Se aplică tuturor denumirilor comerciale, formelor farmaceutice şi concentraţiilor corespunzătoare DCI-ului.
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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M01AB05 DICLOFENACUM COMPR. FILM. ELIB. PREL 100 mg
DICLOTARD(R) 100 mg 100 mg TERAPIA SA
REFEN(R) RETARD 100 mg HEMOFARM S.R.L
VOLTAREN(R) RETARD 100 mg NOVARTIS PHARMA GMBH
M01AB05 DICLOFENACUM SUPOZ. 100 mg
CLAFEN 100 mg 100 mg ANTIBIOTICE SA
DICLOFENAC 100 mg 100 mg SINTOFARM SA
DICLOFENAC SODIC 100 mg 100 mg MAGISTRA C & C
DICLOGESIC 100 SUPOZITOARE 100 mg DAR AL DAWA PHARMA SRL
EPIFENAC 100 mg E.I.P.I.CO. MED S.R.L.
VOLTAREN(R) 100 mg NOVARTIS PHARMA GMBH
M01AB05 DICLOFENACUM SUPOZ. 120 mg
TRATUL 120 120 mg GEROT PHARMAZEUTIKA GMBH
M01AB05 DICLOFENACUM CAPS. ELIB. PREL. 150 mg
DICLOREUM 150 mg 150 mg ALFA WASSERMANN SPA
M01AB05 DICLOFENACUM COMPR. FILM. GASTROREZ. 25 mg
RHEUMAVEK 25 mg FARAN LABORATORIES S.A.
VOLTAREN(R) 25 25 mg NOVARTIS PHARMA GMBH
M01AB05 DICLOFENACUM COMPR. GASTROREZ. 25 mg
EPIFENAC 25 mg E.I.P.I.CO. MED S.R.L.
M01AB05 DICLOFENACUM DRAJ. GASTROREZ. 25 mg
DICLOFENAC 25 mg 25 mg ARENA GROUP SA
M01AB05 DICLOFENACUM SOL. INJ. 25 mg/ml
RHEUMAVEK 25 mg/ml FARAN LABORATORIES S.A.
VOLTAREN(R) 25 mg/ml NOVARTIS PHARMA GMBH
M01AB05 DICLOFENACUM SOL. INJ. 30 mg/ml
TRATUL(R) 30 mg/ml GEROT PHARMAZEUTIKA GMBH
M01AB05 DICLOFENACUM CAPS. GASTROREZ. 50 mg
TRATUL 50 50 mg GEROT PHARMAZEUTIKA GMBH
M01AB05 DICLOFENACUM COMPR. FILM. GASTROREZ. 50 mg
CLAFEN 50 mg 50 mg ANTIBIOTICE SA
DICLOFENAC 50 mg 50 mg AC HELCOR PHARMA SRL
VOLTAREN(R) 50 50 mg NOVARTIS PHARMA GMBH
M01AB05 DICLOFENACUM DRAJ. 50 mg
VOLTAREN RAPID(R) 50 mg NOVARTIS PHARMA GMBH
M01AB05 DICLOFENACUM DRAJ. GASTROREZ. 50 mg
DICLOFENAC 50 mg 50 mg ARENA GROUP SA
M01AB05 DICLOFENACUM SUPOZ. 50 mg
VOLTAREN(R) 50 mg NOVARTIS PHARMA GMBH
M01AB05 DICLOFENACUM SUPOZ. 60 mg
TRATUL 60 60 mg GEROT PHARMAZEUTIKA GMBH
M01AB05 DICLOFENACUM COMPR. ELIB. MODIF. 75 mg
DICLAC(R) 75 ID 75 mg HEXAL AG
M01AB05 DICLOFENACUM SOL. INJ. 75 mg
DICLAC 75 mg HEXAL AG
VURDON 75 mg HELP S.A. PHARMACEUTICALS
M01AB05 DICLOFENACUM SOL. INJ. 75 mg/3 ml
ALMIRAL 75 mg/3 ml MEDOCHEMIE LTD.
DICLOFENAC 75 mg 75 mg/3 ml TERAPIA SA
DICLOFENAC AL I.M. 75 mg/3 ml ALIUD PHARMA GMBH & CO.KG
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SUBLISTA C1 - G22 BOLI ENDOCRINE (GUŞA ENDEMICĂ, INSUFICIENŢA SUPRARENALĂ CRONICĂ, DIABETUL INSIPID, MIXEDEMUL ADULTULUI, TUMORI HIPOFIZARE CU EXPANSIUNE SUPRASELARĂ ŞI TUMORI NEUROENDOCRINE).
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| 525 |G02CB03| CABERGOLINUM** | Protocol: G001C |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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G02CB03 CABERGOLINUM COMPR. 0.5 mg
DOSTINEX 0.5 mg PFIZER EUROPE MA EEG
G02CB03 CABERGOLINUM COMPR. 0.5 mg
DOSTINEX 0.5 mg PFIZER EUROPE MA EEG
Prescriere limitată: Prevenirea apariţiei lactaţiei în lăuzie din motive medicale
Cod restricţie 2659: Hiperprolactinemia patologică pentru care nu este indicată intervenţia chirurgicală
Cod restricţie 2660: Hiperprolactinemia patologică pentru care a fost utilizat tratament chirurgical dar cu rezultate incomplete
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| 526 |H01AX01| PEGVISOMANTUM**** | Protocol: H012E |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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H01AX01 PEGVISOMANTUM LIOF. + SOLV. PT. SOL. 10 mg
INJ.
SOMAVERT 10 mg 10 mg PFIZER LTD.
H01AX01 PEGVISOMANTUM LIOF. + SOLV. PT. SOL. 20 mg
INJ.
SOMAVERT 20 mg 20 mg PFIZER LTD.
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| 527 |H01BA02| DESMOPRESSINUM | |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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H01BA02 DESMOPRESSINUM COMPR. 0.2 mg
MINIRIN 0,2 mg 0.2 mg FERRING AB
Cod restricţie 1678: Diabet insipid.
H01BA02 DESMOPRESSINUM
MINIRIN 0,2 mg 0.2 mg FERRING AB
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| 528 |H01CB02| OCTREOTIDUM**** | Protocol: H008E |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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H01CB02 OCTREOTIDUM COMPR. 100 mg
SANDOSTATIN(R) 0.1 mg/ml NOVARTIS PHARMA GMBH
H01CB02 OCTREOTIDUM PULB. + SOLV. PT. SUSP. 10 mg
INJ. (I.M.) CU ELIB.
PRELUNG.
SANDOSTATIN LAR 10 mg 10 mg NOVARTIS PHARMA GMBH
H01CB02 OCTREOTIDUM PULB. + SOLV. PT. SUSP. 20 mg
INJ. (I.M.) CU ELIB.
PRELU
SANDOSTATIN LAR 20 mg 20 mg NOVARTIS PHARMA GMBH
H01CB02 OCTREOTIDUM PULB. + SOLV. PT. SUSP. 30 mg
INJ. (I.M.) CU ELIB.
PRELUNG.
SANDOSTATIN LAR 30 mg 30 mg NOVARTIS PHARMA GMBH
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| 529 |H01CB03| LANREOTIDUM**** | Protocol: H005E;|
| | | | H006C |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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H01CB03 LANREOTIDUM LIOF. PT. SOL. INJ. + 30 mg
SOLV.
SOMATULINE(R) PR 30 mg 30 mg BEAUFOUR IPSEN PHARMA
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| 530 |H02AA02| FLUDROCORTISONUM | |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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H02AA02 FLUDROCORTISONUM COMPR. 0.1 mg
ASTONIN H 0.1 mg MERCK KGAA
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| 531 |H02AB06| PREDNISOLONUM | |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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H02AB06 PREDNISOLONUM LIOF. + SOLV. PT. SOL. 250 mg
INJ.
SOLU - DECORTIN H 250 250 mg MERCK KGAA
H02AB06 PREDNISOLONUM LIOF. + SOLV. PT. SOL. 50 mg
INJ.
SOLU - DECORTIN H 50 50 mg MERCK KGAA
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| 532 |H02AB07| PREDNISONUM | |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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H02AB07 PREDNISONUM COMPR. 5 mg
N - PREDNISON 5 mg MEDUMAN SA
PREDNISON 5 mg 5 mg SINTOFARM SA
PREDNISON ARENA 5 mg 5 mg ARENA GROUP SA
PREDNISON GEDEON RICHTER 5 mg 5 mg GEDEON RICHTER ROMANIA SA
PREDNISON MAGISTRA 5 mg 5 mg MAGISTRA C & C
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| 533 |H02AB09| HYDROCORTISONUM | |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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H02AB09 HYDROCORTISONUM LIOF. + SOLV. PT. SOL. 100 mg
INJ.
HYDROCORTISONE 100 mg 100 mg HEMOFARM S.R.L
HYDROCORTISONE SUCCINAT SODIC 100 mg E.I.P.I.CO. MED S.R.L.
H02AB09 HYDROCORTISONUM SOL. INJ. I.V. 25 mg/5 ml
HIDROCORTIZON HEMISUCCINAT 25 mg/5 ml ZENTIVA S.A.
H02AB09 HYDROCORTISONUM LIOF. PT. SOL. INJ. + 500 mg
SOLV.
HYDROCORTISONE 500 mg 500 mg HEMOFARM S.R.L.
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| 534 |H03AA01| LEVOTHYROXINUM | |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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H03AA01 LEVOTHYROXINUM COMPR. 100 µg
EUTHYROX(R) 100 100 µg MERCK KGAA
L-THYROXIN 100 BERLIN-CHEMIE 100 µg BERLIN CHEMIE AG MENARINI
GROUP
H03AA01 LEVOTHYROXINUM COMPR. 200 µg
EUTHYROX(R) 200 200 µg MERCK KGAA
H03AA01 LEVOTHYROXINUM COMPR. 25 µg
EUTHYROX(R) 25 25 µg MERCK KGAA
H03AA01 LEVOTHYROXINUM COMPR. 50 µg
EUTHYROX(R) 50 50 µg MERCK KGAA
L-THYROXIN 50 50 µg BERLIN CHEMIE AG MENARINI
GROUP
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| 535 |H03CA01| KALII IODIDUM | |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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H03CA01 KALII IODIDUM COMPR. 100 µg
JODID 100 100 µg MERCK KGAA
H03CA01 KALII IODIDUM COMPR. 200 µg
JODID 200 200 µg MERCK KGAA
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| 536 |G02CB01| BROMOCRIPTINUM | |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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G02CB01 BROMOCRIPTINUM DRAJ. 2.5 mg
BROCRIPTIN 2.5 mg BIOFARM SA
Prescriere limitată: Hiperprolactinemia patologică pentru care nu este indicată intervenţia chirurgicală
Prescriere limitată: Hiperprolactinemia patologică pentru care tratamentul chirurgical utilizat a dus la rezultate incomplete;
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SUBLISTA C1 - G23 BOALA WILSON.
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| 537 |M01CC01| PENICILLAMINUM**(4) | |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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M01CC01 PENICILLAMINUM
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SUBLISTA C1 - G25 BOALA CRONICA DE RINICHI - FAZA PREDIALIZA.
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| 538 |A11CC07| PARICALCITOLUM** | Protocol: A005E |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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A11CC07 PARICALCITOLUM SOL. INJ. 5 µg/ml
ZEMPLAR 5 µg/ml ABBOTT LABORATORIES S.A.
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| 539 |B03AC02| COMPLEX DE HIDROXID DE FER (III) SUCROZA** | Protocol: A010N |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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B03AC02 COMPLEX DE HIDROXID SOL. INJ./PERF. 20 mg/ml
DE FER (III) SUCROZA
VENOFER(R) 20 mg/ml VIFOR FRANCE S.A.
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| 540 |B03XA01| EPOETINUM ALFA** | Protocol: B010N |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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B03XA01 EPOETINUM ALFA SOL. INJ. 10000 ui/ml
EPREX(R) 10000 UI 10000 ui/ml JOHNSON & JOHNSON D.O.O.
B03XA01 EPOETINUM ALFA SOL. INJ. 1000 UI/0.5 ml
EPOKINE 1000 UI/0,5 ml 1000 UI/0.5 ml RENAMED FARMA S.R.L.
EPREX(R) 1000 UI 1000 ui/0.5 ml JOHNSON & JOHNSON D.O.O.
B03XA01 EPOETINUM ALFA SOL. INJ. 2000 UI
EPOPHAR 2000 U.I. 2000 UI GULF PHARMACEUTICAL IND.
S.R.L.
B03XA01 EPOETINUM ALFA SOL. INJ. 2000 ui/0.5 ml
EPOKINE 2000 UI/0,5 ml 2000 UI/0.5 ml RENAMED FARMA S.R.L.
EPREX(R) 2000 UI 2000 ui/0.5 ml JOHNSON & JOHNSON D.O.O.
B03XA01 EPOETINUM ALFA SOL. INJ. 2000 UI/1 ml
EPOKINE 2000 UI/1 ml 2000 UI/1 ml RENAMED FARMA S.R.L.
B03XA01 EPOETINUM ALFA SOL. INJ. 3000 ui/0.3 ml
EPREX(R) 3000 UI 3000 ui/0.3 ml JOHNSON & JOHNSON D.O.O.
B03XA01 EPOETINUM ALFA SOL. INJ. 40000 UI
EPREX(R) 40000 UI 40000 UI JOHNSON & JOHNSON D.O.O.
B03XA01 EPOETINUM ALFA SOL. INJ. 4000 UI
EPOPHAR 4000 U.I. 4000 UI GULF PHARMACEUTICAL IND.
S.R.L.
B03XA01 EPOETINUM ALFA SOL. INJ. 4000 ui/0.4 ml
EPOKINE 4000 UI/0,4 ml 4000 UI/0.4 ml RENAMED FARMA S.R.L.
EPREX(R) 4000 UI 4000 ui/0.4 ml JOHNSON & JOHNSON D.O.O.
B03XA01 EPOETINUM ALFA SOL. INJ. 4000 UI/1 ml
EPOKINE 4000 UI/1 ml 4000 UI/1 ml RENAMED FARMA S.R.L.
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| 541 |B03XA01| EPOETINUM BETA** | Protocol: B009N |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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B03XA01 EPOETINUM BETA SOL. INJ. ÎN SERINGĂ
PREUMPLUTĂ
NEORECORMON 10000 UI 10000 UI/0,6ml ROCHE REGISTRATION L
B03XA01 EPOETINUM BETA SOL. INJ. ÎN SERINGĂ
PREUMPLUTĂ
NEORECORMON 1000 UI 1000 UI/0,3 ml ROCHE REGISTRATION L
B03XA01 EPOETINUM BETA SOL. INJ. ÎN SERINGĂ
PREUMPLUTĂ
NEORECORMON 2000 UI 2000 UI/0,3 ml ROCHE REGISTRATION L
B03XA01 EPOETINUM BETA SOL. INJ. ÎN SERINGĂ 30000 UI/0,6ml
PREUMPLUTĂ
NEORECORMON 30000 UI/0,6 ml 30000 UI/0,6 ml ROCHE REGISTRATION LTD.
B03XA01 EPOETINUM BETA SOL. INJ. ÎN SERINGĂ
PREUMPLUTĂ
NEORECORMON 4000 UI 4000 UI/0,3 ml ROCHE REGISTRATION L
B03XA01 EPOETINUM BETA SOL. INJ. ÎN SERINGĂ
PREUMPLUTĂ
NEORECORMON 5000 UI 5000 UI/0,3 ml ROCHE REGISTRATION L
B03XA01 EPOETINUM BETA SOL. INJ. ÎN SERINGĂ
PREUMPLUTĂ
NEORECORMON 500 UI 500 UI/0,3 ml ROCHE REGISTRATION L
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| 542 |B03XA02| DARBEPOETINUM ALFA** | Protocol: B011N |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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B03XA02 DARBEPOETINUM ALFA SOL. INJ. ÎN SERINGĂ 10 µg/0.4 ml
PREUMPLUTĂ
ARANESP 10 µg/0.4 ml 10 µg/0.4 ml AMGEN EUROPE BV
B03XA02 DARBEPOETINUM ALFA SOL. INJ. ÎN SERINGĂ 100 µg/0.5 ml
PREUMPLUTĂ
ARANESP 100 µg/0.5 ml 100 µg/0.5 ml AMGEN EUROPE BV
B03XA02 DARBEPOETINUM ALFA SOL. INJ. ÎN SERINGĂ 15 µg/0.375 ml
PREUMPLUTĂ
ARANESP 15 µg/0.375 ml 15 µg/0.375 ml AMGEN EUROPE BV
B03XA02 DARBEPOETINUM ALFA SOL. INJ. ÎN SERINGĂ 150 µg/0.3 ml
PREUMPLUTĂ
ARANESP 150 µg/0.3 ml 150 µg/0.3 ml AMGEN EUROPE BV
B03XA02 DARBEPOETINUM ALFA SOL. INJ. ÎN SERINGĂ 20 µg/0.5 ml
PREUMPLUTĂ
ARANESP 20 µg/0.5 ml 20 µg/0.5 ml AMGEN EUROPE BV
B03XA02 DARBEPOETINUM ALFA SOL. INJ. ÎN SERINGĂ 30 µg/0.3 ml
PREUMPLUTĂ
ARANESP 30 µg/0.3 ml 30 µg/0.3 ml AMGEN EUROPE BV
B03XA02 DARBEPOETINUM ALFA SOL. INJ. ÎN SERINGĂ 300 µg/0.6 ml
PREUMPLUTĂ
ARANESP 300 µg/0.6 ml 300 µg/0.6 ml AMGEN EUROPE BV
B03XA02 DARBEPOETINUM ALFA SOL. INJ. ÎN SERINGĂ 40 µg/0.4 ml
PREUMPLUTĂ
ARANESP 40 µg/0.4 ml 40 µg/0.4 ml AMGEN EUROPE BV
B03XA02 DARBEPOETINUM ALFA SOL. INJ. ÎN SERINGĂ 50 µg/0.5 ml
PREUMPLUTĂ
ARANESP 50 µg/0.5 ml 50 µg/0.5 ml AMGEN EUROPE BV
B03XA02 DARBEPOETINUM ALFA SOL. INJ. ÎN SERINGĂ 500 µg/ml
PREUMPLUTĂ
ARANESP 500 µg/ml 500 µg/ml AMGEN EUROPE BV
B03XA02 DARBEPOETINUM ALFA SOL. INJ. ÎN SERINGĂ 60 µg/0.3 ml
PREUMPLUTĂ
ARANESP 60 µg/0.3 ml 60 µg/0.3 ml AMGEN EUROPE BV
B03XA02 DARBEPOETINUM ALFA SOL. INJ. ÎN SERINGĂ 80 µg/0.4 ml
PREUMPLUTĂ
ARANESP 80 µg/0.4 ml 80 µg/0.4 ml AMGEN EUROPE BV
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| 544 |C09CA04| IRBESARTANUM** | Protocol: C008N |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
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CONCENTRAŢIE FIRMA
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C09CA04 IRBESARTANUM COMPR. FILM. 150 mg
APROVEL 150 mg 150 mg SANOFI PHARMA - BRISTOL
MYERS SQUIBB
C09CA04 IRBESARTANUM COMPR. FILM. 300 mg
APROVEL 300 mg 300 mg SANOFI PHARMA - BRISTOL
MYERS SQUIBB
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| 545 |H02AB07| PREDNISONUM | Protocol: H002N |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
__________________________________________________
CONCENTRAŢIE FIRMA
________________________________________________________________________________
H02AB07 PREDNISONUM COMPR. 5 mg
N-PREDNISON 5 mg MEDUMAN SA
PREDNISON 5 mg 5 mg SINTOFARM SA
PREDNISON ARENA 5 mg 5 mg ARENA GROUP SA
PREDNISON GEDEON RICHTER 5 mg 5 mg GEDEON RICHTER ROMANIA SA
PREDNISON MAGISTRA 5 mg 5 mg MAGISTRA C & C
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| 546 |L01AA01| CYCLOPHOSPHAMIDUM | Protocol: L027N |
|_______|_______|____________________________________________|_________________|
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DCI/DENUMIRE COMERCIALĂ FORMA FARM.
__________________________________________________
CONCENTRAŢIE FIRMA
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L01AA01 CYCLOPHOSPHAMIDUM DRAJ. 50 mg
ENDOXAN(R) 50 mg 50 mg BAXTER ONCOLOGY GMBH
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| 547 |L04AA01| CICLOSPORINUM* | Protocol: L028N |
|_______|_______|____________________________________________|_________________|
Monitorizarea atentă a pacienţilor este obligatorie.
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