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      loxoprofen sodium
相关语句
  洛索洛芬钠
    Clinical observation of loxoprofen sodium in treatment of patients with knee osteoarthritis
    洛索洛芬钠治疗膝骨关节炎的临床研究
短句来源
    Objective: To evaluate the efficacy and safety of loxoprofen sodium in treatment of patients with osteoarthritis (OA).
    目的:评价洛索洛芬钠片(乐松)治疗膝骨关节炎(OA)的疗效和安全性。
短句来源
  “loxoprofen sodium”译为未确定词的双语例句
    The clinical evaluation of loxoprofen sodium in the treatment of patients with knee osteoarthritis
    洛索洛芬治疗膝骨关节炎的临床评价
短句来源
    Objective:To study the efficacy and safety of loxoprofen sodium in the treatment of patients with knee osteoarthritis(OA).
    目的 :观察洛索洛芬 (乐松 )治疗膝骨关节炎 (OA)的疗效和安全性。
短句来源
    Methods:114 patients with OA in knees were enrolled in a random order,open trial. Each patient received loxoprofen sodium at a dosage of 60mg, tid, taking after the food.
    方法 :选择 114例膝OA患者 ,口服乐松 ,6 0mg ,tid。
短句来源
    The efficacy and safety of loxoprofen sodium was evaluated prior to and after 3 weeks of medication. The efficacy indices include rest pain index, active pain index, tenderness index, swelling index and activity degree of the knee joint.
    分别在 0周和第 3周末进行疗效和安全性评估 ,疗效指标包括休息时痛、活动痛指数、关节压痛、关节肿胀和关节活动度等 5项指标。
短句来源
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  loxoprofen sodium
In contrast, the combination of enoxacin at 100 mg/kg and either ketoprofen at 125 mg/kg or pranoprofen at 500 mg/kg induced clonic convulsions, while that of enoxacin at 400 mg/kg and loxoprofen sodium at 600 mg/kg induced no convulsion.
例句来源      
The oral administration of ketoprofen, pranoprofen or loxoprofen sodium induced no convulsion up to 1000 mg/kg, 500 mg/kg and 600 mg/kg, respectively, and that of enoxacin induced no convulsion at more than 5000 mg/kg.
例句来源      
Convulsions induced by the combination of enoxacin, a new antimicrobial, and nonsteroidal anti-inflammatory drugs including nimesulide, ketoprofen, pranoprofen and loxoprofen sodium, were investigated in mice.
例句来源      
Oral loxoprofen sodium at a daily dose of 180?mg resulted in rapid symptom resolution.
例句来源      



         Objective:To study the efficacy and safety of loxoprofen sodium in the treatment of patients with knee osteoarthritis(OA).Methods:114 patients with OA in knees were enrolled in a random order,open trial. Each patient received loxoprofen sodium at a dosage of 60mg, tid, taking after the food.The efficacy and safety of loxoprofen sodium was evaluated prior to and after 3 weeks of medication.The efficacy indices include rest pain index, active pain index, tenderness index,...
            目的 :观察洛索洛芬 (乐松 )治疗膝骨关节炎 (OA)的疗效和安全性。方法 :选择 114例膝OA患者 ,口服乐松 ,6 0mg ,tid。分别在 0周和第 3周末进行疗效和安全性评估 ,疗效指标包括休息时痛、活动痛指数、关节压痛、关节肿胀和关节活动度等 5项指标。结果 :完成疗程、资料齐全的患者共 10 6例。经过 3周的治疗 ,乐松对患者5项疗效指标均有明显改善 (P <0 .0 1) ,各项指标的有效率均超过 80 .0 % ;医师和患者对疗效评定的总有效率分别为 89.6 2 %和 91.5 1%。 13例 (12 .2 6 % )患者出现了与药物相关的不良反应 ,全部为胃肠道症状 ,勿需减量或停药 1周内症状消失。无严重的或危及生命的不良反应发生。结论 :乐松具有强大的消炎镇痛作用 ,不良反应轻 ,依从性较好
文摘来源
         Objective: To evaluate the efficacy and safety of loxoprofen sodium in treatment of patients with osteoarthritis (OA). Methods: The study was conducted in 40 patients of OA by a random, open and controlled method. All of them were in line with the criteria of American College of Rheumatology. They were divided to receive oral loxoprofen 60 mg tid or sustained release ibuprofen 300 mg bid for 4 weeks. Results: After 4 weeks treatment, all parameters including active pain of knee, time for w...
            目的:评价洛索洛芬钠片(乐松)治疗膝骨关节炎(OA)的疗效和安全性。方法:选取OA病人40例,每组20例,采用随机、开放、对照法,试验组:口服洛索洛芬钠片60mg,3次/d;对照组:口服布洛芬缓释胶囊300mg,2次/d。疗程为4周。分别观察治疗前后临床指标和炎性实验指标的变化及不良反应。结果:比较两组在治疗前后组内膝关节活动痛、15m行走时间、日常活动能力及病人综合评估等方面,均显示有显著性差异;而组间比较均无显著性差异。两组总有效率无显著性差异。结论:洛索洛芬钠对OA的疗效与布洛芬相当,且不良反应更轻。
文摘来源
 
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