Примери за използване на Severely active на Английски и техните преводи на Български
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Moderately to severely active ulcerative colitis(a disease causing inflammation and ulcers in the lining of the gut).
Table 8 Effects on clinical response in adult patients with moderately to severely active ulcerative colitis, clinical remission and mucosal healing at weeks 8 and 30.
In the treatment of Crohn's disease, Stelara(concentrate for infusion)was compared with placebo in two main studies involving 1,369 patients with moderately to severely active disease.
A total of 573 patients with moderately to severely active Crohn' s disease(CDAI≥ 220≤ 400) received a single infusion of 5 mg/ kg at week 0.
The safety and efficacy of Humira was assessed in an open-label, multicentre study in 32 children(2-< 4 years old or aged 4 and above weighing<15 kg) with moderately to severely active polyarticular JIA.
In patients with moderately to severely active paediatric Crohn's disease, the rate of anti-adalimumab antibody development in patients receiving adalimumab was 3.3%.
The safety and efficacy of ustekinumab was assessed in two randomized,double-blind, placebocontrolled, multicenter studies in adult patients with moderately to severely active ulcerative colitis(Mayo score 6 to 12; Endoscopy subscore≥ 2).
Kevzara is used to treat adults with moderately to severely active rheumatoid arthritis if previous therapy did not work well enough or was not tolerated.
The safety and efficacy of ustekinumab was assessed in three randomized,double-blind, placebo-controlled, multicenter studies in adult patients with moderately to severely active Crohn's disease(Crohn's Disease Activity Index[CDAI] score of≥ 220 and≤ 450).
Entyvio is indicated for the treatment of adult patients with moderately to severely active Crohn's disease who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a tumour necrosis factor-alpha(TNFα) antagonist.
The efficacy and safety of upadacitinib 15 mg once daily was assessed in five Phase 3 randomised, double-blind,multicentre studies in patients with moderately to severely active rheumatoid arthritis and fulfilling the ACR/EULAR 2010 classification criteria(see Table 3).
STELARA is indicated for the treatment of adult patients with moderately to severely active Crohn's disease who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a TNFα antagonist or have medical contraindications to such therapies.
Au The safety and efficacy of Trudexa were assessed in over 1400 patients with moderately to severely active Crohn' s disease(Crohn' s Disease Activity Index(CDAI)≥ 220 and≤ 450) in randomised, double-blind, placebo-controlled studies.
Zessly is indicated for treatment of severely active ulcerative colitis, in children and adolescents aged 6 to 17 years, who have had an inadequate response to conventional therapy including corticosteroids and 6-MP or AZA, or who are intolerant to or have medical contraindications for such therapies.
The safety and efficacy of Humira were assessed in over 1400 patients with moderately to severely active Crohn' s disease(Crohn' s Disease Activity Index(CDAI)≥ 220 and≤ 450) in randomised, double-blind, placebo-controlled studies.
Simponi is indicated for treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy including corticosteroids and 6-mercaptopurine(6-MP) or azathioprine(AZA), or who are intolerant to or have medical contraindications for such therapies.
The safety and efficacy of Humira were assessed in over 1500 patients with moderately to severely active Crohn's disease(Crohn's Disease Activity Index(CDAI) 220 and 450) in randomised, double-blind, placebo-controlled studies.
Hulio is indicated for treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy including corticosteroids and 6-mercaptopurine(6-MP) or azathioprine(AZA), or who are intolerant to or have medical contraindications for such therapies.
The safety and efficacy of multiple doses of Humira were assessed in adult patients with moderately to severely active ulcerative colitis(Mayo score 6 to 12 with endoscopy subscore of 2 to 3) in randomised, double-blind, placebo-controlled studies.
In this study children and adolescents with moderately to severely active pJIA, ages 2 to 17 years(46 patients in the 2 to 5 year age cohort and 173 patients in the 6 to 17 year age cohort) with an inadequate response or intolerance to at least one DMARD, which may have included biologic agents.
STELARA is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic or have medical contraindications to such therapies(see section 5.1).
Cyltezo is indicated for treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy including corticosteroids and 6-mercaptopurine(6-MP) or azathioprine(AZA), or who are intolerant to or have medical contraindications for such therapies.
Hulio is indicated for treatment of moderately to severely active Crohn's disease, in adult patients who have not responded despite a full and adequate course of therapy with a corticosteroid and/or an immunosuppressant; or who are intolerant to or have medical contraindications for such therapies.
Hulio is indicated for the treatment of moderately to severely active Crohn's disease in paediatric patients(from 6 years of age) who have had an inadequate response to conventional therapy including primary nutrition therapy and a corticosteroid and/or an immunomodulator, or who are intolerant to or have contraindications for such therapies.
AMGEVITA is indicated for the treatment of moderately to severely active Crohn's disease in paediatric patients(from 6 years of age) who have had an inadequate response to conventional therapy including primary nutrition therapy and a corticosteroid and/or an immunomodulator, or who are intolerant to or have contraindications for such therapies.