KODEIN 1 A PHARMA 10MG Tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

kodein 1 a pharma 10mg tableta

1 a pharma gmbh, holzkirchen array - 5382 hemihydrÁt kodein-fosfÁtu - tableta - 10mg - kodein

KODEIN 1 A PHARMA 15MG Tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

kodein 1 a pharma 15mg tableta

1 a pharma gmbh, holzkirchen array - 5382 hemihydrÁt kodein-fosfÁtu - tableta - 15mg - kodein

KODEIN 1 A PHARMA 20MG Tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

kodein 1 a pharma 20mg tableta

1 a pharma gmbh, holzkirchen array - 5382 hemihydrÁt kodein-fosfÁtu - tableta - 20mg - kodein

KODEIN 1 A PHARMA 30MG Tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

kodein 1 a pharma 30mg tableta

1 a pharma gmbh, holzkirchen array - 5382 hemihydrÁt kodein-fosfÁtu - tableta - 30mg - kodein

LEVETIRACETAM G.L. PHARMA 1000MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

levetiracetam g.l. pharma 1000mg potahovaná tableta

g.l. pharma gmbh, lannach array - 11237 levetiracetam - potahovaná tableta - 1000mg - levetiracetam

LEVETIRACETAM G.L. PHARMA 500MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

levetiracetam g.l. pharma 500mg potahovaná tableta

g.l. pharma gmbh, lannach array - 11237 levetiracetam - potahovaná tableta - 500mg - levetiracetam

OFLOXACIN UNIMED PHARMA 3MG/ML Ušní/oční kapky, roztok Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

ofloxacin unimed pharma 3mg/ml ušní/oční kapky, roztok

unimed pharma spol. s r.o., bratislava array - 9158 ofloxacin - ušní/oční kapky, roztok - 3mg/ml - antiinfektiva

SOLIFENACIN G.L.PHARMA 10MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

solifenacin g.l.pharma 10mg potahovaná tableta

g.l. pharma gmbh, lannach array - 17227 solifenacin-sukcinÁt - potahovaná tableta - 10mg - solifenacin

SOLIFENACIN G.L.PHARMA 5MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

solifenacin g.l.pharma 5mg potahovaná tableta

g.l. pharma gmbh, lannach array - 17227 solifenacin-sukcinÁt - potahovaná tableta - 5mg - solifenacin

Clopidogrel Taw Pharma (previously Clopidogrel Mylan) Evropská unie - čeština - 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. , , ,.