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   tablets group 的翻译结果: 查询用时:0.138秒
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tablets group
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     The incidence of sanqi tablets group was 24% and there were 10 femoral head necrosis cases,6 of which had hip ache with the VAS (6.41±1.23).
     三七伤药片组股骨头坏死发生率为24%,10例股骨头坏死患者6例出现髋痛,VAS评分为(6.41±1.23)分。
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     Methods: 67 IRS patients were divided into YTT group (33 patients) and Metformin Tablets group (34 patients). After 8 weeks, (Ca2+)I, RBC-MDA, Na+-K+-ATPase and Ca2+-ATPase were compared to those before treatment.
     方法:67例IRS患者根据用药不同随机分为养心通脉片组(33例)和二甲双胍片组(34例),治疗8周,观察比较治疗前后(Ca2+)I、RBC-MDA、Na+-K+-ATPase和Ca2+-ATPase等指标的变化。
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     the total cure and prominent efficiency ratio of Fukeqianjin tablets group is 20.00%,the total efficiency ratio is 85.56%.
     妇科千金片组90例,治愈0例,显效18例(20.00%),有效60例(66.67%),无效13例(14.44%),总愈显率为20.00%,总有效率为85.56%;
短句来源
     Results: The total effective rate of Qingxuanjianyia Tablets group was 82.5% and lower than that of nifedipine group (94.6%) and captoril group(91.5%), but higher than that of atenolol group(75.0%).
     结果 :清眩降压片组降压有效率为 82 .5 % ,低于硝苯地平控释片组 (94.6 % )和卡托普利组 (91.5 % ) ,高于阿替洛尔组 (75 .0 % )。
短句来源
     Patients were randomly divided into a treatment group(Jianpi Huayu Tablets group,n=65) and a control group(Metformin group,n=32) and were administrated for 8 weeks.
     97例患者按2∶1比例随机分为治疗组(健脾化瘀片组)65例和对照组(二甲双胍片组)32例,均服药8周。
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  “tablets group”译为未确定词的双语例句
     Results After treatment, the leukocyte count, lymphocyte proliferation and micronucleus rate of the Shengbai Tablets group were ( 7.470 ±1.852)×10~9/L, (14768.23±8316.86) and (6.02±1.72)‰ respectively, all were significantly better than that of the group without Shengbai Tablets treatment ( P<0.05~0.01).
     结果“生白片”组小鼠的白细胞计数为(7.470±1.852)×109/L,淋巴细胞增殖为(14768.23±8316.86)/min,骨髓细胞微核率为(6.02±1.72)‰,均明显优于血虚模型组(P<0.01)。
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     In losartan potassium tablets group,the decrease of blood pressure was(18.86±14.42)/(13.76±9.69)(mmHg.)
     氯沙坦钾组降压幅度为(18.86±14.42)/(13.76±9.69)mmHg,总有效率为80.95%。 两药均有良好的降压作用及相近的降压疗效(均P>0.05)。
短句来源
     ① Comparison of the general effects of the two treatment methods: The results in the risperidone group and the quetiapine famarate tablets group were close [59%, 53% (χ2=0.731, P > 0.05)].
     ①两治疗方案的总效果比较:利培酮组及富马酸奎硫平组治疗总效果相近犤59%,53%(χ2=0.731,P>0.05)犦。
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     Compared with model group, the expression of brain MAO-B mRNA obviously decreased in DHYZ protective group (0.367 8±0.022 2), DHYZ therapeutic group (0.388 2±0.020 5) and Donepezil Hydrochloride Tablets group (0.377 4±0.031 1), (P < 0.01).
     与模型组相比较,地黄饮子预防组(0.3678±0.0222)、地黄饮子治疗组(0.3882±0.0205)、盐酸多奈哌齐组(0.3774±0.0311)单胺氧化酶B信使核糖核酸的表达明显降低(P<0.01)。
短句来源
     The effect of high dose group is better than Captopril Tablets group.
     各剂量组均有降低Lvw忍W作用,与模型组比较,中剂量组和高剂量组有显著性差异(P<0.05),高剂量组优于卡托普利组。
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  相似匹配句对
     In group K.
     K.
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     . group's.
     而且实验组的增量显著高于控制组的增量。
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     The treatment group was added Shenyankang tablets.
     治疗组 3 0例在对照组方案中加服肾炎康片。
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     the control group: prednisone acetate tablets.
     对照组:强的松口服。
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     Weianlin Tablets
     唯安林片
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  tablets group
Eight patients were treated with the oral solution (Group A, mean age 10.6 years) and five patients with enteric coated tablets (Group B, mean age 16.4 years).
      


2,204 cases of schistosomiasis japonica treated with three formsof nithiocyamine (4-nitro-4'-isothiocyano-diphenyl-amine) from October1976 to October 1978 in Mianzhu (绵竹), Deyang (德阳) counties andQingbaijiang (青白江) area, Sichuan Province were reported. This seriesconsisted mainly of young adults of chiefly commune members and students,the youngest being 5 years old and the oldest 72 years. There were 1,203males and 1, 001 females. Among them, 2, 170 cases were in chronic earlystage, 32 cases in late stage and...

2,204 cases of schistosomiasis japonica treated with three formsof nithiocyamine (4-nitro-4'-isothiocyano-diphenyl-amine) from October1976 to October 1978 in Mianzhu (绵竹), Deyang (德阳) counties andQingbaijiang (青白江) area, Sichuan Province were reported. This seriesconsisted mainly of young adults of chiefly commune members and students,the youngest being 5 years old and the oldest 72 years. There were 1,203males and 1, 001 females. Among them, 2, 170 cases were in chronic earlystage, 32 cases in late stage and 2 cases in acute stage. 194 cases(9. 4%)were complicated with respiratory, gastrointestinal, cardiovascular ornervous system diseases. For treatment nithiocyamine was given orally in 3 forms, namely,microencapsulated tablets (Group A), micropowder (Group B) and droppedpills (Group C). The total dose of the drug given was calculated inmilligrams per kilogram of body weight. In Group A 773 patients weretreated: 4mg/kg given in two days to 54 cases, and 6 mg and 7mg/kg in3 days to 527 cases and 192 cases respectively. In Group B 1, 144 patientswere treated: 3mg/kg given one day to 66 cases, 4mg/kg in two days to220 cases, and 6 mg and 7mg/kg in 3 days to 741 cases and 117 casesrespectively. In Group C 287 patients were treated: 3.5 mg and 4mg/kg given in 3 days to 77 cases and 210 cases respectively. All the 2,204 cases except 229 which were admitted to the regularhospital were treated in their own communes. During medication all thepatients in the communes were observed for 7 days, then followed up for18 days after being discharged. The side effects of the drug which usuallyappeared after the first, the second or the third treating day wereobserved and recorded daily. Their manifestations were on central nervoussystem, such as dizziness, fatigue, stagger, vertigo and headache, etc.,and on gastrointestinal tract such as abdominal pain, nausea, anorexiaand diarrhea, etc. The side effects of the drug were more prominent infemale than in male. The children were least affected. Patients in GroupA, i.e., with microencapsulated tablets showed lesser side effects thanthose in Group B and C. Side effects, if any, subsided naturally in 2-3days after medication. The normal daily life was not affected duringmedication. The late and complicated cases underwent the course oftreatment smoothly without serious side effects. Liver function tests were done in a number of the patients selectedat random before and after medication. The tests revealed that the liverfunction of the patients tested was impaired to a certain extent aftermedication. This showed that this drug might have impaired the livercells but only very mildly. Among the patients 13 cases developed jaundice.The incidence was found to be 0.59%. Clinical results were justified by hatching test for 3 times after thetreatment for 3 months and 6 months. The results showed that the curerate was only about 60% in Group A with a total dose of 4mg/kg andGroup B 3-4mg/kg and Group C 3.5mg/kg. Thus, these dosages were notfurther used because of the relatively low cure rate. As to Group A witha total dose of 6mg and 7mg/kg, the cure rates were 82.1% and 86.7%respectively. Group B with a total dose of 6mg and 7mg/kg being 80.9%and 87.1% respectively. Group C with a total dose of 4mg/kg, the curerate was 81.8% There were no statistic differences found among these 3groups. But the microencapsulated tablets have the following advantages:accuracy of dosage, convenience in administration, mild side effect and equalefficacy in comparison to the other two forms of this drug. Therefore, weconsider that the microencapsulated tablet is the form of choice.

本文报告用硝硫氰胺的微囊片、微粉及滴丸三种剂型治疗血吸虫病2,204例的临床观察。经3~6月的疗效考核证实三种剂型的疗效相等,均在80%以上。作者认为微囊片型具有剂量准确,服用方便,疗效与其他二型相等而付作用比其他二型轻的优点,是值得推广的一种剂型。

Fu-Ning-Di pills is a new preparation composed of the essential oil of Radix Angelicae Sinensis. Upon pharmacologcal experiments, it was reported to be able to inhibit the uterine contraction of the isolated uterus of rabbit.Altogether eighty cases of primary and secondary dysmenorrhea were treated by Fu-Ning-Di pills 10 bid just for one day at the onset of the malady; with fifteen cases administering placebo pills and forty five cases administering tablets of extact of Radix Angelicae Sinensis both serving...

Fu-Ning-Di pills is a new preparation composed of the essential oil of Radix Angelicae Sinensis. Upon pharmacologcal experiments, it was reported to be able to inhibit the uterine contraction of the isolated uterus of rabbit.Altogether eighty cases of primary and secondary dysmenorrhea were treated by Fu-Ning-Di pills 10 bid just for one day at the onset of the malady; with fifteen cases administering placebo pills and forty five cases administering tablets of extact of Radix Angelicae Sinensis both serving as control groups.The relief rates of the above three gro ups were 86.2%, 53.3% and 33.3% respectively; differences between the rate of Fu-Ning-Di pills group and the rates of placebo pills group and the radix extract tablets group both showed remarkable statistical significance as calculated dy the grade index method, p0.0l in both cases. Clinical observation also revealed that almost no side effect could be seen following administration of the Fu-Ning-Di pills.

一种当归挥发油新制剂腹宁滴丸,据药理实验报告能抑制兔离体子宫的自动节律运动。作者等试用以治疗80例原发性和继发性痛经患者(10毫克,痛经开始时顿服或于同日再服一次),并分别以空白对照丸和当归浸羔片作对照(分别应用于15和45例)。结果,上述三组患者服药后的缓解有效率分别为86.2%、53.3%和33.3%;按等级指数法进行统计学处理,腹宁滴丸与空白对照丸,腹宁滴刃与当归浸羔片之间的差异均具有非常显著的统计学意义。临床观察还提示,服用腹宁滴丸者几乎没有副作用。

The relative bioavailability of oral preparations of iron sorbitolby hemoglobin regeneration method in rats suffered from iron-deficiency anemiawas investigated. The result showed that during regeneration period the averagehemoglobin content of tablet group and oral solution group increased from8.20g% to 13.06g%,and 8.29g% to 12.77g% respectively. The relative bioavai-lability of the two group was 103.6% and 109%, respectively. On preliminaryclinical trial, the hemoglobin of patients increased...

The relative bioavailability of oral preparations of iron sorbitolby hemoglobin regeneration method in rats suffered from iron-deficiency anemiawas investigated. The result showed that during regeneration period the averagehemoglobin content of tablet group and oral solution group increased from8.20g% to 13.06g%,and 8.29g% to 12.77g% respectively. The relative bioavai-lability of the two group was 103.6% and 109%, respectively. On preliminaryclinical trial, the hemoglobin of patients increased significantly.

通过贫血大鼠模型血红蛋白恢复效应,研究了山梨醇铁片剂与口服液的相对生物利用度。实验结果表明,山梨醇铁片剂和口服液可分别使贫血大鼠血红蛋白提升4.86%和4.48%,相对生物利用度分别为103.6%和109%。临床初步应用表明,本品口服吸收良好,患者血红蛋白明显上升。

 
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