Plavix Evropska unija - slovenščina - EMA (European Medicines Agency)

plavix

sanofi winthrop industrie - klopidogrel vodikov sulfat - stroke; peripheral vascular diseases; atrial fibrillation; myocardial infarction; acute coronary syndrome - antitrombotična sredstva - 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. preprečevanje atherothrombotic in thromboembolic dogodkov v atrijska fibrillationin odraslih bolnikov z atrijsko fibrilacijo, ki imajo vsaj en dejavnik tveganja za žilne dogodke, niso primerni za zdravljenje z vitaminom k antagonisti in ki imajo nizko tveganje krvavitve, clopidogrel je indiciran v kombinaciji s asa za preprečevanje atherothrombotic in thromboembolic dogodkov, vključno z možgansko kap.

Olanzapine Cipla (previously Olanzapine Neopharma) Evropska unija - slovenščina - EMA (European Medicines Agency)

olanzapine cipla (previously olanzapine neopharma)

cipla (eu) limited - olanzapin - schizophrenia; bipolar disorder - psiholeptiki - adultsolanzapine je primerna za zdravljenje shizofrenije. olanzapin je učinkovita pri ohranjanju klinično izboljšanje, med nadaljevanje terapije pri bolnikih, ki so pokazali začetni odziv zdravljenje. olanzapin je primerna za zdravljenje zmerno do hudo manične epizode. pri bolnikih, katerih manične epizode se je odzvala na olanzapin zdravljenje, olanzapin, je indicirano za preprečevanje ponovitve pri bolnikih z bipolarno motnjo.

Rapilysin Evropska unija - slovenščina - EMA (European Medicines Agency)

rapilysin

actavis group ptc ehf - reteplaza - miokardni infarkt - antitrombotična sredstva - rapilysin is indicated for the thrombolytic treatment of suspected myocardial infarction with persistent st elevation or recent left bundle branch block within 12 hours after the onset of acute-myocardial-infarction (ami) symptoms.

Adakveo Evropska unija - slovenščina - EMA (European Medicines Agency)

adakveo

novartis europharm limited - crizanlizumab - anemija, srčna celica - other hematological agents - adakveo is indicated for the prevention of recurrent vaso occlusive crises (vocs) in sickle cell disease patients aged 16 years and older. it can be given as an add on therapy to hydroxyurea/hydroxycarbamide (hu/hc) or as monotherapy in patients for whom hu/hc is inappropriate or inadequate.

Cancidas (previously Caspofungin MSD) Evropska unija - slovenščina - EMA (European Medicines Agency)

cancidas (previously caspofungin msd)

merck sharp & dohme b.v. - caspofungin (as acetate) - candidiasis; aspergillosis - antimikotiki za sistemsko uporabo - treatment of invasive candidiasis in adult or paediatric patients;treatment of invasive aspergillosis in adult or paediatric patients who are refractory to or intolerant of amphotericin b, lipid formulations of amphotericin b and / or itraconazole. refractoriness is defined as progression of infection or failure to improve after a minimum of seven days of prior therapeutic doses of effective antifungal therapy;empirical therapy for presumed fungal infections (such as candida or aspergillus) in febrile, neutropaenic adult or paediatric patients.

Dutrebis Evropska unija - slovenščina - EMA (European Medicines Agency)

dutrebis

merck sharp dohme limited - lamivudine, raltegravir kalij - okužbe z virusom hiv - antivirals for systemic use, antivirals for treatment of hiv infections, combinations - dutrebis je naveden v kombinaciji z drugimi anti‑retroviral zdravili za zdravljenje okužbe z virusom človeške imunske pomanjkljivosti (hiv‑1) pri odraslih, mladostnikih in otroci v starosti od 6 let in tehtanje vsaj 30 kg brez sedanjosti ali preteklosti dokaz virusne odpornostjo na protivirusna zdravila institucij (sklop prenos integraze) in nrti (nukleozidni zaviralec reverzne transkriptaze) razredov (glej točki 4. 2, 4. 4 in 5.

Iscover Evropska unija - slovenščina - EMA (European Medicines Agency)

iscover

sanofi winthrop industrie - klopidogrel - stroke; peripheral vascular diseases; atrial fibrillation; myocardial infarction; acute coronary syndrome - antitrombotična sredstva - sekundarno preprečevanje atherothrombotic eventsclopidogrel je navedeno v:izobraževanje odraslih bolnikih, ki trpijo za miokardni infarkt (od nekaj dni do manj kot 35 dni), ischaemic kap (od 7 dni do manj kot 6 mesecev) ali sedež periferne arterijske bolezni. za odrasle bolnike, ki trpijo za akutni koronarni sindrom:non-st segmentu višinskih akutni koronarni sindrom (nestabilna angina pektoris ali ne-q-val, miokardni infarkt), vključno z bolniki, ki opravljajo stent umestitev po perkutani koronarni intervenciji, v kombinaciji z acetilsalicilne kisline (asa). st segment elevation acute myocardial infarction, in combination with asa in patients undergoing percutaneous coronary intervention (including patients undergoing a stent placement) 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. preprečevanje atherothrombotic in thromboembolic dogodkov v atrijska fibrillationin odraslih bolnikov z atrijsko fibrilacijo, ki imajo vsaj en dejavnik tveganja za žilne dogodke, niso primerni za zdravljenje z antagonisti vitamina k (vka) in ki imajo nizko tveganje krvavitve, clopidogrel je indiciran v kombinaciji s asa za preprečevanje atherothrombotic in thromboembolic dogodkov, vključno z možgansko kap.

ANASTROZOL ACCORD 1 mg filmsko obložene tablete Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

anastrozol accord 1 mg filmsko obložene tablete

accord healthcare - anastrozol - filmsko obložena tableta - anastrozol 1 mg / 1 tableta - anastrozol

ANASTROZOL ACCORD 1 mg filmsko obložene tablete Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

anastrozol accord 1 mg filmsko obložene tablete

accord healthcare - anastrozol - filmsko obložena tableta - anastrozol 1 mg / 1 tableta - anastrozol

ANASTROZOL ACCORD 1 mg filmsko obložene tablete Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

anastrozol accord 1 mg filmsko obložene tablete

accord healthcare - anastrozol - filmsko obložena tableta - anastrozol 1 mg / 1 tableta - anastrozol