solution for infusion - 1mg/ml - cisplatin (0015663271) 1mg - cisplatin

DEPRIM (200MG/40MG ) /5ML ORAL SUSPENSION Κύπρος - Ελληνικά - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

deprim (200mg/40mg ) /5ml oral suspension

remedica ltd (0000003171) aharnon str., lemesos, 3056 - trimethoprim; sulfamethoxazole - oral suspension - (200mg/40mg ) /5ml - trimethoprim (0000738705) 40mg; sulfamethoxazole (0000723466) 200mg - sulfamethoxazole and trimethoprim

DEPRIM 400MG/80MG TABLETS Κύπρος - Ελληνικά - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

deprim 400mg/80mg tablets

remedica ltd (0000003171) aharnon str., lemesos, 3056 - sulfamethoxazole; trimethoprim - tablets - 400mg/80mg - sulfamethoxazole (0000723466) 400mg; trimethoprim (0000738705) 80mg - sulfamethoxazole and trimethoprim