Πολωνία - Πολωνικά - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

teva b.v. - rosuvastatinum + acidum acetylsalicylicum - kapsułki twarde - 10 mg + 100 mg

Πολωνία - Πολωνικά - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

teva b.v. - rosuvastatinum + acidum acetylsalicylicum - kapsułki twarde - 20 mg + 100 mg

Ευρωπαϊκή Ένωση - Πολωνικά - EMA (European Medicines Agency)

taw pharma (ireland) limited - chlorowodorek klopidogrelu - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - Środki przeciwzakrzepowe - , , , , 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. , , ,.

Ευρωπαϊκή Ένωση - Πολωνικά - EMA (European Medicines Agency)

sanofi winthrop industrie - clopidogrel, acetylsalicylic acid - acute coronary syndrome; myocardial infarction - Środki przeciwzakrzepowe - duoplavin jest wskazany do wtórnego zapobiegania incydentom miażdżycowym u dorosłych pacjentów przyjmujących już klopidogrel i kwas acetylosalicylowy (asa). duoplavin is a fixed-dose combination medicinal product for continuation of therapy in: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 (pci);st segment elevation acute myocardial infarction (stemi) in patients undergoing a stent placement) or medically treated patients eligible for thrombolytic/fibrinolytic therapy. aby uzyskać więcej informacji, proszę odnieść się do rozdziału 5.

Ευρωπαϊκή Ένωση - Πολωνικά - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - zmodyfikowany żywy wirus grypy bydlęcej typu 1, niecytopatyczny szczep rodzicielski ke-9 i zmodyfikowany wirus żywej bydła, biegunka typu 2, niecytopatyczny szczep macierzysty ny-93 - immunomodulatorów dla byka, żywe szczepionki wirusowe - dla aktywnej immunizacji bydła od 3 miesiąca życia w celu zmniejszenia hipertermia i, aby zminimalizować spadek liczby białych krwinek jest spowodowany wirusowej biegunki bydła (bvdv-1 i bvdv-2), i zmniejszyć wydzielanie wirusa i viremia spowodowanych bvdv-2. do czynnej immunizacji bydła przeciwko bvdv-1 i bvdv-2, w celu zapobiegania narodzinom stale zakażonych cieląt spowodowanych przez zakażenie przez łożysko.

Ευρωπαϊκή Ένωση - Πολωνικά - EMA (European Medicines Agency)

sanofi winthrop industrie - wodorosiarczan klopidogrelu - stroke; peripheral vascular diseases; atrial fibrillation; myocardial infarction; acute coronary syndrome - Środki przeciwzakrzepowe - 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. zapobieganie aterotrombotičeskih i zakrzepowo-zatorowych w przypadku migotania fibrillationin dorosłych pacjentów z migotaniem przedsionków, które mają co najmniej jeden czynnik ryzyka występowania naczyniowych zdarzeń, nie nadają się do leczenia witaminy-do-antagonistów i które mają niskie ryzyko krwawienia, klopidogrel jest wskazany w skojarzeniu z asa w celu zapobiegania aterotrombotičeskih i zakrzepowo-zatorowych, w tym udaru mózgu.

Ευρωπαϊκή Ένωση - Πολωνικά - EMA (European Medicines Agency)

janssen-cilag international n.v.   - palmitynian paliperydonu - schizofrenia - psycholeptyki - byannli (previously paliperidone janssen-cilag international) a 6 monthly injection, is indicated for the maintenance treatment of schizophrenia in adult patients who are clinically stable on 1 monthly or 3 monthly paliperidone palmitate injectable products (see section 5.

Ευρωπαϊκή Ένωση - Πολωνικά - EMA (European Medicines Agency)

mylan ireland limited - sitagliptin hydrochloride monohydrate, metformin hydrochloride - diabetes mellitus, type 2 - leki stosowane w cukrzycy - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride mylan is indicated as an adjunct to diet and exercise to improve glycaemic control in patients inadequately controlled on their maximal tolerated dose of metformin alone or those already being treated with the combination of sitagliptin and metformin. sitagliptin/metformin hydrochloride mylan is indicated in combination with a sulphonylurea (i. potrójnej terapii skojarzonej), jako uzupełnienie diety i ćwiczeń fizycznych u pacjentów niedostatecznie kontrolowanych o ich maksymalnej tolerowanej dawki sulfonylomocznika z metforminą i. sitagliptin/metformin hydrochloride mylan is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparg) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparg agonist. sitagliptin/metformin hydrochloride mylan is also indicated as add-on to insulin (i. , triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in patients when stable dose of insulin and metformin alone do not provide adequate glycaemic control.

Ευρωπαϊκή Ένωση - Πολωνικά - EMA (European Medicines Agency)

accord healthcare s.l.u. - metformin hydrochloride, sitagliptin hydrochloride monohydrate - diabetes mellitus, type 2 - leki stosowane w cukrzycy - for adult patients with type 2 diabetes mellitus:it is indicated as an adjunct to diet and exercise to improve glycaemic control in patients inadequately controlled on their maximal tolerated dose of metformin alone or those already being treated with the combination of sitagliptin and metformin. it is indicated in combination with a sulphonylurea (i. potrójnej terapii skojarzonej), jako uzupełnienie diety i ćwiczeń fizycznych u pacjentów niedostatecznie kontrolowanych o ich maksymalnej tolerowanej dawki sulfonylomocznika z metforminą i. it is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparγ) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparγ agonist. it is also indicated as add-on to insulin (i. , triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in patients when stable dose of insulin and metformin alone do not provide adequate glycaemic control.

Πολωνία - Πολωνικά - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

adamed pharma s.a. - sitagliptin hydrochloride monohydrate + metformini hydrochloridum - tabletki o zmodyfikowanym uwalnianiu - 100 mg + 1000 mg