on the reimbursement of medicinal products and foodstuffs for special medical purposes
According to Article 15 (10) of Act No. 48 / 1997 Coll., on Public Health Insurance, and amending and supplementing certain related laws, as amended by Act No. 438 / 2004 Coll., hereinafter referred to as "the Act":
(a) medicinal products and foodstuffs for special medical purposes fully covered by public health insurance (hereinafter referred to as "health insurance") listed in Annex 1 thereto,
(b) the amount of the reimbursement of each active substance belonging to the groups of active substances referred to in Annex 2 to the Act, as set out in Annex 1 to this Decree;
(c) the amount of food payments for special medical purposes, containing active substances from groups of active substances as listed in Annex 2 to the Act, as listed in Annex 1 to this Decree;
(d) the level of reimbursement of individually prepared medicinal products, radiopharmaceuticals and transfusions of health insurance products listed in Annex 1 thereto;
(e) restrictions and symbols setting out the conditions for the prescription of medicinal products and foodstuffs for special medical purposes covered by health insurance, including restrictions and symbols for the use of medicinal products and foodstuffs for special medical purposes in the provision of healthcare at specialised centres listed in Annex 2 to this Regulation.
The amount of the remuneration set out in Annex 1 to this Regulation and the limits and symbols set out in Annex 2 to this Regulation shall also apply where medicinal products are used in accordance with specific legislation1) in specialised centres of pediatric oncology, which have a contract with health insurance companies to treat this type of medicinal product for the treatment of paediatric cancer in cases where use is not mentioned in the Summary of Product Data (2).
The following shall be deleted:
1. Decree No. 532 / 2005 Coll., on the reimbursement of medicinal products and foodstuffs for special medical purposes.
2. Decree No. 37 / 2006 Coll., amending Decree No. 532 / 2005 Coll., on the reimbursement of medicines and foodstuffs for special medical purposes.
3. Decree No. 368 / 2006 Coll., amending Decree No. 532 / 2005 Coll., on the reimbursement of medicines and foodstuffs for special medical purposes.
4. Decree No. 387 / 2006 Coll., amending Decree No. 532 / 2005 Coll., on the reimbursement of medicines and foodstuffs for special medical purposes.
5. Decree No. 621 / 2006 Coll., amending Decree No. 532 / 2005 Coll., on the reimbursement of medicines and foodstuffs for special medical purposes.
This Decree shall take effect on 1 April 2007.
Příloha č. 1
Annex No 1 to Decree No 63 / 2007 Coll.
Medicinal products, including individually prepared medicinal products, radiopharmaceuticals and transfusion products, and food for special medical purposes fully covered by health insurance, the amount of payments of active substances and the amount of food payments for special medical purposes
Číslo
řádku
vyhlášky | Označení
ATC a
V06XX | Název léčivé látky | Cesta podání | Množství | Název
jedn. | Úhrada v Kč | Omezení |
|---|
|
| 1 | Stomatologika |
|
| 1.0 | | Stomatologika dále neuvedená | Veškeré | 1,00 | BA | 0,01 | |
|
| 1.1 | A01AA01 | fluorid sodný | p.o. | 1.10 | MG | 0,01 | |
|
| 1.2 | A01AB10 | natamycin | lok. | 20.00 | MG | 7,31 | |
|
| 1.3 | A01AB03 | chlorhexidin | lok. | 1 000.00 | ML | 174,64 | H |
|
| 1.4 | A01AC01 | triamcinolon | lok. | 1.00 | GM | 13,38 | L/DER,STO,ORL |
|
| 1.5 | A01AC02 | dexametason | lok. | 1.00 | GM | 12,31 | L/DER,STO,ORL |
| 0021695 | DEXALTIN ORAL PASTE | orm pst 10x5gm/5mg | ENK | D |
| 0096959 | DEXALTIN ORAL PASTE | pst 10x5gm/5mg | NKU | J |
| 2 | adsorbční antacida a protivředová léčiva ze skupiny H2-blokátorů, perorální podání |
|
| 2.0 | | Adsobční anatacida a protivředová léčiva ze skupiny H2-blokátorů dále neuvedená | p.o. | 1,00 | BA | 0,01 | |
|
| 2.1 | A02AD | kombinace hliníku, vápníku a hořčíku (pevné lékové formy) | p.o. | 10.00 | DF | 0,01 | |
|
| 2.2 | A02AD | kombinace hliníku, vápníku a hořčíku (tekuté lékové formy) | p.o. | 50.00 | ML | 0,01 | |
|
| 2.3 | A02AD01 | kombinace hliníku, vápníku a hořčíku (obvyklé kombinace solí - pevné lékové formy) | p.o. | 10.00 | DF | 0,01 | |
|
| 2.4 | A02AD01 | kombinace hliníku, vápníku a hořčíku (obvyklé kombinace solí - tekuté lékové formy) | p.o. | 50.00 | ML | 0,01 | |
|
| 2.5 | A02AD04 | hydrotalcit (pevné lékové formy) | p.o. | 10.00 | DF | 0,01 | |
|
| 2.6 | A02AD04 | hydrotalcit (tekuté lékové formy) | p.o. | 50.00 | ML | 0,01 | |
|
| 2.7 | A02BA01 | cimetidin | p.o. | 0.80 | GM | 3,11 | |
| | | | | | | |
| 2.8 | A02BA02 | ranitidin nad 75 mg v 1tbl | p.o. | 0.30 | GM | 3,11 | |
| 0047471 | RANISAN 150 MG | por tblflm60x150mg | PMP | CZ |
| 0096283 | ULCOSAN | tbl obd 30x150mg | IXP | CZ |
| 2.9 | A02BA03 | famotidin 20 mg a výše v 1 tabletě | p.o. | 40.00 | MG | 3,11 | |
| 0047862 | FAMOSAN 20 MG | por tbl flm100x20mg | PMP | CZ |
| 0047863 | FAMOSAN 40 MG | por tbl flm 100x40mg | PMP | CZ |
| 0059596 | FAMOSAN 40 MG | por tbl flm 50x40mg | PMP | CZ |
| 3 | protivředová léčiva ze skupiny inhibitorů protonové pumpy a ostatní protivředová léčiva |
|
| 3.0 | | Protivředová léčiva skupiny inhibitorů protonové pumpy a ostatní protivředová léčiva dále neuvedená | Veškeré | 1,00 | BA | 0,01 | |
|
| 3.1 | A02BA01 | cimetidin | parent. | 0.80 | GM | 31,33 | H |
|
| 3.2 | A02BA02 | ranitidin | parent. | 0.30 | GM | 66,88 | H |
|
| 3.3 | A02BA03 | famotidin | parent. | 40.00 | MG | 66,88 | H |
|
| 3.4 | A02BC01 | omeprazol | parent. | 20.00 | MG | 163,92 | H |
| 0076644 | LOSEC 40 MG | inf sic 5x40mg | AZC | S |
| 3.5 | A02BC01 | omeprazol (do 10 mg v jedné dávce včetně) | p.o. | 20.00 | MG | 9,45 | |
| 0023786 | LOSEPRAZOL 10 MG | por cps etd 14x10mg | PMP | CZ |
| 0023787 | LOSEPRAZOL 10 MG | por cps etd 28x10mg | PMP | CZ |
| 0030659 | ORTANOL 10 MG | por cps dur 56x10mg | LEK | SLO |
| 3.6 | A02BC01 | omeprazol (nad 10 mg do 20mg v jedné dávce včetně) | p.o. | 20.00 | MG | 6,03 | |
| 0017103 | LOSEPRAZOL 20 MG | por cps etd 14x20mg | PMP | CZ |
| 0017104 | LOSEPRAZOL 20 MG | por cps etd 28x20mg | PMP | CZ |
| 0098625 | OMEPRAZOL-RATIOPHARM 20 MG | por cps etd 15x20mg | MCK | D |
| 0098626 | OMEPRAZOL-RATIOPHARM 20 MG | por cps etd 30x20mg | MCK | D |
| 0098628 | OMEPRAZOL-RATIOPHARM 20 MG | por cpsetd 100x20mg | MCK | D |
| 3.7 | A02BC01 | omeprazol (více než 20 mg v jedné dávce) | p.o. | 20.00 | MG | 3,91 | |
| 0023788 | LOSEPRAZOL 40 MG | por cps etd 14x40mg | PMP | CZ |
| 0023789 | LOSEPRAZOL 40 MG | por cps etd 28x40mg | PMP | CZ |
| 3.8 | A02BC02 | pantoprazol | p.o. | 40.00 | MG | 6,03 | |
| 3.9 | A02BC02 | pantoprazol | parent. | 40.00 | MG | 163,92 | H |
| 3.10 | A02BC03 | lansoprazol (do 15 mg v jedné dávce včetně) | p.o. | 30.00 | MG | 9,45 | |
| 3.11 | A02BC03 | lansoprazol (nad 15 mg do 30 mg v jedné dávce včetně) | p.o. | 30.00 | MG | 6,03 | |
| 3.12 | A02BC05 | esomeprazol (do 20mg v jedné dávce včetně) | p.o. | 30.00 | MG | 13,01 | L/GIT,INT,GER |
| 3.13 | A02BC05 | esomeprazol (nad 20mg v jedné dávce ) | p.o. | 30.00 | MG | 7,22 | L/GIT,INT,GER |
| 3.14 | A02BC05 | esomeprazol | parent. | 30.00 | MG | 163,92 | H |
| 3.15 | A02BX02 | sukralfát | p.o. | 4.00 | GM | 6,78 | |
| 4 | spasmolytika, perorální podání |
|
| 4.0 | | Spasmolytika dále neuvedená | p.o. | 1,00 | BA | 0,01 | |
|
| 4.1 | A03AA04 | mebeverin | p.o. | 0.30 | GM | 4,83 | |
|
| 4.2 | A03AB06 | otilonium bromid | p.o. | 0.12 | GM | 12,14 | |
|
| 4.3 | A03AD01 | papaverin | p.o. | 0.10 | GM | 0,66 | |
|
| 4.4 | A03AD02 | drotaverin | p.o. | 0.10 | GM | 4,79 | |
| 0017933 | NO-SPA FORTE | tbl 10x80mg | CPW | H |
| 4.5 | A03BA01 | atropin | p.o. | 1.50 | MG | 0,48 | |
|
| 4.6 | A03BB01 | butylskopolamin | p.o. | 60.00 | MG | 13,89 | |
| 5 | spasmolytika, ostatní cesty aplikace |
|
| 5.0 | | Spasmolytika dále neuvedená | Ostatní cesty aplikace | 1,00 | BA | 0,01 | |
|
| 5.1 | A03AD01 | papaverin | parent. | 0.10 | GM | 17,53 | |
|
| 5.2 | A03AD02 | drotaverin | parent. | 0.10 | GM | 24,97 | |
|
| 5.3 | A03BA01 | atropin (1 mg a více v 1 ampuli) | parent. | 1.50 | MG | 8,09 | |
| 0000394 | ATROPIN BIOTIKA 1MG | inj 10x1 ml/1 mg | HBS | SK |
| 5.4 | A03BA01 | atropin (do 1mg v 1 ampuli) | parent. | 1.50 | MG | 14,81 | |
|
| 5.5 | A03BB01 | butylskopolamin | p.rect. | 60.00 | MG | 14,33 | |
|
| 5.6 | A03BB01 | butylskopolamin | parent. | 60.00 | MG | 36,77 | |
| 6 | anticholinergika a spasmolytika v kombinaci s analgetiky |
|
| 6.0 | | Anticholinergika a spasmolytika v kombinaci s analgetiky, dále neuvedená | veškeré | 1,00 | BA | 0,01 | |
|
| 6.1 | A03DA02 | pitofenon kombinace s analgetiky | p.rect. | 2.00 | DF | 13,70 | |
| 0091517 | ALGIFEN SUP | rct sup 5 | LEX | CZ |
| 6.2 | A03DA02 | pitofenon kombinace s analgetiky | parent. | 2.00 | DF | 43,25 | |
|
| 6.3 | A03DA02 | pitofenon kombinace s analgetiky (pevné lékové formy) | p.o. | 2.00 | DF | 4,02 | |
|
| 6.4 | A03DA02 | pitofenon kombinace s analgetiky (tekuté lékové formy) | p.o. | 2.00 | ML | 4,02 | |
|
| 6.5 | A03EA | antispasmodika, psycholeptika, analgetika v komb. | p.rect. | 2.00 | DF | 12,43 | |
|
| 7 | prokinetika, antiflatulencia, perorální podání |
| 7.0 | | Prokinetika, antiflatulencia dále neuvedená | p.o. | 1,00 | BA | 0,01 | |
|
| 7.1 | A03AX13 | silikony (pevné lékové formy) | p.o. | 0.50 | GM | 8,63 | |
|
| 7.2 | A03AX13 | silikony (tekuté lékové formy) | p.o. | 0.50 | GM | 14,69 | |
|
| 7.3 | A03AX58 | alverin (kombinace se silikony) | p.o. | 0.18 | GM | 6,76 | |
|
| 7.4 | A03FA | itoprid | p.o. | 0.15 | GM | 22,23 | L/GIT,INT,PED |
| 7.5 | A03FA01 | metoclopramid hydrochlorid | p.o. | 30.00 | MG | 3,67 | |
| 0056696 | MCP HEXAL 10 | tbl 100x10mg | SFS | D |
| 7.6 | A03FA03 | domperidon | p.o. | 30.00 | MG | 3,87 | |
| 8 | prokinetika, ostatní cesty aplikace |
|
| 8.0 | | Prokinetika dále neuvedená | Ostatní cesty aplikace | 1,00 | BA | 0,01 | |
|
| 8.1 | A03FA01 | metoclopramid | p.rect. | 30.00 | MG | 40,56 | |
|
| 8.2 | A03FA01 | metoclopramid | parent. | 30.00 | MG | 20,69 | O |
| 0093105 | DEGAN | inj 50x2ml/10mg | LEK | SLO |
| 8.3 | A03FA03 | domperidon | p.rect. | 0.12 | GM | 40,56 | |
| 9 | antiemetika, perorální podání |
|
| 9.0 | | Antiemetika dále neuvedená | p.o. | 1,00 | BA | 0,01 | |
|
| 9.1 | A04AA01 | ondansetron (pevné lékové formy do 4 mg v jedné tabletě včetně) | p.o. | 16.00 | MG | 385,74 | P |
| 0021342 | ONDANSETRON-TEVA 4 MG | por tbl flm 10x4mg | PHM | NL |
| 9.2 | A04AA01 | ondansetron (pevné lékové formy nad 4 mg v jedné tabletě) | p.o. | 16.00 | MG | 285,90 | P |
| 0021353 | ONDANSETRON-TEVA 8 | MG | por tbl flm 10x8mg | PHM | NL |
| 0041206 | ONDANSETRON EBEWE | 8 MG POTTAB | por tbl flm 50x8mg | PPN | GR |
| 0041208 | ONDANSETRON EBEWE | 8 MG POTTAB | por tbl flm 100x8mg | PPN | GR |
| 9.3 | A04AA01 | ondansetron (tekuté lékové formy) | p.o. | 16.00 | MG | 604,00 | P |
|
| 9.4 | A04AA02 | granisetron | p.o. | 2.00 | MG | 285,90 | P |
Ondansetron, granisetron a palonosetron jsou hrazeny u pacientů s nauzeou a zvracením v důsledku silného uvolnění serotoninu, navozeného cytotoxickou chemoterapií a radioterapií.
| 9.5 | A04AD | různá antiemetika (meklozin) | p.o. | 50.00 | MG | 3,23 | |
|
| 9.6 | A04AD | různá antiemetika (theoklát embraminu) | p.o. | 50.00 | MG | 3,23 | |
|
| 9.7 | A04AD | různá antiemetika (theoklát moxastinu) | p.o. | 0.10 | GM | 3,23 | |
|
| 9.8 | A04AD12 | aprepitant (80 mg a více v jedné dávce) | p.o. | 1.00 | DF | 385,74 | P |
Aprepitant je v síle 80 a 125 mg hrazen po dobu 3dnů jako součást léčebného režimu zahrnujícího kortikosteroid a antagonistu 5-HT3 (setrony) u pacientů s nauzeou a zvracením v souvislosti s vysoce emetogenní protinádorovou chemoterapií, založené na bázi cisplatiny, v další linii po selhání léčby setrony.
| 10 | antiemetika, ostatní cesty aplikace |
|
| 10.0 | | Antiemetika dále neuvedená | Ostatní cesty aplikace | 1,00 | BA | 0,01 | |
|
| 10.1 | A04AA | palonosetron | parent. | 1 | DF | 2 749,14 | P |
| 0028441 | ALOXI | ivn injsol250rg/5ml | HBP | IRL |
| 10.2 | A04AA01 | ondansetron (léková forma čípků) | p.rect. | 16.00 | MG | 553,61 | P |
|
| 10.3 | A04AA01 | ondansetron (do 4 mg v jedné ampuli včetně) | parent. | 16.00 | MG | 764,19 | P |
|
| 10.4 | A04AA01 | ondansetron (nad 4 mg v jedné ampuli) | parent. | 16.00 | MG | 616,33 | P |
| 0015828 | EMESET | inj sol 5x4ml/8mg | SDD | CZ |
| 10.5 | A04AA02 | granisetron | parent. | 3.00 | MG | 404,59 | P |
| 11 | hepatika a hepatoprotektiva a další léčiva působící na žlučové cesty nebo játra |
|
| 11.0 | | Hepatika a hepatoprotektiva a další léčiva působící na žlučové cesty nebo játra, dále neuvedená | Veškeré | 1,00 | BA | 0,01 | |
|
| 11.1 | A05AA02 | kyselina ursodeoxycholová | p.o. | 0.75 | GM | 19,79 | L/GIT,INF |
|
| 11.2 | A05AX | jiná léčiva onemocnění žlučníku (fenipentol) | p.o. | 3.00 | DF | 2,14 | |
| 0022108 | FEBICHOL | por cps mol50x100mg | NOZ | CZ |
| 11.3 | A05AX02 | hymekromon | p.o. | 1.20 | GM | 5,82 | |
|
| 11.4 | A05BA | léčiva onemocnění jater (fosfolipidy) | p.o. | 4.00 | DF | 6,18 | |
|
| 11.5 | A05BA | léčiva onemocnění jater (fosfolipidy) | parent. | 1.00 | DF | 41,75 | H |
|
| 11.6 | A05BA | léčiva onemocnění jater (silymarin v kombinaci) | p.o. | 0.21 | GM | 2,90 | |
|
| 11.7 | A05BA03 | silymarin | parent. | 0.35 | GM | 2 291,90 | H |
|
| 11.8 | A05BA03 | silymarin (do 70 mg včetně v jedné tabletě) | p.o. | 0.21 | GM | 2,90 | |
|
| 11.9 | A05BA03 | silymarin (nad 70 mg v jedné tabletě) | p.o. | 0.21 | GM | 2,32 | |
| 12 | laxativa a další léčiva k očištění střeva |
|
| 12.0 | | Laxativa a další léčiva k očištění střeva dále neuvedená | Veškeré | 1,00 | BA | 0,01 | |
|
| 12.1 | A06AD11 | laktulóza | p.o. | 6.70 | GM | 2,97 | P |
Lactulose is prescribed by qastroenterologist and pediatrician in patients with:
2. Non-specific intestinal inflammation
3. heavy forms of constipation
| 12.2 | A06AD15 | macrogol | p.o. | 4.00 | DF | 213,47 | |
|
| 12.3 | A06AG10 | sorbitol v kombinaci s kont. laxativem | p.rect. | 2.00 | DF | 166,73 | |
| 0092489 | YAL | sol 10x67.5ml | TRM | D |
| 13 | Antidiarhoika, antiinfekční a protizánětlivá léčiva gastrointestinálního traktu, perorální podání |
|
| 13.0 | | Antidiarhoika, antiinfekční a protizánětlivá léčiva gastrointestinálního traktu dále neuvedená | p.o. | 1,00 | BA | 0,01 | |
|
| 13.1 | A07AA11 | rifaximin | p.o. | 0.80 | GM | 83,07 | P |
Rifaximin is prescribed in the following indications:
(1) hepatic encephalopathy,
2) prophylaxis in colorectal surgery,
3) pseudomembranose colitis,
4) bacterial infection associated with non-specific inflammatory bowel disease (i. e. Crohn 's disease and ulcerative colitis) susceptible to rifaximin.
| 13.2 | A07BC05 | diosmectit (plv. susp.) | p.o. | 1.00 | DF | 3,77 | L/PED, INF |
|
| 13.3 | A07EA06 | budesonid | p.o. | 9.00 | MG | 84,29 | P |
Oral budesonide prescribes a gastroenterologist or internist in an acute attack, or chronic phase of Crohn 's disease, affecting ileum or colon ascendens, particularly where there is a need to treat steroids while minimising their systemic effects.
| 13.4 | A07EB01 | natrium kromoglykát | p.o. | 800.00 | MG | 71,01 | P |
The sodium cromoglycate is prescribed by an allergologist and a clinical immunologist in evidence of food allergy accompanied by severe local or general symptoms which cannot be fully corrected by the elimination of food allergens, based on an allergenic examination of skin potential exposure test or a specific IgE of antibodies.
| 0085932 | NALCROM | cps 100x100mg | ILC | I |
| 13.5 | A07EC01 | sulfasalazin | p.o. | 2.00 | GM | 14,80 | L/GIT,INT,REV, GER |
| 0002159 | SULFASALAZIN K | por tbl flm50x500mg | KRK | SLO |
| 0004304 | SULFASALAZIN K-EN | por tblent100x500mg | KRK | SLO |
| 13.6 | A07EC02 | mesalazin (léková forma - sáčky) | p.o. | 1.50 | GM | 35,03 | P |
Mesalazine per os - pharmaceutical format- sachets is the first-choice aminosalicylate in non-specific intestinal inflammation (Crohn 's disease) affecting the upper gastrointestinal tract, small intestine and adjacent colon (ileocolitis) in children under 3 years of age and in patients with swallowing disorder. It is not a first-choice aminosalicylate for the location of non-specific intestinal inflammation in the colon; is indicated after failure of other aminosalicylates.
| 13.7 | A07EC02 | mesalazin (potahované tablety) | p.o. | 1.50 | GM | 21,75 | L/GIT,INT,GER |
| 0075567 | SALOFALK 500 | tbl obdent100x500mg | FAK | D |
| 0093235 | SALOFALK 250 | tbl ent 100x250mg | FAK | D |
| 13.8 | A07EC02 | mesalazin (tablety s řízeným uvolňováním) | p.o. | 1.50 | GM | 35,03 | P |
Mesalazine powder - modified-release tablets: is a first-choice aminosalicylate in non-specific intestinal inflammation (Crohn 's disease) affecting the upper gastrointestinal tract, small intestine and adjacent colon (ileocolitis). It is not a first-choice aminosalicylate for the location of non-specific intestinal inflammation in the colon, it is indicated here after failure of other aminosalicylates.
| 13.9 | A07FA | protiprůjmové mikroorganismy (Escherichia coli), lékové formy tobolek | p.o. | 2.00 | DF | 24,57 | L/PED |
| 0066065 | MUTAFLOR 20MG | cps ent 20x20mg | ARP | D |
| 13.10 | A07FA | protiprůjmové mikroorganismy (Escherichia coli), tekuté lékové formy | p.o. | 1.00 | DF | 42.99 | L/PED, INF |
|
| 13.11 | A07FA01 | organismy produkující kyselinu mléčnou, pevné lékové formy | p.o. | 4.00 | DF | 3,77 | L/PED, INF |
|
| 13.12 | A07FA01 | organismy produkující kyselinu mléčnou, tekuté lékové formy | p.o. | 2.00 | ML | 3,47 | L/PED, INF |
| 0009158 | HYLAK FORTE | sol 1x30ml | MCK | D |
| 0009159 | HYLAK FORTE | sol 1x100ml | MCK | D |
| 13.13 | A07FA02 | saccharomyces boulardii sicatus | p.o. | 1.00 | DF | 5,38 | P |
Medicinal products containing Saccharomyces boulardii sic. are prescribed for the treatment of infectious diarrhoea, prophylaxis and the treatment of diarrhoea in patients fed with gastric or enteral nutrition using a probe.
| 14 | antidiarhoika, antiinfekční a protizánětlivá léčiva gastrointestinálního traktu, ostatní cesty aplikace |
|
| 14.0 | | Antidiarhoika, antiinfekční a protizánětlivá léčiva gastrointestinálního traktu dále neuvedená | Ostatní cestyaplikace | 1,00 | BA | 0,01 | |
|
| 14.1 | A07EA06 | budesonid | p.rect. | 2.00 | MG | 216,73 | L/GIT,INT,GER |
|
| 14.2 | A07EC02 | mesalazin (čípky do 250 mg včetně) | p.rect. | 1.50 | GM | 108,77 | L/GIT |
|
| 14.3 | A07EC02 | mesalazin (čípky nad 250 mg) | p.rect. | 1.50 | GM | 92,80 | L/GIT |
| 0075569 | SALOFALK 500 | sup 30x500mg | FAK | D |
| 14.4 | A07EC02 | mesalazin (enema) do 1 gm včetně v 1 lahvičce | p.rect. | 1.50 | GM | 101,65 | L/GIT |
| 0045744 | PENTASA 1 G | rct sus 7x1gm | FEI | DK |
| 14.5 | A07EC02 | mesalazin (enema) nad 1gm v 1 lahvičce | p.rect. | 1.50 | GM | 60.00 | L/GIT |
| 15 | digestiva včetně enzymových přípravků |
|
| 15.0 | | Digestiva včetně enzymových přípravků dále neuvedená | Veškeré | 1,00 | BA | 0,01 | |
|
| 15.1 | A09AA | enzymové přípravky (s pankreatinem, dle obsahu lipázy) | p.o. | 5 000.00 | U | 0,01 | |
|
| 15.2 | A09AA02 | multienzymy (dle obsahu lipázy: do 10 000U včetně v jedné tabletě nebo kapsli) | p.o. | 5 000.00 | U | 1,44 | P |
Multienzymes up to 10,000 lipase In one tablet, cystic fibrosis is prescribed for paediatric patients up to 10 kg of their body weight.
| 15.3 | A09AA02 | multienzymy (dle obsahu lipázy: nad 10 000 do 19 999 U v jedné tabletě) | p.o. | 5 000.00 | U | 0,01 | |
|
| 15.4 | A09AA02 | multienzymy (dle obsahu lipázy: 20 000U v jedné tabletě) | p.o. | 5 000.00 | U | 1,37 | P |
Multienzymes as gastro-resistant tablets containing 20,000 lipase In patients with an algic form of chronic pancreatitis, they are prescribed using at least one of the following methods: ERCP, EUS, CT, MRCP, peroperatively, in patients with pancreatic cancer and after pancreatic resection.
| 0040378 | PANZYNORM FORTE-N | por tbl flm 30 | KRK | SLO |
| 0040379 | PANZYNORM FORTE-N | por tbl flm 100 | KRK | SLO |
| 15.5 | A09AA02 | multienzymy (dle obsahu lipázy: nad 20000U v jedné tabletě) - formy mikropelet | p.o. | 5 000.00 | U | 1,91 | P |
Multienzymes in the form of micropellets are prescribed in patients with cystic fibrosis and chronic pancreatitis with at least one of the following methods: ERCP, EUS, CT, MRCP, peroperatively, in patients with pancreatic cancer and pancreatic resection.
| 0054534 | PANZYTRAT 25 000 | por cps dur 50-sklo | NOA | D |
| 15.6 | A09AA02 | multienzymy (dle lipázy, nad 20.000 U v jedné tabletě) | p.o. | 5 000.00 | U | 0,01 | |
| 16 | insuliny krátkodobě působící |
|
| 16.0 | | Insuliny krátkodobě působící dále neuvedené | Veškeré | 1,00 | BA | 0,01 | |
|
| 16.1 | A10AB01 | insulin lidský rychle účinkující 100 U/ml, cartridge | parent. | 40.00 | U | 21,50 | L/DIA |
|
| 16.2 | A10AB01 | insulin lidský rychle účinkující 100 U/ml, cartridge v jednorázovém aplikátoru | parent. | 40.00 | U | 26,00 | P |
Diabetes mellitus treated with insulin in people with defined visual impairment determined on the basis of ophthalmologist examination - decrease in visual acuity below 0.4 on a better eye with optimal correction and at a value of visual acuity up to close of more than 10 Jg with optimal correction, which can clearly not be used by other applicators due to visual impairment.
| 16.3 | A10AB01 | insulin lidský rychle účinkující, lahv. | parent. | 40.00 | U | 16,17 | |
| 0044576 | HUMULIN R 100 M.J./ML | inj 1x10ml/1ku | LIL | F |
| 0047193 | HUMULIN R 100 M.J./ML | inj 1x10ml/1ku | LPF | D |
| 17 | insuliny střednědobě působící včetně kombinací |
|
| 17.0 | | Insuliny střednědobě působící včetně kombinací dále neuvedené | Veškeré | 1,00 | BA | 0,01 | |
|
| 17.1 | A10AD01 | insulin lidský kombinace středně a rychle účinného 100U/ml, cartridge | parent. | 40.00 | U | 21,50 | L/DIA |
|
| 17.2 | A10AD01 | insulin lidský kombinace středně a rychle účinného 100U/ml, cartridge v jednorázovém aplikátoru | parent. | 40.00 | U | 26,00 | P |
Diabetes mellitus treated with insulin in people with defined visual impairment determined on the basis of ophthalmologist examination - decrease in visual acuity below 0.4 on a better eye with optimal correction and at a value of visual acuity up to close of more than 10 Jg with optimal correction, which can clearly not be used by other applicators due to visual impairment.
| 17.3 | A10AD01 | insulin lidský kombinace středně a rychle účinného, lahv. | parent. | 40.00 | U | 16,17 | |
| 40878 | INSULIN-HM MIX 30 | inj 1x10ml/1ku | ZEH | CZ |
| 18 | insuliny dlouhodobě působící |
|
| 18.0 | | Insuliny dlouhodobě působící dále neuvedené | Veškeré | 1,00 | BA | 0,01 | |
| 18.1 | A10AC01 | insulin lidský středně dlouze účinkující 100U/ml, cartridge | parent. | 40.00 | U | 21,50 | L/DIA |
|
| 18.2 | A10AC01 | insulin lidský středně dlouze účinkující 100U/ml, cartridge v jednorázovém aplikátoru | parent. | 40.00 | U | 26,00 | P |
Diabetes mellitus treated with insulin in people with defined visual impairment determined on the basis of ophthalmologist examination - decrease in visual acuity below 0.4 on a better eye with optimal correction and at a value of visual acuity up to close of more than 10 Jg with optimal correction, which can clearly not be used by other applicators due to visual impairment.
| 18.3 | A10AC01 | insulin lidský středně dlouze účinkující, lahv. | parent. | 40.00 | U | 16,17 | |
| 0044567 | HUMULIN N 100 M.J./ML | inj 1x10ml/1ku | LIL | F |
| 0047195 | HUMULIN N 100 M.J./ML | inj 1x10ml/1ku | LPF | D |
| 18.4 | A10AE01 | insulin lidský dlouhodobě účinkující | parent. | 40.00 | U | 16,17 | |
| 19 | analoga insulinů a insuliny používané k aplikaci pomocí insulinové pumpy |
|
| 19.0 | | Analoga insulinů a insuliny používané k aplikaci pomocí insulinové pumpy dále neuvedená | Veškeré | 1,00 | BA | 0,01 | |
|
| 19.1 | A10AB04 | insulin-lispro krátce působící, cartridge 100U/ML | parent. | 40.00 | U | 26,24 | P |
|
| 19.2 | A10AB04 | insulin-lispro krátce působící, lahv. | parent. | 40.00 | U | 25,70 | P |
|
| 19.3 | A10AB05 | insulin-aspart krátce působící, cartridge 100U/ML | parent. | 40.00 | U | 26,24 | P |
|
| 19.4 | A10AB05 | insulin-aspart krátce působící, lahv. | parent. | 40.00 | U | 25,70 | P |
|
| 19.5 | A10AB06 | insulin glulisin, cartridge 100U/ML | parent. | 40.00 | U | 26,24 | P |
A short-acting insulin analogue (insulin aspart, insulin lispro, insulin glulisine) prescribes a diabetic as a 2nd choice in diabetic patients with insufficient compensation for classic human insulin (HbA1c greater than 6.0% according to IFCC or severe hypoglycaemia). Insulin analogues should be replaced by human insulin if there is no evidence of improvement in glycaemic control within 3 months (decrease in mean HbA1c by at least 10% or a significant reduction in the frequency of hypoglycaemia).
| 19.6 | A10AB01 | insulin lidský rychle účinkující pro aplikaci do insulinových pump | parent. | 40.00 | U | 28.56 | L/DIA |
| 28001 | VELOSULIN 100 IU/ML | inj sol 1x10ml/1ku | NOO | DK |
| 19.7 | A10AD04 | insulin lispro, kombinace středně a rychle účinného, cartridge | parent. | 40.00 | U | 26,24 | P |
|
| 19.8 | A10AD05 | insulin aspart, kombinace středně a rychle účinného, cartridge | parent. | 40.00 | U | 26,24 | P |
The combination of short-term and medium-term insulin analogue (insulin aspart, insulin lispro) prescribes a diabetic as a 2nd choice in diabetic patients with insufficient compensation in the treatment of classic human insulin (HbA1c greater than 6.0% according to IFCC or severe hypoglycaemia). Insulin analogues should be replaced by human insulin if there is no evidence of improvement in glycaemic control within 3 months (decrease in mean HbA1c by at least 10% or a significant reduction in the frequency of hypoglycaemia).
| 19.9 | A10AE04 | insulin glargin, dlouhodobě účinný, lahv. | parent. | 40.00 | U | 26,67 | P |
|
| 19.10 | A10AE04 | insulin glargin, dlouhodobě účinný, cartridge | parent. | 40.00 | U | 43,01 | P |
| | | | | | | |
| 19.11 | A10AE05 | insulin detemir, dlouhodobě účinný, cartridge | parent. | 40.00 | U | 43,01 | P |
The long-acting insulin analogue (insulin glargine, insulin detemir) is prescribed in diabetes centres or ambulatory diabetic patients on the recommendation of a diabetes centre only as a second choice in patients treated with intensified insulin therapy, who are indicated to be treated with an insulin pump (repeated hypoglycaemia, dilute diabetes with evidence of unsatisfactory compensation, requiring long-term effective insulin multiple daily). Insulin analogues are not indicated.
| 20 | perorální antidiabetika ze skupiny biguanidů a glitazonů |
|
| 20.0 | | Perorální antidiabetika ze skupiny biguanidů a glitazonů dále neuvedená | Veškeré | 1,00 | BA | 0,01 | |
|
| 20.1 | A10BA02 | metformin hydrochlorid | p.o. | 2.00 | GM | 5,48 | |
| 0011114 | METFORMIN-TEVA 850 MG | por tbl flm30x850mg | BER | GB |
| 0011123 | METFORMIN-TEVA 850 MG | por tblflm 90x850mg | BER | GB |
| 0030294 | ADIMET | tbl obd 60x850mg | MCK | D |
| 0064641 | ADIMET | tbl obd 30x850mg | MCK | D |
| 0064642 | ADIMET | tbl obd 120x850mg | MCK | D |
| 0085231 | ADIMET 1000 | por tblflm60x1000mg | MCK | D |
| 0096087 | METFORMIN-TEVA 500 MG | por tblflm 60x500mg | BER | GB |
| 0112628 | METFORMIN-TEVA 850 MG | por tbl flm60x850mg | TEU | GB |
| 20.2 | A10BD02 | metformin a glibenklamid - kombinace | p.o. | 3.00 | DF | 4,17 | |
|
| 20.3 | A10BD03 | metformin a roziglitazon v kombinaci 500 mg a 1 mg | p.o. | 1.00 | DF | 8,27 | P |
|
| 20.4 | A10BD03 | metformin a roziglitazon v kombinaci 500 mg a 2 mg | p.o. | 1.00 | DF | 15,18 | P |
|
| 20.5 | A10BD03 | metformin a roziglitazon v kombinaci 1000 mg a 2 mg | p.o. | 1.00 | DF | 16,55 | P |
|
| 20.6 | A10BD03 | metformin a roziglitazon v kombinaci 1000 mg a 4 mg | p.o. | 1.00 | DF | 30,36 | P |
Metformin and rosiglitazone in combination are prescribed by a 2-choice diabetic after unsuccessful treatment with metformin in patients with type 2 diabetes and obesity (BMI > 30 kg / m2) with insulin resistance.
Treatment is discontinued unless there is evidence of an improvement in glycaemic control by at least 10% (decrease in HbA1c by at least 10%) within 6 months.
| 20.7 | A10BF01 | akarboza | p.o. | 0.30 | GM | 10,03 | |
|
| 20.8 | A10BG02 | rosiglitason s obsahem 4 mg v jedné tabletě | p.o. | 1.00 | DF | 27,62 | P |
|
| 20.9 | A10BG02 | rosiglitason s obsahem 8 mg v jedné tabletě | p.o. | 1.00 | DF | 41,32 | P |
|
| 20.10 | A10BG03 | pioglitazon s obsahem 15 mg v jedné tabletě | p.o. | 1.00 | DF | 27,62 | P |
|
| 20.11 | A10BG03 | pioglitazon s obsahem od 30 mg do 45 mg v jedné tabletě včetně | p.o. | 1.00 | DF | 41,32 | P |
Thiazolidinedione derivatives are prescribed by a diabetic in a subsequent choice following unsuccessful metformin therapy or in combination with a sulphonylurea in patients with type 2 diabetes and obesity (BMI > 30 kg / m2) and with insulin resistance. Treatment is discontinued unless there is evidence of improvement in glycaemic control by at least 10% (decrease in HbA1c by at least 10%) within 6 months.
1 tbl rosiglitazone containing 4 mg or 8 mg or 1 tbl pioglitazone containing 15 mg, 30 mg or 45 mg daily, respectively.
| 21 | perorální antidiabetika ze skupiny sulfonylurey a meglitinidů, případně další antidiabetika |
|
| 21.0 | | Perorální antidiabetika ze skupiny sulfonylurey a meglitinidů, případně další antidiabetika dále neuvedená | Veškeré | 1,00 | BA | 0,01 | |
|
| 21.1 | A10BB01 | glibenklamid (do 1 mg v jedné tabletě včetně) | p.o. | 10.00 | MG | 2,25 | |
|
| 21.2 | A10BB01 | glibenklamid (nad 1 mg v jedné tabletě) | p.o. | 10.00 | MG | 0,84 | |
|
| 21.3 | A10BB01 | glibenklamid (mikronizované formy, do 1,75 mg včetně v jedné tabletě) | p.o. | 7.00 | MG | 1,34 | |
| 0094523 | GLUCOBENE 1.75 MG | tbl 120x1.75mg | MCK | D |
| 21.4 | A10BB01 | glibenklamid (mikronizované formy, nad 1,75 mg v jedné tabletě) | p.o. | 7.00 | MG | 0,84 | |
| 0094525 | GLUCOBENE 3.5 MG | tbl 120x3.5mg | MCK | D |
| 21.5 | A10BB03 | tolbutamid | p.o. | 1.50 | GM | 2,27 | |
|
| 21.6 | A10BB07 | glipizid | p.o. | 10.00 | MG | 3,71 | |
| 0087110 | ANTIDIAB | tbl 30x5mg | KRK | SLO |
| 21.7 | A10BB08 | gliquidon | p.o. | 60.00 | MG | 4,10 | |
|
| 21.8 | A10BB09 | gliklazid | p.o. | 0.16 | GM | 4,10 | |
|
| 21.9 | A10BB09 | gliklazid, retardované lékové formy | p.o. | 2.00 | DF | 4,10 | |
|
| 21.10 | A10BB12 | glymepirid do 2 mg v jedné tabletě včetně | p.o. | 2.00 | MG | 4,10 | |
| 0044647 | GLIMEPIRID-RATIOPHARM 2 MG | por tbl nob 30x2mg | MCK | D |
| 0101740 | GLIMEPIRID ACTAVIS 2 MG | por tbl nob 30x2mg | ASZ | M |
| 21.11 | A10BB12 | glymepirid nad 2 mg do 4 mg v jedné tabletě včetně | p.o. | 2.00 | MG | 3,07 | |
| 0024134 | GLIMEPIRID-RATIOPHARM 4 MGZZ | por tbl nob 30x4mg | MCK | D |
| 0044899 | GLIMEPIRID-RATIOPHARM 3 MG | por tbl nob 30x3mg | MCK | D |
| 0101750 | GLIMEPIRID ACTAVIS 3 MG | por tbl nob 30x3mg | ASZ | M |
| 21.12 | A10BB12 | glymepirid nad 4 mg v jedné tabletě | p.o. | 2.00 | MG | 2,30 | |
|
| 21.13 | A10BX02 | repaglinid | p.o. | 1.00 | DF | 4,10 | L/DIA |
|
| 21.14 | A10BX03 | nateglinid | p.o. | 1.00 | DF | 4,10 | L/DIA |
| 22 | vitamin A nebo D včetně jejich kombinací, perorální podání |
|
| 22.0 | | Vitamin A nebo D včetně jejich kombinací dále neuvedený | p.o. | 1,00 | BA | 0,01 | |
|
| 22.1 | A11CA01 | retinol (vitamin A) | p.o. | 50.00 | KU | 1,09 | |
|
| 22.2 | A11CC01 | ergocalciferol (pevné lékové formy) | p.o. | 6.00 | KU | 0,53 | |
| 0000353 | VITAMIN D SLOVAKOFARMA | cps 1x300ku | SLO | SK |
| 22.3 | A11CC01 | ergokalciferol (tekuté lékové formy, do 200 U/ml včetně) | p.o. | 6.00 | KU | 12,80 | |
|
| 22.4 | A11CC01 | ergokalciferol (tekuté lékové formy, nad 200 U/ml) | p.o. | 6.00 | KU | 0,74 | |
| 0000716 | INFADIN | gtt 1x10ml/100mg | SLO | SK |
| 22.5 | A11CC02 | dihydrotachysterol | p.o. | 1.00 | MG | 16,74 | |
| 0014320 | TACHYSTIN | por gtt sol 1x20ml | CUA | D |
| 22.6 | A11CC03 | alfakalcidol do 0,50 rg včetně | p.o. | 1.00 | RG | 13,12 | P |
|
| 22.7 | A11CC03 | alfakalcidol nad 0,50 rg | p.o. | 1.00 | RG | 12,37 | P |
|
| 22.8 | A11CC04 | kalcitriol | p.o. | 1.00 | RG | 24,74 | P |
Alfakalcidol and calcitriol p.o. are prescribed by an internist, endocrinologist, urologist, pediatrician, rhematologist, orthoped, gynecologist, geriatr, nephrologist and physician in the dialysis unit in patients:
(a) a senile or osteoporotic fracture which has developed during vitamin D and calcium-free therapy;
(b) induced by the treatment of glucocorticoids,
(c) at a high dose of corticosteroids (7,5 mg prednisone daily and greater) with elevated PTH levels resistant to vitamin D and calcium therapy.
2. for the treatment of renal osteodystrophy with chronic renal insufficiency (particularly in patients on dialysis).
3. with vitamin D resistant curvature.
5. With hypoparathyroidism or pseudo-hypoparathyroidism resistant to vitamin D and calcium.
| 22.9 | A11CC05 | cholekalciferol - pevné lékové formy | p.o. | 0.50 | MG | 1,02 | |
|
| 22.10 | A11CC05 | cholekalciferol - tekuté lékové formy | p.o. | 0.50 | MG | 3,71 | |
| 0012023 | VIGANTOL | por gtt sol 1x10ml | MEC | D |
| 23 | vitamin A nebo D včetně jejich kombinací, ostatní cesty aplikace |
|
| 23.0 | | Vitamin A nebo D včetně jejich kombinací dále neuvedený | Ostatní cesty aplikace | 1,00 | BA | 0,01 | |
|
| 23.1 | A11CA01 | retinol (vitamin A) | parent. | 50.00 | KU | 10,16 | |
|
| 23.2 | A11CC07 | paricalcitolum | parent. | 2.50 | RG | 329,87 | O/P |
Paricalcitol is indicated in patients on dialysis if:
1. the serum PTH concentration is greater than 450pg / ml despite treatment with calcitriol for 3 months,
2. failure of calcitriol (hypercalcaemia on calcitriol - greater than 2,7 mmol / l and hyperphosphataemia greater than 2,5 mmol / l; phosphocalcatic product greater than 6,5),
3. extraoseal calcification with advanced hyperparathyroidism is present.
Treatment conditions are:
1. sonographically proven enlarged parathyroid organs,
2. Verified Hemodialysis Efficacy (Kt / V greater than 1,2).
| 0016881 | ZEMPLAR 5 MCG/ML | inj sol 5x2ml | ABB | I |
| 23.3 | A11CC01 | ergokalciferol | parent. | 6.00 | KU | 0,74 | |
| 0000405 | CALCIFEROL BIOTIKA FORTE | inj sol 1x1ml/7.5mg | BTA | SK |
| 0056677 | CALCIFEROL BIOTIKA FORTE | inj sol 5x1ml/7.5mg | BTA | SK |
| 23.4 | A11CC04 | kalcitriol | parent. | 1.00 | RG | 154,69 | O/P |
Parenteral calcitriol is prescribed by an internist, an endocrinologist, a urologist, a pediatrician and a physician in a dialysis unit in patients:
Comments 0