1) Fuatlin Cream
扶他林乳膏
2) Diclofenac emulsion
扶他林乳剂
1.
Methods Forty-six subjects were randomized into two groups: treatment group in which 23 cases were treated by electroacupuncture and control group in which 23 cases were treated with Diclofenac emulsion,with a course of four weeks.
方法设治疗组和对照组各23例,治疗组采用电针治疗为主,对照组以外用扶他林乳剂治疗,疗程均为4周。
3) Votalin emulsion
扶他林乳胶剂
1.
Objective To compare and research the clinical effect of Bitongxiao ointment and Votalin emulsion in curing acute soft tissue injury.
目的比较研究痹痛消膏和扶他林乳胶剂治疗急性软组织损伤的临床疗效。
4) Diclofenac
扶他林
1.
Methods:A total of 32 rabbits randomly divided into for groups: the control group ,the model group ,the Diclofenac group ,the SKXXF group .
方法:32只日本大耳兔随机分成四组:空白组,模型组,扶他林组,中药熏洗组,手术方法制作兔膝骨性关节炎模型,造模成功后中药熏洗组给予中药熏洗汤治疗4周,扶他林组给予扶他林外搽4周。
2.
Methods 60 patients were randomly divided into treatment group treated with Tongxinluo combined with Allopurinol Tablets and control group treated with Diclofenac combined with Allopurinol Tablets.
方法将60例患者随机分成2组,治疗组以通心络联合别嘌醇片治疗;对照组以扶他林片联合别嘌醇片治疗,2组均以4周为1个疗程。
3.
Methods:One hundred and five patients were randomly divided into WMG(the western medicine group of Diclofenac),CMMG(the Chinese Materia Medica group) and CMG(combined medicine group), with 35,32 and 38 patients respectively, according to the time sequence of seeing doctor.
方法:105例患者按就诊先后时间顺序随机进入西药扶他林组(35例)、中药组(32例)和联合用药组(38例)。
5) votalin
扶他林
1.
Methods Eighty-eight patients with pain were divided into treatment group with flexible nanoliposomes of diclofen and control group with votalin(diclofenac potassium gel).
方法:将88例关节肌肉疼痛患者随机分为2组,分别局部外用双氯芬酸柔性纳米脂质体或外用扶他林乳胶剂(即双氯芬酸乳胶剂),疗程2周,观察各项临床指标并比较其疗效。
2.
Methods A total of 133 parturients who requested postpaitum analgesia were randomly allocated to five groups and received placebo,Sumidon,Votalin,Di-hydroetorphine (DHE) and Qxiprofenum respectively.
方法 选取要求镇痛的产妇133人,随机分为5组,即安慰剂组、去痛片组、扶他林组、二氢埃托啡组 (DHE组) 及布洛芬组,施行双盲对照研究。
3.
Methods:90 cases prophase patients were randomly divided into treatment group that treated with Huangqin Xiaojia Decoction and control group that treated with Votalin,to measure Blood Sedimentation,thyroid gland functions and so on respectively pretherapy and post-treatment,to observe difference of pyretolysis time,pain extinction time and subsiding swelling time between two group.
方法:将早期亚急性甲状腺炎患者90例随机分为治疗组和对照组,治疗组予黄芩消甲汤,对照组用扶他林治疗,治疗前后分别测血沉、甲状腺功能等,观察两组退热时间、疼痛消失时间、甲肿消肿时间的差别。
6) lindame ointment
林旦乳膏
补充资料：林旦乳膏
【通用名称】
林旦乳膏
【其他名称】
林旦乳膏 林旦乳膏 拼音名：Lindan Rugao 英文名：Lindane Cream 书页号：2000年版二部-378 本品含林旦(C6H6Cl6)应为标示量的90.0％～110.0％。
【性状】
本品为乳剂型基质的白色软膏。
【鉴别】
取本品约1g(相当于林旦10mg)，加氯仿20ml，振摇溶解，滤过，滤液蒸发至干，残渣加 丙酮 1ml溶解，取澄清液作为供试品溶液；另取林旦对照品，加丙酮制成每1ml中约含10mg的溶液，作为对 照品 溶液。照薄层色谱法(附录Ⅴ B)试验，吸取上述两种溶液各5μl，分别点于同一硅胶G薄层板上，以丁 酮-正已 烷(7:93)为展开剂，展开后，晾干，喷以0.5％邻联二茴香胺丙酮溶液，置紫外光灯下10分钟，在可见 光下 检视。供试品所显主斑点的颜色和位置应与对照品的主斑点相同。
【检查】
α-异构体 取含量测定项下的供试品溶液，照林旦项下的方法，自“另取林旦对照品适 量”起，依法测定，应符合规定。 其他 应符合软膏剂项下有关的各项规定(附录Ⅰ F)。
【含量测定】
照气相色谱法(附录Ⅴ E)测定。 色谱条件与系统适用性试验 用2m玻璃色谱柱，以硅酮(OV-17)为固定相，涂布浓度为2％；柱温 为 190℃；检测器为电子捕获检测器。 测定法 取本品适量(约相当于林旦10mg)，精密称定，置100ml量瓶中，加丙酮溶解并稀释至刻 度，精 密量取1ml，置50ml量瓶中，加环已烷稀释至刻度，精密量取1ml，置10ml量瓶中，加环已烷稀释至刻 度，摇 匀，精密量取适量注入气相色谱仪，测定；另取林旦对照品，同法测定。按外标法计算，即得。
【类别】
同林旦。
【规格】
1％
【贮藏】
密闭，置阴凉处保存。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条