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diclofenac
相关语句
  双氯芬酸
    Severe hepatitis induced by diclofenac sodium
    双氯芬酸钠引起重型肝炎
短句来源
    Hyperpyrexia attributed to use of diclofenac sodium / lidocaine injection
    双氯芬酸钠/利多卡因注射液引起高热反应
短句来源
    RESULTS: The effective rates of flurbiprofen and diclofenac for rheumatoid arthritis and osteoarthritis group were 86%, 87% and 85%, 80% ( P >0.05).
    结果 :在氟比洛芬组中类风湿关节炎组和骨关节炎组的疗效分别为 86%和 85% ,双氯芬酸组为87%和 80 % ,2组差异无显著意义 (P >0 .0 5)。
短句来源
    Thirty patients of diclofenac group [M 6, F 24; age 44 a±10 a(26~64 a)] were treated with diclofenac tablets 50 mg, po , qd×4 wk.
    双氯芬酸组 30例 ,男性 6例 ,女性 2 4例 ,年龄 4 4a± 10a(2 6~ 64a) ,给双氯芬酸 5 0mg ,po ,qd× 4wk。
短句来源
    CLINICAL STUDY ON THERAPEUTIC EFFECT OF DICLOFENAC SODIUM GEL(DSG)ON PATIENTS WITH RHEUMATOID ARTHRITIS
    外用双氯芬酸钠凝胶治疗类风湿性关节炎的临床研究
短句来源
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  “diclofenac”译为未确定词的双语例句
    METHODS : The control group of 32 patients (M 6,F 26; age 46 a±s3 a,course of disease 4.1 a±1.0 a) and sinomenine group of 32 patients (M 7,F 25, age 46 a±4 a, course of disease 4.6 a±1.6 a) were continued to use the non-steroidal anti-inflammatory drugs (indometacin,diclofenac).
    方法 :对照组 32例 (男性 6例、女性 2 6例 ,年龄 4 6a±s3a ,病程 4 .1a± 1.0a) ; 青藤碱组 32例 (男性 7例 ,女性 2 5例 ,年龄 4 6a± 4a ,病程 4 .6a± 1.6a)。
短句来源
    RESULTS: The efficacy rates of meloxicam and diclofenac sodium in rheumatoid arthritis and osteoarthritis group were 86.00%,80,00%and 83.3396.80.00% (P>0.05).
    结果:在治疗组中类风湿关节炎组和骨关节炎组的疗效分别为86%和80%,对照组为83.33%和80%,两组无显著差异(P>0.05)。
短句来源
    RESULTS:The efficacy rates of nimesulide and diclofenac sodium in rheumatoid arthritis and osteoarthritis group were 84.00%, 80.00% and 83.33%, 80.00% ( P <0.05).
    结果 :在治疗组中类风湿关节炎组和骨关节炎组的疗效分别为 84%和80 % ,对照组为 83.33 %和 80 % ,两组无显著差异 (P >0 .0 5 )。
短句来源
    The incidence of CI side-effect in celecoxib group was lower than that in diclofenac group(Fisher′s exact test, P=0.233).
    譻研究者对疾病的总体评价,两组差值为0.05,其95%CI为-0.59~0.49; 譼对照组发生胃肠道不良事件3起,治疗组未报告胃肠道不良事件(Fisher精确概率检验,P=0.233)。
短句来源
    Comparative study on efficacy and safety of celecoxib and diclofenac in the treatment of osteoarthritis and rheumatoid arthritis
    塞来昔布治疗类风湿关节炎和骨关节炎有效性和安全性的临床研究
短句来源
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  diclofenac
Diclofenac (25 mg kg-1) and meloxicam (7.5 mg kg-1) produced 9.3 and 19.6 mm2 ulcer areas in stomachs of rats, respectively, when used alone, but when combined with nimesulide diclofenac and meloxicam did not cause any injury in rat stomachs.
      
While ranitidine at 100 mg kg-1 dose prevented diclofenac-induced ulcer formation, it reduced meloxicam-induced ulcer formation significantly.
      
Determination of diclofenac in pharmaceuticals and urine samples using a membrane sensor based on the ion associate of diclofena
      
The potentiometric response characteristics of a diclofenac selective electrode, based on ion association in different plasticizers, were compared.
      
The potentiometric unit presented a linear response toward diclofenac concentrations between 1 × 10-5 - 5 × 10-2 mol L-1, with slopes of approximately 60 mV dec-1, and exhibited a response time of 3 s.
      
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To study the efficacy and safety of diclofenac sodium gel (DSG) in patients with rheumatoid arthritis (RA),radomized,controlled,single-blind clinical trial of DSG versus indomathacin embrocation (IE) were studied. The results indicated that the total efficacy rates of DSG and IE were 71.64% and 61.82% respectively after two weeks'treatment.The incidences of adverse effects associated with DSG and IE were 10.44% and 36.36%.These results suggest that DSG had a similar efficacy with IE in the treatment of...

To study the efficacy and safety of diclofenac sodium gel (DSG) in patients with rheumatoid arthritis (RA),radomized,controlled,single-blind clinical trial of DSG versus indomathacin embrocation (IE) were studied. The results indicated that the total efficacy rates of DSG and IE were 71.64% and 61.82% respectively after two weeks'treatment.The incidences of adverse effects associated with DSG and IE were 10.44% and 36.36%.These results suggest that DSG had a similar efficacy with IE in the treatment of patients with RA, but its adverse effects were significantly lower than that of IE.

为观察双氯芬酸钠凝胶外用治疗类风湿关节炎(RA)的疗效和安全性,我们对其与阳性对照药吲哚美辛擦剂治疗122例RA进行了随机、单盲,平行性和多中心的临床验证。结果表明:双氯芬酸钠凝胶治疗67例RA的总有效率为71.64%,不良反应发生率为10.44%;吲哚美辛擦剂治疗55例RA的总有效率为61.82%不良反应发生率为36.6%。提示两药的疗效相近,但前者的不良反应发生率明显低于后者。

AIM: To observe the effect and adverse reaction of sinomenine combined with methotrexate in treating rheumatoid arthritis.METHODS : The control group of 32 patients (M 6,F 26; age 46 a±s3 a,course of disease 4.1 a±1.0 a) and sinomenine group of 32 patients (M 7,F 25, age 46 a±4 a, course of disease 4.6 a±1.6 a) were continued to use the non-steroidal anti-inflammatory drugs (indometacin,diclofenac).Control group took methotrexate 15 mg, po qw ,sinomenine group took sinomenine 20 mg,po tid and methotrexate...

AIM: To observe the effect and adverse reaction of sinomenine combined with methotrexate in treating rheumatoid arthritis.METHODS : The control group of 32 patients (M 6,F 26; age 46 a±s3 a,course of disease 4.1 a±1.0 a) and sinomenine group of 32 patients (M 7,F 25, age 46 a±4 a, course of disease 4.6 a±1.6 a) were continued to use the non-steroidal anti-inflammatory drugs (indometacin,diclofenac).Control group took methotrexate 15 mg, po qw ,sinomenine group took sinomenine 20 mg,po tid and methotrexate 7.5 mg, po, qw. Three days later, the dosage of sinomenine was increased to 40 mg,tid .After 1 mo the non-steroidal antiinflammatory drug was reduced to half of its original dosage for both groups, and it was stopped after 2 mo.Three months was a course of treatment.RESULTS: In the control group the excellent response rate was 31%, effective rate 56% and the improvement rate 13%;sinomenine group that were 38%,59%,3%,respectively. The rate of adverse reaction was 47% in the control group and 12% in the sinomenine group. CONCLUSION: Sinomenine combined with methotrexate can reduce dosage of the drugs in treating rheamatoid arthritis, increase the appropriateness of patient treatment, and decrease the adverse reaction.

目的 :观察青藤碱和甲氨蝶呤联合治疗类风湿关节炎的疗效和不良反应。方法 :对照组 32例 (男性 6例、女性 2 6例 ,年龄 4 6a±s3a ,病程 4 .1a± 1.0a) ;青藤碱组 32例 (男性 7例 ,女性 2 5例 ,年龄 4 6a± 4a ,病程 4 .6a± 1.6a)。 2组原有非甾类抗炎药 (吲哚美辛、双氯芬酸 )继续应用。对照组加服甲氨蝶呤 15mg ,qw ;青藤碱组加服青藤碱 2 0mg ,tid +甲氨蝶呤 7.5mg ,qw。 3d后无不良反应 ,青藤碱加至 4 0mg ,tid。 2组于 1mo时非甾类抗炎药减半 ,2mo停用。 3mo为一个疗程。结果 :对照组显效 31% ,有效 56% ,改善 13% ;青藤碱组显效 38% ,有效 59% ,改善 3%。不良反应对照组4 7% ,青藤碱组 12 %。结论 :联合用药可减少治疗类风湿关节炎的用药剂量 ,增加病人治疗的顺应性和减少不良反应

AIM: To observe the efficacy of the flurbiprofen in treating rheumatoid arthritis, osteoarthritis and ankylosing spondylitis. METHODS: Eighty patients with rheumatoid arthritis were radomly divided into 2 groups. Fifty patients (M 9,F 41;age 47 a± s 12 a) of flurbiprofen group were treated with flurbiprofen 50 mg, po ,tid for 4 wk; 30 patients (M 5, F 25; age 46 a±10 a) of diclofenac group were treated with diclofenac 25 mg, po , tid for 4 wk. Forty patients with osteoarthritis were also...

AIM: To observe the efficacy of the flurbiprofen in treating rheumatoid arthritis, osteoarthritis and ankylosing spondylitis. METHODS: Eighty patients with rheumatoid arthritis were radomly divided into 2 groups. Fifty patients (M 9,F 41;age 47 a± s 12 a) of flurbiprofen group were treated with flurbiprofen 50 mg, po ,tid for 4 wk; 30 patients (M 5, F 25; age 46 a±10 a) of diclofenac group were treated with diclofenac 25 mg, po , tid for 4 wk. Forty patients with osteoarthritis were also divided into 2 groups. Twenty patients (M 6, F 14; age 56 a±12 a) of flurbiprofen group were treated with flurbiprofen 50 mg, po , tid for 4 wk; the other patients (M 7, F 13; age 56 a± s 12 a) of diclofenac group were treated with diclofenac 25 mg, po, tid for 4 wk. Thirty eight patients with ankylosing spondylitis (M 33, F 5; age 33 a±11 a) were treated with flurbiprofen 100 mg, po , tid for 4 wk. RESULTS: The effective rates of flurbiprofen and diclofenac for rheumatoid arthritis and osteoarthritis group were 86%, 87% and 85%, 80% ( P >0.05). For ankylosing spondylitis group the effective rate of flurbiprofen was 79%. The rates of adverse reaction of flurbiprofen and diclofenac groups were respectively 19% and 30%. The rates of adverse reaction of flurbiprofen was lower than dicolofenac ( P < 0.05 ). CONCLUSION: Flurbiprofen is efficacious and safe in treating rheumatoid arthritis, osteoarthritis and ankylosing spondylitis.

目的 :观察氟比洛芬治疗类风湿关节炎、骨关节炎及强直性脊柱炎的疗效和不良反应。方法 :80例类风湿关节炎病人随机分为氟比洛芬组 50例 ,双氯芬酸组 30例。 4 0例骨关节炎病人分为氟比洛芬组 2 0例 ,双氯芬酸组 2 0例。氟比洛芬组口服氟比洛芬 50mg ,po ,tid× 4wk ;双氯芬酸组口服双氯芬酸 2 5mg ,po ,tid× 4wk。 38例强直性脊柱炎均为氟比洛芬组 ,口服氟比洛芬 10 0mg ,po ,tid×4wk。结果 :在氟比洛芬组中类风湿关节炎组和骨关节炎组的疗效分别为 86%和 85% ,双氯芬酸组为87%和 80 % ,2组差异无显著意义 (P >0 .0 5)。强直性脊柱炎组的疗效为 79%。不良反应发生率氟比洛芬组和双氯芬酸组分别为 19%和 30 % ,氟比洛芬组明显低于双氯芬酸组 (P <0 .0 5)。结论 :氟比洛芬是一种安全有效的新型非甾体消炎止痛药

 
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