ROSUVASTATIN TEVA PHARMA 40MG Potahovaná tableta 체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

rosuvastatin teva pharma 40mg potahovaná tableta

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SUNITINIB G.L. PHARMA 12,5MG Tvrdá tobolka 체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

sunitinib g.l. pharma 12,5mg tvrdá tobolka

g.l. pharma gmbh, lannach array - 17420 sunitinib - tvrdá tobolka - 12,5mg - sunitinib

SUNITINIB G.L. PHARMA 25MG Tvrdá tobolka 체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

sunitinib g.l. pharma 25mg tvrdá tobolka

g.l. pharma gmbh, lannach array - 17420 sunitinib - tvrdá tobolka - 25mg - sunitinib

SUNITINIB G.L. PHARMA 50MG Tvrdá tobolka 체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

sunitinib g.l. pharma 50mg tvrdá tobolka

g.l. pharma gmbh, lannach array - 17420 sunitinib - tvrdá tobolka - 50mg - sunitinib

TERIFLUNOMIDE G.L. PHARMA 14MG Potahovaná tableta 체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

teriflunomide g.l. pharma 14mg potahovaná tableta

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Clopidogrel Taw Pharma (previously Clopidogrel Mylan) 유럽 연합 - 체코어 - EMA (European Medicines Agency)

clopidogrel taw pharma (previously clopidogrel mylan)

taw pharma (ireland) limited - hydrochlorid klopidogrelu - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - antitrombotické činidla - , , , , 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. , , ,.

CABAZITAXEL G.L. PHARMA 20MG/ML Koncentrát pro infuzní roztok 체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

cabazitaxel g.l. pharma 20mg/ml koncentrát pro infuzní roztok

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AGOMELATINE G.L.PHARMA 25MG Potahovaná tableta 체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

agomelatine g.l.pharma 25mg potahovaná tableta

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SOLIFENACIN G.L.PHARMA 10MG Potahovaná tableta 체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

solifenacin g.l.pharma 10mg potahovaná tableta

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SOLIFENACIN G.L.PHARMA 5MG Potahovaná tableta 체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

solifenacin g.l.pharma 5mg potahovaná tableta

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