1. 甲氧氯普胺可有多种制剂,包括:片剂、糖浆和注射液。
Metoclopramide is available in a variety of formulations including tablets, syrups and injections.

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2. 目的:观察胃复安(甲氧氯普胺)治疗急性偏头痛的疗效。
Objective to observe the effects of metoclopramide in the treatment of acute migraine headache.

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3. 目的制备由氧氯普胺速释层与萘普生钠缓释层组成的双层片。
OBJECTIVE to prepare bilayer tablet, which consists of a metoclopramide rapid release layer and a naproxen sodium sustained release layer.

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4. 氧氯普胺通过促进胃肌肉的蠕动以增加胃向小肠排空的速率起作用。
Metoclopramide works by speeding up the movement of the stomach muscles, thus increasing the rate at which the stomach empties into the intestines.

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5. 目的:观察氟虫腈对小鼠离体胃平滑肌的作用及普胺对其的影响。
Objective To observe the effect of fipronil on contractile activity of the isolated gastric muscle strips in mice and the influence of paspertin on it.

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6. 然而,对于某些病人,当停止服用氧氯普胺后其症状可以部分或完全缓解。
However, in some patients, symptoms may lessen or resolve after metoclopramide treatment is stopped.

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7. 除非在极少数收益被认为大于风险的情况下,都应避免长期应用甲氧氯普胺。
The chronic use of metoclopramide therapy should be avoided in all but rare cases where the benefit is believed to outweigh the risk.

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8. 所述的止吐药剂为格拉司琼、昂丹司琼、托烷司琼、阿瑞匹坦或普胺。
The compound preparation is prepared from the rolipram and the granisetron, the ondansetron, the tropisetron, the aprepitant or the metoclopramide.

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9. 近期的产品标签已对长期应用氧氯普胺可导致迟发型运动障碍的风险提出警示。
Current product labeling warns of the risk of tardive dyskinesia with chronic metoclopramide treatment.

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10. 结果:甲氧氯普胺治疗肾绞痛的总有效率(86.0%)明显高于心痛定(75.6%)。
RESULTS: The global response rate of metoclopramide (86. 0%) is significantly superior to isosorbide dinitrate (75. 6%).

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11. 他们将这些数据和同时期母亲和婴儿的医院记录进行了联系,查看了婴儿中甲氧氯普胺使用和不良结果之间的关联。
They linked that with maternal and infant hospital records during the same period of time, looking at associations between the use of metoclopramide and adverse outcomes in the babies.

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12. 采用松香、三胺和环丙烷为原料,溶剂法合成了阳离子松香。
The cationic rosin was synthesized by solvent method, with rosin, trimethylamine and epoxy chloropropane as raw materials.

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13. 聚环氧氯丙烷—二胺与PAC复配,不仅可使絮凝效果更佳,而且可降低处理成本。
Using polyamine flocculants with PAC, not only shows better flocculation performance, but also can lower the water treatment cost.

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14. 以环氧氯丙烷和三胺为原料,常温下合成活性中间体失水甘油基三化铵(GTA)。
Using trimethylamine and epichlorohydrin as raw materials, an active intermediate, glycidyl trimethyl ammonium chloride (GTA), was synthesized at ambient temperature.

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15. 综合研究结果表明,聚环氧氯丙烷—二胺是一种高效多功能的有机絮凝剂。
The experimental results show that polyamine polymers are organic flocculants with high performance and multi-function.

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16. 以环氧氯丙烷、二胺为反应单体,过硫酸钾-亚硫酸钠为引发剂合成了小阳离子聚合物粘土稳定剂pta。
Minor cationic polymer clay stabilizer PTA was synthesized with epichlorohydrin and dimethylamine as monomers and potassium persulfate - sodium sulfite as initiating agent.

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17. 结果表明,阳离子度、分子量以及聚合物的结构是影响聚环氧氯丙烷—二胺絮凝效果的重要因素。
The experimental results show that the cationicity, the molecular weight and the structure have a great effect on the flocculation efficiency of polyamine flocculants.

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18. 研究了木质素与环氧氯丙烷、三胺合成木质素季铵盐的工艺。
Synthesis of cationic lignin flocculant by lignin, epichlorohydrin and trimethylamine was obtained.

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19. 以三胺、环丙烷和聚乙烯醇为原料,合成出季铵型阳离子聚乙烯醇。
Using trimethylamine, epoxy chloropropane and poly (vinyl alcohol) as materials, the quaternary cationic poly (vinyl alcohol) was synthesized.

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20. 以丙烯酸、二胺、环氧氯丙烷为原料,通过曼尼希反应制得两性离子单体。
Amphoteric monomer is prepared with acrylic acid, dimethylamine, and chloroethanol by Mannich reaction.

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21. 最后,研究了叔辛胺和环氧氯丙烷反应得到的1-叔辛基-3-羟基氮杂环丁烷盐酸盐的磺酰化和硝化的反应性。
At Iast, the possibility of the 1-tert-octyl-3-hydroxyl azetidine's hydrochloric salt methyl-sulfuric-acyl reaction and nitration reaction is studied.

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22. 以邻甲氧基苯酚与对*为原料,经四步反应合成6-(2-甲氧基)-1,4-二氢-4-代-3-喹啉羧酸乙酯。经抗鸡球虫实验证明具有抗球虫效果。
The compound 6-(2-methoxy phenoxy)-1, 4-dihydrogen-4-oxo-3-ethyl quinoline carboxylate is prepared with o-methoxyphenol and p-chloronitrobenzene as materials and through four-step reaction.

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23. 以邻甲氧基苯酚与对*为原料,经四步反应合成6-(2-甲氧基)-1,4-二氢-4-代-3-喹啉羧酸乙酯。经抗鸡球虫实验证明具有抗球虫效果。
The compound 6-(2-methoxy phenoxy)-1, 4-dihydrogen-4-oxo-3-ethyl quinoline carboxylate is prepared with o-methoxyphenol and p-chloronitrobenzene as materials and through four-step reaction.

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