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uključujući jedan ili više DMARD-a.
including one or more DMARDs.
neuspjeh s 1 ili više DMARD-om.
had failed 1 or more DMARDs.
Lijek Cimzia također je uspoređen s placebom u 879 bolesnika s aktivnim reumatoidnim artritisom koji nikad nisu primili liječenje DMARD-ima.
Cimzia was also compared with placebo in 879 adults with active rheumatoid arthritis who had never received treatment with DMARDs.
Nije potrebno prilagođavati dozu kada se ovaj lijek koristi u kombinaciji s drugim DMARD-ima, kortikosteroidima, salicilatima,
No dose adjustment is required when used in combination with other DMARDs, corticosteroids, salicylates,
ne preporučuje se kombinacija s drugim DMARD-ima npr. metotreksatom.
haematotoxicity), combination with another DMARD(e.g. methotrexate) is not advisable.
Premalo je podataka iz kliničkih ispitivanja da bi se u potpunosti mogla procijeniti sigurnost sekvencijske primjene drugih DMARD-a(uključujući TNF-inhibitore
There are limited data from clinical trials to fully assess the safety of the sequential use of other DMARDs(including TNF inhibitors
Lijek RoActemra primijenjen injekcijom pod kožu ispitan je u dvama ispitivanjima kojima je bilo obuhvaćeno 1 918 bolesnika s umjerenim do teškim oblikom reumatoidnog artritisa u slučajevima kada prethodna terapija DMARD-om nije bila uspješna.
RoActemra given by injection under the skin has been investigated in two studies involving 1,918 patients with moderate to severe rheumatoid arthritis where previous treatment with DMARD had not worked well.
jest 6,2% kod bolesnika liječenih tocilizumabom u dozi od 8 mg/kg i DMARD-om.
is 6.2% in patients treated with 8 mg/kg tocilizumab+ DMARD.
u pedijatrijskih bolesnika u dobi od 6 godina i starijih koji su nedostatno odgovorili na druge DMARD-e, uključujući najmanje jedan TNF-inhibitor.
older who have had an insufficient response to other DMARDs including at least one TNF inhibitor.
U posljednjem ispitivanju bolesnika koji nikad nisu primili terapiju DMARD-ima, u gotovo 29% bolesnika(189 od 655)
In the last study in patients who had never received treatment with DMARDs, almost 29% of patients(189 out of 655)
DMARD- Antireumatski lijek koji modificira tijek bolesti.
DMARD- Disease modifying anti-rheumatic drug.
Bolesnici koji su uzimali DMARD, NSAID ili kortikosteroide mogli su ih nastaviti uzimati u stabilnoj dozi.
Patients receiving DMARDs, NSAIDS, or corticosteroids could continue them on stable doses.
Apremilast se primjenjivao kao monoterapija(34,8%) ili u kombinaciji sa stabilnim dozama malomolekulskih DMARD lijekova 65, 2.
Apremilast was used as a monotherapy(34.8%) or in combination with stable doses of small molecule DMARDs 65.2.
Odgovori opaženi u skupini liječenoj apremilastom bili su slični u bolesnika koji jesu i onih koji nisu istodobno primali DMARD lijekove, uključujući metotreksat.
Responses observed in the apremilast treated group were similar in patients receiving and not receiving concomitant DMARDs, including MTX.
U 24. tjednu opaženo je statistički značajno poboljšanje u vrijednostima hemoglobina kod bolesnika liječenih tocilizumabom u usporedbi s bolesnicima liječenima DMARD lijekovima p< 0, 0001.
Statistically significant improvements in haemoglobin levels were observed with tocilizumab compared with DMARDs(p< 0.0001) at week 24.
Leflunomid je indiciran u liječenju odraslih bolesnika s: aktivnim reumatoidnim artritisom kao antireumatik koji modificira tijek bolesti(DMARD od engl. disease-modifying antirheumatic drug), aktivnim psorijatičnim artritisom.
Leflunomide is indicated for the treatment of adult patients with: active rheumatoid arthritis as a"disease-modifying antirheumatic drug"(DMARD). active psoriatic arthrit is.
Cimzia se može također primjenjivati i samostalno, ako liječenje metotreksatom nije primjereno. teškog, aktivnog i progresivnog reumatoidnog artritisa koji nije prethodno liječen metotreksatom ili drugim antireumatskim lijekovima koji modificiraju tijek bolesti DMARD.
Cimzia can also be given alone when treatment with methotrexate is not appropriate. severe, active and progressive rheumatoid arthritis that has not been previously treated with methotrexate or other DMARDs.
Ukupno 76,4% bolesnika bilo je prethodno liječeno samo malomolekulskim DMARD lijekovima, a 22,4% bolesnika bilo je prethodno liječeno biološkim DMARD lijekovima, uključujući 7,8% onih kojima je prethodna terapija biološkom DMARD terapijom bila neuspješna.
A total of 76.4% of patients were previously treated with only small-molecule DMARDs and 22.4% of patients were previously treated with biologic DMARDs, which includes 7.8% who had a therapeutic failure with a prior biologic DMARD.
DMARD-ovi(biološki ili ne biološki)
DMARDs(biologic or non-biologic)
Za napomenuti je kako neki lijekovi protiv povišenog pritiska i DMARD-ovi mogu štetiti razvoju ploda.
Some blood pressure medicines and DMARDs can harm the development of the foetus.