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["0006200","TRAMAL INJEKČNÍ ROZTOK 50 MG/1 ML","INJ SOL 5X50 MG/1ML","INJ","SOL","5X1ML","50MG/ML","AMP","GNG","D","65/078/91-S/C","","NAR","R","OP","","",62.33,"Z","O","","","","","","X","","","","","","","","","N02AX02","","","X","","","0,3","GM",0.8333,"","","","01012010","01012010",0,"","0","R","",85.7,"","",""]
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["0010381","AZITROX 250","POR TBL FLM 6X250MG","POR","TBL FLM","6","250MG","BLI","ZNP","CZ","15/272/01-C","","NAR","R","OP","","",183.21,"Z","","","","","","","","","","","","","","","","J01FA10","08082001","25082011","","","","0,3","GM",{"v":5,"d":"5.0000"},"","","","01012010","01012010",30,"","1","R","",219.91,"","",""]
["0010382","AZITROX 500","POR TBL FLM 3X500MG","POR","TBL FLM","3","500MG","BLI","ZNP","CZ","15/273/01-C","","NAR","R","OP","","",183.21,"Z","","","","","","","","","","","","","","","","J01FA10","08082001","25082011","","","07092010","0,3","GM",{"v":5,"d":"5.0000"},"","","","01012010","01012010",30,"","1","R","",219.91,"","",""]
["0011139","CLEXANE","INJ SOL 2X0.2ML/2KU","INJ","SOL","2X0.2ML","2KU/0.2ML","ISP","LVN","F","16/250/93-C","","NAR","B","MCV",96.11,"S",89.48,"S","","","P","Nízkomolekulární hepariny nižší síly s obsahem enoxaparinu jsou v ambulantní péči hrazeny - \n1. v indikaci zahájení léčby hluboké žilní trombózy potvrzené doplerovským vyšetřením nebo při silném klinickém podezření na hlubokou žilní trombózu před tím, než jsou známy výsledky diagnostických testů, a to v monoterapii nebo spolu s warfarinem do dosažení jeho terapeutického účinku (INR 2,0), nebo při nutnosti ambulantního převedení z warfarinu na nízkomolekulární hepariny (tzv.překlenovací léčba) \n2. v prevenci srážení krve v mimotělním oběhu, zejména při hemodialýze a hemofiltraci \n3. v prevenci žilního tromboembolismu v perioperačním období v délce 10 dní, po vysoce rizikových operacích (totální náhrada kyčelního kloubu, endoprotéza kolenního kloubu, stav po operaci zlomeniny horního konce stehenní kosti, rozsáhlé operace pro zhoubný nádor)  se doba profylaxe prodlužuje na 28 dní \n4. pro léčbu stavů vyžadujících antikoagulační léčbu v průběhu gravidity a šestinedělí či před plánovanou transplantací srdce\n 5. v prevenci a léčbě hluboké žilní trombózy u nemocných s prokázaným vrozeným či získaným hyperkoagulačním stavem, u nichž nelze stabilizovat požadované snížení koagulačních faktorů perorálními antikoagulancii či při nemožnosti nebo dokumentované kontraindikaci tato antikoagulancia podat \n6. u nemocných se zvýšeným rizikem tromboembolické nemoci indikovaných k zahájení léčby warfarinem z jiných indikací (fibrilace síní aj.) k potlačení prvotního prokoagulačního působení warfarinu po dobu 2-3 dnů či nejdéle do dosažení terapeutického účinku (INR 2,0)\n","","","","","","","","","12/1","12","1","B01AB05","","30112010","","","","2","KU",{"v":2,"d":"2.0000"},"4","KU",89.48,"01102010","01102010",11.29,"","1","R","",143.78,"",143.78,""]
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["0015591","ARTEOPTIC 2%","OPH GTT SOL 1X5ML","OPH","GTT SOL","1X5ML","20MG/ML","LGT","NAI","CZ","64/979/97-C","","NAR","B","MCV",104.46,"Z",90.91,"Z","L","OPH","","","","","","","","","","","","","","S01ED05","","30112012","","","","0,2","ML",{"v":25,"d":"25.0000"},"","","","01012010","01012010",15.91,"","1","R","",156.27,"",156.27,""]
["0015770","METVIX","DRM CRM 1X2GM","DRM","CRM","2GM","160MG/GM","TUB","GAS","F","44/185/04-C","","CMS","R","MCV",5070.35,"Z",7365.38,"S","S","","P","Methylaminolevulinát předepisuje dermatolog jako součást léčebného výkonu v léčbě superficiálního vícečetného bazocelulárního karcinomu jako poslední možnost  po vyčerpání  léčebných možností jinými dostupnými léčivými prostředky  nebo postupy.","","","","","","","","","","","","L01XD03","01122004","","X","","","","","","1","GM","","01012010","01102010",0,"","0","R","",6524.18,"",6524.18,""]
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["0024722","TAMIPRO","POR CPS PRO 30X0.4MG","POR","CPS PRO","30","0.4MG","TBC","JSA","PL","87/027/07-C","","CMS","R","OP","","",284.58,"Z","","","P","","","","","","","","","","","","","G04CA02","24012007","31122011","","","","0,4","MG",{"v":30,"d":"30.0000"},"","","","01012010","01012010",0,"","U","R","",553.01,"","",""]
["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","","","X","","","","","","500","MG","","01012010","01102010",0,"","0","R","",38629.98,"",38629.98,""]
["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","","","X","","","","","","41","MG","","01042010","01102010",0,"","0","R","",38937.48,"",38937.48,""]
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["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","","31082012","","","","1","KU",{"v":3,"d":"3.0000"},"1000","IU","","01102010","01102010",0,"","0","R","",809.55,"",809.55,""]
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["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","11112009","09122014","","","","7,5","MG",{"v":20,"d":"20.0000"},"10","MG","","01052010","01102010",0,"","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",1158,"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","11112009","04122014","","","","7,5","MG",{"v":40,"d":"40.0000"},"10","MG","","01052010","01102010",0,"","U","R","",1701,"",1701,""]
["0127011","PROMEMORE 10 MG","POR TBL FLM 90X10MG","POR","TBL FLM","90","10MG","BLI","SVS","CZ","06/774/09-C","","NAR","R","MCV",4116,"S",3474,"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","11112009","04122014","","","","7,5","MG",{"v":120,"d":"120.0000"},"10","MG","","01052010","01102010",0,"","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",1382.7,"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","20052009","11012014","","","","","","","14","MG",664.1,"01102010","01022010",0,"","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",4609,"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","20052009","11012014","","","","","","","14","MG",664.1,"01102010","01022010",0,"","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",13591.1,"S",13825.9,"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","20052009","11012014","","","","","","","14","MG",664.1,"01102010","01022010",0,"","0","R","",16419.87,"",16419.87,""]
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["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","29102009","30052014","","18082010","","50","MG",{"v":98,"d":"98.0000"},"20","MG","","01012010","01102010",0,"","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","29102009","30052014","","","","50","MG",{"v":28,"d":"28.0000"},"20","MG","","01012010","01102010",0,"","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","29102009","30052014","","","","50","MG",{"v":98,"d":"98.0000"},"20","MG","","01012010","01102010",0,"","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","","",126.2,"S","","","","","","","","","","","","","25/3","25","3","C09CA01","29102009","30052014","","18082010","","50","MG",{"v":56,"d":"56.0000"},"20","MG","","01012010","01102010",0,"","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","29102009","30052014","","18082010","","50","MG",{"v":196,"d":"196.0000"},"20","MG","","01012010","01102010",0,"","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","","",126.2,"S","","","","","","","","","","","","","25/3","25","3","C09CA01","29102009","30052014","","","","50","MG",{"v":56,"d":"56.0000"},"20","MG","","01012010","01102010",0,"","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","29102009","30052014","","","","50","MG",{"v":196,"d":"196.0000"},"20","MG","","01012010","01102010",0,"","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",4609,"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","27022008","14122012","","09082010","","","","","14,4","MG","","01102010","01022010",0,"","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",13827,"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","27022008","14122012","","09082010","","","","","14,4","MG","","01102010","01022010",0,"","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","","31032014","","","","","","","","","","01092010","01012010",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",1064.4,"S",1443.69,"Z","O","INT,KAR,GER","","","","","","","","","","","","","","C01EB10","","31082010","","","","15","MG",{"v":2.4,"d":"2.4000"},"","","","01102010","01012010",0,"","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","","30112011","","","","2","GM",{"v":2.5,"d":"2.5000"},"3000","MG",31.96,"01102010","01102010",0,"","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","19022003","31072013","","","","50","MG",{"v":28,"d":"28.0000"},"","","","01012010","01012010",0,"","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",368,"S",159.27,"S","","","","","","","","","","","","","","","","C09BA04","25022009","30042012","","","","1","DF",{"v":30,"d":"30.0000"},"","","","01102010","01102010",0,"","U","R","",536.6,"",536.6,""]
["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",477.8,"S","","","","","","","","","","","","","","","","C09BA04","25022009","30042012","","","","1","DF",{"v":90,"d":"90.0000"},"","","","01102010","01102010",0,"","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","20012010","24112014","","","","75","MG",{"v":30,"d":"30.0000"},"75","MG","","01102010","01102010",0,"","U","R","",393.92,"",532.48,""]
["0142164","AZIBIOT 500 MG","POR TBL FLM 3X500MG","POR","TBL FLM","3","500MG","BLI","KRK","SLO","15/409/07-C","","NAR","R","OP","","",126.6,"S","","","","","","","","","","","","","55/1","55","1","J01FA10","12092007","30092012","","","","0,3","GM",{"v":5,"d":"5.0000"},"500","MG/D",23.55,"01012010","01012010",30,"","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",104.8,"Z",25.76,"Z","","","","","","","","","","","","","","","","C05CA04","","30092013","","","","","","","","","","01012010","01012010",67.83,"","P","F","",156.78,"",156.78,""]
["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","04072007","20022011","","","","5","MG",{"v":30,"d":"30.0000"},"5","MG","","01012010","01102010",0,"","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","04072007","20022011","","","","5","MG",{"v":100,"d":"100.0000"},"5","MG","","01012010","01102010",0,"","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","04072007","20022011","","","","5","MG",{"v":60,"d":"60.0000"},"5","MG","","01012010","01102010",0,"","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","04072007","20022011","","","","5","MG",{"v":200,"d":"200.0000"},"5","MG","","01012010","01102010",0,"","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",246.9,"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","17022010","30072012","","","","10","MG",{"v":30,"d":"30.0000"},"5","MG","","01102010","01102010",0,"","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",823,"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","17022010","30072012","","","","10","MG",{"v":100,"d":"100.0000"},"5","MG","","01102010","01102010",0,"","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",329.1,"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","17022010","30072012","","","","10","MG",{"v":60,"d":"60.0000"},"5","MG","","01102010","01102010",0,"","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",1097,"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","17022010","30072012","","","","10","MG",{"v":200,"d":"200.0000"},"5","MG","","01102010","01102010",0,"","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",878.6,"S",438.9,"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","17022010","30072012","","","","10","MG",{"v":120,"d":"120.0000"},"5","MG","","01102010","01102010",0,"","U","R","",1216.4,"",1216.4,""]
["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",1463,"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","17022010","30072012","","","","10","MG",{"v":400,"d":"400.0000"},"5","MG","","01102010","01102010",0,"","U","R","",3844.7,"",3844.7,""]
["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","","",185.1,"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","24022010","30062012","","23082010","","20","MG",{"v":15,"d":"15.0000"},"10","MG",5.61,"01012010","01072010",0,"","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","","",617,"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","24022010","30062012","","23082010","","20","MG",{"v":50,"d":"50.0000"},"10","MG",5.61,"01012010","01072010",0,"","U","R","",702.6,"","",""]
["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","","",246.9,"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","24022010","30062012","","23082010","","20","MG",{"v":30,"d":"30.0000"},"10","MG",5.61,"01012010","01072010",0,"","U","R","",293.1,"","",""]
["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","","",823,"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","24022010","30062012","","23082010","","20","MG",{"v":100,"d":"100.0000"},"10","MG",5.61,"01012010","01072010",0,"","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","","",329.1,"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","24022010","30062012","","23082010","","20","MG",{"v":60,"d":"60.0000"},"10","MG",5.61,"01012010","01072010",0,"","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","","",1097,"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","24022010","30062012","","23082010","","20","MG",{"v":200,"d":"200.0000"},"10","MG",5.61,"01012010","01072010",0,"","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","","",438.9,"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","24022010","30062012","","23082010","","20","MG",{"v":120,"d":"120.0000"},"10","MG",5.61,"01012010","01072010",0,"","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","","",1463,"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","24022010","30062012","","23082010","","20","MG",{"v":400,"d":"400.0000"},"10","MG",5.61,"01012010","01072010",0,"","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","24022010","03102011","","","","30","MG",9.3333,"20","MG","","01012010","01102010",0,"","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","24022010","03102011","","","","30","MG",32.6667,"20","MG","","01012010","01102010",0,"","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","24022010","03102011","","","","30","MG",18.6667,"20","MG","","01012010","01102010",0,"","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","24022010","03102011","","","","30","MG",65.3333,"20","MG","","01012010","01102010",0,"","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","24022010","03102011","","","","30","MG",37.3333,"20","MG","","01012010","01102010",0,"","U","R","",236.1,"","",""]
["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","24022010","03102011","","","","30","MG",130.6667,"20","MG","","01012010","01102010",0,"","U","R","",818.29,"","",""]
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["0155865","SUMAMED FORTE SIRUP","POR PLV SUS 1X15ML","POR","PLV SUS","15ML","40MG/ML","LAG","TPP","CZ","15/352/92-B/C","","NAR","R","OP","","",137.88,"Z","","","","","","","","","","","","","","","","J01FA10","","30062012","","","","0,3","GM",{"v":2,"d":"2.0000"},"","","","01012010","01012010",12,"","1","R","",188.72,"","",""]
["0155866","SUMAMED FORTE SIRUP","POR PLV SUS 1X37,5ML","POR","PLV SUS","37,5ML","40MG/ML","LAG","TPP","CZ","15/352/92-B/C","","NAR","R","OP","","",333.95,"Z","","","","","","","","","","","","","","","","J01FA10","","30062012","","","","0,3","GM",{"v":5,"d":"5.0000"},"","","","01012010","01012010",30,"","1","R","",437.49,"","",""]
["0155867","SUMAMED SIRUP","POR PLV SUS 1X20ML","POR","PLV SUS","20ML","20MG/ML","LAG","TPP","CZ","15/352/92-A/C","","NAR","R","OP","","",94.49,"Z","","","","","","","","","","","","","","","","J01FA10","","30062012","","","","0,3","GM",1.3333,"","","","01012010","01012010",8,"","1","R","",119.52,"","",""]
["0155868","SUMAMED","POR CPS DUR 6X250MG","POR","CPS DUR","6","250MG","BLI","TPP","CZ","15/226/90-C","","NAR","R","OP","","",183.21,"Z","","","","","","","","","","","","","","","","J01FA10","","31102010","","","","0,3","GM",{"v":5,"d":"5.0000"},"","","","01012010","01012010",30,"","1","R","",293.67,"","",""]
["0162008","PRESTARIUM NEO COMBI 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","R","MCV",368,"S",159.27,"S","","","","","","","","","","","","","","","","C09BA04","25022009","14012014","","","","1","DF",{"v":30,"d":"30.0000"},"","","","01102010","01102010",0,"","U","R","",536.6,"",536.6,""]
["0162012","PRESTARIUM NEO COMBI 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","R","MCV",1379.42,"S",477.8,"S","","","","","","","","","","","","","","","","C09BA04","25022009","14012014","","","","1","DF",{"v":90,"d":"90.0000"},"","","","01102010","01102010",0,"","U","R","",1864.96,"",1864.96,""]
["0162898","ORCAL NEO 5 MG","POR TBL NOB 30X5MG","POR","TBL NOB","30 BLI I","5MG","BLI","DOZ","CZ","83/361/07-C","","CMS","R","OP","","",57.32,"S","","","","","","","","","","","","","24/1","24","1","C08CA01","04072007","20022011","","","","5","MG",{"v":30,"d":"30.0000"},"5","MG","","01012010","01102010",0,"","U","R","","","","",""]
["0162908","ORCAL NEO 5 MG","POR TBL NOB 100X5MG","POR","TBL NOB","100 BLI I","5MG","BLI","DOZ","CZ","83/361/07-C","","CMS","R","OP","","",191.07,"S","","","","","","","","","","","","","24/1","24","1","C08CA01","04072007","20022011","","","","5","MG",{"v":100,"d":"100.0000"},"5","MG","","01012010","01102010",0,"","U","R","","","","",""]
["0162932","ORCAL NEO 10 MG","POR TBL NOB 30X10MG","POR","TBL NOB","30 BLI I","10MG","BLI","DOZ","CZ","83/362/07-C","","CMS","R","OP","","",76.41,"S","","","","","","","","","","","","","24/1","24","1","C08CA01","04072007","20022011","","","","5","MG",{"v":60,"d":"60.0000"},"5","MG","","01012010","01102010",0,"","U","R","","","","",""]
["0162942","ORCAL NEO 10 MG","POR TBL NOB 100X10MG","POR","TBL NOB","100 BLI I","10MG","BLI","DOZ","CZ","83/362/07-C","","CMS","R","OP","","",254.69,"S","","","","","","","","","","","","","24/1","24","1","C08CA01","04072007","20022011","","","","5","MG",{"v":200,"d":"200.0000"},"5","MG","","01012010","01102010",0,"","U","R","","","","",""]
["0163069","AMARYL 1 MG","POR TBL NOB 30X1MG","POR","TBL NOB","30","1MG","BLI","SFK","CZ","18/232/97-C","","CMS","R","OP","","",57.2,"Z","","","","","","","","","","","","","","","","A10BB12","","31032012","","","","2","MG",{"v":15,"d":"15.0000"},"","","","01012010","01012010",0,"","U","R","","","","",""]
["0163077","AMARYL 2 MG","POR TBL NOB 30X2MG","POR","TBL NOB","30","2MG","BLI","SFK","CZ","18/233/97-C","","CMS","R","OP","","",114.39,"Z","","","","","","","","","","","","","","","","A10BB12","","31032012","","","","2","MG",{"v":30,"d":"30.0000"},"","","","01012010","01012010",0,"","U","R","","","","",""]
["0163085","AMARYL 3 MG","POR TBL NOB 30X3MG","POR","TBL NOB","30","3MG","BLI","SFK","CZ","18/234/97-C","","CMS","R","OP","","",128.48,"Z","","","","","","","","","","","","","","","","A10BB12","","31032012","","","","2","MG",{"v":45,"d":"45.0000"},"","","","01012010","01012010",0,"","U","R","","","","",""]
["0163093","AMARYL 4 MG","POR TBL NOB 30X4MG","POR","TBL NOB","30","4MG","BLI","SFK","CZ","18/235/97-C","","CMS","R","OP","","",171.31,"Z","","","","","","","","","","","","","","","","A10BB12","","31032012","","","","2","MG",{"v":60,"d":"60.0000"},"","","","01012010","01012010",0,"","U","R","","","","",""]
["0163191","CEFUROXIM TEVA 250 MG","POR TBL FLM 10X250MG","POR","TBL FLM","10","250MG","BLI","TPP","CZ","15/329/06-C","","NAR","R","MCV",154.69,"S",131.19,"S","","","","","","","","","","","","","53/2","53","2","J01DC02","30082006","31082011","","","","0,5","GM",{"v":5,"d":"5.0000"},"1","GM",34.98,"01102010","01092010",0,"","U","R","",231.26,"",231.26,""]
["0163387","TESSYRON 75 MG POTAHOVANÉ TABLETY","POR TBL FLM 90X75MG","POR","TBL FLM","90","75MG","BLI","GDB","H","16/021/10-C","","CMS","R","MCV",2105.94,"S",1181.76,"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","","","X","","","","","","13/1","13","1","B01AC04","20012010","24112014","","","","75","MG",{"v":90,"d":"90.0000"},"75","MG","","01102010","01102010",0,"","U","R","",1181.76,"",2799.99,""]
["0163761","FINASTERID ACTAVIS 5 MG","POR TBL FLM 30X5MG","POR","TBL FLM","30 I","5MG","BLI","PGZ","A","87/442/06-C","","CMS","B","OP","","",261.04,"S","E","URN","","","","","","","","","","","46/2","46","2","G04CB01","15112006","17022011","","","","5","MG",{"v":30,"d":"30.0000"},"5","MG",8.7,"","01082010",0,"","U","R","","","","",""]
["0164070","ZEPPELITON 5 MG","POR TBL NOB 30X5MG","POR","TBL NOB","30","5MG","BLI","PGZ","A","83/140/07-C","","RMS","R","OP","","",57.32,"S","","","","","","","","","","","","","24/1","24","1","C08CA01","28022007","28022012","","01082010","","5","MG",{"v":30,"d":"30.0000"},"5","MG",1.74,"01012010","01082010",0,"","U","R","",57.25,"","",""]
["0164071","ZEPPELITON 10 MG","POR TBL NOB 30X10MG","POR","TBL NOB","30","10MG","BLI","PGZ","A","83/141/07-C","","RMS","R","OP","","",76.41,"S","","","","","","","","","","","","","24/1","24","1","C08CA01","28022007","28022012","","01082010","","5","MG",{"v":60,"d":"60.0000"},"5","MG",1.74,"01012010","01082010",0,"","U","R","",76.35,"","",""]
["0164997","ELTROXIN 100 MCG","POR TBL NOB 100X0.1MG","POR","TBL NOB","100","0.1MG","TBC","AUO","D","56/125/79-C","","NAR","R","MCV",80.96,"Z",81.83,"Z","","","","","","","","","","","","","","","","H03AA01","","","X","","","0,15","MG",66.6667,"0,2","MG",0.76,"01102010","01102010",0,"","U","R","",121.12,"",121.12,""]
["0169048","HYPLAFIN 5 MG","POR TBL FLM 30X5MG","POR","TBL FLM","30 I","5MG","BLI","PGZ","A","87/442/06-C","","CMS","R","OP","","",261.04,"S","E","URN","","","","","","","","","","","46/2","46","2","G04CB01","15112006","17022011","","01092010","","5","MG",{"v":30,"d":"30.0000"},"5","MG",8.7,"","01082010",0,"","U","R","",260.77,"","",""]
["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","","30112012","","","","0,2","ML",{"v":25,"d":"25.0000"},"","","","01012010","01012010",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","","30112012","","","","0,2","ML",{"v":75,"d":"75.0000"},"","","","01012010","01012010",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",43.5,"S","","","","","","","","","","","","","","","","B03AD02","","31122012","","","","","","","1","TBL",2.89,"01082009","01012010",0,"","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",101.8,"S",145,"S","","","","","","","","","","","","","","","","B03AD02","","31122012","","","","","","","1","TBL",2.89,"01082009","01012010",0,"","U","R","",142.68,"",152.29,""]
["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","30052007","31052012","","","","20","MG",{"v":15,"d":"15.0000"},"10","MG",5.61,"","01032010",0,"","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","30052007","31052012","","","","20","MG",{"v":30,"d":"30.0000"},"10","MG",5.61,"","01032010",0,"","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","30052007","31052012","","","","20","MG",{"v":60,"d":"60.0000"},"10","MG",5.61,"","01032010",0,"","U","R","",329,"","",""]
["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","29112006","","X","","","","","","","","","01012010","01012010",0,"","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","29112006","","X","","","","","","","","","01012010","01012010",0,"","0","R","","","","",""]