目的合成非甾体类抗炎药奥沙普秦。
Objective to synthesize nonsteroidal anti-inflammatory drug oxaprozin.
使用非甾体类抗炎药物或者抗高血压药物。
Use nonsteroidal anti-inflammatory drugs or antihypertensive drugs.
他说：“不同的非甾体类抗炎药作用不同。
There are differences in the various NSAIDs and these differences might well confer differences in cardiovascular risk.
非甾体类抗炎药可以控制疼痛和炎症反应。
Non-steroidal anti-inflammatory drugs to control pain and inflammation.
目的探讨非甾体类抗炎药致上消化道大出血的治疗方法。
Objective To detect the methods of treating upper alimentary canal massive hemorrhage result in taking NSAIDs(nonsteroidal anti-inflammatory drugs).
对OA的治疗目前常用非甾体类抗炎药和多糖类软骨保护剂。
Non-steroidal anti-inflammatory drugs and chondroprotective agents are now used in the therapy of OA.
结论奥曲肽是治疗非甾体类抗炎药致上消化道大出血的理想药物。
Conclusion Octreotide is an idea drug with treating upper alimentary canal massive hemorrhage.
非甾体类抗炎药治疗能缓解60 - 80%患者脊柱的炎性疼痛。
NSA therapy alleviates inflammatory pain of spine in 60 to 80% of patients.
像医学布洛芬、阿斯匹林是一种非甾体类抗炎药——一个非甾体抗炎药。
Like the medicine ibuprofen, aspirin is an NSAID — a non-steroidal anti-inflammatory drug.
我们给他进行了颈圈治疗，并且让他服用非甾体类抗炎药和阿仑膦酸。
We treated him with a cervical collar, non-steroidal anti-inflammatory agents and alendronate.
非甾体类抗炎药(NSAID)有严重的胃肠道和心血管系统的不良反应。
Gastrointestinal and cardiovascular adverse effects are well-recognized sequelae of non-steroidal anti-inflammatory drugs (NSAID).
非甾体类抗炎药具有解热、镇痛、抗炎等作用，应用于临床已有一个多世纪。
Non-steroidal anti-inflammatory drugs have many effects in relieving fever and pain and anti-inflammatory, which have been applied in clinic for more than one century.
比较在非甾体类抗炎药基础上用和不用甲氨蝶呤对类风湿性关节炎临床疗效的影响。
To compare the non-steroidal anti-inflammatory drugs based on methotrexate for rheumatoid arthritis with and without clinical impact.
根据最近的研究证明，长期的非甾体类抗炎药治疗可以改善本病患者脊柱的骨质破坏。
According to the most recent findings, long-term administration of NSA can affect also X-ray progression.
骨关节炎处理可以舒缓疼痛，止痛剂、抗炎药物，例如皮质激素治疗，非甾体类抗炎药物。
Osteoarthritis is treated with analgesics to relieve pain, anti-inflammatory agents, such as corticosteroids, and nonsteroidal anti-inflammatory drugs.
目的：比较半导体激光和抗生素与非甾体类抗炎药联合应用在治疗牙根管充填后疼痛的疗效。
Objective: to compare the effect of the semiconductor laser on the pain behind RCT with the antibiotic combined the nonsteroidal anti inflammatory agents.
痛力克是一种非甾体类抗炎药，曾被口服，肌注和静脉给药试图预防和减轻疼痛，减少对阿片类药物的需求。
Ketorolac, a nonsteroidal anti-inflammatory agent, has been administered orally, intramuscularly, and intravenously in an attempt to prevent and relieve pain and reduce opioid requirements.
这些药物的结构和西乐葆相似，作为COx - 2受体拮抗剂是非甾体类抗炎药专门的一种分类的一部分。
Those drugs, structurally similar to Celebrex, are part of a special subset of the NSAID class known as Cox-2 inhibitors.
了解这些指标的意义将有助于我们筛选出那些最有可能从服用阿司匹林或非甾体类抗炎药等化学预防中受益的人群。
A better understanding of the significance of these markers will help us identify individuals most likely to benefit from chemoprevention using aspirin or NSAIDs.
很多人认为典型的治疗方式，像非甾体类抗炎药凝胶和膏药，可缓解疼痛而不像片剂一样伴有胃和心脏方面的副作用。
Many think that topical treatments, like NSAID gels and patches, may relieve pain without as many adverse effects for the stomach and heart as pills.
此研究结果发布在BMJ的网络杂志上，结论是非甾体类抗炎药显著增加常规服用该药的患者的心血管事件发生的风险。
The study, published online in the BMJ, concludes that NSAIDs significantly increase the risk of cardiovascular events in patients who take them regularly.
目的：新型非甾体类抗炎药氯诺昔康能否降低大鼠切口疼痛，并探讨其可能的作用机制，主要研究其是否存在脊髓中枢作用机制。
Objective: to study whether or not lornoxicam reduced pain in the rat incision model and to discuss the possible mechanism, mainly discuss the mechanism of spinal cord center.
此外，定期服用阿司匹林或非甾体类抗炎药降低患结直肠肿瘤的风险主要是表现在那些stnfr—2基准水平较高的参与者身上。
In addition, the reduced risk of developing colorectal tumors associated with regularly taking aspirin or NSAIDs was primarily seen among participants with high baseline sTNFR-2 levels.
例如，juni医生说他以前的观察发现，仅25到50的患者需要使用一年的非甾体类抗炎药治疗。其可导致增加一例心脏病发作和中风的患者。
For example, juni says his review found that only 25 to 50 patients would need to be treated with NSAIDs for one year to cause one additional event such as a heart attack or stroke.
PAR - 2可能由肥大细胞分泌的类胰蛋白酶激活而参与非甾体抗炎药致小肠损伤的发病过程。
PAR-2 may be activated by tryptase released from mast cells and participate in the pathogenesis of small intestinal injury as induced by non-steroidal antiinflammatory drugs.
PAR - 2可能由肥大细胞分泌的类胰蛋白酶激活而参与非甾体抗炎药致小肠损伤的发病过程。
PAR-2 may be activated by tryptase released from mast cells and participate in the pathogenesis of small intestinal injury as induced by non-steroidal antiinflammatory drugs.
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