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["0026544","MABTHERA 500 MG","INF CNC SOL 1X50ML","IVN","INF CNC SOL","1X50ML","10MG/ML","VIA","RRG","GB","EU/1/98/067/002","","EUR","R","MCV",32820.63,"Z",37217.04,"S","S","","P","Rituximab předepisuje onkolog, hematolog, revmatolog:\n1) u dosud neléčených nemocných s folikulárním lymfomem III. a IV. klinického stadia v kombinaci s chemoterapií\n2) u difúzního velkobuněčného nehodgkinského maligního lymfomu B řady CD 20 pozitivní v kombinaci s režimem CHOP (cyklofosfamid, doxorubicin, vinkristin, prednizolon)\n3) u nemocných s folikulárním lymfomem III. a IV. klinického stadia, kteří se nacházejí ve druhém či dalším relapsu po chemoterapii nebo jejichž nádor je chemoresistentní \n4) jako udržovací léčba u pacientů s relabovaným/ refrakterním folikulárním lymfomem, kteří odpovídají na indukční chemoterapeutickou léčbu s nebo bez léčivého přípravku s obsahem rituximabu, jednou za 3 měsíce, dokud nedojde k progresi onemocnění nebo nejdéle po dobu dvou let\n5) pro léčbu pacientů s dříve neléčenou a relabující/refrakterní chronickou lymfatickou leukémií v kombinaci s chemoterapií \n6) u těžké aktivní revmatoidní arthritidy v kombinaci s metothrexátem u dospělých pacientů, kteří vykazovali nepřiměřenou reakci nebo nesnášenlivost na terapii nemoc modifikujícími protirevmatickými léky (DMARD), včetně jedné nebo více terapií inhibitory tumor nekrotizujícího faktoru (TNF)\n","","","","","","","","","","","","L01XC02",null,null,"X",null,null,"","","","500","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","0","R","",38629.98,"",38629.98,""]
["0026651","NEOCLARITYN 5 MG","POR TBL FLM 30X5MG","POR","TBL FLM","30","5MG","BLI","SBS","B","EU/1/00/161/011","","EUR","R","MCV",226.86,"S",{"v":129.6,"d":"129.60"},"S","","","","","","","","","","","","","96/2","96","2","R06AX27",null,null,"X",null,null,"5","MG",{"v":30,"d":"30.0000"},"5","MG",4.32,"2008-11-01","2010-01-01",205.55,"","1","R","",336.85,"",336.85,""]
["0026652","NEOCLARITYN 5 MG","POR TBL FLM 50X5MG","POR","TBL FLM","50","5MG","BLI","SBS","B","EU/1/00/161/012","","EUR","R","MCV",399.32,"S",{"v":216,"d":"216.00"},"S","","","","","","","","","","","","","96/2","96","2","R06AX27",null,null,"X",null,null,"5","MG",{"v":50,"d":"50.0000"},"5","MG",4.32,"2008-11-01","2010-01-01",342.58,"","1","R","",579.32,"",579.32,""]
["0027357","PREVENAR","INJ SUS 1X0.5MLSTŘ+J","IMS","INJ SUS","0.5ML ST+J","0.5ML","ISP","WYV","B","EU/1/00/167/006","","EUR","R","MCV",1184.19,"Z",{"v":1613.7,"d":"1613.70"},"V","A","","P","","I","","","","","","","","","","","J07AL02",null,"2011-02-03","",null,"2010-09-30","","","","","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","0","R","",{"v":1613.7,"d":"1613.70"},"1099",{"v":1613.7,"d":"1613.70"},""]
["0028274","ALIMTA 500 MG","INF PLV CSL 1X500MG","IVN","INF PLV CSL","1","500MG/LAH","VIA","ELH","NL","EU/1/04/290/001","","EUR","R","MCV",33086.87,"S",28493.06,"S","S","","P","Pemetrexed je indikován:\n1) v kombinační léčbě s cisplatinou u pacientů s neresekovatelným maligním mezoteliomem pleury, 2) v 1. linii léčby v kombinaci s cisplatinou lokálně pokročilého nebo metastazujícího karcinomu plic pouze diagnosticky prokázaného adenokarcinomu a velkobuněčného morfologického typu. Přípravek je podáván až do progrese onemocnění, nicméně z prostředků veřejného zdravotního pojištění jsou hrazeny maximálně 4 cykly léčby, \n3) v 2. linii léčby lokálně pokročilého nebo metastazujícího nemalobuněčného karcinomu plic jiného histologického typu než predominantně z dlaždicových buněk \n","","","","","","","","","","","","L01BA04",null,null,"X",null,null,"","","","41","MG","","2010-04-01","2010-10-01",{"v":0,"d":"0.00"},"","0","R","",38937.48,"",38937.48,""]
["0028880","AZOMYR 0,5 MG/ML","POR SOL 1X120ML+LŽ","POR","SOL","120ML+LŽ","0.5MG/ML","LAG","SBS","B","EU/1/00/157/063","","EUR","R","MCV",141.54,"S",51.84,"S","","","","","","","","","","","","","96/2","96","2","R06AX27",null,null,"X",null,null,"5","MG",{"v":12,"d":"12.0000"},"5","MG",4.32,"2008-11-01","2010-01-01",82.22,"","1","R","",211.74,"",211.74,""]
["0028913","NEOCLARITYN 0,5 MG/ML","POR SOL 1X120ML+LŽ","POR","SOL","120ML+LŽ","0.5MG","LAG","SBS","B","EU/1/00/161/063","","EUR","R","MCV",141.54,"S",51.84,"S","","","","","","","","","","","","","96/2","96","2","R06AX27",null,null,"X",null,null,"5","MG",{"v":12,"d":"12.0000"},"5","MG",4.32,"2008-11-01","2010-01-01",82.22,"","1","R","",211.74,"",211.74,""]
["0029224","BINOCRIT 1000 IU/0,5 ML","SDR+IVN INJ SOL 1X0.5ML","IVN","INJ SOL","1X0.5ML","2000UT/ML","ISP","SZK","A","EU/1/07/410/001","","EUR","R","MCV",191.96,"S",222.54,"S","A","","P","Erytropoetin alfa předepisuje onkolog, hematolog, internista, nefrolog nebo pediatr:\n1. k léčbě klinicky významné anémie (s hladinou hemoglobinu nižší než 90 g/l, s vyššími hodnotami při manifestních příznacích anémie) u pacientů zařazených do dialyzačního programu, pacientů s chronickým renálním selháním, pacientů s nádorovým onemocněním po radikální cytostatické léčbě nebo ozáření\n2. k léčbě anémie u pacientů s aplastickou anémií, erythroblastoftýzou, myelodysplastickým syndromem a anémií po transplantaci kostní dřeně\n","","","","","","","","","18/1","18","1","B03XA01",null,"2012-08-31","",null,null,"1","KU",{"v":1,"d":"1.0000"},"1000","IU","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","0","R","",285.79,"",285.79,""]
["0029225","BINOCRIT 1000 IU/0,5 ML","SDR+IVN INJ SOL 6X0.5ML","IVN","INJ SOL","6X0.5ML","2000UT/ML","ISP","SZK","A","EU/1/07/410/002","","EUR","R","MCV",1143.57,"S",1335.27,"S","A","","P","Erytropoetin alfa předepisuje onkolog, hematolog, internista, nefrolog nebo pediatr:\n1. k léčbě klinicky významné anémie (s hladinou hemoglobinu nižší než 90 g/l, s vyššími hodnotami při manifestních příznacích anémie) u pacientů zařazených do dialyzačního programu, pacientů s chronickým renálním selháním, pacientů s nádorovým onemocněním po radikální cytostatické léčbě nebo ozáření\n2. k léčbě anémie u pacientů s aplastickou anémií, erythroblastoftýzou, myelodysplastickým syndromem a anémií po transplantaci kostní dřeně\n","","","","","","","","","18/1","18","1","B03XA01",null,"2012-08-31","",null,null,"1","KU",{"v":6,"d":"6.0000"},"1000","IU","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","0","R","",1561.42,"",1561.42,""]
["0029226","BINOCRIT 2000 IU/1,0 ML","SDR+IVN INJ SOL 1X1.0ML","IVN","INJ SOL","1X1.0ML","2000UT/ML","ISP","SZK","A","EU/1/07/410/003","","EUR","R","MCV",383.77,"S",445.09,"S","A","","P","Erytropoetin alfa předepisuje onkolog, hematolog, internista, nefrolog nebo pediatr:\n1. k léčbě klinicky významné anémie (s hladinou hemoglobinu nižší než 90 g/l, s vyššími hodnotami při manifestních příznacích anémie) u pacientů zařazených do dialyzačního programu, pacientů s chronickým renálním selháním, pacientů s nádorovým onemocněním po radikální cytostatické léčbě nebo ozáření\n2. k léčbě anémie u pacientů s aplastickou anémií, erythroblastoftýzou, myelodysplastickým syndromem a anémií po transplantaci kostní dřeně\n","","","","","","","","","18/1","18","1","B03XA01",null,"2012-08-31","",null,null,"1","KU",{"v":2,"d":"2.0000"},"1000","IU","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","0","R","",558.11,"",558.11,""]
["0029227","BINOCRIT 2000 IU/1,0 ML","SDR+IVN INJ SOL 6X1.0ML","IVN","INJ SOL","6X1.0ML","2000UT/ML","ISP","SZK","A","EU/1/07/410/004","","EUR","R","MCV",2319.17,"S",2670.53,"S","A","","P","Erytropoetin alfa předepisuje onkolog, hematolog, internista, nefrolog nebo pediatr:\n1. k léčbě klinicky významné anémie (s hladinou hemoglobinu nižší než 90 g/l, s vyššími hodnotami při manifestních příznacích anémie) u pacientů zařazených do dialyzačního programu, pacientů s chronickým renálním selháním, pacientů s nádorovým onemocněním po radikální cytostatické léčbě nebo ozáření\n2. k léčbě anémie u pacientů s aplastickou anémií, erythroblastoftýzou, myelodysplastickým syndromem a anémií po transplantaci kostní dřeně\n","","","","","","","","","18/1","18","1","B03XA01",null,"2012-08-31","",null,null,"1","KU",{"v":12,"d":"12.0000"},"1000","IU","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","0","R","",3074.42,"",3074.42,""]
["0029228","BINOCRIT 3000 IU/0,3 ML","SDR+IVN INJ SOL 1X0.3ML","IVN","INJ SOL","1X0.3ML","10000UT/ML","ISP","SZK","A","EU/1/07/410/005","","EUR","R","MCV",570.38,"S",667.63,"S","A","","P","Erytropoetin alfa předepisuje onkolog, hematolog, internista, nefrolog nebo pediatr:\n1. k léčbě klinicky významné anémie (s hladinou hemoglobinu nižší než 90 g/l, s vyššími hodnotami při manifestních příznacích anémie) u pacientů zařazených do dialyzačního programu, pacientů s chronickým renálním selháním, pacientů s nádorovým onemocněním po radikální cytostatické léčbě nebo ozáření\n2. k léčbě anémie u pacientů s aplastickou anémií, erythroblastoftýzou, myelodysplastickým syndromem a anémií po transplantaci kostní dřeně\n","","","","","","","","","18/1","18","1","B03XA01",null,"2012-08-31","",null,null,"1","KU",{"v":3,"d":"3.0000"},"1000","IU","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","0","R","",809.55,"",809.55,""]
["0029229","BINOCRIT 3000 IU/0,3 ML","SDR+IVN INJ SOL 6X0.3ML","IVN","INJ SOL","6X0.3ML","10000UT/ML","ISP","SZK","A","EU/1/07/410/006","","EUR","R","MCV",3420.49,"S",{"v":4005.8,"d":"4005.80"},"S","A","","P","Erytropoetin alfa předepisuje onkolog, hematolog, internista, nefrolog nebo pediatr:\n1. k léčbě klinicky významné anémie (s hladinou hemoglobinu nižší než 90 g/l, s vyššími hodnotami při manifestních příznacích anémie) u pacientů zařazených do dialyzačního programu, pacientů s chronickým renálním selháním, pacientů s nádorovým onemocněním po radikální cytostatické léčbě nebo ozáření\n2. k léčbě anémie u pacientů s aplastickou anémií, erythroblastoftýzou, myelodysplastickým syndromem a anémií po transplantaci kostní dřeně\n","","","","","","","","","18/1","18","1","B03XA01",null,"2012-08-31","",null,null,"1","KU",{"v":18,"d":"18.0000"},"1000","IU","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","0","R","",4461.44,"",4461.44,""]
["0029230","BINOCRIT 4000 IU/0,4 ML","SDR+IVN INJ SOL 1X0.4ML","IVN","INJ SOL","1X0.4ML","10000UT/ML","ISP","SZK","A","EU/1/07/410/007","","EUR","R","MCV",760.75,"S",890.18,"S","A","","P","Erytropoetin alfa předepisuje onkolog, hematolog, internista, nefrolog nebo pediatr:\n1. k léčbě klinicky významné anémie (s hladinou hemoglobinu nižší než 90 g/l, s vyššími hodnotami při manifestních příznacích anémie) u pacientů zařazených do dialyzačního programu, pacientů s chronickým renálním selháním, pacientů s nádorovým onemocněním po radikální cytostatické léčbě nebo ozáření\n2. k léčbě anémie u pacientů s aplastickou anémií, erythroblastoftýzou, myelodysplastickým syndromem a anémií po transplantaci kostní dřeně\n","","","","","","","","","18/1","18","1","B03XA01",null,"2012-08-31","",null,null,"1","KU",{"v":4,"d":"4.0000"},"1000","IU","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","0","R","",1060.84,"",1060.84,""]
["0029231","BINOCRIT 4000 IU/0,4 ML","SDR+IVN INJ SOL 6X0.4ML","IVN","INJ SOL","6X0.4ML","10000UT/ML","ISP","SZK","A","EU/1/07/410/008","","EUR","R","MCV",{"v":4482.7,"d":"4482.70"},"S",5341.06,"S","A","","P","Erytropoetin alfa předepisuje onkolog, hematolog, internista, nefrolog nebo pediatr:\n1. k léčbě klinicky významné anémie (s hladinou hemoglobinu nižší než 90 g/l, s vyššími hodnotami při manifestních příznacích anémie) u pacientů zařazených do dialyzačního programu, pacientů s chronickým renálním selháním, pacientů s nádorovým onemocněním po radikální cytostatické léčbě nebo ozáření\n2. k léčbě anémie u pacientů s aplastickou anémií, erythroblastoftýzou, myelodysplastickým syndromem a anémií po transplantaci kostní dřeně\n","","","","","","","","","18/1","18","1","B03XA01",null,"2012-08-31","",null,null,"1","KU",{"v":24,"d":"24.0000"},"1000","IU","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","0","R","",5793.46,"",5793.46,""]
["0029232","BINOCRIT 5000 IU/0,5 ML","SDR+IVN INJ SOL 1X0.5ML","IVN","INJ SOL","1X0.5ML","10000UT/ML","ISP","SZK","A","EU/1/07/410/009","","EUR","R","MCV",950.87,"S",1112.72,"S","A","","P","Erytropoetin alfa předepisuje onkolog, hematolog, internista, nefrolog nebo pediatr:\n1. k léčbě klinicky významné anémie (s hladinou hemoglobinu nižší než 90 g/l, s vyššími hodnotami při manifestních příznacích anémie) u pacientů zařazených do dialyzačního programu, pacientů s chronickým renálním selháním, pacientů s nádorovým onemocněním po radikální cytostatické léčbě nebo ozáření\n2. k léčbě anémie u pacientů s aplastickou anémií, erythroblastoftýzou, myelodysplastickým syndromem a anémií po transplantaci kostní dřeně\n","","","","","","","","","18/1","18","1","B03XA01",null,"2012-08-31","",null,null,"1","KU",{"v":5,"d":"5.0000"},"1000","IU","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","0","R","",{"v":1311.8,"d":"1311.80"},"",{"v":1311.8,"d":"1311.80"},""]
["0029233","BINOCRIT 5000 IU/0,5 ML","SDR+IVN INJ SOL 6X0.5ML","IVN","INJ SOL","6X0.5ML","10000UT/ML","ISP","SZK","A","EU/1/07/410/010","","EUR","R","MCV",5674.43,"S",6676.33,"S","A","","P","Erytropoetin alfa předepisuje onkolog, hematolog, internista, nefrolog nebo pediatr:\n1. k léčbě klinicky významné anémie (s hladinou hemoglobinu nižší než 90 g/l, s vyššími hodnotami při manifestních příznacích anémie) u pacientů zařazených do dialyzačního programu, pacientů s chronickým renálním selháním, pacientů s nádorovým onemocněním po radikální cytostatické léčbě nebo ozáření\n2. k léčbě anémie u pacientů s aplastickou anémií, erythroblastoftýzou, myelodysplastickým syndromem a anémií po transplantaci kostní dřeně\n","","","","","","","","","18/1","18","1","B03XA01",null,"2012-08-31","",null,null,"1","KU",{"v":30,"d":"30.0000"},"1000","IU","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","0","R","",7228.54,"",7228.54,""]
["0029234","BINOCRIT 6000 IU/0,6 ML","SDR+IVN INJ SOL 1X0.6ML","IVN","INJ SOL","1X0.6ML","10000UT/ML","ISP","SZK","A","EU/1/07/410/011","","EUR","R","MCV",1140.89,"S",1335.27,"S","A","","P","Erytropoetin alfa předepisuje onkolog, hematolog, internista, nefrolog nebo pediatr:\n1. k léčbě klinicky významné anémie (s hladinou hemoglobinu nižší než 90 g/l, s vyššími hodnotami při manifestních příznacích anémie) u pacientů zařazených do dialyzačního programu, pacientů s chronickým renálním selháním, pacientů s nádorovým onemocněním po radikální cytostatické léčbě nebo ozáření\n2. k léčbě anémie u pacientů s aplastickou anémií, erythroblastoftýzou, myelodysplastickým syndromem a anémií po transplantaci kostní dřeně\n","","","","","","","","","18/1","18","1","B03XA01",null,"2012-08-31","",null,null,"1","KU",{"v":6,"d":"6.0000"},"1000","IU","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","0","R","",1557.98,"",1557.98,""]
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["0118762","FINASTERID ORION 5 MG POTAHOVANÉ TABLETY","POR TBL FLM 100X5MG","POR","TBL FLM","100","5MG","BLI","ORN","SF","87/343/07-C","","CMS","R","OP","","",870.12,"S","E","URN","","","","","","","","","","","46/2","46","2","G04CB01","2007-06-06","2011-04-30","","2008-01-02",null,"5","MG",{"v":100,"d":"100.0000"},"5","MG",{"v":8.7,"d":"8.70"},null,"2010-08-01",{"v":0,"d":"0.00"},"","U","R","",1321.08,"","",""]
["0121385","GRANISETRON TEVA 1 MG/1 ML","INJ+INF CNC SOL 1X1ML/1MG","INJ+INF","CNC SOL","1AMP","1MG/1ML","AMP","TPP","CZ","20/237/08-C","","CMS","R","MCV",122.53,"S",62.64,"S","","","P","Granisetron  je indikován u pacientů s nauzeou a zvracením v důsledku silného uvolňování serotoninu, navozeného cytotoxickou chemoterapií a radioterapií.","","","","","","","","","4/2","4","2","A04AA02","2008-05-21","2012-08-31","",null,null,"3","MG",0.3333,"3","MG","","2010-10-01","2010-10-01",26.88,"","1","R","",{"v":183.3,"d":"183.30"},"",{"v":183.3,"d":"183.30"},""]
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["0121410","GRANISETRON TEVA 3 MG/3 ML","INJ+INF CNC SOL 5X3ML/3MG","INJ+INF","CNC SOL","5AMP","3MG/3ML","AMP","TPP","CZ","20/238/08-C","","CMS","R","MCV",1555.22,"S",939.62,"S","","","P","Granisetron  je indikován u pacientů s nauzeou a zvracením v důsledku silného uvolňování serotoninu, navozeného cytotoxickou chemoterapií a radioterapií.","","","","","","","","","4/2","4","2","A04AA02","2008-05-21","2012-08-31","",null,null,"3","MG",{"v":5,"d":"5.0000"},"3","MG","","2010-10-01","2010-10-01",403.25,"","1","R","",2091.22,"",2091.22,""]
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["0125338","AZIBIOT 500 MG","POR TBL FLM 3X500MG","POR","TBL FLM","3","500MG","BLI","ICH","CZ","15/409/07-C","","NAR","B","OP","","",{"v":126.6,"d":"126.60"},"S","","","","","","","","","","","","","55/1","55","1","J01FA10","2007-09-12","2011-03-31","","2008-05-01",null,"0,3","GM",{"v":5,"d":"5.0000"},"500","MG",23.55,"2010-01-01","2010-01-01",{"v":30,"d":"30.00"},"","1","R","",202.96,"","",""]
["0125339","LEKOPROST","POR TBL FLM 100X5MG","POR","TBL FLM","100","5MG","BLI","GDB","H","87/010/03-C","","NAR","R","OP","","",870.12,"S","E","URN","","","","","","","","","","","46/2","46","2","G04CB01","2003-01-22","2013-02-18","",null,null,"5","MG",{"v":100,"d":"100.0000"},"5","MG",{"v":8.7,"d":"8.70"},null,"2010-08-01",{"v":0,"d":"0.00"},"","U","R","","","","",""]
["0127005","PROMEMORE 5 MG","POR TBL FLM 30X5MG","POR","TBL FLM","30","5MG","BLI","SVS","CZ","06/773/09-C","","NAR","R","MCV",734.75,"S",868.57,"S","E","NEU, PSY, GER","P","Léčivý přípravek je předepisován u pacientů, u kterých je diagnosticky vyloučena demence jiného typu než Alzheimerova a potvrzena diagnóza Alzheimerovy demence se stupněm postižení vyjádřeným dle škály MMSE (Mini-Mental State Examination) v rozmezí dosaženého skóre 25 - 13 bodů včetně. Po 12. týdnech (3 měsíce) od zahájení podávání donepezilu je provedeno další vyšetření pacienta škálou MMSE. Léčba donepezilem je indikována při setrvání skóre, nebo jeho poklesu o nejvíce 2 body ve srovnání s hodnotou MMSE dosahovanou pacientem před zahájením léčby donepezilem. Další kontroly MMSE jsou prováděny nejméně po každých 3 měsících léčby. Léčba donepezilem není indikována u pacientů, u nichž po 6, 9 atd. měsících od zahájení léčby nedojde k objektivně prokazatelnému terapeutickému účinku (tj. zastavení progrese anebo pokles menší než 2 body dle škály MMSE oproti původnímu stavu) a dále při zjištěném skóre škály MMSE 12 bodů. Tato kritéria se vztahují i na léčbu pacientů trvající v rámci stanovených kritérií déle než 9 měsíců.","","","","","","","","","87/1","87","1","N06DA02","2009-11-11","2014-12-09","",null,null,"7,5","MG",{"v":20,"d":"20.0000"},"10","MG","","2010-05-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",1026.52,"",1026.52,""]
["0127009","PROMEMORE 10 MG","POR TBL FLM 30X10MG","POR","TBL FLM","30","10MG","BLI","SVS","CZ","06/774/09-C","","NAR","R","MCV",1252.02,"S",{"v":1158,"d":"1158.00"},"S","E","NEU, PSY, GER","P","Léčivý přípravek je předepisován u pacientů, u kterých je diagnosticky vyloučena demence jiného typu než Alzheimerova a potvrzena diagnóza Alzheimerovy demence se stupněm postižení vyjádřeným dle škály MMSE (Mini-Mental State Examination) v rozmezí dosaženého skóre 25 - 13 bodů včetně. Po 12. týdnech (3 měsíce) od zahájení podávání donepezilu je provedeno další vyšetření pacienta škálou MMSE. Léčba donepezilem je indikována při setrvání skóre, nebo jeho poklesu o nejvíce 2 body ve srovnání s hodnotou MMSE dosahovanou pacientem před zahájením léčby donepezilem. Další kontroly MMSE jsou prováděny nejméně po každých 3 měsících léčby. Léčba donepezilem není indikována u pacientů, u nichž po 6, 9 atd. měsících od zahájení léčby nedojde k objektivně prokazatelnému terapeutickému účinku (tj. zastavení progrese anebo pokles menší než 2 body dle škály MMSE oproti původnímu stavu) a dále při zjištěném skóre škály MMSE 12 bodů. Tato kritéria se vztahují i na léčbu pacientů trvající v rámci stanovených kritérií déle než 9 měsíců.","","","","","","","","","87/1","87","1","N06DA02","2009-11-11","2014-12-04","",null,null,"7,5","MG",{"v":40,"d":"40.0000"},"10","MG","","2010-05-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",{"v":1701,"d":"1701.00"},"",{"v":1701,"d":"1701.00"},""]
["0127011","PROMEMORE 10 MG","POR TBL FLM 90X10MG","POR","TBL FLM","90","10MG","BLI","SVS","CZ","06/774/09-C","","NAR","R","MCV",{"v":4116,"d":"4116.00"},"S",{"v":3474,"d":"3474.00"},"S","E","NEU, PSY, GER","P","Léčivý přípravek je předepisován u pacientů, u kterých je diagnosticky vyloučena demence jiného typu než Alzheimerova a potvrzena diagnóza Alzheimerovy demence se stupněm postižení vyjádřeným dle škály MMSE (Mini-Mental State Examination) v rozmezí dosaženého skóre 25 - 13 bodů včetně. Po 12. týdnech (3 měsíce) od zahájení podávání donepezilu je provedeno další vyšetření pacienta škálou MMSE. Léčba donepezilem je indikována při setrvání skóre, nebo jeho poklesu o nejvíce 2 body ve srovnání s hodnotou MMSE dosahovanou pacientem před zahájením léčby donepezilem. Další kontroly MMSE jsou prováděny nejméně po každých 3 měsících léčby. Léčba donepezilem není indikována u pacientů, u nichž po 6, 9 atd. měsících od zahájení léčby nedojde k objektivně prokazatelnému terapeutickému účinku (tj. zastavení progrese anebo pokles menší než 2 body dle škály MMSE oproti původnímu stavu) a dále při zjištěném skóre škály MMSE 12 bodů. Tato kritéria se vztahují i na léčbu pacientů trvající v rámci stanovených kritérií déle než 9 měsíců.","","","","","","","","","87/1","87","1","N06DA02","2009-11-11","2014-12-04","",null,null,"7,5","MG",{"v":120,"d":"120.0000"},"10","MG","","2010-05-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",5333.61,"",5333.61,""]
["0131859","PACLITAXEL KABI 6 MG/ML KONCENTRÁT PRO PŘÍPRAVU INFUZNÍHO ROZTOKU","INF CNC SOL 1X5ML/30MG","INF","CNC SOL","1X5ML","6MG/ML","VIA","FRK","CZ","44/410/09-C","","CMS","R","MCV",1359.16,"S",{"v":1382.7,"d":"1382.70"},"S","A","ONK","P","Paclitaxel předepisuje onkolog u pacientů: 1. a) v primární kombinované chemoterapii časných stadií\nkarcinomu ovaria zvýšeného rizika (I.a,b, G3, Ic, G2-3) nebo pokročilých stadií karcinomu ovaria, b)\npo selhání primární léčby karcinomů ovaria senzitivních k cisplatině (při recidivě v odstupu delším než\n6 měs.), 2. a) s generalizovaným karcinomem prsu v další linii po selhání standardní léčby, b) v první\nvolbě pro kombinovanou chemoterapii generalizovaného karcinomu prsu s postižením jedné\nmetastatické lokalizace (játra, plíce) u premenopauzálních žen ER neg. , c) v adjuvantním podání v\npřípadě postižených lymfatických uzlin u pre- a perimenopauzálních pacientek s neg. estrogen.\nreceptory. 3. v terapii nemalobuněčného karcinomu plic u chemoterapií nepředléčených nemocných při\nradikálním léčebném záměru","","","","","","","","","63/1","63","1","L01CD01","2009-05-20","2014-01-11","",null,null,"","","","14","MG",{"v":664.1,"d":"664.10"},"2010-10-01","2010-02-01",{"v":0,"d":"0.00"},"","0","R","",1838.89,"",1838.89,""]
["0131861","PACLITAXEL KABI 6 MG/ML KONCENTRÁT PRO PŘÍPRAVU INFUZNÍHO ROZTOKU","INF CNC SOL 1X16.7ML/100.2MG","INF","CNC SOL","1X16.7ML","6MG/ML","VIA","FRK","CZ","44/410/09-C","","CMS","R","MCV",4530.28,"S",{"v":4609,"d":"4609.00"},"S","A","ONK","P","Paclitaxel předepisuje onkolog u pacientů: 1. a) v primární kombinované chemoterapii časných stadií\nkarcinomu ovaria zvýšeného rizika (I.a,b, G3, Ic, G2-3) nebo pokročilých stadií karcinomu ovaria, b)\npo selhání primární léčby karcinomů ovaria senzitivních k cisplatině (při recidivě v odstupu delším než\n6 měs.), 2. a) s generalizovaným karcinomem prsu v další linii po selhání standardní léčby, b) v první\nvolbě pro kombinovanou chemoterapii generalizovaného karcinomu prsu s postižením jedné\nmetastatické lokalizace (játra, plíce) u premenopauzálních žen ER neg. , c) v adjuvantním podání v\npřípadě postižených lymfatických uzlin u pre- a perimenopauzálních pacientek s neg. estrogen.\nreceptory. 3. v terapii nemalobuněčného karcinomu plic u chemoterapií nepředléčených nemocných při\nradikálním léčebném záměru","","","","","","","","","63/1","63","1","L01CD01","2009-05-20","2014-01-11","",null,null,"","","","14","MG",{"v":664.1,"d":"664.10"},"2010-10-01","2010-02-01",{"v":0,"d":"0.00"},"","0","R","",5853.12,"",5853.12,""]
["0131863","PACLITAXEL KABI 6 MG/ML KONCENTRÁT PRO PŘÍPRAVU INFUZNÍHO ROZTOKU","INF CNC SOL 1X50ML/300MG","INF","CNC SOL","1X50ML","6MG/ML","VIA","FRK","CZ","44/410/09-C","","CMS","R","MCV",{"v":13591.1,"d":"13591.10"},"S",{"v":13825.9,"d":"13825.90"},"S","A","ONK","P","Paclitaxel předepisuje onkolog u pacientů: 1. a) v primární kombinované chemoterapii časných stadií\nkarcinomu ovaria zvýšeného rizika (I.a,b, G3, Ic, G2-3) nebo pokročilých stadií karcinomu ovaria, b)\npo selhání primární léčby karcinomů ovaria senzitivních k cisplatině (při recidivě v odstupu delším než\n6 měs.), 2. a) s generalizovaným karcinomem prsu v další linii po selhání standardní léčby, b) v první\nvolbě pro kombinovanou chemoterapii generalizovaného karcinomu prsu s postižením jedné\nmetastatické lokalizace (játra, plíce) u premenopauzálních žen ER neg. , c) v adjuvantním podání v\npřípadě postižených lymfatických uzlin u pre- a perimenopauzálních pacientek s neg. estrogen.\nreceptory. 3. v terapii nemalobuněčného karcinomu plic u chemoterapií nepředléčených nemocných při\nradikálním léčebném záměru","","","","","","","","","63/1","63","1","L01CD01","2009-05-20","2014-01-11","",null,null,"","","","14","MG",{"v":664.1,"d":"664.10"},"2010-10-01","2010-02-01",{"v":0,"d":"0.00"},"","0","R","",16419.87,"",16419.87,""]
["0134110","LOSARTAN ORION 50 MG","POR TBL FLM 28X50MG","POR","TBL FLM","28 BLI I","50MG","BLI","ORN","SF","58/718/09-C","","CMS","R","OP","","",94.68,"S","","","","","","","","","","","","","25/3","25","3","C09CA01","2009-10-29","2014-05-30","","2010-08-18",null,"50","MG",{"v":28,"d":"28.0000"},"20","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",131.65,"","",""]
["0134111","LOSARTAN ORION 50 MG","POR TBL FLM 98X50MG","POR","TBL FLM","98 BLI I","50MG","BLI","ORN","SF","58/718/09-C","","CMS","R","OP","","",331.37,"S","","","","","","","","","","","","","25/3","25","3","C09CA01","2009-10-29","2014-05-30","","2010-08-18",null,"50","MG",{"v":98,"d":"98.0000"},"20","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",414.59,"","",""]
["0134112","LOSARTAN ORION 50 MG","POR TBL FLM 28X50MG","POR","TBL FLM","28 BLI II","50MG","BLI","ORN","SF","58/718/09-C","","CMS","R","OP","","",94.68,"S","","","","","","","","","","","","","25/3","25","3","C09CA01","2009-10-29","2014-05-30","",null,null,"50","MG",{"v":28,"d":"28.0000"},"20","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",131.65,"","",""]
["0134113","LOSARTAN ORION 50 MG","POR TBL FLM 98X50MG","POR","TBL FLM","98 BLI II","50MG","BLI","ORN","SF","58/718/09-C","","CMS","R","OP","","",331.37,"S","","","","","","","","","","","","","25/3","25","3","C09CA01","2009-10-29","2014-05-30","",null,null,"50","MG",{"v":98,"d":"98.0000"},"20","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",414.59,"","",""]
["0134114","LOSARTAN ORION 100 MG","POR TBL FLM 28X100MG","POR","TBL FLM","28 BLI I","100MG","BLI","ORN","SF","58/719/09-C","","CMS","R","OP","","",{"v":126.2,"d":"126.20"},"S","","","","","","","","","","","","","25/3","25","3","C09CA01","2009-10-29","2014-05-30","","2010-08-18",null,"50","MG",{"v":56,"d":"56.0000"},"20","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",166.06,"","",""]
["0134115","LOSARTAN ORION 100 MG","POR TBL FLM 98X100MG","POR","TBL FLM","98 BLI I","100MG","BLI","ORN","SF","58/719/09-C","","CMS","R","OP","","",441.72,"S","","","","","","","","","","","","","25/3","25","3","C09CA01","2009-10-29","2014-05-30","","2010-08-18",null,"50","MG",{"v":196,"d":"196.0000"},"20","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",525.69,"","",""]
["0134116","LOSARTAN ORION 100 MG","POR TBL FLM 28X100MG","POR","TBL FLM","28 BLI II","100MG","BLI","ORN","SF","58/719/09-C","","CMS","R","OP","","",{"v":126.2,"d":"126.20"},"S","","","","","","","","","","","","","25/3","25","3","C09CA01","2009-10-29","2014-05-30","",null,null,"50","MG",{"v":56,"d":"56.0000"},"20","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",166.06,"","",""]
["0134117","LOSARTAN ORION 100 MG","POR TBL FLM 98X100MG","POR","TBL FLM","98 BLI II","100MG","BLI","ORN","SF","58/719/09-C","","CMS","R","OP","","",441.72,"S","","","","","","","","","","","","","25/3","25","3","C09CA01","2009-10-29","2014-05-30","",null,null,"50","MG",{"v":196,"d":"196.0000"},"20","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",525.69,"","",""]
["0136072","PACLITAXEL ACTAVIS 6 MG/ML","INF CNC SOL 1X16.7ML/100MG","INF","CNC SOL","1X16.7ML/100MG","6MG/ML","VIA","ACK","IS","44/048/08-C","","CMS","R","MCV",2558.79,"S",{"v":4609,"d":"4609.00"},"S","A","ONK","P","Paclitaxel předepisuje onkolog u pacientů: 1. a) v primární kombinované chemoterapii časných stadií karcinomu ovaria zvýšeného rizika (I.a,b, G3, Ic, G2-3) nebo pokročilých stadií karcinomu ovaria,    b) po selhání primární léčby karcinomů ovaria senzitivních k cisplatině (při recidivě v odstupu delším než 6 měs.), 2. a) s generalizovaným karcinomem prsu v další linii po selhání standardní léčby, b) v první volbě pro kombinovanou chemoterapii generalizovaného karcinomu prsu s postižením jedné metastatické lokalizace (játra, plíce) u premenopauzálních žen ER neg. , c) v adjuvantním podání v případě postižených lymfatických uzlin u pre- a perimenopauzálních pacientek s neg. estrogen. receptory. 3. v terapii nemalobuněčného karcinomu plic u chemoterapií nepředléčených nemocných při radikálním léčebném záměru","","","","","","","","","63/1","63","1","L01CD01","2008-02-27","2012-12-14","","2010-08-09",null,"","","","14,4","MG","","2010-10-01","2010-02-01",{"v":0,"d":"0.00"},"","0","R","",3380.87,"",3380.87,""]
["0136078","PACLITAXEL ACTAVIS 6 MG/ML","INF CNC SOL 1X50ML/300MG","INF","CNC SOL","1X50ML/300MG","6MG/ML","VIA","ACK","IS","44/048/08-C","","CMS","R","MCV",9090.06,"S",{"v":13827,"d":"13827.00"},"S","A","ONK","P","Paclitaxel předepisuje onkolog u pacientů: 1. a) v primární kombinované chemoterapii časných stadií karcinomu ovaria zvýšeného rizika (I.a,b, G3, Ic, G2-3) nebo pokročilých stadií karcinomu ovaria,    b) po selhání primární léčby karcinomů ovaria senzitivních k cisplatině (při recidivě v odstupu delším než 6 měs.), 2. a) s generalizovaným karcinomem prsu v další linii po selhání standardní léčby, b) v první volbě pro kombinovanou chemoterapii generalizovaného karcinomu prsu s postižením jedné metastatické lokalizace (játra, plíce) u premenopauzálních žen ER neg. , c) v adjuvantním podání v případě postižených lymfatických uzlin u pre- a perimenopauzálních pacientek s neg. estrogen. receptory. 3. v terapii nemalobuněčného karcinomu plic u chemoterapií nepředléčených nemocných při radikálním léčebném záměru","","","","","","","","","63/1","63","1","L01CD01","2008-02-27","2012-12-14","","2010-08-09",null,"","","","14,4","MG","","2010-10-01","2010-02-01",{"v":0,"d":"0.00"},"","0","R","",11211.16,"",11211.16,""]
["0137120","MAGNESIUM 250 MG PHARMAVIT","POR TBL EFF 20","POR","TBL EFF","20","250MG","TBC","WAV","CZ","39/214/94-C","","NAR","R","MCV",39.79,"Z",52.92,"Z","L","INT,NEU,PSY,GYN,GER","","","","","","","","","","","","","","A12CC30",null,"2014-03-31","",null,null,"","","","","","","2010-09-01","2010-01-01",3.98,"","1","F","",59.53,"",59.53,""]
["0137238","ADENOCOR","INJ SOL 6X2ML/6MG","INJ","SOL","6X2ML","3MG/ML","VIA","SFK","CZ","13/574/95-C","","NAR","R","MCV",{"v":1064.4,"d":"1064.40"},"S",1443.69,"Z","O","INT,KAR,GER","","","","","","","","","","","","","","C01EB10",null,"2010-08-31","",null,null,"15","MG",{"v":2.4,"d":"2.4000"},"","","","2010-10-01","2010-01-01",{"v":0,"d":"0.00"},"","0","R","",1459.53,"",1459.53,""]
["0137276","EXACYL","POR SOL 5X10ML/1GM","POR","SOL","5X10ML","100MG/ML","AMP","SFK","CZ","16/402/91-S/C","","NAR","R","MCV",60.57,"S",53.25,"S","","","","","","","","","","","","","16/1","16","1","B02AA02",null,"2011-11-30","",null,null,"2","GM",{"v":2.5,"d":"2.5000"},"3000","MG",31.96,"2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",90.61,"",90.61,""]
["0137495","ASENTRA 50","POR TBL FLM 28X50MG","POR","TBL FLM","28","50MG","BLI","KRK","SLO","30/062/03-C","/PI/001/08","SOU","R","OP","","",260.92,"Z","","","","","","","","","","","","","","","","N06AB06","2003-02-19","2013-07-31","",null,null,"50","MG",{"v":28,"d":"28.0000"},"","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","U","R","","","","",""]
["0138194","NOLITERAX 10 MG/2,5 MG","POR TBL FLM 30","POR","TBL FLM","30","10 MG/2.5 MG","TBC","SVE","F","58/215/09-C","","CMS","B","MCV",{"v":368,"d":"368.00"},"S",159.27,"S","","","","","","","","","","","","","","","","C09BA04","2009-02-25","2012-04-30","",null,null,"1","DF",{"v":30,"d":"30.0000"},"","","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",{"v":536.6,"d":"536.60"},"",{"v":536.6,"d":"536.60"},""]
["0138198","NOLITERAX 10 MG/2,5 MG","POR TBL FLM 90","POR","TBL FLM","90","10 MG/2.5 MG","TBC","SVE","F","58/215/09-C","","CMS","B","MCV",1379.42,"S",{"v":477.8,"d":"477.80"},"S","","","","","","","","","","","","","","","","C09BA04","2009-02-25","2012-04-30","",null,null,"1","DF",{"v":90,"d":"90.0000"},"","","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",1864.96,"",1864.96,""]
["0141308","TESSYRON 75 MG POTAHOVANÉ TABLETY","POR TBL FLM 30X75MG","POR","TBL FLM","30","75MG","BLI","GDB","H","16/021/10-C","","CMS","R","MCV",364.98,"S",393.92,"S","","","P","Klopidogrel předepisuje internista, neurolog , kardiolog a angiolog -\n1) u alergie a prokazatelné intolerance kyseliny acetylsalicylové či při necitlivosti na kyselinu\nacetylsalicylovou prokázanou agregometricky v indikaci snížení rizika\nkardiovaskulárních příhod u nemocných po ischemické mozkové příhodě (včetně TIA), u nemocných\ns ischemickou chorobou srdeční či s ischemickou chorobou dolních končetin\n2) v prevenci recidivy mozkové příhody u nemocných po ischemické mozkové příhodě (včetně TIA),\nkterá se objevila při léčbě kyselinou acetylsalicylovou\n3) v prevenci opakující se trombózy v arterio-venózní spojce u hemodialyzovaných nemocných při léčbě\nkyselinou acetylsalicylovou\n4) po intravaskulárních intervencích s vysokým rizikem trombózy (implantace stentu, rotablace,\nendarterektomie, přímá koronární angioplastika a angioplastika magistrálních tepen) obvykle v kombinaci\ns kyselinou acetylsalicylovou po dobu jednoho měsíce či u tzv.?potahovaných? stentů uvolňujících\nsirolimus či paclitaxel po dobu 9 měsíců","","","X","","","","","","13/1","13","1","B01AC04","2010-01-20","2014-11-24","",null,null,"75","MG",{"v":30,"d":"30.0000"},"75","MG","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",393.92,"",532.48,""]
["0142006","AUGMENTIN 1 G","POR TBL FLM 14X1GM","POR","TBL FLM","14","1GM","BLI","GSB","SK","15/644/96-C","/PI/001/08","SOU","R","OP","","",224.46,"Z","","","","","","","","","","","","","","","","J01CR02",null,"2013-07-31","",null,null,"1","GM",{"v":14,"d":"14.0000"},"","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","U","R","","","","",""]
["0142164","AZIBIOT 500 MG","POR TBL FLM 3X500MG","POR","TBL FLM","3","500MG","BLI","KRK","SLO","15/409/07-C","","NAR","R","OP","","",{"v":126.6,"d":"126.60"},"S","","","","","","","","","","","","","55/1","55","1","J01FA10","2007-09-12","2012-09-30","",null,null,"0,3","GM",{"v":5,"d":"5.0000"},"500","MG/D",23.55,"2010-01-01","2010-01-01",{"v":30,"d":"30.00"},"","1","R","",202.96,"","",""]
["0142306","VENORUTON FORTE","POR TBL NOB 30X500MG","POR","TBL NOB","30","500MG","BLI","NFL","P","85/244/95-C","/PI/001/08","SOU","R","MCV",{"v":104.8,"d":"104.80"},"Z",25.76,"Z","","","","","","","","","","","","","","","","C05CA04",null,"2013-09-30","",null,null,"","","","","","","2010-01-01","2010-01-01",67.83,"","P","F","",156.78,"",156.78,""]
["0142806","PLAVOCORIN","POR TBL FLM 28X75MG II","POR","TBL FLM","28 II","75MG","BLI","DOZ","CZ","16/722/09-C","","CMS","R","MCV",521.28,"S",367.66,"S","","","P","Klopidogrel předepisuje internista, neurolog , kardiolog a angiolog ?\n1) u alergie a prokazatelné intolerance kyseliny acetylsalicylové či při necitlivosti na kyselinu\nacetylsalicylovou prokázanou agregometricky v indikaci snížení rizika kardiovaskulárních\npříhod u nemocných po ischemické mozkové příhodě (včetně TIA), u nemocných\ns ischemickou chorobou srdeční či s ischemickou chorobou dolních končetin\n2) v prevenci recidivy mozkové příhody u nemocných po ischemické mozkové příhodě (včetně\nTIA), která se objevila při léčbě kyselinou acetylsalicylovou\n3) v prevenci opakující se trombózy v arterio-venózní spojce u hemodialyzovaných\nnemocných při léčbě kyselinou acetylsalicylovou\n4) po intravaskulárních intervencích s vysokým rizikem trombózy (implantace stentu,\nrotablace, endarterektomie, přímá koronární angioplastika a angioplastika magistrálních\ntepen) obvykle v kombinaci s kyselinou acetylsalicylovou po dobu jednoho měsíce či u\ntzv.?potahovaných? stentů uvolňujících sirolimus či paclitaxel po dobu 9 měsíců","","","X","","","","","","13/1","13","1","B01AC04","2009-10-29","2011-12-23","","2010-08-02",null,"75","MG",{"v":28,"d":"28.0000"},"500","MG",13.13,"2010-08-01","2010-08-01",{"v":0,"d":"0.00"},"","U","R","",367.66,"",744.74,""]
["0142874","DOCETAXEL EBEWE 10 MG/ML KONCENTRÁT PRO PŘÍPRAVU INFUZNÍHO ROZTOKU","INF CNC SOL 1X2ML/20MG","INF","CNC SOL","1X2ML","10MG/ML","VIA","EBP","A","44/081/10-C","","CMS","R","MCV",2872.04,"S",{"v":2149.2,"d":"2149.20"},"S","A","ONK","P","Docetaxel je indikován u pacientů:\n1) v 1. linii u metastatického karcinomu prsu,\n2) u karcinomu prsu vysoce rizikových pacientek (N1-2) v kombinaci TAC (docetaxel, doxorubicin, cyklofosfamid) jako adjuvantní terapie,\n3) v 2. linii u lokálně pokročilého nebo metastazujícího nemalobuněčného karcinomu plic po selhání předchozí chemoterapie,\n4) v 1. linii v kombinaci s cisplatinou v léčbě neresekovatelného, lokálně pokročilého nebo metastazujícího nemalobuněčného karcinomu plic, kteří pro toto onemocnění nebyly dosud léčeni chemoterapií,\n5) v kombinaci s prednisonem nebo prednisolonem u metastazujícího hormonorezistentního karcinomu prostaty.\n","","","","","","","","","63/1","63","1","L01CD02","2010-01-27","2014-09-23","",null,null,"","","","6,1","MG","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","0","R","",3773.69,"",3773.69,""]
["0142877","DOCETAXEL EBEWE 10 MG/ML KONCENTRÁT PRO PŘÍPRAVU INFUZNÍHO ROZTOKU","INF CNC SOL 1X8ML/80MG","INF","CNC SOL","1X8ML","10MG/ML","VIA","EBP","A","44/081/10-C","","CMS","R","MCV",11503.71,"S",{"v":8596.8,"d":"8596.80"},"S","A","ONK","P","Docetaxel je indikován u pacientů:\n1) v 1. linii u metastatického karcinomu prsu,\n2) u karcinomu prsu vysoce rizikových pacientek (N1-2) v kombinaci TAC (docetaxel, doxorubicin, cyklofosfamid) jako adjuvantní terapie,\n3) v 2. linii u lokálně pokročilého nebo metastazujícího nemalobuněčného karcinomu plic po selhání předchozí chemoterapie,\n4) v 1. linii v kombinaci s cisplatinou v léčbě neresekovatelného, lokálně pokročilého nebo metastazujícího nemalobuněčného karcinomu plic, kteří pro toto onemocnění nebyly dosud léčeni chemoterapií,\n5) v kombinaci s prednisonem nebo prednisolonem u metastazujícího hormonorezistentního karcinomu prostaty.\n","","","","","","","","","63/1","63","1","L01CD02","2010-01-27","2014-09-23","",null,null,"","","","6,1","MG","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","0","R","",14008.94,"",14008.94,""]
["0144309","AMLODIPINE STICHTING 5 MG","POR TBL NOB 30X5MG","POR","TBL NOB","30 BLI I","5MG","BLI","DOZ","CZ","83/361/07-C","","CMS","B","OP","","",57.32,"S","","","","","","","","","","","","","24/1","24","1","C08CA01","2007-07-04","2011-02-20","",null,null,"5","MG",{"v":30,"d":"30.0000"},"5","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","","","","",""]
["0144319","AMLODIPINE STICHTING 5 MG","POR TBL NOB 100X5MG","POR","TBL NOB","100 BLI I","5MG","BLI","DOZ","CZ","83/361/07-C","","CMS","B","OP","","",191.07,"S","","","","","","","","","","","","","24/1","24","1","C08CA01","2007-07-04","2011-02-20","",null,null,"5","MG",{"v":100,"d":"100.0000"},"5","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","","","","",""]
["0144339","AMLODIPINE STICHTING 10 MG","POR TBL NOB 30X10MG","POR","TBL NOB","30 BLI I","10MG","BLI","DOZ","CZ","83/362/07-C","","CMS","B","OP","","",76.41,"S","","","","","","","","","","","","","24/1","24","1","C08CA01","2007-07-04","2011-02-20","",null,null,"5","MG",{"v":60,"d":"60.0000"},"5","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","","","","",""]
["0144349","AMLODIPINE STICHTING 10 MG","POR TBL NOB 100X10MG","POR","TBL NOB","100 BLI I","10MG","BLI","DOZ","CZ","83/362/07-C","","CMS","B","OP","","",254.69,"S","","","","","","","","","","","","","24/1","24","1","C08CA01","2007-07-04","2011-02-20","",null,null,"5","MG",{"v":200,"d":"200.0000"},"5","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","","","","",""]
["0145129","AMLODIPIN IVOWEN 5 MG","POR TBL NOB 30X5MG","POR","TBL NOB","30","5MG","BLI","IWC","IRL","83/354/10-C","","CMS","B","OP","","",57.32,"S","","","","","","","","","","","","","24/1","24","1","C08CA01","2010-05-12","2013-01-31","",null,null,"5","MG",{"v":30,"d":"30.0000"},"5","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","","","","",""]
["0145133","AMLODIPIN IVOWEN 5 MG","POR TBL NOB 100X5MG","POR","TBL NOB","100","5MG","BLI","IWC","IRL","83/354/10-C","","CMS","B","OP","","",191.07,"S","","","","","","","","","","","","","24/1","24","1","C08CA01","2010-05-12","2013-01-31","",null,null,"5","MG",{"v":100,"d":"100.0000"},"5","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","","","","",""]
["0145144","AMLODIPIN IVOWEN 10 MG","POR TBL NOB 30X10MG","POR","TBL NOB","30","10MG","BLI","IWC","IRL","83/355/10-C","","CMS","B","OP","","",76.41,"S","","","","","","","","","","","","","24/1","24","1","C08CA01","2010-05-12","2013-01-31","",null,null,"5","MG",{"v":60,"d":"60.0000"},"5","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","","","","",""]
["0145148","AMLODIPIN IVOWEN 10 MG","POR TBL NOB 100X10MG","POR","TBL NOB","100","10MG","BLI","IWC","IRL","83/355/10-C","","CMS","B","OP","","",254.69,"S","","","","","","","","","","","","","24/1","24","1","C08CA01","2010-05-12","2013-01-31","",null,null,"5","MG",{"v":200,"d":"200.0000"},"5","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","","","","",""]
["0145256","ROSUVASTATIN TEVA 10 MG","POR TBL FLM 30X10MG","POR","TBL FLM","30","10MG","BLI","TPP","CZ","31/140/10-C","","CMS","R","MCV",536.07,"S",{"v":246.9,"d":"246.90"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA07","2010-02-17","2012-07-30","",null,null,"10","MG",{"v":30,"d":"30.0000"},"5","MG","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",764.26,"",764.26,""]
["0145261","ROSUVASTATIN TEVA 10 MG","POR TBL FLM 100X10MG","POR","TBL FLM","100","10MG","BLI","TPP","CZ","31/140/10-C","","CMS","R","MCV",1778.34,"S",{"v":823,"d":"823.00"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA07","2010-02-17","2012-07-30","",null,null,"10","MG",{"v":100,"d":"100.0000"},"5","MG","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",2378.37,"",2378.37,""]
["0145266","ROSUVASTATIN TEVA 20 MG","POR TBL FLM 30X20MG","POR","TBL FLM","30","20MG","BLI","TPP","CZ","31/141/10-C","","CMS","R","MCV",881.06,"S",{"v":329.1,"d":"329.10"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA07","2010-02-17","2012-07-30","",null,null,"10","MG",{"v":60,"d":"60.0000"},"5","MG","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",1219.65,"",1219.65,""]
["0145271","ROSUVASTATIN TEVA 20 MG","POR TBL FLM 100X20MG","POR","TBL FLM","100","20MG","BLI","TPP","CZ","31/141/10-C","","CMS","R","MCV",2637.26,"S",{"v":1097,"d":"1097.00"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA07","2010-02-17","2012-07-30","",null,null,"10","MG",{"v":200,"d":"200.0000"},"5","MG","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",3479.27,"",3479.27,""]
["0145276","ROSUVASTATIN TEVA 40 MG","POR TBL FLM 30X40MG","POR","TBL FLM","30","40MG","BLI","TPP","CZ","31/142/10-C","","CMS","R","MCV",{"v":878.6,"d":"878.60"},"S",{"v":438.9,"d":"438.90"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA07","2010-02-17","2012-07-30","",null,null,"10","MG",{"v":120,"d":"120.0000"},"5","MG","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",{"v":1216.4,"d":"1216.40"},"",{"v":1216.4,"d":"1216.40"},""]
["0145281","ROSUVASTATIN TEVA 40 MG","POR TBL FLM 100X40MG","POR","TBL FLM","100","40MG","BLI","TPP","CZ","31/142/10-C","","CMS","R","MCV",2928.67,"S",{"v":1463,"d":"1463.00"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA07","2010-02-17","2012-07-30","",null,null,"10","MG",{"v":400,"d":"400.0000"},"5","MG","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",{"v":3844.7,"d":"3844.70"},"",{"v":3844.7,"d":"3844.70"},""]
["0145551","ROSUMOP 10 MG","POR TBL FLM 30X10MG","POR","TBL FLM","30","10MG","BLI","DOZ","CZ","31/364/10-C","","CMS","R","MCV",266.46,"S",{"v":246.9,"d":"246.90"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","X","","","","","","28/1","28","1","C10AA07","2010-05-12","2014-07-31","",null,null,"10","MG",{"v":30,"d":"30.0000"},"5","MG","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",{"v":246.9,"d":"246.90"},"",394.78,""]
["0145558","ROSUMOP 10 MG","POR TBL FLM 100X10MG","POR","TBL FLM","100","10MG","BLI","DOZ","CZ","31/364/10-C","","CMS","R","MCV",1760.06,"S",{"v":823,"d":"823.00"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","X","","","","","","28/1","28","1","C10AA07","2010-05-12","2014-07-31","",null,null,"10","MG",{"v":100,"d":"100.0000"},"5","MG","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",{"v":823,"d":"823.00"},"",2354.85,""]
["0145567","ROSUMOP 20 MG","POR TBL FLM 30X20MG","POR","TBL FLM","30","20MG","BLI","DOZ","CZ","31/365/10-C","","CMS","R","MCV",441.78,"S",{"v":329.1,"d":"329.10"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l","","","X","","","","","","28/1","28","1","C10AA07","2010-05-12","2014-07-31","",null,null,"10","MG",{"v":60,"d":"60.0000"},"5","MG","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",{"v":329.1,"d":"329.10"},"",637.24,""]
["0145574","ROSUMOP 20 MG","POR TBL FLM 100X20MG","POR","TBL FLM","100","20MG","BLI","DOZ","CZ","31/365/10-C","","CMS","R","MCV",2610.14,"S",{"v":1097,"d":"1097.00"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","X","","","","","","28/1","28","1","C10AA07","2010-05-12","2014-07-31","",null,null,"10","MG",{"v":200,"d":"200.0000"},"5","MG","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",{"v":1097,"d":"1097.00"},"",3445.27,""]
["0145583","ROSUMOP 40 MG","POR TBL FLM 30X40MG","POR","TBL FLM","30","40MG","BLI","DOZ","CZ","31/366/10-C","","CMS","R","MCV",{"v":878.6,"d":"878.60"},"S",{"v":438.9,"d":"438.90"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","X","","","","","","28/1","28","1","C10AA07","2010-05-12","2014-07-31","",null,null,"10","MG",{"v":120,"d":"120.0000"},"5","MG","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",{"v":438.9,"d":"438.90"},"",{"v":1216.4,"d":"1216.40"},""]
["0145590","ROSUMOP 40 MG","POR TBL FLM 100X40MG","POR","TBL FLM","100","40MG","BLI","DOZ","CZ","31/366/10-C","","CMS","R","MCV",{"v":2929,"d":"2929.00"},"S",{"v":1463,"d":"1463.00"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","X","","","","","","28/1","28","1","C10AA07","2010-05-12","2014-07-31","",null,null,"10","MG",{"v":400,"d":"400.0000"},"5","MG","","2010-10-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",{"v":1463,"d":"1463.00"},"",3845.12,""]
["0147063","APO-ATORVASTATIN 10 MG POTAHOVANÉ TABLETY","POR TBL FLM 30X10MG","POR","TBL FLM","30","10MG","TBC","ATX","NL","31/182/10-C","","CMS","R","OP","","",{"v":185.1,"d":"185.10"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA05","2010-02-24","2012-06-30","","2010-08-23",null,"20","MG",{"v":15,"d":"15.0000"},"10","MG",5.61,"2010-01-01","2010-07-01",{"v":0,"d":"0.00"},"","U","R","",219.66,"","",""]
["0147065","APO-ATORVASTATIN 10 MG POTAHOVANÉ TABLETY","POR TBL FLM 100X10MG","POR","TBL FLM","100","10MG","TBC","ATX","NL","31/182/10-C","","CMS","R","OP","","",{"v":617,"d":"617.00"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA05","2010-02-24","2012-06-30","","2010-08-23",null,"20","MG",{"v":50,"d":"50.0000"},"10","MG",5.61,"2010-01-01","2010-07-01",{"v":0,"d":"0.00"},"","U","R","",{"v":702.6,"d":"702.60"},"","",""]
["0147073","APO-ATORVASTATIN 20 MG POTAHOVANÉ TABLETY","POR TBL FLM 30X20MG","POR","TBL FLM","30","20MG","TBC","ATX","NL","31/183/10-C","","CMS","R","OP","","",{"v":246.9,"d":"246.90"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA05","2010-02-24","2012-06-30","","2010-08-23",null,"20","MG",{"v":30,"d":"30.0000"},"10","MG",5.61,"2010-01-01","2010-07-01",{"v":0,"d":"0.00"},"","U","R","",{"v":293.1,"d":"293.10"},"","",""]
["0147075","APO-ATORVASTATIN 20 MG POTAHOVANÉ TABLETY","POR TBL FLM 100X20MG","POR","TBL FLM","100","20MG","TBC","ATX","NL","31/183/10-C","","CMS","R","OP","","",{"v":823,"d":"823.00"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA05","2010-02-24","2012-06-30","","2010-08-23",null,"20","MG",{"v":100,"d":"100.0000"},"10","MG",5.61,"2010-01-01","2010-07-01",{"v":0,"d":"0.00"},"","U","R","",927.45,"","",""]
["0147083","APO-ATORVASTATIN 40 MG POTAHOVANÉ TABLETY","POR TBL FLM 30X40MG","POR","TBL FLM","30","40MG","TBC","ATX","NL","31/184/10-C","","CMS","R","OP","","",{"v":329.1,"d":"329.10"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA05","2010-02-24","2012-06-30","","2010-08-23",null,"20","MG",{"v":60,"d":"60.0000"},"10","MG",5.61,"2010-01-01","2010-07-01",{"v":0,"d":"0.00"},"","U","R","",386.49,"","",""]
["0147085","APO-ATORVASTATIN 40 MG POTAHOVANÉ TABLETY","POR TBL FLM 100X40MG","POR","TBL FLM","100","40MG","TBC","ATX","NL","31/184/10-C","","CMS","R","OP","","",{"v":1097,"d":"1097.00"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA05","2010-02-24","2012-06-30","","2010-08-23",null,"20","MG",{"v":200,"d":"200.0000"},"10","MG",5.61,"2010-01-01","2010-07-01",{"v":0,"d":"0.00"},"","U","R","",1229.14,"","",""]
["0147093","APO-ATORVASTATIN 80 MG POTAHOVANÉ TABLETY","POR TBL FLM 30X80MG","POR","TBL FLM","30","80MG","TBC","ATX","NL","31/185/10-C","","CMS","R","OP","","",{"v":438.9,"d":"438.90"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA05","2010-02-24","2012-06-30","","2010-08-23",null,"20","MG",{"v":120,"d":"120.0000"},"10","MG",5.61,"2010-01-01","2010-07-01",{"v":0,"d":"0.00"},"","U","R","",505.75,"","",""]
["0147095","APO-ATORVASTATIN 80 MG POTAHOVANÉ TABLETY","POR TBL FLM 100X80MG","POR","TBL FLM","100","80MG","TBC","ATX","NL","31/185/10-C","","CMS","R","OP","","",{"v":1463,"d":"1463.00"},"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA05","2010-02-24","2012-06-30","","2010-08-23",null,"20","MG",{"v":400,"d":"400.0000"},"10","MG",5.61,"2010-01-01","2010-07-01",{"v":0,"d":"0.00"},"","U","R","",1628.64,"","",""]
["0147554","SIMVASTATIN ORION 10 MG","POR TBL FLM 28X10MG","POR","TBL FLM","28","10MG","BLI","ORN","SF","31/201/10-C","","CMS","R","OP","","",117.88,"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA01","2010-02-24","2011-10-03","",null,null,"30","MG",9.3333,"20","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",134.64,"","",""]
["0147555","SIMVASTATIN ORION 10 MG","POR TBL FLM 98X10MG","POR","TBL FLM","98","10MG","BLI","ORN","SF","31/201/10-C","","CMS","R","OP","","",412.58,"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA01","2010-02-24","2011-10-03","",null,null,"30","MG",32.6667,"20","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",495.68,"","",""]
["0147558","SIMVASTATIN ORION 20 MG","POR TBL FLM 28X20MG","POR","TBL FLM","28","20MG","BLI","ORN","SF","31/202/10-C","","CMS","R","OP","","",157.08,"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA01","2010-02-24","2011-10-03","",null,null,"30","MG",18.6667,"20","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",178.02,"","",""]
["0147559","SIMVASTATIN ORION 20 MG","POR TBL FLM 98X20MG","POR","TBL FLM","98","20MG","BLI","ORN","SF","31/202/10-C","","CMS","R","OP","","",549.78,"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA01","2010-02-24","2011-10-03","",null,null,"30","MG",65.3333,"20","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",633.45,"","",""]
["0147562","SIMVASTATIN ORION 40 MG","POR TBL FLM 28X40MG","POR","TBL FLM","28","40MG","BLI","ORN","SF","31/203/10-C","","CMS","R","OP","","",209.72,"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA01","2010-02-24","2011-10-03","",null,null,"30","MG",37.3333,"20","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",{"v":236.1,"d":"236.10"},"","",""]
["0147563","SIMVASTATIN ORION 40 MG","POR TBL FLM 98X40MG","POR","TBL FLM","98","40MG","BLI","ORN","SF","31/203/10-C","","CMS","R","OP","","",734.02,"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných s dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté kardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5% (toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je nejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace aterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0 mmol/l.","","","","","","","","","28/1","28","1","C10AA01","2010-02-24","2011-10-03","",null,null,"30","MG",130.6667,"20","MG","","2010-01-01","2010-10-01",{"v":0,"d":"0.00"},"","U","R","",818.29,"","",""]
["0149779","VANTAVO 70 MG/2800 IU","POR TBL NOB 4","POR","TBL NOB","4","","BLI","MSD","GB","EU/1/09/572/002","","EUR","R","MCV",560.72,"Z",510.38,"Z","","","P","","","","","","","","","","","","","M05BB03",null,"2014-10-20","",null,null,"10","MG",{"v":28,"d":"28.0000"},"","","","2010-01-01","2010-01-01",286.42,"","1","R","",{"v":796.8,"d":"796.80"},"",{"v":796.8,"d":"796.80"},""]
["0149781","VANTAVO 70 MG/2800 IU","POR TBL NOB 12","POR","TBL NOB","12","","BLI","MSD","GB","EU/1/09/572/004","","EUR","R","MCV",1832.24,"Z",1531.15,"Z","","","P","","","","","","","","","","","","","M05BB03",null,"2014-10-20","",null,null,"10","MG",{"v":84,"d":"84.0000"},"","","","2010-01-01","2010-01-01",859.26,"","1","R","",2447.74,"",2447.74,""]
["0150726","THYMOGLOBULINE","INF PLV SOL 1X25MG","INF","PLV SOL","1","5MG/ML","AMP","GZE","NL","59/222/89-C","","NAR","R","MCV",3126.24,"Z",2667.24,"Z","U","J10","","","","","","","","","","","","","","L04AA04",null,"2009-10-31","",null,null,"","","","","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","0","R","",4092.45,"",4092.45,""]
["0150760","GABANOX 400 MG TVRDÉ TOBOLKY","POR CPS DUR 100X400MG","POR","CPS DUR","100","400MG","BLI","DOZ","CZ","21/523/07-C","","CMS","R","OP","","",{"v":1320.8,"d":"1320.80"},"Z","L","PSY,NEU","","","","","","","","","","","","","","N03AX12","2007-08-22","2012-04-10","",null,null,"1,8","GM",22.2222,"","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","U","R","",{"v":1320.8,"d":"1320.80"},"","",""]
["0150767","GABANOX 300 MG TVRDÉ TOBOLKY","POR CPS DUR 100X300MG","POR","CPS DUR","100","300MG","BLI","DOZ","CZ","21/522/07-C","","CMS","R","OP","","",{"v":990.6,"d":"990.60"},"Z","L","PSY,NEU","","","","","","","","","","","","","","N03AX12","2007-08-22","2012-04-10","",null,null,"1,8","GM",16.6667,"","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","U","R","",990.59,"","",""]
["0150782","GABANOX 100 MG TVRDÉ TOBOLKY","POR CPS DUR 100X100MG","POR","CPS DUR","100","100MG","BLI","DOZ","CZ","21/521/07-C","","CMS","R","OP","","",{"v":330.2,"d":"330.20"},"Z","L","PSY,NEU","","","","","","","","","","","","","","N03AX12","2007-08-22","2012-04-10","",null,null,"1,8","GM",5.5555,"","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","U","R","",330.19,"","",""]
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["0169251","TROMBEX 75 MG POTAHOVANÉ TABLETY","POR TBL FLM 30X75MG","POR","TBL FLM","30","75MG","BLI","ZNP","CZ","16/351/09-C","","RMS","R","MCV",660.82,"Z",{"v":468.3,"d":"468.30"},"S","","","P","Klopidogrel předepisuje internista, neurolog , kardiolog a angiolog -\n1) u alergie a prokazatelné intolerance kyseliny acetylsalicylové či při necitlivosti na kyselinu acetylsalicylovou prokázanou agregometricky v indikaci snížení rizika kardiovaskulárních příhod u nemocných po ischemické mozkové příhodě (včetně TIA), u nemocných s ischemickou chorobou srdeční či s ischemickou chorobou dolních končetin\n2) v prevenci recidivy mozkové příhody u nemocných po ischemické mozkové příhodě (včetně TIA), která se objevila při léčbě kyselinou acetylsalicylovou\n3) v prevenci opakující se trombózy v arterio-venózní spojce u hemodialyzovaných nemocných při léčbě kyselinou acetylsalicylovou\n4) po intravaskulárních intervencích s vysokým rizikem trombózy (implantace stentu, rotablace, endarterektomie, přímá koronární angioplastika a angioplastika magistrálních tepen) obvykle v kombinaci s kyselinou acetylsalicylovou po dobu jednoho měsíce či u tzv.\"potahovaných\" stentů uvolňujících sirolimus či paclitaxel po dobu 9 měsíců\n","","","",{"v":915,"d":"915.00"},"","","P","","13/1","13","1","B01AC04","2009-04-15","2014-03-31","",null,null,"75","MG",{"v":30,"d":"30.0000"},"75","MG",14.52,"2010-01-01","2010-01-01",{"v":0,"d":"0.00"},{"v":0,"d":"0.00"},"U","R","",928.93,"",928.93,""]
["0169252","TROMBEX 75 MG POTAHOVANÉ TABLETY","POR TBL FLM 90X75MG","POR","TBL FLM","90","75MG","BLI","ZNP","CZ","16/351/09-C","","RMS","R","MCV",3156.35,"Z",{"v":1404.9,"d":"1404.90"},"S","","","P","Klopidogrel předepisuje internista, neurolog , kardiolog a angiolog -\n1) u alergie a prokazatelné intolerance kyseliny acetylsalicylové či při necitlivosti na kyselinu acetylsalicylovou prokázanou agregometricky v indikaci snížení rizika kardiovaskulárních příhod u nemocných po ischemické mozkové příhodě (včetně TIA), u nemocných s ischemickou chorobou srdeční či s ischemickou chorobou dolních končetin\n2) v prevenci recidivy mozkové příhody u nemocných po ischemické mozkové příhodě (včetně TIA), která se objevila při léčbě kyselinou acetylsalicylovou\n3) v prevenci opakující se trombózy v arterio-venózní spojce u hemodialyzovaných nemocných při léčbě kyselinou acetylsalicylovou\n4) po intravaskulárních intervencích s vysokým rizikem trombózy (implantace stentu, rotablace, endarterektomie, přímá koronární angioplastika a angioplastika magistrálních tepen) obvykle v kombinaci s kyselinou acetylsalicylovou po dobu jednoho měsíce či u tzv.\"potahovaných\" stentů uvolňujících sirolimus či paclitaxel po dobu 9 měsíců\n","","","",{"v":2745,"d":"2745.00"},"","","P","","13/1","13","1","B01AC04","2009-04-15","2014-03-31","",null,null,"75","MG",{"v":90,"d":"90.0000"},"75","MG",14.52,"2010-01-01","2010-01-01",{"v":0,"d":"0.00"},{"v":0,"d":"0.00"},"U","R","",4130.21,"",4130.21,""]
["0169253","TROMBEX 75 MG POTAHOVANÉ TABLETY","POR TBL FLM 28X75MG","POR","TBL FLM","28","75MG","BLI","ZNP","CZ","16/351/09-C","","RMS","R","MCV",616.77,"Z",437.08,"S","","","P","Klopidogrel předepisuje internista, neurolog , kardiolog a angiolog -\n1) u alergie a prokazatelné intolerance kyseliny acetylsalicylové či při necitlivosti na kyselinu acetylsalicylovou prokázanou agregometricky v indikaci snížení rizika kardiovaskulárních příhod u nemocných po ischemické mozkové příhodě (včetně TIA), u nemocných s ischemickou chorobou srdeční či s ischemickou chorobou dolních končetin\n2) v prevenci recidivy mozkové příhody u nemocných po ischemické mozkové příhodě (včetně TIA), která se objevila při léčbě kyselinou acetylsalicylovou\n3) v prevenci opakující se trombózy v arterio-venózní spojce u hemodialyzovaných nemocných při léčbě kyselinou acetylsalicylovou\n4) po intravaskulárních intervencích s vysokým rizikem trombózy (implantace stentu, rotablace, endarterektomie, přímá koronární angioplastika a angioplastika magistrálních tepen) obvykle v kombinaci s kyselinou acetylsalicylovou po dobu jednoho měsíce či u tzv.\"potahovaných\" stentů uvolňujících sirolimus či paclitaxel po dobu 9 měsíců\n","","","",{"v":854,"d":"854.00"},"","","P","","13/1","13","1","B01AC04","2009-04-15","2014-03-31","",null,null,"75","MG",{"v":28,"d":"28.0000"},"75","MG",14.52,"2010-01-01","2010-01-01",{"v":0,"d":"0.00"},{"v":0,"d":"0.00"},"U","R","",870.79,"",870.79,""]
["0169302","ARTEOPTIC 2%","OPH GTT SOL 1X5ML","OPH","GTT SOL","1X5ML","20MG/ML","LGT","LTF","F","64/979/97-C","","NAR","R","MCV",104.46,"Z",90.91,"Z","L","OPH","","","","","","","","","","","","","","S01ED05",null,"2012-11-30","",null,null,"0,2","ML",{"v":25,"d":"25.0000"},"","","","2010-01-01","2010-01-01",15.91,"","1","R","",156.27,"",156.27,""]
["0169303","ARTEOPTIC 2%","OPH GTT SOL 3X5ML","OPH","GTT SOL","3X5ML","20MG/ML","LGT","LTF","F","64/979/97-C","","NAR","R","MCV",215.65,"Z",272.72,"Z","L","OPH","","","","","","","","","","","","","","S01ED05",null,"2012-11-30","",null,null,"0,2","ML",{"v":75,"d":"75.0000"},"","","","2010-01-01","2010-01-01",47.73,"","1","R","",320.45,"",320.45,""]
["0169451","FERRETAB COMP.","POR CPS DUR 30","POR","CPS DUR","30","","BLI","GCL","A","12/1148/97-C","","NAR","R","MCV",32.12,"S",{"v":43.5,"d":"43.50"},"S","","","","","","","","","","","","","","","","B03AD02",null,"2012-12-31","",null,null,"","","","1","TBL",2.89,"2009-08-01","2010-01-01",{"v":0,"d":"0.00"},"","U","R","",48.05,"",48.05,""]
["0169452","FERRETAB COMP.","POR CPS DUR 100","POR","CPS DUR","100","","BLI","GCL","A","12/1148/97-C","","NAR","R","MCV",{"v":101.8,"d":"101.80"},"S",{"v":145,"d":"145.00"},"S","","","","","","","","","","","","","","","","B03AD02",null,"2012-12-31","",null,null,"","","","1","TBL",2.89,"2009-08-01","2010-01-01",{"v":0,"d":"0.00"},"","U","R","",142.68,"",152.29,""]
["0169459","GEMCITABIN TEVA 200 MG","INF PLV SOL 1X200MG","IVN","INF PLV SOL","1","200MG/LAH","LAG","TPP","CZ","44/363/07-C","","NAR","R","MCV",712.64,"Z",853.74,"Z","B","","P","","","","","","","","","","","","","L01BC05","2007-06-13","2012-06-30","",null,null,"","","","","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","0","R","",997.33,"",997.33,""]
["0169460","GEMCITABIN TEVA 1 G","INF PLV SOL 1X1000MG","IVN","INF PLV SOL","1","1000MG/LAH","LAG","TPP","CZ","44/364/07-C","","NAR","R","MCV",3448.84,"Z",{"v":4268.7,"d":"4268.70"},"Z","B","","P","","","","","","","","","","","","","L01BC05","2007-06-13","2012-06-30","",null,null,"","","","","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","0","R","",{"v":4497,"d":"4497.00"},"",{"v":4497,"d":"4497.00"},""]
["0169465","BISATUM 10 MG","POR TBL FLM 30X10MG","POR","TBL FLM","3X10","10MG","BLI","TPP","CZ","31/323/07-C","","NAR","R","OP","","",185.13,"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných\ns dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté\nkardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5%\n(toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je\nnejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace\naterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0\nmmol/l.","","","","","","","","","28/1","28","1","C10AA05","2007-05-30","2012-05-31","",null,null,"20","MG",{"v":15,"d":"15.0000"},"10","MG",5.61,null,"2010-03-01",{"v":0,"d":"0.00"},"","U","R","",185.13,"","",""]
["0169467","BISATUM 20 MG","POR TBL FLM 30X20MG","POR","TBL FLM","3X10","20 MG","BLI","TPP","CZ","31/324/07-C","","NAR","R","OP","","",246.84,"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných\ns dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté\nkardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5%\n(toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je\nnejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace\naterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0\nmmol/l.","","","","","","","","","28/1","28","1","C10AA05","2007-05-30","2012-05-31","",null,null,"20","MG",{"v":30,"d":"30.0000"},"10","MG",5.61,null,"2010-03-01",{"v":0,"d":"0.00"},"","U","R","",246.83,"","",""]
["0169469","BISATUM 40 MG","POR TBL FLM 30X40MG","POR","TBL FLM","3X10","40 MG","BLI","TPP","CZ","31/325/07-C","","NAR","R","OP","","",329.01,"S","","","P","Atorvastatin, simvastatin, fluvastatin, lovastatin, pravastatin a rosuvastatin je indikován u nemocných\ns dyslipidemií a manifestní aterosklerózou či diabetem nebo v případě, že celkové desetileté\nkardiovaskulární riziko úmrtí nemocného dle systému SCORE (platného pro ČR) je větší nebo rovno 5%\n(toto riziko musí být při iniciaci léčby uvedeno ve zdravotnické dokumentaci). Pro účinnost léčby je\nnejvýznamnějším ukazatelem LDL-cholesterol, jehož cílová hodnota je stanovena u osob bez manifestace\naterosklerózy či bez diabetu na 2,5 mmol/l a u osob s manifestací aterosklerózy či s diabetem na 2,0\nmmol/l.","","","","","","","","","28/1","28","1","C10AA05","2007-05-30","2012-05-31","",null,null,"20","MG",{"v":60,"d":"60.0000"},"10","MG",5.61,null,"2010-03-01",{"v":0,"d":"0.00"},"","U","R","",{"v":329,"d":"329.00"},"","",""]
["0169471","OXALIPLATIN PLIVA 5 MG/ML","INF PLV SOL 1X50MG","INF","PLV SOL","1 VIA","50MG/VIA","VIA","TPP","CZ","44/484/06-C","","RMS","R","OP","","",4581.64,"Z","B","","P","","","","","","","","","","","","","L01XA03","2006-11-29",null,"X",null,null,"","","","","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","0","R","","","","",""]
["0169472","OXALIPLATIN PLIVA 5 MG/ML","INF PLV SOL 1X100MG","INF","PLV SOL","1 VIA","100MG/VIA","VIA","TPP","CZ","44/484/06-C","","RMS","R","OP","","",9163.29,"Z","B","","P","","","","","","","","","","","","","L01XA03","2006-11-29",null,"X",null,null,"","","","","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","0","R","","","","",""]
["0169495","IMURAN","INJ PLV SOL 1X50MG","INJ","PLV SOL","1","50MG/LAH","VIA","AUO","D","59/189/70-C","","NAR","R","MCV",330.17,"Z",{"v":446.4,"d":"446.40"},"Z","U","J10","","","","","","","","","","","","","","L04AX01",null,"2010-07-31","",null,null,"150","MG",0.3333,"","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","0","R","",{"v":485,"d":"485.00"},"",{"v":485,"d":"485.00"},""]
["0169673","CALTRATE PLUS","POR TBL FLM 30","POR","TBL FLM","30","","TBC","PCV","A","39/385/00-C","","NAR","R","OP","","",{"v":89,"d":"89.00"},"Z","","","","","","","","","","","","","","","","A12AX",null,"2010-07-31","",null,null,"","","","","","","2010-01-01","2010-01-01",47.35,"","1","F","","","","",""]
["0500154","VELMETIA 50 MG/1000 MG","POR TBL FLM 56X50MG/1000MG","POR","TBL FLM","56 (4X14)","50MG/1000MG","BLI","MSD","GB","EU/1/08/456/010","","EUR","R","MCV",989.04,"Z",1314.04,"S","L","DIA","P","Přípravek je indikován u pacientů, u nichž použití maximálních tolerovaných dávek metforminu a/nebo sulfonylurey po dobu alespoň 3 měsíců společně s režimovými opatřeními nevedlo k uspokojivé kompenzaci diabetu definované jako hladina HbA1c nižší než 6,0% dle IFCC. Nedojde-li k prokazatelnému zlepšení kompenzace diabetu o 7% či vyšší pokles hladiny HbA1c při kontrole po 6 měsících léčby, přípravek není dále indikován.","","","","","","","","","","","","A10BD07",null,"2013-07-18","",null,null,"2","DF",{"v":28,"d":"28.0000"},"","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","U","R","",1362.18,"",1362.18,""]
["0500161","EFFICIB 50 MG/850 MG","POR TBL FLM 56X50MG/850MG","POR","TBL FLM","56 (4X14)","50MG/850MG","BLI","MSD","GB","EU/1/08/457/003","","EUR","R","MCV",966.33,"Z",1306.76,"S","L","DIA","P","Přípravek je indikován u pacientů, u nichž použití maximálních tolerovaných dávek metforminu a/nebo sulfonylurey po dobu alespoň 3 měsíců společně s režimovými opatřeními nevedlo k uspokojivé kompenzaci diabetu definované jako hladina HbA1c nižší než 6,0% dle IFCC. Nedojde-li k prokazatelnému zlepšení kompenzace diabetu o 7% či vyšší pokles hladiny HbA1c při kontrole po 6 měsících léčby, přípravek není dále indikován.","","","","","","","","","","","","A10BD07",null,"2013-07-18","",null,null,"2","DF",{"v":28,"d":"28.0000"},"","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","U","R","",1306.54,"",1332.21,""]
["0500168","EFFICIB 50 MG/1000 MG","POR TBL FLM 56X50MG/1000MG","POR","TBL FLM","56 (4X14)","50MG/1000MG","BLI","MSD","GB","EU/1/08/457/010","","EUR","R","MCV",989.04,"Z",1314.04,"S","L","DIA","P","Přípravek je indikován u pacientů, u nichž použití maximálních tolerovaných dávek metforminu a/nebo sulfonylurey po dobu alespoň 3 měsíců společně s režimovými opatřeními nevedlo k uspokojivé kompenzaci diabetu definované jako hladina HbA1c nižší než 6,0% dle IFCC. Nedojde-li k prokazatelnému zlepšení kompenzace diabetu o 7% či vyšší pokles hladiny HbA1c při kontrole po 6 měsících léčby, přípravek není dále indikován.","","","","","","","","","","","","A10BD07",null,"2013-07-18","",null,null,"2","DF",{"v":28,"d":"28.0000"},"","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","U","R","",1362.18,"",1362.18,""]
["0500171","EFFICIB 50 MG/1000 MG","POR TBL FLM 196X50MG/1000MG","POR","TBL FLM","196 (14X14)","50MG/1000MG","BLI","MSD","GB","EU/1/08/457/013","","EUR","R","MCV",{"v":3491.1,"d":"3491.10"},"Z",2627.71,"S","L","DIA","P","Přípravek je indikován u pacientů, u nichž použití maximálních tolerovaných dávek metforminu a/nebo sulfonylurey po dobu alespoň 3 měsíců společně s režimovými opatřeními nevedlo k uspokojivé kompenzaci diabetu definované jako hladina HbA1c nižší než 6,0% dle IFCC. Nedojde-li k prokazatelnému zlepšení kompenzace diabetu o 7% či vyšší pokles hladiny HbA1c při kontrole po 6 měsících léčby, přípravek není dále indikován.","","","","","","","","","","","","A10BD07",null,"2013-07-18","",null,null,"2","DF",{"v":98,"d":"98.0000"},"","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","U","R","",4549.99,"",4549.99,""]
["0500649","EFFICIB 50 MG/850 MG","POR TBL FLM 196X50MG/850MG","POR","TBL FLM","196 (2X98)","50MG/850MG","BLI","MSD","GB","EU/1/08/457/015","","EUR","R","MCV",3432.85,"Z",2583.87,"S","L","DIA","P","Přípravek je indikován u pacientů, u nichž použití maximálních tolerovaných dávek metforminu a/nebo sulfonylurey po dobu alespoň 3 měsíců společně s režimovými opatřeními nevedlo k uspokojivé kompenzaci diabetu definované jako hladina HbA1c nižší než 6,0% dle IFCC. Nedojde-li k prokazatelnému zlepšení kompenzace diabetu o 7% či vyšší pokles hladiny HbA1c při kontrole po 6 měsících léčby, přípravek není dále indikován.","","","","","","","","","","","","A10BD07",null,"2013-07-18","",null,null,"2","DF",{"v":98,"d":"98.0000"},"","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","U","R","",4476.94,"",4476.94,""]
["0500652","VELMETIA 50 MG/1000 MG","POR TBL FLM 196X50MG/1000MG","POR","TBL FLM","196 (2X98)","50MG/1000MG","BLI","MSD","GB","EU/1/08/456/016","","EUR","R","MCV",{"v":3491.1,"d":"3491.10"},"Z",2627.71,"S","L","DIA","P","Přípravek je indikován u pacientů, u nichž použití maximálních tolerovaných dávek metforminu a/nebo sulfonylurey po dobu alespoň 3 měsíců společně s režimovými opatřeními nevedlo k uspokojivé kompenzaci diabetu definované jako hladina HbA1c nižší než 6,0% dle IFCC. Nedojde-li k prokazatelnému zlepšení kompenzace diabetu o 7% či vyšší pokles hladiny HbA1c při kontrole po 6 měsících léčby, přípravek není dále indikován.","","","","","","","","","","","","A10BD07",null,"2013-07-18","",null,null,"2","DF",{"v":98,"d":"98.0000"},"","","","2010-01-01","2010-01-01",{"v":0,"d":"0.00"},"","U","R","",4549.99,"",4549.99,""]