全英文临床药理学问题答案完整版
临床药理复习题及答案
临床药理复习题及答案临床药理第二部分名词解释1.临床试验(clinical trial):指任何在人体(病人或健康志愿者)进行药物的系统性研究,以证实或揭示试验药物的作用、不良反应及/或试验药物的吸收、分布、代谢和排泄,目的是确定试验药物的疗效与安全性。
2. 知情同意(Informed Consent):指向受试者告知一项试验的各方面情况后,受试者自愿确认其同意参加该项临床试验的过程,须以签名和注明日期的知情同意书作为文件证明。
3. 监查员(Monitor):由申办者任命并对申办者负责的具备相关知识的人员,其任务是监查和报告试验的进行情况和核实数据。
4. 病例报告表(Case Report Form,CRF):指按试验方案所规定设计的一种文件,用以记录每一名受试者在试验过程中的数据。
5.多中心临床试验(multicenter clinical trial ):由多位研究者按同一试验方案在不同地点和单位同时进行的临床试验。
各中心同期开始与结束试验。
多中心试验由一位主要研究者总负责,并作为临床试验各中心间的协调研究者。
6.临床试验标准操作规程(standard operation procedure, SOP):有效地实施和完成某一临床试验中每项工作所拟定的标准和详细的书面规程。
第三部分简答题一、临床药理学的任务有哪些?临床药理学学科任务1.教学与培训2.新药临床研究与评价3.市场药物的再评价4.药物不良反应监察5.临床药理服务6.技术与咨询服务二、何谓临床药理学?临床药理学(clinica1 pharmacology)是以人体为对象,研究药物与机体(包括人体和病原体)相互作用规律的学科。
这种相互作用包括药物对机体的作用和机体对药物的作用。
临床药理学既是药理学的一个分支,也是临床医学的一个分支。
临床药理学涉及到基础医学、临床医学和药学的研究领域,是一门具有广泛学科交叉特点的桥梁学科。
临床药理学以药理学和临床医学为基础,其范围涉及临床用药科学研究的各个领域,包括临床药效学、临床药动学、新药临床试验、临床疗效评价、不良反应监测、药物相互作用以及病原体对药物的耐药性等方面。
临床药理学习题及答案(28)
临床药理学习题及答案(28)1.对传染病确诊意义最大的试验是:A.补体结合试验B.中和试验C.反向试验D.显凝试验E.特异性抗体IgM正确答案为:E2.苯妥英钠与双香豆素合用,后者作用A.减弱B.起效快C.增强D.吸收增强E.作用时间长正确答案为:A3.西司他丁与亚胺培南配伍的主要目的是A.保护亚胺培南免受内酰胺酶破坏B.降低亚胺培南的不良反应C.防止亚胺培南在肝中代谢D.防止亚胺培南在肾中代谢E.扩大亚胺培南的抗菌谱正确答案为:D4.女,45岁,因卵巢癌行根治术,输血400mL,3个月后体查发现血清ALTl50u/L,进一步检查血清丙肝抗体阳性,其正确的治疗方案是A.以“保肝”支持治疗为主B.“保肝”支持治疗阿昔洛韦治疗C.“保肝”支持治疗猪苓多糖治疗D.“保肝”支持治疗α干扰素治疗E.“保肝”支持治疗强的松治疗正确答案为:D5.按照我国《药品注册管理办法》的规定,负责对药品申报注册资料进行形式审查的部门是A.国家食品药品监督管理局B.省级食品药品监督管理局C.市级食品药品监督管理局D.县级食品药品监督管理局E.国家药典委员会正确答案为:B6.药物进入人体后,化学结构发生变化,属于A.构效关系B.生物转化C.药物结构归一D.毒性物质转化E.毒物生成与解毒过程。
正确答案为:B7.临床有一定资料表明对胎儿有危害,但治疗孕妇疾病的疗效肯定,又无替代药物,其效益明显超过其危害,再考虑应用的一类药是A.A类B.B类C.C类D.D类E.X类正确答案为:D8.阿昔单抗的作用机制为A.抑制磷酸二酯酶B.抑制腺苷的摄取,激活腺苷环化酶是cAMP浓度增高C.阻断血小板膜糖蛋白受体D.抑制血栓素A2(TXA2)合酶,使合成减少E.使血管内皮产生PGI2增多正确答案为:C9.Fisger提出的三项基本原则是A.随机、对照、盲法B.对照、盲法、重复C.盲法、重复、安慰剂D.重复、安慰剂、随机E.随机、对照、重复正确答案为:E10.与氨基糖苷类药物合用,易引起患者呼吸麻痹的药物是A.青霉素B.甲苯磺丁尿C.琥珀胆碱D.卡托普利E.西米替丁正确答案为:C11.霍乱病人依据下列哪些情况分为轻、中、重三型A.发热,腹泻,脱水程度,血压及尿量等B.腹泻,呕吐,血压,脉搏及尿量等C.脱水程度,血压,脉搏及尿量等D.腹泻,呕吐,脱水程度及尿量等E.脱水程度,腹痛,血压、脉搏及尿量等正确答案为:C12.对产生超广谱β-内酰胺酶的细菌感染的患者进行治疗时宜首选哪类抗生素A.碳青霉烯类B.氯霉素类C.大环内酯类D.氨基糖苷类E.喹诺酮类正确答案为:A13.临床药理学的研究内容不包括A.药效学B.药动学C.毒理学研究D.临床试验E.动物实验正确答案为:E14.下列哪项不是钩体病重症表现A.脑水肿、昏迷B.肺弥漫性出血C.眼部虹膜睫状体炎D.肾功能衰竭E.肝功能衰竭正确答案为:C15.患者,女,71岁,结肠手术后深静脉留置导管并应用广谱抗生素,1个月后突然畏寒,高热,血压70/60mmHg,尿量16ml/h,血象,白细胞总数18×109CP为15mmol/L。
临床药理学习题及答案(114)
临床药理学习题及答案(114)1.四环素类药物与钙、镁、铝、铋等无机盐类抗酸药合用会降低四环素类药物的抗菌效果,是由于A.在吸收方面的相互作用B.在分布方面的相互作用C.在代谢方面的相互作用D.在排泄方面的相互作用E.在药效学方面的相互作用正确答案为:A2.扎莫特罗属于A.β受体激动剂B.β受体部份激动剂C.β受体拮抗剂D.α受体激动剂E.α受体拮抗剂正确答案为:B3.苯巴比妥钠在碱性尿中A.解离少,再吸收少,排泄快B.解离多,再吸收多,排泄慢C.解离少,再吸收多,排泄慢D.解离多,再吸收少,排泄快E.解离多,再吸收少,排泄慢正确答案为:D4.有关HIV感染的抗病毒治疗,下列描述不正确的是A.单一用药易产生耐药,需要联合用药治疗B.可选择的药物有核苷类、非核苷类逆转录酶抑制剂及蛋白酶抑制剂C.能够有效地抑制HIV复制,免疫损伤得到一定的重建D.不能清除HIV及根治AIDSE.所有HIV感染者均应抗HIV治疗正确答案为:E5.对多数传染来说,最少见的传染过程的表现是A.病原体被清除B.隐性感染C.显性感染D.病原携带状态E.潜伏性感染正确答案为:C6.男,24岁,1年前经常出现寒战、发热、头疼,退热时大汗淋漓,退热后体温恢复正常,自觉明显好转,每2天发作1次,而近半年左右发作停止。
体检发现脾脏肿大,血涂片检查有间日疟原虫,应给予下列何种治疗:A.氯喹阿的平B.阿的平伯氨喹C.乙胺嘧啶伯氨喹D.磺胺类E.氯喹伯氨喹正确答案为:C7.女,22岁,因间歇寒战高热入院,血涂片中找到间日疟原虫,幼时有蚕豆黄病史,目前怀孕3个月,最适宜的治疗是:A.乙胺嘧啶B.伯胺喹啉C.甲氟喹D.奎宁E.氯喹正确答案为:E8.某药半衰期为10 小时,一次给药后,药物在体内基本消除的时间为A.10小时左右B.20小时左右C.1天左右D.2天左右E.5天左右正确答案为:D9.下列哪种不属于抗菌药物的应用严加控制的情况A.病毒性疾病B.不明原因发热C.抗菌药物的预防应用D.严重烧伤的患者E.皮肤、粘膜局部应用抗菌药物正确答案为:D10.患者男性,18岁,寒战、稽留高热6天,伴意识障碍3天入院,有蚕豆病史,查体:昏睡状态,皮肤巩膜黄染,脾大,血常规:WBC 12×109/L,HB62g/L,N 82%。
临床药理学题库(有答案)
临床药理学题库(有答案)1.临床药理学的重点研究包括药效学、药动学、毒理学、新药的临床研究与评价以及药物相互作用。
2.临床药理学的研究内容包括药效学、药动学与生物利用度研究、毒理学研究、临床试验与药物相互作用研究。
3.临床药理学试验必须遵循XXX提出的三项基本原则,即随机、对照、盲法。
4.正确的描述是:安慰剂在临床药理研究中有实际的意义,临床试验中应设立双盲法,单盲法指对病人保密而非医生,安慰剂在试验中也可能引起不良反应,新药的随机对照试验必须使用安慰剂。
5.药物代谢动力学的临床应用包括给药方案的调整及进行TDM、给药方案的设计及观察ADR、进行TDM和观察ADR、测定生物利用度及ADR、测定生物利用度、进行TDM和观察ADR。
6.临床药理学研究的内容不包括剂型改造。
7.安慰剂可用于某些作用较弱或专用于治疗慢性疾病的药物的阴性对照药、治疗轻度精神忧郁症、已证明有安慰剂效应的慢性疼痛病人、一些证实不需用药的病人,但不包括危重、急性病人。
8.药物代谢动力学研究的内容包括新药体内过程及给药方案、比较新药与已知药的疗效。
9.影响药物吸收的因素包括药物所处环境的pH值、病人的精神状态、肝、肾功能状态、药物血浆蛋白率高低以及肾小球滤过率高低。
10.在碱性尿液中,弱碱性药物解离多、重吸收少、排泄快。
11.地高辛血浆半衰期为33小时,按逐日给予治疗剂量,血中达到稳定浓度的时间为9天。
12.不正确的描述是:药物血浆半衰期能反映体内药量的消除速度。
C.通常涉及数百名病人D.研究药物的药代动力学特征E.确定药物的最佳给药途径和剂量37.新药临床Ⅲ期试验的目的是()A.评价药物的安全性B.评价药物的疗效C.评价药物的毒副反应D.评价药物的药代动力学特征E.评价药物的最佳给药途径和剂量38.新药临床Ⅳ期试验的目的是()A.评价药物的安全性B.评价药物的疗效C.评价药物的药代动力学特征D.评价药物的毒副反应E.评价药物的最佳给药途径和剂量39.以下哪项不属于新药研发的前期研究()A.药理学实验B.毒理学实验C.药代动力学实验D.临床试验E.化学合成40.以下哪项不属于新药研发的后期研究()A.Ⅰ期临床试验B.Ⅱ期临床试验C.Ⅲ期临床试验D.Ⅳ期临床试验E.化学合成48.老年人使用胰岛素后容易出现低血糖或昏迷,原因是内分泌系统变化对药效学的影响。
药理学英文作业及答案
药理学作业----周师兄General principles1. Which route of administration is most likely to subject a drug to a first-pass effect?a. Intravenousb. Inhalationalc. Orald. Sublingual (SL)e. Intramuscular2. Two drugs may act on the same tissue or organ through independent receptors, resulting in effects in opposite directions. This is known asa. Physiologic antagonismb. Chemical antagonismc. Competitive antagonismd. Irreversible antagonisme. Dispositional antagonism3. If a drug is repeatedly administered at dosing intervals that are equal to its elimination half-life, the number of doses required for the plasma concentration of the drug to reach the steady state isa. 2 to 3b. 4 to 5c. 6 to 7d. 8 to 9e. 10 or more4. The pharmacokinetic value that most reliably reflects the amount of drug reaching the target tissue after oral administration is thea. Peak blood concentrationb. Time to peak blood concentrationc. Product of the V d and the first-order rate constantd. V de. Area under the blood concentration-time curve (AUC)5. Of the following, which is a phase II biotransformation reaction?a. Sulfoxide formationb. Nitro reductionc. Ester hydrolysisd. Sulfate conjugatione. Deamination6. The greater proportion of the dose of a drug administered orally will be absorbed in the small intestine. However, on the assumption that passive transport of the nonionized form of a drug determines its rate of absorption, which of the following compounds will be absorbed to the least extent in the stomach?a. Ampicillin (pKa = 2.5)b. Aspirin (pKa= 3.0)c. Warfarin (pKa = 5.0)d. Phenobarbital (pKa = 7.4)e. Propranolol (pKa = 9.4)7. Of the following characteristics, which is unlikely to be associated with the process of facilitated diffusion of drugs?a. The transport mechanism becomes saturated at high drug concentrationsb. The process is selective for certain ionic or structural configurations of the drugc. If two compounds are transported by the same mechanism, one will competitively inhibit the transport of the otherd. The drug crosses the membrane against a concentration gradient and the process requires cellular energye. The transport process can be inhibited noncompetitively by substances that interfere with cellular metabolism8. Which of the following is unlikely to be associated with oral drug administration of an enteric-coated dosage form?a Irritation to the gastric mucosa with nausea and vomitingb Destruction of the drug by gastric acid or digestive enzymesc. Unpleasant taste of the drugd. Formation of nonabsorbable drug-food complexese. Variability in absorption caused by fluctuations in gastric emptying time9. Which of the following is classified as belonging to the tyrosine kinase family of receptors?a. GABA -A receptorb. β-adrenergic receptorc. Insulin receptord. Nicotinic II receptore. Hydrocortisone receptor2.Explanation of terms1、Bioavailability2、Hepatoenteral circulation3、Half-life time4、50% lethal dose5、Absorption6、Ateady state plasma concentration7、Pharmacokinetics8、Pharmacodynamics9、adverse effect10、antagonist11、potency12、symptomatic treatment13、therapeutic index14、first-pass effect(elimination)15、enzyme inhibitor16、etiological treatment17、median effective dose18、side effects19、dose- effect relationship20、structure activity relationship21、tolerance22、tachyphylaxis1. Describe factors affecting absorption of drug.2. Describe receptor characters.3. Which is the most common process for drug transfer across cell membranes and point out its characteristics.4. List the characteristics of plasma protein binding of drugs.5. What is the hepatic microsomal enzymes? List their main characteristics.6. What is the difference between the action and the effect of a drug?7. Use receptor-action theory to elucidate what is the difference between the competitive antagonist and the non-competitive antagonist.1.c 2c. 3b 4e 5d 6e 7d 8d 9c 1生物利用度:是药物活性成分从制剂释放吸收进入血液循环的程度和速度。
临床药理学习题及答案(100)
临床药理学习题及答案(100)1.防治青霉素G过敏反应的措施A.注意询问过敏史B.做皮肤过敏试验C.先用肾上腺素预防D.出现过敏性休克时选肾上腺素E.换用半合成青霉素正确答案为:ABD2.决定是否TDM进行的原则A.药效指标不明确的药B.寻找合适的药C.血药浓度与药效间的关系适合于病情D.疗程不明确E.实施新的治疗方案正确答案为:AC3.按药物不良反应的可能度,可定义为“可能(possible)”是指A.经停药证实,但未经再次用药证实B.不良反应发生在用药后符合合理的时间顺序C.可用药物相互作用解释所发生的反应D.可能符合,也可能不符合已知的反应方式E.可由患者的临床表现或已知的药物反应特征解释正确答案为:BDE4.药物经过生物转化后A.可以成为有活性药物B.有利于肾血管重吸收C.脂溶性升高D.失去药理活性E.极性升高正确答案为:ADE5.妊娠期用药原则A.应尽早用药B.单药有效的避免联合用药C.有疗效肯定的老药避免用尚难确定的新药D.小剂量有效的避免用大剂量E.以上均不是正确答案为:BCDE6.关于病原体感染机体后的表现,就流行性脑脊髓膜炎而言,下列哪些叙述不正确A.病原携带状态最常见,隐性感染次之,显性感染占比例最少B.显性感染最常见,病原携带状态次之,隐性感染占比例最少C.显性感染最常见,隐性感染次之,病原携带状态占比例最少D.隐性感染最常见,病原携带状态次之,显性感染占比例最少E.隐性感染最常见,显性感染次之,病原携带状态占比例最少正确答案为:ABCE7.下列哪些传染病,外周血白细胞总数常常是升高的?A.伤寒B.流行性出血热C.登革热D.流行性乙型脑炎E.恙虫病正确答案为:BD8.哪些是动物源性传染病:A.狂犬病B.伤寒C.鼠疫D.钩体病E.恙虫病正确答案为:ACDE9.医院感染的医源性传播包括哪些?A.输液制品B.患者的分泌物C.诊疗器械及设备D.一次性医疗用品E.工作人员与病人接触正确答案为:ACD10.中毒性菌痢的临床特征是:A.急性高热,反复惊厥,昏迷B.腹痛、腹泻明显C.迅速发生休克.呼吸衰竭D.大便常规捡查发现大量炎性细胞E.脑脊液化验正常正确答案为:ACDE11.患者因“高热2天,头痛呕吐2小时”就诊,考虑“流行性脑脊髓膜炎”,下列哪些条件支持该诊断:A.夏秋季发病率增高B.脑脊液检查:白细胞计数轻度升高,淋巴细胞增高为主C.脑脊液革兰氏染色见革兰氏阴性双球菌D.脑脊液革兰氏染色见革兰氏阳性双球菌E.脑脊液检查蛋白升高明显正确答案为:CE12.肾综合征出血热期血常规检查可见哪些变化?A.白细胞计数升高B.可见异型淋巴细胞C.发热后期血红蛋白和红细胞计数可升高D.血小板计数下降E.可见异型血小板正确答案为:ABCDE13.必须对患者进行消化道隔离的传染病包括:A.伤寒B.细菌性痢疾C.阿米巴病D.甲型肝炎E.戊型肝炎正确答案为:ABCDE14.下列哪些药物增加胃酸分泌A.组胺B.阿托品C.乙酰胆碱D.毛果芸香碱E.西米替丁正确答案为:ACD15.黄疸型肝炎与钩体病的鉴别点有A.无流行病学史B.无眼结膜充血C.白细胞计数多升高D.无腓肠肌压痛E.以食欲不振等消化道症状为主正确答案为:ABDE16.妊娠期可选用的抗感染药物A.头孢菌素类B.大环内酯类抗生素C.青霉素类D.磷霉素E.氯霉素正确答案为:ABCD17.氯喹的临床适应证包括A.间日疟B.恶性疟C.阿米巴肝脓肿D.阿米巴肝炎E.系统性红斑狼疮正确答案为:BCE18.哮喘、支气管炎和肺气肿患者的呼吸困难症状严重发作具有显著的昼夜节律性,凌晨最为多见,因为A.过敏性患者呼吸道对抗原敏感性于夜间增高B.呼吸道在夜间对乙酰胆碱和组织胺敏感性增高C.夜间血清糖皮质激素水平降低D.夜间血中肾上腺素水平下降E.夜间呼吸道交感神经张力下降正确答案为:ABCDE19.脑型疟疾的处理哪项正确的是:A.20%甘露醇脱水B.止痉镇静C.盐酸奎宁滴注D.口服伯胺喹啉E.维持水电解质和酸碱平衡正确答案为:ABCE20.两性霉素B的应用注意点包括A.静脉滴注液应新鲜配制B.静滴前常服解热镇痛药和抗组胺药C.静滴液内加小量糖皮质激素D.避光滴注E.定期查血钾,血、尿常规等正确答案为:ABE。
临床药理学(附习题及答案)
第1章绪论一、学习目标1. 掌握:临床药理学的概念,主要研究内容及主要职能。
2.了解:临床药理学的发展趋势。
二、学习内容1.临床药理学(clinical pharmacology)是一门以基础药理学和临床医学为基础,主要以人体为研究对象,研究药物的治疗作用、不良反应、药物在体内的浓度变化规律等,包括临床药效学、临床药代学、新药的临床实验、临床疗效评价、药物不良反应监测及药物的相互作用等内容。
2.临床药理学的研究内容:临床药效学、临床药动学、毒理学、临床试用、药物相互作用。
3.临床药理学的主要职能:新药的药效学和毒理学评价;药代动力学研究;治疗药物监测;临床药理学的教学与培训;指导临床合理用药。
三、本章重点、要点临床药物动力学的基本理论、新药临床研究与评价的主要内容。
四、建议学习策略在熟练掌握临床药理学概念的基础上,理解临床药理学的主要研究内容及其主要职能。
五、章节练习1.临床药理学的概念2.临床药理学的研究内容答案要点1.临床药理学(clinical pharmacology)是一门以基础药理学和临床医学为基础,主要以人体为研究对象,研究药物的治疗作用、不良反应、药物在体内的浓度变化规律等,包括临床药效学、临床药代学、新药的临床实验、临床疗效评价、药物不良反应监测及药物的相互作用等内容。
2. 临床药理学的研究内容主要包括:药效学研究,药动学与生物利用度研究,毒理学研究,临床试验研究,药物相互作用研究。
第2章临床药动学一、学习目标1.掌握:药动学主要参数的概念和意义,及静脉注射一房室模型药动学参数的求算。
2.了解:临床给药方案的制订方法。
二、学习内容(一)、药物的体内过程及其影响因素1、吸收吸收是指药物从给药部位进入血液循环的过程。
(1)消化道内吸收(2)影响药物从消化道吸收的主要因素:药剂学因素、生物学因素、首关效应(3)消化道外吸收:从注射部位吸收、从皮肤粘膜吸收、从鼻粘膜、支气管或肺泡吸收2、分布分布是指吸收入血的药物随血流转运至组织器官的过程。
(完整版)《临床药理学》名词解释和问答(考试后总结版)
1. 临床药理学:是药理学的分支,时研究药物在人体内作用规律和人体与药物间相互作用过程的一门学科2.消除半衰期:药物的消除半衰期是指药物在体内消除一半所需要的时间,或血药浓度下降一半所需要的时间。
3.时间药理学:时间药理学是研究药物与生物周期相互关系的一门学科。
其主要研究内容包括机体的昼夜节律对药物作用或体内过程的影响,药物对机体昼夜节律的影响。
5.国家基本药物:指一个国家根据各自国情,按照符合实际的科学标准从临床各类药品中遴选出的疗效可靠、不良反应较轻、质量稳定、价格合理、使用方便的药品。
6.临床试验:评价新药的疗效和毒性为国家食品药品监督管理局批准新药生产提供科学依据,我国新药的临床试验分为Ⅰ、Ⅱ、Ⅲ、Ⅳ期,各类新药视类别不同进行Ⅰ、Ⅱ、Ⅲ、Ⅳ期临床试验。
7.不良事件:在使用药物治疗期间发生的不良医疗事件,它不一定和治疗有因果关系8.药物耐受性:指人体在重复用药条件下形成的一种对药物的反应性逐渐减弱的状态。
在此状态下,该药原用剂量的效应明显减弱,必须增加剂量方可获原用剂量的相同效应。
9.不良反应:是药物在正常用法和用量时由药物引起的不良和不期望产生的反应包括副作用毒性反应、依赖性、特异质反应、过敏反应、致畸、致癌和致突变反应。
10.生物利用度:用药代动力学原理来评价和研究药物进入血循环的速度和程度,是评价药物有效性的指标。
通常用药时曲线下浓度、达峰时间、峰值血药浓度来表示。
11.处方药POM:指必需凭执业医师处方才可在正规药店或药房调配、购买和使用的药品12.药物滥用drug abuse:指人们背离医疗、预防和保健目的,间断或不见断地自行过量用药行为。
这种用药具有无节制反复用药地特征,往往导致对用药个人精神和身体地危害。
13. 非处方药OTC:指经过国家药品监督管理部门批准,不需要凭执业医师处方,消费者可自行判断购买和使用的药品14. TDM治疗药物:在药代动力学原理的指导下,应用灵敏快速的分析技术,测定血液中或其他体液中药物浓度,研究药物浓度与疗效及毒性间的关系,进而设计或调整给药方案。
临床药理学习题及答案(9)
临床药理学习题及答案(9)1.氯霉素属于下列药物分类中的哪一类A.A类B.B类C.C类D.D类E.X类正确答案为:C2.下列肝炎患者相关检查项目中,最能提示肝硬化的是A.ALT中度升高B.TBil中度升高C.ALB下降D.AFP升高E.CHE下降正确答案为:C3.医院感染中可以通过空气传播的传染病有哪些?A.水痘B.登革热C.乙脑D.伤寒E.HIV正确答案为:A4.何种表现是强心苷中毒的表现A.S-T段下移B.Q-T间期间缩短C.T波倒置或低平D.地高辛血药浓度>3.0ng/mlE.洋地黄毒苷血药浓度>20ng/ml正确答案为:D5.青霉素皮试反应的峰值时间位于A.04﹕32B.10﹕22C.14﹕32D.18﹕45E.23﹕32正确答案为:E6.从严格意义上讲,与药物的药理作用强度密切相关的是A.药物的总剂量B.游离型药物浓度C.结合型药物浓度D.血药浓度E.体液中药物浓度正确答案为:B7.构成传染必须具备的条件是:A.传染源、传播途径、易感人群B.传染源、易感人群C.病原的毒力、数量D.病原体、人体E.自然因素、社会因素正确答案为:A8.洗手的目的是(),切断通过手传播感染的途径。
A.去除手上大部分常住菌B.去除手上所有常住菌C.去除手上污垢和大部分暂住菌D.去除手上污垢和所有暂住菌E.抑制微生物的快速再生正确答案为:C9.治疗药物监测的内容不包括A.原型药物B.游离药物C.活性代谢物D.药物半衰期E.药物对应体正确答案为:E10.在胆汁中浓度较高的抗菌药物为A.氯霉素B.万古霉素C.利福平D.多粘菌素BE.庆大霉素正确答案为:C11.某男, 50岁。
食欲减退、腹胀、黄疸一个月。
腹软, 轻压痛, 肝脾均可触及,•有移动性浊音。
HBsAg(-), IgM抗HBc(+), 抗HBe(+), WBC 14.2×109/L,中性0.85, A/G=0.7, 胆红素350μmol/L, ALT 45U/L, PT 30秒, 血钠126μmol/L, 血钾3.5μmol/L。
临床药理学习题及答案(40)
临床药理学习题及答案(40)1.关于药物依赖性的治疗正确的是A.实施个体化的脱毒治疗B.美沙酮替代治疗C.可乐定替代治疗D.让患者完全脱离原来的环境E.努力改变患者的生活方式正确答案为:ABCDE2.对于药物依赖进行治疗的方法是A.完全停用致依赖药物B.减少致依赖药物使用C.有效康复治疗D.同类型药物替代递减治疗E.心理治疗和对症处理正确答案为:ACDE3.碳酸锂抗躁狂症的机制可能是A.抑制去极化和Ca2+依赖的NA和DA从神经末梢释放B.不影响或促进5-HT的释放C.摄取突触间隙中儿茶酚胺,并增加其灭活D.抑制腺苷酸环化酶和磷脂酶C所介导的反应等E.阻断M受体正确答案为:ABCD4.下列关于合并用药的说法正确的是A.合并用药要“少而精”B.能用一种药物治疗就尽量不用两种C.合并药物越多,不良反应越多D.药物相互作用都是有害的E.配伍变化是指体外的配伍禁忌正确答案为:ABCE5.关于甲氟喹下列说法正确的是A.是由奎宁改造而得到的衍生物B.可以杀灭红细胞内期的疟原虫滋养体C.用于疟疾的症状性预防D.与长效磺胺和乙胺嘧啶合用可增加治疗E.有精神病史者禁用正确答案为:ABCDE6.以下哪些感染病毒感染易慢性化A.HAVB.HBVC.HCVD.HDVE.HEV正确答案为:BC7.为克服水肿治疗中利尿药抵抗,常可采用的措施A.多次应用最小有效量或连续静滴高效利尿药B.当利尿药抵抗出现于肾功不全时,使用的高效利尿药增加剂量C.联合应用作用于肾小管不同节段的利尿药D.联合应用作用于肾小管相同节段的利尿药E.当利尿药抵抗出现于心功不全时,可先用卡托普利后再用利尿药正确答案为:ABCE8.新生儿用药的主要特有反应有哪些A.对药物的超敏反应B.药物导致的溶血和黄疸C.出血D.新生儿窒息和惊厥E.高铁血红蛋白血症正确答案为:ABCDE9.以下哪些药物可作为复合麻醉药A.山梗菜碱B.地西泮C.硫喷妥钠D.贝美格E.呢可刹米正确答案为:BC10.属于老年性功能变化的是A.肌肉萎缩B.视力听力下降C.细胞结构改变D.免疫力下降E.心肺功能减退正确答案为:BDE11.地高辛对心衰的治疗作用有A.正性肌力作用B.负性传导作用C.负性频率作用D.使心脏体积缩小E.使Q-T期延长正确答案为:ABCD12.院内感染败血症中占重要地位的是A.大量应用广谱抗菌素诱发的真菌败血症B.恶性肿瘤化疗后革兰阴性杆菌败血症C.长期应用肾上腺皮质激素诱发的真菌败血症D.静脉导管留置引起的葡萄球菌败血症E.留置尿管诱发的大肠埃希菌败血症正确答案为:ABCDE13.下面对受体的认识,哪些是正确的A.受体是首选与药物直接反应的化学基团B.药物必须与全部受体结合后才能发挥药物最大效应C.受体兴奋的后果可能是效应器官功能的兴奋,也可能是抑制D.受体与激动药及拮抗药都能结合E.经常处于代谢转换状态正确答案为:ACDE14.我国临床疗效评价(assessment of response)一般采用四级评定标准是A.无效B.改善C.经济D.进步E.明显进步正确答案为:ABDE15.药物的作用机制与干扰叶酸代谢有关的是A.甲氨蝶呤B.乙胺嘧啶C.磺胺类D.甲氧苄啶E.四环素正确答案为:ABCD16.影响生物利用度的因素是A.剂型因素B.物理因素C.化学因素D.生理因素E.食物因素正确答案为:ADE17.以下哪些生物学现象受各种内在生物节律控制A.睡眠习惯B.运动能力C.激素分泌D.细胞增殖E.说话方式正确答案为:ABCD18.下列哪些类药物通常需要进行TDM的是A.抗肿瘤药B.抗癫痫药C.抗高血压药D.抗心律失常药E.强心苷类正确答案为:ABDE19.麻疹的并发症有A.支气管肺炎B.心肌炎C.喉炎D.脑炎E.亚急性硬化性全脑炎正确答案为:ABCDE20.18岁女性患者,因“发热、皮疹4天”入院,起病前1周曾到草地上野餐。
药理学英文试题(含答案)
1山东大学医学院(2005 ——2006 学年第二学期)2003 级医学七年制药理学期末考试试题(A 卷)二、选择题:(A 型每题0.5 分,X 型每题1分, 共50 分)Type A choice questions (only one answer is correct)1. Which of the following is classified as belong to the G proteincoupling receptors?A. GABAA receptorB. b adrenergicreceptorC. insulin receptorD. nicotinic II receptorE. hydrocortisone receptor2. Which of the following is unlikely to be associated with oral drug administration of anentericcoateddosage form?A. irritation to the gastric mucosa with nausea and vomitingB. destruction of the drug by gastric acid or digestive enzymesC. unpleasant taste of the drugD. formation of nonabsorbable drugfood complexesE. variability in absorption caused by fluctuations in gastric emptying time3. Which of the following compounds will be absorbed to the least extent in the stomach?A. ampicillin (pKa=2.5)B. aspirin (pKa=3.0)C. warfarin (pKa=5.0)D. Phenobarbital (pKa=7.4)E. propranolol (pKa=9.4)4. Which of the following terms is most likely to be associated w ith “a rapid reduction in theeffect of a given dose of a drug after only one or two doses”?A. supersensitivityB. tachyphylaxisC. toleranceD. hyposensitivityE. anaphylaxis5. A weak acidic drug with 4.4 of pKa, if the stomach juice pH is 1.4, plasma pH is 7.4, whenthe distribution balance is reached, the drug concentration ratio between plasma and stomachjuice isA. 100B. 0.001C. 1000D. 10000E. 0.016. In this graph,drugs A,B and C are analogs,thenA. A has a greater potency than BB. A has a greater efficacy than CC. B has less potency than CD. A has a greater potency than CE. B has a greater efficacy than C7. Aspirin is a weak acid with 3.5 of pKa, what percentage of lipidsolubleform will be in thestomach juice with 2.5 of pH?A. 0.99%B. 9%C. 9.09%D. 90.9%E. 99.9%8. The contractile effect of various doses of norepinephrine (NE) (X) alone on vascular smoothmuscle is represented in the figure below. When combined with an antagonist (IC or INC), ashift in the doseresponsecurve occurs. The curve labeled X+INC would mostly likely occurwhen vascular smooth muscle is treated with NE in the presenA. terazosinB. phentolamineC. labetalolD. phenoxybenzamineE. prazosinBAC效应Log 剂量49. The reversible cholinesterase inhibitor indicated in the treatment of Alzheimer’s disease isA. tacrineB. edrophoniumC. neostigmineD. pyridostigmineE. ambenonium10. A predictably dangerous side effect of nadolol that constitutes a contraindication to itsclinical use in susceptible patients is the induction ofA. hypertensionB. cardiac arrhythmiaC. asthmatic attacksD. respiratory depressionE. hypersensitivity11. Epinephrine may be mixed with certain anesthetics, such as procaine, in order toA. stimulate local wound repairB. promote hemostasisC. enhance their interaction with neural membranes and their ability to depress nerveconductionD. retard their systemic absorptionE. facilitate their distribution along nerves12. A 58yearoldmale with angina is treated with atenolol. Select the mechanism of action of atenolol A. a adrenergicagonistB. a adrenergicantagonistC. b adrenergicagonistD. b adrenergicantagonistE. mixed a and b antagonist13. A male patient is brought to the emergency department following ingestion of an unknownsubstance. He is found to have an elevated temperature, hot and flushed skin, dilated pupils,and tachycardia. Of the following, which would most likely cause these findings?5A. propranololB. tolazolineC. prazosinD. donepezilE. atropine14. A 65yearoldmale has a blood pressure of 170/105mmHg. Which of the following wouldbe effective in lowering this patient’s blood pressure?A. terbutalineB. dobutamineC. pancuroniumD. prazosinE. scopolamine15. Which of the following can be used in shock for increasing cardiac output and renal bloodflow?A. norepinephrineB. epinephrineC. dopamineD. phenylephrineE. methoxamine16. All of the following statements are related with succinylcholine EXCEPTA. have muscle fasciculation before muscle relaxationB. have no ganglionic blocking actions at therapeutic doseC. can be antagonized by neostigmineD. elevate blood potassium concentrationE. assistant agents of anesthetics17. The agent which is effective for prostatic hyperplasia but has no effect on blood pressure isA. terazosinB. tamsulosinC. phenoxybenzamineD. regitineE. prazosin18. Which of the following statements is correct?A. Diazepam induce the drug metabolizing enzymes.B. All benzodiazepines show antiepileptic actions.C. All benzodiazepines have sedative effects.D. Benzodiazepines readily produce general anesthesia.E. Benzodiazepines directly open chloride channels.19. Which of the following statements is correct?A. Chlorpromazine is indicated in treating the nausea of levodopa treatment.B. Vitamin B6 increases the effectiveness of levodopa.6C. Administration of dopamine is an effective treatment of Parkinson’s disease.D. Levodopainducednausea is reduced by carbidopa.E. Nonspecific MAOinhibitorsare a useful adjunct to levodopa therapy. 20. Which of the following is common to the tricyclic antidepressants and MAO inhibitors?A. They can produce sedation.B. They produce physical dependence.C. They show strong interaction with certain foods.D. They can produce postural hypotension.E. They decrease availability of epinephrine in the synaptic cleft21. The antipsychotic drugs:A. are equally effective against the positive and negative symptoms of schizophreniaB. can cause blurred vision, urinary retention and other signs of muscarinic blockadeC. bind selectively to D2dopaminergic receptors.D. have antiparkinsonism effects similar to levodopa.E. have a rapid onset of antipsychotic action.22. All of the following are observed in patients taking neuroleptic agents EXCEPT:A. sexual dysfunction.B. bronchial asthmaC. altered endocrine function.D. constipation.E. orthostatic hypotension23. Which of the following statements about morphine is INCORRECT?A. It is used therapeutically to relieve pain caused by severe head injury.B. Its withdrawal symptoms can be relieved by methadone.C. It causes constipation.D. It is most effective by parenteral administration.E. It rapidly enters many body tissues, including the fetus of a pregnant woman. 24. Which of the following statements concerning phenytoin is INCORRECT?A. causes less sedation than phenobarbital.B. causes gingival hyperplasia.C. may cause megaloblastic anemiaD. is excreted unchanged in the urine.E. The plasma halflifeincreases as the dose is increased.25. Which of the following drugs is contraindicated in the patients with epilepsy?A. PhenobarbitalB. imipramineC. digoxinD. chlorpromazineE. aspirin26. The agent which is effective for various epilepsy is7A. diazepamB. sodium phenytoinC. sodium valproateD. PhenobarbitalE. ethosuximide27. All of the following produce a significant decrease in peripheral resistance EXCEPT:A. chronic administration of diureticsB. hydralazineC. ACE inhibitorsD. βRblockersE. calcium channel blockers28. Which of the following hypertensive patients is most suitble for primary therapy withhydrochlorothiazide?A. patients with goutB. patients with hyperlipidemiaC. young hypertensive patients with rapid resting heart rateD. patients with impaired renal functionE. elderly patients29. Regarding antihypertensive drugs, which of the following statements is WRONG?A. Hydrochlorothiazide can increase activity of renninB. Propranolol can decrease secretion of renninC. Sodium nitroprusside lowers BP rapidly by releasing NO.D. Clonidine stimulates α2receptorand imidazoline receptorE. Diuretics decreased BP mainly by increasing water and sodium excretion from thekidneys.30. Which of the following drugs occurs orthostatic hypotension most frequently in first use:A. clonidineB. nifedipineC. propranololD. enalaprilE. prazosin31. The reason that digoxin can reduce the ventricular rate of atrial fibrillation patient is:A. decreasing automaticity of ventriclesB. decreasing automaticity of atriaC. reducing the conduction of AVnodeD. improving cardiac ischemiaE. shortening the effective refractory period of atria32. All of the following measures can be used in the treatment of digoxininduced arrhythmiaEXCEPTA. stopping digoxin administration8B. diuretic agents such as furosemide are used to promote the excretion of digoxinC. phenytoin administrationD. atropine administrationE. lidocaine administration33. Which of the following effects of digoxin can NOT be seen in failure heart?A. slowing sinus rhythmB. increasing the oxygen consumption of myocardiaC. increasing the cardiac outputD. increasing the cardiac contractilityE. shortening atrial ERP34. A 70 year oldfemale is treated with sublingual nitroglycerin for her occasional bouts of angina. Which of the following is involved in the action of nitroglycerin?A. αadrenergicactivityB. phosphodiesterase activityC. phosphorylation of light chains of myosinD. norepinephrine releaseE. cGMP increased35. The therapeutic effect of β adrenergic receptor blockers such as propranolol in anginapectoris is believed to be primarily the result ofA. reduced production of catecholaminesB. dilation of the coronary vasculatureC. decreased requirement for myocardial oxygenD. increased peripheral resistanceE. increased sensitivity to catecholamines36. A 69yearoldmale with angina develops severe constipation following treatment withA. nitroglycerinB. gemfibrozil(吉非贝齐)C. propranololD. captoprilE. verapamil37. Which of the following drugs has relatively few electrophysiologic effects on normalmyocardial tissue but suppresses the arrhythmogenic tendencies of ischemic myocardialtissue?A. VerapamilB. LidocaineC. QuinidineD. PropranololE. Procainamide38. The firstline drug for treating acute attack of reentrant supraventricular tachycardia isA. adenosine9B. lidocaineC. quinidineD. digoxinE. procainamide39. Which of the following drugs is NOT suitable to treat the patient with angina pectorisaccompanied with asthma?A. nifedipineB. isosorbide dinitrateC. nitroglycerinD. verapamilE. propranolol40. Which of the following drugs decreases de novo cholesterol biosynthesis by inhibiting theenzyme HMG CoA reductase?A. nicotinic acidB. gemfibrozilC. lovastatinD. cholestyramine(考来烯胺)E. probucol41.Which of the following drugs can be used for Diabetics(typeⅡ)with renal insufficiencyA. gliclazideB. tolbutamideC. glibornurideD. gliquidoneE. glipizide42. The contraindication of Glucocorticoids isA. septicemiaB. iritisC. dermatomyositisD. epidemic parotitis(流行性腮腺炎)E. peptic ulcer43. Antiasthmatic that could inhibit leukotrienes release and increase cerebral blood flow isA. zileutonB. pemirolastC. ibudilastD. zafirlukastE. montelukast44. Which of the following statements about acetazolamide is WRONG?A. diuretic actionB. depresss the intracranial pressureC. acidify blood10D. alkalized urineE. hyperkalemia45. Which of the following drugs could promote macrophage production and enhance thenonspecific immunologic functionA. erythropoietinB. thrombopoietinC. MCSFD. MultiCSFE. GCSF46. Which of the following can be used for megaloblastic anemiaA. folic acidB. folic acid +VitB12C. folic acid +VitB6D. folic acid +VitB12 +VitB6E. folic acid +VitB12+VitB6+VitC47. A ll of the following are true about hydrochlorothiazide EXCEPTA. It can be used to treat hypercalcinuriaB. It can lead to hypoglycemiaC. It can increase the secretion of K + then cause hypokalemiaD. It can decrease blood pressure mildlyE. It can decrease the urinary output of diabetes insipidus patients48. Which of the statements about thiourea is WRONG?A. They inhibit synthesis of thyroxineB. They have immunosuppressive effectC. Propylthiouracil stimulates T4 transform to T3D. They can cause thyroid enlargement when long term usedE. They can excrete from milk and pass through placenta barrier49. The antibiotics which are potent against the pseudomonas aeruginosa areA. carbenicillin, polymyxin, gentamycin and tobramycineB. kanamycin, tobramycine, polymyxin and erythromycinC. amikacin, gentamycin, polymyxin and oxacillinD. amikacin, gentamycin, chloramphenicol and spectinomycinE. carbenicillin, ampicillin, Cephalexin and polymyxin50. Which of the following compatibility administration is correct?A. streptomycin + gentamicinB. penicillin + gentamicinC. streptomycin + furosemideD. penicillin + tetracyclineE. penicillin + chloramphenicol 51.Clavulanic acid can inhibit which one of the following enzymes?11A.Dihydrofolate synthetase B.peptidoglycan synthetaseC.βlactamaseD.DNA polymeraseE.dihydrofolate reductase52.The agent which can relieve AIDS and AIDS correlating syndrome isA. idoxuridineB. zidovudineC. acyclovirD. ribavirinE. adenine arabinoside53.Which of the following imidazoles have NO effect on fungus ?A. metronidazoleB. miconazoleC. clotrimazoleD. fluconazolE. ketoconazole54.Herxheimer reaction is caused by penicillin when it is used to treat:A.lobar pneumoniaB.tetanusC.viridans endocarditisD.bacterial meningitis E.leptospirosis55. Of the following, which is the best agent to use in pregnant patient with urinary tractinfection (UTI ) caused by Chlamydia trachomatis?A. tetracyclineB. levofloxacinC. gentamycinD. erythromycinE. SMZTMP56. The t1/2 of which of the following tetracyclines remains unchanged when the drug isadministered to an anuric patientA. methacyclineB. oxytetracyclineC. doxycyclineD. tetracyclineE. none of the above57. A 45yearoldfemale being treated for a chronic UTI develops acute alcohol intolerance.Which of the following agents could have caused this intolerance?A. cefoperazone12B. amoxicillinC. SMZD. norfloxacinE. tetracycline58. A patient with a pneumonia has a sputum culture that is positive for a staphylococcalstrain that is b lactamase positive.Which is the best choice of penicillin therapy in this patient?A. ampicillinB. oxacillinC. penicillin VD. penicillin GE. carbenicillin59. A 75 year oldwoman is hospitalized for pneumonia and treated with an intravenousantibiotic. On day three, she develops severe diarrhea. Stool is positive for Clostridiumdifficile toxin. What is the best treatment?A. clindamycinB. cefaclorC. metronidazoleD. erythromycinE. doxycycline60. The mechanism of action of chloramphenicol as an antibiotic is that itA. binds to the 30s ribosome subunitB. binds to the 50s ribosome subunitC. prevents cell membrane developmentD. inhibits cell wallsynthesisE. inhibits RNA polymeraseType X choice questions (one or more answers are correct)1. If the plasma concentration of a drug declines with “first orderkinetics”, it means thatA. There is only one metabolic path for drug dispositionB. The half lifeis the same regardless of plasma concentrationC. The drug is largely metabolized in the liver after oral administration and has low bioavailabilityD. The rate of elimination is proportional to the plasma concentrationE. the metabolic ability has reached saturation.2. Of the following, which will be blockedby atropine and scopolamine?A. bradycardiaB. salivary secretionC. bronchoconstriction13D. skeletal muscle contractionE. miosis3. The agents which can be used to treat glaucoma haveA. timololB. pindololC. physostigmineD. acetazolamideE. pilocarpine4. A 34yearoldwoman with schizophrenia has been treated for several years with variousdrugs. She is now being treated with fluphenazine and complains of amenorrhea(闭经) andgalactorrhea(溢乳). Which of the following drugs would be appropriate to switch her medication toA. haloperidolB. risperidone (利培酮)C. olanzapine (奥氮平)D. clozapineE. thioridazine5. Which of the following drugs may cause dependence?A. methadoneB. naloxoneC. ibuprofenD. buspironeE. diazepam6. Which of the following drugs can be used in treatment of depressive disorder?A. imipramineB. fluoxetineC. perphenazineD. selegilineE. paroxetine7. The agents which are effective in the treatment of Parkinson’s disease are A. pirenzepineB. amantadineC. anisodamineD. levodopaE. scopolamine8. Which of the following statements about the treatment of chronic heart failure are right?A. Patients with evidence of fluid retention should receive a diuretic.B. Treatment with an ACE inhibitor and a βRblocker should be initiated and maintained unless specifically contraindicated.C. Digoxin may be added if needed to reduce symptoms or to slow the ventricular repsonse14in patients with rapid atrial fibrillation. D. Patients with severe heart failure should also receive a βRblockerE. Spironolactone may reduce mortality in patients with severe heart failure9. Precautions advisable when using lovastatin includeA. serum transaminase measurementsB. renal function studiesC. acoustic measurementD. serum creatinine kinase measurementsE. monthly complete blood counts10. Precautions advisable when using amiodarone includeA. serum transaminase measurementsB. renal function studiesC. acoustic measurementD. serum T3、T4 measurementsE. Xraychest check11. In a hypertensive patient who is taking insulin to treat diabetes, which of the followingdrugs is to be used with extra caution and advice to the patient?A. prazosinB. hydralazineC. propranololD. captoprilE. losartan12. Drugs that can enhance the sensitivity of insulin includeA. repaglinideB. rosiglitazoneC. pioglitazoneD. acarboseE. metformin13. The antiinflammatory mechanisms of glucocorticoids (GCS) includeA. GCS combined with GRE ,induce synthesis of ACEB. GCS combined with GRE ,induce synthesis of lipocortin1C. GCS combined with nGRE ,inhibit the expression of ICAM1and ELAM1D. GCS promote the apoptosis of inflammatory cellE. GCS combined with steroid receptor of cell membrane and mitochondrial membrane.14. Which of the following statements about cimetidine are WRONGA. increase the secreation of gastric acidB. block androgen receptorC. enhance the immunologic functionD. induce acne(痤疮)E. treat zolingerEllisonsyndrom and countercurrent esophagitis 1515. Which of the following megaloblastic amemia are NOT the indication of folic acidA. megaloblastic anemia caused by AIDSB. megaloblastic anemia caused by TMPC. megaloblastic anemia caused by MTXD. megaloblastic anemia caused by pyrimethamine(乙胺嘧啶)E. megaloblastic anemia caused by malignant tumor 16. The drugs which can protect gastric mucosa and inhibit helicobacter pylori includeA. omeprazoleB. sucralfateC. colloidal bismuth subcitrateD. cimetidineE. pirenzepine17. Quinolones can NOT be used to patients whoA. have epilepsy historyB. are in growth and development periodC. are taking antiacidD. are pregnantE. are allergic to penicillin18.Besides their antibacterial activity, macrolides agents alsoA.promote gastrointestinal motility B.have strong immunosuppressive action C.be used to treat bronchial asthma D.expel parasite in intestinal tract E.have antitumor action19.Of the following, the true statements about Rifampin areA. it can produce resistance to mycobacterium tuberculosis when administered onlyB. it is effective on chlamydia trachomatisC. it has no effect on Staphylococcus aureusD. it is inductor of liver drug enzymeE. it can interfere with RNA synthesis20. The agents that can inhibit bacterial protein synthesis includeA. clindamycinB. streptomycinC. amantadineD. isoniazideE. azithromycin二、选择题1.A2.E3.E4.B5.C6.D7.D8.D9.A 10.C 11.D 12.D 13.E14.D 15.C 16.C 17.B 18.C 19.D 20.D 21.B 22.B 23.A 24.D 25.D 26.C 27.D28.E 29.E 30.E 31.C 32.B 33.B 34.E 35.C 36.E 37.B 38.A 39.E40.C 41.D 42.E 43.C 44.E 45.C 46.E 47.B 48.C 49.A 50.B 51.C52.B 53.A 54.E 55.D 56.C 57.A 58.B 59.C 60.B 61.BD 62.ABCE63.ACDE 64.BCD 65.AE 66.ABDE 67.BDE 68.ABCE 69.AD 70.ADE71.CD 72.BC 73.ABCDE 74.AD 75.BCD 76.ABC 77.ABCD78.ABCDE 79.ABDE 80ABE山东大学医学院(2006 ——2007 学年第二学期)2004 级临床医学七年制药理学期末考试试题(A 卷)一、选择题:(A 型每题0.5 分,X 型每题1 分, 共50 分)Type A Choice questions (only one answer is correct)1.A drug with t1/2 3 hours is given intravenously, the steady state of plasma concentrationcan be expected withinA.3 hrsB.8 hrsC.10 hrsD.15 hrsE.20 hrs2.Which of the following is true for a drug whose elimination from plasma shows first orderkinetics?A. the half lifeof the drug is proportional to the drug concentration in plasmaB. the amount eliminated per unit time is constantC. the rate of elimination is proportional to the plasma concentrationD. elimination involves a rate limiting enzyme reaction operating at its maximal velocityE. a plot of drug concentration versus time is a straight line3.A drug eliminated with first order kinetics, the concentration of the drug in plasma is200mg/L, at 10 o ’ clock in the morning after administration of a single dose, the drug plasmaconcentration is 25 mg/L, at 10 o ’ clock on second day morning, its t1/2 isA.4hB.6hC.12hD.24hE.8h4. Aspirin is a weak acid with 4.5 of pKa, what percentage of lipidsolubleform will be in thestomach juice with 2.5 of pH?A. 0.99%B. 9%C. 9.09%D. 90.9%E. 99.0%5. In this graph,drugs A,B and C are analogs,thenA. A has a greater potency than BB. A has a greater efficacy than CC. B has less potency than CD. A has a greater potency than CE. B has a greater efficacy than C6. Which of the following statements is correct?A. if 10mg of drug A produces the same response as 100mg of drug B, drug A is moreefficacious than drug B.B. the greater the efficacy, the greater the potency of a drugC. in selecting a drug, potency is usually more important than efficacyD. a competitive antagonist increases ED50E. variation in response to a drug among different individuals is most likely to occur with adrug showing a large therapeutic index7. Among the following drugs, which will be excreted most quickly in acidic urine?A. a weak acid drug with pKa of 5.5B. a weak base drug with pKa of 7.5C. a weak base drug with pKa of 4.5D. a weak acid drug with pKa of 3.5E. a weak base drug with pKa of 6.58. The mechanism of treating phenobarbital poisoning with bicarbonate sodium is that itA. neutralizes PhenobarbitalB. stimulates Phenobarbital transference from the brain to the plasmaC. alkalinizes urine fluid, prevents Phenobarbital from reuptake, and stimulates excretion ofdrugD. both B and C are rightE. both A and C are right9. After repeated administration of phenobarbital sodium, the patients complainthe drug is less useful, this phenomenon is calledA. toleranceB. resistanceC. dependenceD. side reactionE. residual effect10. The effect of pilocarpine on eye isA. miosis, increase intraocular pressure, paralysis of accommodationB. miosis, decrease intraocular pressure, spasm of accommodationC. mydriasis, decrease intraocular pressure, paralysis of accommodationD. mydriasis, increase intraocular pressure, spasm of accommodationE. mydriasis, increase intraocular pressure, paralysis of accommodation11. All of the following statements are related with succinylcholine EXCEPTA. have muscle fasciculation before muscle relaxationB. have no ganglionic blocking actions at therapeutic doseC. can be antagonized by neostigmineD. elevate blood potassium concentrationE. assistant agents of anesthetics12. A male patient is brought to the emergency department following ingestion of an unknownsubstance. He is found to have an elevated temperature, hot and flushed skin, dilated pupils,and tachycardia. Of the following, which would most likely cause these findings?A. propranololB. tolazolineC. prazosinD. organophosphateE. atropine13. A predictably dangerous side effect of metoprolol that constitutes a contraindication to itsclinical use in susceptible patients is the induction ofA. hypertensionB. cardiac arrhythmiaC. asthmatic attacksD. angina pectorisE. hypersensitivity414. Which of the following therapeutic projects would be used in the treatment of patient withserious organophosphate intoxication? A.atropine + norepinephrine B.atropine+ neostigmineC.atropine + pralidoxime iodide D.atropine + epinephrineE.atropine + morphine15. The released norepinephrine is disposed mainly byA.the metabolism in the liver B.enzymatic inactivationC.reuptake by the neuronal terminal D.hydrolysisE. MAO and COMT in the circulation16. The elevated blood pressure caused byepinephrine may be reversed by A.propranololB.phentolamineC.norepinephrineD.nicotineE.atropine17. Epinephrine may be mixed with certain anesthetics, such as procaine, in order toA. stimulate local wound repairB. increase the potency of the local anestheticsC. enhance their interaction with neural membranes and their ability to depress nerveconductionD. retard their systemic absorptionE. facilitate their distribution along nerves 18.Which is correct description about the βadrenoceptoreffect?A.both cardiac excitation and bronchial dilation belong to β1 effectB.both cardiac excitation and bronchial dilation belong to β2 effectC.both cardiac excitation and vascular dilation belong to β1 effectD.both cardiac excitation and vascular dilation belong to β2 effe ctE.both vascular dilation and bronchial dilation belong to β2 effect19. Which is NOT the indication of phentolamine?A.shockB.diagnosis of pheochromacytoma C.male sexual dysfunctionD.primary hypertensionE.peripheral vascular occlusive disorders20. Chlorpromazine can be used forA. hypertensionB.hypothermic anesthesiaC. epilepsyD. comaE. coronary heart disease21. Which of the following statements about aspirin is incorrect?A. its analgesia is due to inhibition of PG synthesisB. it is mainly used to relieve headache and other dull painC. its main adverse effect is GI reactionD. it can inhibit lipoxidaseE. it inhibits the synthesis of both PGI2 and TXA222. Extrapyramidal symptoms caused by chlorpromazine is due toA. blocking DA receptor in midbrainlimbic systemB. inhibiting αreceptorin brainC. inhibiting DA receptor in tuberoinfunfibular pathwayD. inhibiting M receptorin CNSE. blocking DA receptor in nigro striatal pathway23. The main reason for the combination use of levodopa with carbidopa isA. to increase the absorption of LdopaB. to inhibit levodopa decarboxylation in the peripheryC. to inhibit MAOD. to inhibit COMTE. to increase Ldopaconverting to dopamine directly24. A three month oldinfant is brought to the emergency room with seizures of thetonicclonictype. His mother reports that these seizures have been occurring for 50min. The treatment of choice isA. DiazepamB. phenytoinC. phenobarbitalD. carbamazepineE. valproate sodium25. Which one of the following analgesic drugs can be used for artificial。
药学英语试题及答案
药学英语试题及答案一、选择题(每题2分,共20分)1. The term "pharmacology" refers to the study of:A. The origin of drugsB. The effects of drugs on the bodyC. The synthesis of drugsD. The distribution of drugs答案:B2. Which of the following is not a route of drug administration?A. OralB. IntravenousC. InhalationD. Electrolysis答案:D3. The half-life of a drug is the time it takes for the concentration of the drug in the body to:A. DoubleB. TripleC. QuadrupleD. Decrease by half答案:D4. Which of the following is a common side effect of antibiotics?A. Dry mouthB. DiarrheaC. InsomniaD. All of the above答案:B5. The abbreviation "IV" stands for:A. IntravenousB. IntramuscularC. IntraperitonealD. Intradermal答案:A6. The term "bioavailability" refers to the:A. Percentage of a drug that is absorbed into the systemic circulationB. Percentage of a drug that is excreted unchangedC. Percentage of a drug that is metabolized in the liverD. Percentage of a drug that is stored in fat tissues答案:A7. Which of the following is a type of drug interaction?A. SynergismB. AntagonismC. PotentiationD. All of the above答案:D8. The therapeutic index of a drug is a measure of its:A. EfficacyB. SafetyC. Cost-effectivenessD. Taste答案:B9. The term "prodrug" refers to a drug that:A. Is already active when administeredB. Requires metabolic activation to become activeC. Is a combination of two drugsD. Is a drug that has been discontinued答案:B10. Which of the following is a method for enhancing drug solubility?A. Salt formationB. Coating with a polymerC. MicronizationD. All of the above答案:D二、填空题(每空1分,共20分)1. The ________ of a drug refers to its ability to reach the site of action in the body.答案:pharmacokinetics2. A drug that is administered as a liquid and is intended to be swallowed is called a ________.答案:solution3. The ________ of a drug is the maximum amount that can be given without causing harmful effects.答案:therapeutic dose4. A drug that is used to treat a specific disease or condition is called a ________.答案:therapeutic agent5. The ________ of a drug is the minimum amount that will produce a therapeutic effect.答案:therapeutic dose6. A drug that is used to prevent a disease or condition is called a ________.答案:prophylactic agent7. The ________ of a drug is the study of its effects on biological systems.答案:pharmacodynamics8. A drug that is used to alleviate symptoms without treating the underlying cause is called a ________.答案:symptomatic agent9. The ________ of a drug is the process by which it isremoved from the body.答案:elimination10. A drug that is used to treat a wide range of conditionsis called a ________.答案:broad-spectrum agent三、简答题(每题10分,共40分)1. Explain the difference between a generic drug and a brand-name drug.答案:A generic drug is a copy of a brand-name drug that has the same dosage form, safety, strength, quality, performance characteristics, and intended use. A brand-name drug is the original version of a drug that has beendeveloped by a pharmaceutical company and is protected by a patent.2. What are the factors that can influence the absorption ofa drug?答案:Factors that can influence the absorption of a drug include the route of administration, the formulation of the drug, the presence of food in the stomach, the pH of the gastrointestinal tract, and the individual's health status.3. Describe the process of drug metabolism.答案:Drug metabolism is the process by which the body breaks down and eliminates drugs. It typically involves two phases: Phase I reactions, which involve oxidation, reduction, or hydrolysis to make the drug more polar, and Phase。
临床药理学试题及答案
临床药理学试题及答案【篇一:临床药理学题库(有答案)】临床药理学研究的重点()a. 药效学b. 药动学c. 毒理学d. 新药的临床研究与评价e. 药物相互作用2.临床药理学研究的内容是()a.药效学研究b.药动学与生物利用度研究c. 毒理学研究d. 临床试验与药物相互作用研究e. 以上都是3. 临床药理学试验中必须遵循fisher提出的三项基本原则是()a.随机、对照、盲法b.重复、对照、盲法c.均衡、盲法、随机 d.均衡、对照、盲法e.重复、均衡、随机4.正确的描述是()a. 安慰剂在临床药理研究中无实际的意义b. 临床试验中应设立双盲法c. 临床试验中的单盲法指对医生保密,对病人不保密d. 安慰剂在试验中不会引起不良反应e. 新药的随机对照试验都必须使用安慰剂5. 代谢动力学的临床应用是()a. 给药方案的调整及进行tdmb. 给药方案的设计及观察adrc. 进行tdm和观察adrd. 测定生物利用度及adre. 测定生物利用度,进行tdm和观察adr6.临床药理学研究的内容不包括()a. 药效学b. 药动学c. 毒理学d. 剂型改造e. 药物相互作用7.安慰剂可用于以下场合,但不包括 ( )a. 用于某些作用较弱或专用于治疗慢性疾病的的阴性对照药b. 用于治疗轻度精神忧郁症,配合暗示,可获得疗效c. 已证明有安慰剂效应的慢性疼痛病人,可作为间歇治疗期用药d. 其它一些证实不需用药的病人,如坚持要求用药者e. 危重、急性病人8. 代谢动力学研究的内容是()a. 新药的毒副反应b. 新药的疗效c. 新药的不良反应处理方法d. 新药体内过程及给药方案e.比较新药与已知药的疗效9. 影响吸收的因素是()b. 病人的精神状态c. 肝、肾功能状态d. 血浆蛋白率高低e. 肾小球滤过率高低10. 在碱性尿液中弱碱性药物()a.解离多,重吸收少,排泄快b. 解离少,重吸收少,排泄快c. 解离多,重吸收多,排泄快d. 解离少,重吸收多,排泄慢e. 解离多,重吸收少,排泄慢11.地高辛血浆半衰期为33小时,按逐日给予治疗剂量,血中达到稳定浓度的时间是()a. 15天b. 12天c. 9天d. 6天e. 3天12. 有关血浆半衰期的描述,不正确的是()a. 是血浆中浓度下降一半所需的时间b. 血浆半衰期能反映体内药量的消除速度c. 血浆半衰期在临床可作为调节给药方案的参数d. 1次给药后,约4-5个半衰期已基本消除e. 血浆半衰期的长短主要反映病人肝功能的改变13. 生物利用度检验的3个重要参数是()a. auc、css、vdc. tmax、cmax、vdd. auc、tmax、csse. cmax、vd、cssa.与血浆蛋白结合 b.首过效应c.css d.vd e.auc14. 设计给药方案时具有重要意义( b )15. 存在饱和和置换现象( a )16. 可反映吸收程度( e )17. 开展治疗监测主要的目的是()最佳治疗剂量,制定个体化给药方案b. 处理不良反应c. 进行新药药动学参数计算d. 进行药效学的探讨e. 评价新药的安全性18.下例给药途径,按吸收速度快慢排列正确的是()a. 吸入>舌下>口服>肌注b. 吸入>舌下>肌注>皮下c. 舌下>吸入>肌注>口服d. 舌下>吸入>口服>皮下e. 直肠>舌下>肌注>皮肤 19.血浆白蛋白与发生结合后,正确的描述是() a. 与血浆白蛋白结合是不可逆的失去药理学活性 c. 肝硬化、营养不良等病理状态不影响与血浆蛋白的结合情况d. 与血浆蛋白结合后不利于吸收e. 血浆蛋白结合率高的药物,药效作用时间缩短20.不正确的描述是()a.胃肠道给药存在着首过效应 b.舌下给药存在着明显的首过效应c.直肠给药可避开首过效应d.消除过程包括代谢和排泄e.vd大小反映在体内分布的广窄程度21. 下面哪个药物不是目前临床常须进行tdm的药物()a. 地高辛b. 庆大霉素c. 氨茶碱d. 普罗帕酮e. 丙戊酸钠22、下面哪个测定方法不是供临床血药浓度测定的方法()a. 高效液相色谱法b. 气相色谱法c. 荧光偏振免疫法d. 质谱法e. 放射免疫法23. 多剂量给药时,tdm的取样时间是:()a.稳态后的峰浓度,下一次用药后2小时b.稳态后的峰浓度,下一次用药前1小时c. 稳态后的谷浓度,下一次给药前d. 稳态后的峰浓度,下一次用药前e. 稳态后的谷浓度,下一次用药前1小时24. 关于是否进行tdm的原则的描述错误的是:()a. 病人是否使用了适用其病症的合适药物?b. 血药浓度与药效间的关系是否适用于病情?c. 药物对于此类病症的有效范围是否很窄?d. 疗程长短是否能使病人在治疗期间受益于tdm?e. 血药浓度测定的结果是否会显著改变临床决策并提供更多的信息?25.地高辛药物浓度超过多少应考虑是否药物中毒()a.1.0ng/ml b. 1.5ng/mld. 3.0ng/mle. 2.5ng/ml【篇二:《临床药理学》试题及答案】ass=txt>姓名:学号:分数:一、名词解释题(每题2分,共10分)1、药物2、对因治疗3、抗菌谱4、副作用5、 ed50二、单选题(每小题只有一个答案是正确的,每题1分,共20分)1、连续用药后机体对药物的反应性降低,称为()a、耐药性b、耐受性c、抗药性d、依赖性2、以下何项不是毛果芸香碱对眼的作用()a、缩瞳b、降眼压c、视远物不清楚d、调节麻痹3、、以下何种化合物中毒不能用碱性液洗胃()a、硫酸镁b、对硫磷c、对氧磷d、敌百虫4、、以下何项不是阿托品的临床应用()a、麻醉前给药b、验光配镜c、虹膜睫状体炎d、支气管哮喘5、、心收力弱、尿少的休克宜选用()a、肾上腺素b、麻黄碱c、多巴胺d、阿托品6、、以下何项不是安定的作用()a、镇静b、麻醉c、抗焦虑d、催眠a、心得安b、哌唑嗪c、酚妥拉明d、拉贝洛尔8、以下何项不是氢氯噻嗪类的临床适应症()a、中度心性水肿b、尿崩症c、高血压d、脑水肿9、硫脲类作用机理是抑制以下何种酶活性()a、胆碱酯酶b、环加氧酶c、maod、过氧化物酶10、急性骨髓炎宜选用()a、红霉素b、四环素c、庆大霉素d、克林霉素11、肾功能不良的病人绿脓杆菌感染可选用()a、多粘菌素eb、头孢哌酮c、氨苄西林d、庆大霉素12、铁剂用于治疗()a、溶血性贫血b、巨幼红细胞性贫血c、再生障碍性贫血d、小细胞低色素性贫血13、肝素过量时的拮抗药物是()a、维生素kb、维生素cc、鱼精蛋白d、氨甲苯酸14、治疗阵发性室上性心动过速的最佳药物是( )a、奎尼丁b、维拉帕米c、苯妥英钠d、普鲁卡因胺15、高血压合并消化性溃疡者宜选用( )a、甲基多巴b、可乐定c、利血平d、dhct16、下述哪项不属氯丙嗪的药理作用()a、抗精神病作用b、使体温调节失灵c、镇吐作用d、激动多巴胺受体17、诊治嗜铬细胞瘤应选用()a、肾上腺素b、异丙肾上腺素c、麻黄碱d、酚妥拉明18、属于弱效利尿药的是()a、呋塞米b、氢氯噻嗪c、氯噻酮d、螺内酯19、青霉素治疗肺部感染是()a、对因治疗b、对症治疗c、局部作用d、全身治疗20、n2受体兴奋引起的主要效应是()a.、脏抑制 b、神经节兴奋 c、骨骼肌收缩 d、支气管平滑肌收缩三、多选题(每小题正确答案有两个或两个以上,每题2分,共10分)1、氨基糖甙类抗生素的不良反应有()a、肾毒b、耳毒c、过敏反应d、神经肌肉传导阻滞2、下列联合用药不正确的是()a、青霉素+红霉素b、吗啡+镇疼新c、硝酸甘油+普萘洛尔d、强心甙+钙剂3、属于静止期杀菌的抗生素有()a 、氨基糖苷类b 、四环素类c 、青霉素类 d、多粘菌素类4、下列不良反应搭配正确的是( )a、吗啡------成瘾性b、四环素----抑制骨骼的造血功能c、胰岛素-------低血糖d、青霉素-----过敏性休克5、普萘洛尔的作用有( )a、抗甲亢作用b、抗心律失常c、抗高血压d、抗心绞痛四、填空题(每空1分,共20分)1、传出神经系统两种主要递质是____________ 和_____________。
临床药理学题库(有答案)
临床药理学试题1.临床药理学研究的重点〔〕A. 药效学B. 药动学C. 毒理学D. 新药的临床研究与评价E. 药物相互作用2.临床药理学研究的容是〔〕A.药效学研究B.药动学与生物利用度研究C. 毒理学研究D. 临床试验与药物相互作用研究E. 以上都是3. 临床药理学试验中必须遵循Fisher提出的三项根本原则是〔〕A.随机、对照、盲法 B.重复、对照、盲法 C.均衡、盲法、随机D.均衡、对照、盲法 E.重复、均衡、随机4.正确的描述是〔〕A. 抚慰剂在临床药理研究中无实际的意义B. 临床试验中应设立双盲法C. 临床试验中的单盲法指对医生,对病人不D. 抚慰剂在试验中不会引起不良反响E.新药的随机对照试验都必须使用抚慰剂5. 药物代动力学的临床应用是〔〕A. 给药方案的调整及进展TDMB. 给药方案的设计及观察ADRC. 进展TDM和观察ADRD. 测定生物利用度及ADRE. 测定生物利用度,进展TDM和观察ADR6.临床药理学研究的容不包括〔〕A. 药效学B. 药动学C. 毒理学D. 剂型改造E. 药物相互作用7.抚慰剂可用于以下场合,但不包括 ( )A. 用于*些作用较弱或专用于治疗慢性疾病的药物的阴性对照药B. 用于治疗轻度精神忧郁症,配合暗示,可获得疗效C. 已证明有抚慰剂效应的慢性疼痛病人,可作为间歇治疗期用药D. 其它一些证实不需用药的病人,如坚持要求用药者E. 危重、急性病人8. 药物代动力学研究的容是〔〕A. 新药的毒副反响B. 新药的疗效C. 新药的不良反响处理方法D. 新药体过程及给药方案E.比拟新药与药的疗效9. 影响药物吸收的因素是〔〕A. 药物所处环境的pH值B. 病人的精神状态C. 肝、肾功能状态D. 药物血浆蛋白率上下E. 肾小球滤过率上下10. 在碱性尿液中弱碱性药物〔〕A.解离多,重吸收少,排泄快B. 解离少,重吸收少,排泄快C. 解离多,重吸收多,排泄快D. 解离少,重吸收多,排泄慢E. 解离多,重吸收少,排泄慢11.地高辛血浆半衰期为33小时,按逐日给予治疗剂量,血中到达稳定浓度的时间是〔〕A. 15天B. 12天C. 9天D. 6天E. 3天12. 有关药物血浆半衰期的描述,不正确的选项是〔〕A. 是血浆中药物浓度下降一半所需的时间B. 血浆半衰期能反映体药量的消除速度C. 血浆半衰期在临床可作为调节给药方案的参数D. 1次给药后,约4-5个半衰期已根本消除E. 血浆半衰期的长短主要反映病人肝功能的改变13. 生物利用度检验的3个重要参数是〔〕A. AUC、Css、Tma*、Cma*、VdD. AUC、Tma*、CssE. Cma*、Vd、CssA.药物与血浆蛋白结合 B.首过效应C.Css D.VdE.AUC14.设计给药方案时具有重要意义(B)15.存在饱和和置换现象(A)16.可反映药物吸收程度(E)17. 开展治疗药物监测主要的目的是〔〕A.对有效血药浓度围狭窄的药物进展血药浓度监测,从而获得最正确治疗剂量,制定个体化给药方案B. 处理不良反响C. 进展新药药动学参数计算D. 进展药效学的探讨E. 评价新药的平安性18.下例给药途径,按吸收速度快慢排列正确的选项是〔〕A. 吸入>舌下>口服>肌注B. 吸入>舌下>肌注>皮下C. 舌下>吸入>肌注>口服D. 舌下>吸入>口服>皮下E. 直肠>舌下>肌注>皮肤19.血浆白蛋白与药物发生结合后,正确的描述是〔〕A. 药物与血浆白蛋白结合是不可逆的B. 药物暂时失去药理学活性C. 肝硬化、营养不良等病理状态不影响药物与血浆蛋白的结合情况D. 药物与血浆蛋白结合后不利于药物吸收E. 血浆蛋白结合率高的药物,药效作用时间缩短20.不正确的描述是〔〕A.胃肠道给药存在着首过效应B.舌下给药存在着明显的首过效应C.直肠给药可避开首过效应 D.消除过程包括代和排泄E.Vd 大小反映药物在体分布的广窄程度21. 下面哪个药物不是目前临床常须进展TDM的药物〔〕A. 地高辛B. 庆大霉素C. 氨茶碱D. 普罗帕酮E. 丙戊酸钠22、下面哪个测定方法不是供临床血药浓度测定的方法〔〕A. 高效液相色谱法B. 气相色谱法C. 荧光偏振免疫法D. 质谱法E. 放射免疫法23. 多剂量给药时,TDM的取样时间是:〔〕A.稳态后的峰浓度,下一次用药后2小时B.稳态后的峰浓度,下一次用药前1小时C. 稳态后的谷浓度,下一次给药前D. 稳态后的峰浓度,下一次用药前E. 稳态后的谷浓度,下一次用药前1小时24. 关于是否进展TDM的原则的描述错误的选项是:〔〕A. 病人是否使用了适用其病症的适宜药物?B. 血药浓度与药效间的关系是否适用于病情?C. 药物对于此类病症的有效围是否很窄?D. 疗程长短是否能使病人在治疗期间受益于TDM?E. 血药浓度测定的结果是否会显著改变临床决策并提供更多的信息?25.地高辛药物浓度超过多少应考虑是否药物中毒〔〕A.1.0ng/ml B. 1.5ng/ml D. 3.0ng/mlE. 2.5ng/ml26.茶碱的有效血药浓度围正确的选项是〔〕A.0-10μg/ml B.15-30μg/ml C.5-10μg/mlμg/ml27.哪两个药物具有非线性药代动力学特征:〔〕A.茶碱、苯妥英钠B.地高辛、丙戊酸钠C.茶碱、地高辛D.丙戊酸、苯妥英钠 E.安定、茶碱28. 受体是:〔〕A. 所有药物的结合部位B. 通过离子通道引起效应C. 细胞膜、胞浆或细胞核的蛋白组分D. 细胞膜、胞浆或细胞核的结合体E. 第二信使作用部位29. 药物与受体特异结合后,产生冲动或阻断效应取决于:A. 药物作用的强度B. 药物剂量的大小C. 药物的脂溶性D.药物的在活性 E. 药物与受体的亲和力30. 遗传异常主要表现在:〔〕A. 对药物肾脏排泄的异常B. 对药物体转化的异常C. 对药物体分布的异常D. 对药物肠道吸收的异常E. 对药物引起的效应异常31. 缓释制剂的目的:〔〕A. 控制药物按零级动力学恒速释放、恒速吸收B. 控制药物缓慢溶解、吸收和分布,使药物缓慢到达作用部位C. 阻止药物迅速溶出,到达比拟稳定而持久的疗效D. 阻止药物迅速进入血液循环,到达持久的疗效E. 阻止药物迅速到达作用部位,到达持久的疗效32. 老年患者给药剂量一般规定只用成人剂量的:〔〕33. 新药临床试验应遵循下面哪个质量规:〔〕E. ISO34. 治疗作用初步评价阶段为〔〕A.Ⅰ期临床试验B.Ⅱ期临床试验 C.Ⅲ期临床试验 D.Ⅳ期临床试验 E. 扩大临床试验35.新药临床Ⅰ期试验的目的是〔〕A. 研究人对新药的耐受程度B. 观察出现的各种不良反响C. 推荐临床给药剂量D. 确定临床给药方案E. 研究动物及人对新药的耐受程度以及新药在机体的药物代动力学过程36.对新药临床Ⅱ期试验的描述,正确项是〔〕A. 目的是确定药物的疗效适应证和毒副反响B. 是在较大围进展疗效的评价C. 是在较大围进展平安性评价D. 也称为补充临床试验E. 针对小儿、孕妇、哺乳期妇女、老人及肝肾功能不良者进展特殊临床试验37. 关于新药临床试验描述错误的选项是:〔〕A. Ⅰ期临床试验时要进展耐受性试验B. Ⅲ期临床试验是扩大的多中心临床试验C. Ⅱ期临床试验设计应符合代表性、重复性、随机性和合理性四个原则D. Ⅳ期临床试验即上市后临床试验,又称上市后监察E. 临床试验最低病例数要求:Ⅰ期20~50例,Ⅱ期100例,Ⅲ期300例,Ⅳ期2000例38. 妊娠期药代动力学特点:〔〕A. 药物吸收缓慢B. 药物分布减小C. 药物血浆蛋白结合力上升D. 代无变化 E. 药物排泄无变化39. 药物通过胎盘的影响因素是:〔〕A. 药物分子的大小和脂溶性B. 药物的解离程度C. 与蛋白的结合力D. 胎盘的血流量E.以上都是40. 根据药物对胎儿的危害,药物可分为哪几类:A. ABCDE C. ABCDD.ABC*E.ABCDE*41. 妊娠多少周药物致畸最敏感:〔〕A. 1~3周左右B. 2~12周左右C.3~12周左右D. 3~10周左右 E. 2~10周左右42. 以下哪种药物应用于新生儿可引起灰婴综合征〔〕A. 庆大霉素B. 氯霉素C. 甲硝唑D.青霉素 E. 氧氟沙星43. 以下哪个药物能连体双胎:〔〕A. 克霉唑B. 制霉菌素C. 酮康唑D. 灰黄霉素E. 以上都不是44. 以下不是哺乳期禁用的药物的是:〔〕A. 抗肿瘤药B. 锂制剂C. 头孢菌素类D. 抗甲状腺药E. 喹诺酮类45. 以下哪组药物在新生儿中使用时要进展监测:〔〕A. 庆大霉素、头孢曲松钠B. 氨茶碱、头孢曲松钠C. 鲁米那、氯霉素D. 地高辛、头孢呋辛钠E. 地高辛、头孢曲松钠46. 新生儿黄疸的药物治疗,选择苯巴比妥和尼可刹米的原因描述错误的选项是:〔〕A. 两药均为药酶诱导剂B. 主要是诱导肝细胞微粒体,减少葡萄糖醛酸转移酶的合成C. 两药联用比单用效果好D. 单独使用尼可刹米不如苯巴比妥E. 新生儿肝微粒酶少,需要用药酶诱导剂47. 老年人服用地西泮引起的醒后困倦或定位不准反响为:〔〕A. 免疫功能变化对药效学的影响B. 心血管系统变化对药效学的影响C. 神经系统变化对药效学的影响D. 分泌系统变化对药效学的影响E. 用药依从性对药效学的影响48. 老年人使用胰岛素后易出现低血糖或昏迷为:〔〕A. 免疫功能变化对药效学的影响B. 心血管系统变化对药效学的影响C. 神经系统变化对药效学的影响D. 分泌系统变化对药效学的影响E. 用药依从性对药效学的影响49. 以下关于老年患者用药根本原则表达不正确的选项是〔〕A. 可用可不用的药以不用为好B. 宜选用缓、控释药物制剂C. 用药期间应注意食物的选择D. 尽量简化治疗方案E. 注意饮食的合理选择和搭配50. 老年患者抗菌药物使用原则描述正确的选项是:〔〕A. 老年患者常有肝功障碍,主要经肝灭活的抗生素如氯霉素、红霉素、四环素等,应慎用或禁用。
临床药理学名词解释和简答题英文版
临床药理学名词解释和简答题英文版一、名词解释1、临床药理学(clinical pharmacology)临床药理学是研究药物在人体内作用规律和人体与药物间相互作用的一门交叉学科。
阐述药物代谢动力学、药物效应动力学、不良反应的性质和机制,以及药物相互作用的规律等。
是促进医药结合,基础与临床结合,指导临床合理用药,提高临床治疗水平,推动医学与药理学发展为目的的学科。
2、半衰期(half-time period)通常指血浆半衰期,是药物在体内分布达到平衡后血浆药物浓度下降50%所需要的时间,是常用来反映药物消除快慢的药动学参数。
3、曲线下面积(area under the curve, AUC)药物从零时间至所有原形药物全部消除这段时间的药-时曲线下总面积,反映药物进入血循环总量。
4、不良反应(adverse drug reaction, ADR)合格药品在正常用法用量下出现的与用药目的无关或意外的有害反应。
5、药物代谢动力学(Pharmacokinetics, PK)药物在机体的影响下所发生的变化及其规律,称为药物代谢动力学。
临床药动学:研究药物在人体的动力学,提供药物的剂量与药物体内浓度之间的关系,为制定给药方案、必要时根据患者具体情况或通过血药浓度监测结果调整给药方案提供依据,达到提高疗效降低不良反应的目的。
6、治疗药物监测(Therapeutic drug monitoring, TDM)通过应用现代分析技术测定体液(通常为血液样本)中的药物浓度,结合对药物疗效及不良反应的观察,运用药动学原理设计或调整给药方案,以达到提高疗效,降低不良反应,实现个体化给药的目的。
7、清除率(clearance,CL)清除率是机体对药物的消除速率的一种表示方法,即单位时间内机体从血浆内将药物消除的能力。
8、时量曲线(药时曲线,drug concentration-time curve)时间为横坐标,药物浓度(或对数浓度)为纵坐标绘制的图形。
临床药理学课后习题
临床药理学课后习题临床六班侯佳影考试题型:选择40分包括单选B型题简答25分5小题问答20分2题名解15分5个考试范围:选择每章节老师给的单选大题老师给的课后习题考试时间:第十周成绩=平时(30%包括考勤10分和论文20分)+末考(70%)第一章绪论名词解释1临床药理学Clinical pharmacology:是研究药物在人体内作用规律和人体与药物间相互作用过程的一门交叉学科。
2.新药new drug:指化学结构、药品组分或药理作用不同于现有药品的药物。
3.临床试验Clinical trial指对任何在人中进行试验的药品的系统性研究,以证实或揭示试验药品的作用、不良反应及试验药品的吸收、分布、代谢情况。
4.盲法blind trial technigue按试验方案规定,不让参与研究的受试者、研究者以及其他工作人员知道病人所接受到是何种处理,从而避免对试验结果的人为干扰5.安慰剂placeb是由乳糖或淀粉之类没有活性物质经加工制成与试验药物在外观上完全一样的制剂。
二、临床药理学的研究内容包括哪些?1临床药效学研究✓定义:研究药物对人体(包括老、幼、正常人与病人)生理与生化功能的影响和临床效应,以及药物的作用原理。
✓目的:确定治疗剂量观察剂量、疗程和给药途径与疗效的关系2临床药动学✓定义:研究药物在正常人与患者体内的吸收、分布、代谢和排泄的规律性。
✓意义:建立数学模式定量描述体内药动学变化规律。
便于临床医师正确揭示血药浓度测定结果。
制定个体化给药方案。
3毒理学研究✓内容:在研究药物疗效时同时观察药物可能发生的副作用、中毒反应、过敏反应和继发性反应等。
✓目的:确定药物安全性先用动物研究再研究人的潜在毒性4临床试验定义:指对任何在人中进行试验的药品的系统性研究,以证实或揭示试验药品的作用、不良反应及试验药品的吸收、分布、代谢情况。
目的:确定试验药品的疗效和安全信息。
⏹意义:评价新药的疗效和毒性,均必须通过临床试验做出最后判断⏹实施:我国1999年5月1日实施《药品审批办法》将我国新药的临床试验分为四期⏹过程:方案设计、组织实施、监查、稽查、记录、分析总结和报告5药物相互作用研究✓定义:指两种或两种以上的药物合并或先后序贯使用时,所引起的药物作用和效应的变化。
《临床药理学》参考答案.doc
1 •稳态血药浓度:药物在连续恒速给药(如静脉输注)或分次恒量给药的过程中,血药浓度会逐渐增高,经4〜5个半衰期可达稳定而有效的血药浓度,此时纱物吸收速度与消除速度达到平衡,血药浓度相对稳定在一定水平,这时的血药浓度称为稳态血药浓度。
2.药源性疾病:指在药物使用过程中,如预防、诊断或治疗中,通过各种途径进入人体后诱发的生理生化过程紊乱、结构变化等异常反应或疾病,是药物不良反应的后果.3•治疗药物监测(therapeutic drug monitoring,简称 TDM):是在药代动力学原理的指导下,应用现代化的分析技术,测定血液中或其他体液中药物浓度,用于药物治疗的指导与评价.4.累积系数:绝对牛:物利用度:是吸收进入血液循环的药量占总给药剂量的分数,其计算方法和原理是在同一受实者中不同的时间进行静脉注射和血管外给药,测定血纟勺浓度,计算AUC.5.和对生物利用度:是一种受实制剂与已知的参比制剂的吸收分数的比较,其测定方法和原理是在同一受实者中不同时期分别给予两种制剂后,测定血药浓度。
6•配伍禁忌:是指两种以上药物混合使用或药物制成制剂时,发生体外的相互作用,出现使药物中和、水解、破坏失效等理化反应,这时可能发生浑浊、沉淀、产生气体及变色等外观异常的现象。
7.负荷剂量:凡使首次给药时血药浓度达到稳态水平。
8.抗生素后效应:是指细菌与抗生素短暂接触,当药物浓度下降低于最低抑菌浓度(MIC)或消除后,细菌的生长仍受到持续抑制的效应。
9•表观分布容积(apparent volume of distribution, Vd):是指当药物在体内达动态平衡后,体内药量与血药浓度之比值称为表观分布容积。
特异质反应一idiosyncratic reaction:由于用药者有先天性遗传异常,对于某些药物反应特别敏感,出现的反应性质可能与某些常人不同的反应。
10.双盲双模:双盲,就是指研究者和病人都不知道使用的是哪组药,这样更有利于体现试验的真实性。
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临床药理学问题答案鸣谢:沈剑波、王海林、孙俊龙、张玉鑫、汤晨雪、吴慧、郑雅、戴璐、方淼、孔亚男、张舒文、徐阳、蔡水灵、刘珊等同学的无私奉献整理:临床小胖子一、please illusrate how to develop a new drug(p4)Most new drugs or drug products are discovered or developed through the following approaches:(1)identification or elucidation of a new drug target;(2)Rational design of a new molecule based on an understanding of biologic mechanisms and drug receptor structure;(3)Screening for biologic activity of large numbers of natural products,banks of previously discovered chemical entities,or large libraries of peptides,nucleic acids,and other organic molecules;(4)Chemical modification of a known active molecule,resulting in a me-too analog.Steps(1) and (2) are often carried out in academic research laboratories ,but the costs of steps(3) and (4) usually ensure that industry carries them out.二、Please tell the meaning of loading dose and maintenance dose?(p17)Loading dose is one or a sevies of doses that may be given at the onset of therapy with the aim of achieving the target arcentration vapidly .a loading dose may be desirable if the time required to attain steady state by the administration of drug at a anstant rate is long relative to the temporal demands of the condition being treaded.Maintenance dose : Maintenance dose is the dose that continues to keep the drug in the dosing therapeatic range. In most clinical situations, drugs are administered in a sevies of repetitive doses or as a wntinuous infusion to maintain a steady state concentration of drug associated with the therapeatic window. Calculation of the appropriate maintain dosage is a primary goal. To maintain the chosen steady state or target concentration, the rate of drug administration is adjusted such that the rate of input equals the rate of loss.三、Please tell the classification of ADR?(p24)ADR can be divided into three groups according to onset ①acute:within 60 minutes②sub-acute:1 to 24 hours③latent:≥2 days. It can also be divided into another three groups because of severity ①mild:bothersome but requires no change in therapy ②moderate:require change in therapy,addition treatment, hospitalization ③severe:disabling or life-threatening四,How to access ADR(p33)ADR can be evaluated by causality assessment .You can access the ADR from the following aspects:1.If the reaction had prior reports?2.temporal relationship3.de-challenge4.re-challenge5.Close-response relationship6.Alternative etiologies7.Objective confirmation8.If the patient had past history of reaction to same or similar medication .According to the results,the ADR can have four outcomes:highly probable,probable,possible and doubtful.五,what’s the sympoms of schizophrenia.(p39)Postitive symptoms:1.Delusions2.Hallucinations3.Thought disorder4.Abnormal.disorganized behaviour5.CatatoniaNegative symptoms:1.withdrawal from social contacts2.Flatten of emotional response3.Anhedonia(en inability to experience pleasure)4.Reluctance to perform everyday tasks.In addition,deficits in cognitive function are often present together with anxiety,guilt,depression and self punishment.A characteristic feature of schizophrenia is a defect in “selective attention”.Whereas a normal individual quickly accommodates to stimuli of a familiar or inconsequential nature,and responds only to stimuli that are unexpected or significant,the ability of schizophrenic patients to discriminate between significant and insignificant stimuli seems to be impaired六.what kinds of antidepressant drugs are used in clinic?(p53)Antidepressant drugs fall into the following categories:1.Inhibitors of monoamine uptakeSelective serotonin (5-HT) reuptake inhibitors (SSRJs): fluoxetine, fluvoxamine, paroxetine, sertraline, citalopram, escitalopramClassical tricyclic antidepressants (TCAs): imipramine, desipramine, amitriptyline, nortriptyline, clomipramine; varying in their ability to inhibit noradrenaline and 5-HT reuptakeNoradrenaline reuptake inhibitors: bupropion, reboxetine, atomoxetineNewer, mixed 5-HT and noradrenaline reuptake inhabitors: bupropion, desvenlafaxine, duloxetine, milnacipran 2.Monoamine receptor antagonistsDrugs such as mirtazapine, trazodone, mianserin are non-selective and inhibit a range of amine receptors including a2 adrenoceptors and 5-HT2 receptors. They may also have weak effects on monoamine uptake3.Monoamine oxidase inhibitors(MAOIs)Irreversible, non-competitive inhibitors: phenelzine, tranylcypromine,which are non-selective with respect to the MAO-A and -B subtypesReversible, MAO-A-selective inhibitors: moclobemide个人觉得只需答第1点即可。