rikalpa 1mcg měkká tobolka
av medical cz s.r.o., praha array - 15512 parikalcitol - měkká tobolka - 1mcg - parikalcitol
rikalpa 2mcg měkká tobolka
av medical cz s.r.o., praha array - 15512 parikalcitol - měkká tobolka - 2mcg - parikalcitol
torad 200mg/245mg potahovaná tableta
av medical cz s.r.o., praha ČeskÁ republika - 15579 emtricitabin; 16950 tenofovir-disoproxil-fumarÁt - potahovaná tableta - 200mg/245mg - tenofovir-disoproxil a emtricitabin
xindus 10mg potahovaná tableta
av medical cz s.r.o., praha ČeskÁ republika - 17116 rivaroxaban - potahovaná tableta - 10mg - rivaroxaban
xindus 15mg potahovaná tableta
av medical cz s.r.o., praha ČeskÁ republika - 17116 rivaroxaban - potahovaná tableta - 15mg - rivaroxaban
xindus 20mg potahovaná tableta
av medical cz s.r.o., praha ČeskÁ republika - 17116 rivaroxaban - potahovaná tableta - 20mg - rivaroxaban
xindus 2,5mg potahovaná tableta
av medical cz s.r.o., praha ČeskÁ republika - 17116 rivaroxaban - potahovaná tableta - 2,5mg - rivaroxaban
(18f)fdg-fr 300-3100mbq/ml injekční roztok
alliance medical rp berlin gmbh, berlin array - 10981 fludeoxyglukosa-(18f) - injekční roztok - 300-3100mbq/ml - fludeoxyglukosa-(18f)
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. , , ,.
datscan
ge healthcare b.v. - ioflupan (123 i) - tomography, emission-computed, single-photon; lewy body disease; parkinson disease; alzheimer disease - diagnostické radiofarmaka - tento léčivý přípravek je určen pouze pro diagnostické účely. datscan je indikován pro zjišťování ztráty funkčních zakončení dopaminergních neuronů ve striatu:u dospělých pacientů s klinicky nejisté parkinsonské syndromy, například ty s časné příznaky, s cílem pomoci odlišit esenciální tremor od parkinsonské syndromy související s idiopatickou parkinsonovou chorobou, mnohočetnou systémovou atrofií a progresivní supranukleární obrna. datscan není schopen rozlišovat mezi parkinsonovou chorobou, mnohočetnou systémovou atrofií a progresivní supranukleární obrna. u dospělých pacientů, pomoci odlišit pravděpodobné demence s lewyho tělísky od alzheimerovy choroby. datscan není schopen rozlišovat mezi demence s lewyho tělísky parkinsonova choroba a demence.