A. National retail guided price sales
B. Zero-profit sales
C. increase the price by 5% on the basis of the purchase price.
D. Increase the price by 10% on the basis of the purchase price.
E. increase the price on the basis of the purchase price 15%.
Correct answer: b
Analysis of the answer: Item 12 of the "Implementation Opinions on Establishing the National Essential Drug System": In counties (cities, districts) where the basic drug system is implemented, the basic drugs equipped and used by grass-roots medical and health institutions organized by the government are sold at zero rate. All localities should implement relevant government subsidy policies in accordance with state regulations.
Best multiple-choice questions: the questions are in the front and the options are in the back. There are five alternative answers, A, B, C, D and E, of which only one is the best answer, and the rest are interference answers. Candidates must choose the answer that best fits the meaning of the question among the five options.
22. According to the Measures for the Administration of Drug Registration, those who apply for supplementary drugs are
A. application for registration of change of dosage form of listed drugs
B. Application for registration of change of administration route of listed drugs
C. Application for registration of new indications for listed drugs
D. Application for adding the original examination and approval items to the listed drugs
E. Application for registration of drugs produced abroad for sale in China.
Correct answer: D.
Analysis of the answer: Article 12 of the Measures for the Administration of Drug Registration: Supplementary application refers to the registration application for changing, adding or canceling the original approved items or contents after the application for new drugs, generic drugs and imported drugs is approved.
Best multiple-choice questions: the questions are in the front and the options are in the back. There are five alternative answers, A, B, C, D and E, of which only one is the best answer, and the rest are interference answers. Candidates must choose the answer that best fits the meaning of the question among the five options.
23. Where a medical institution needs to use narcotic drugs and psychotropic substances of Category I, which of the following departments should it apply for a stamp card for purchasing narcotic drugs and psychotropic substances of Category I?
A. the State Council drug supervision and administration department
B. Provincial drug supervision and administration departments
C. Municipal drug supervision and administration department
D. Municipal health administrative departments with districts
E. Health authorities in the State Council
Correct answer: D.
Item 4 of the Management Regulations on the Purchase and Use of Seal Cards for Narcotic Drugs and Psychotropic Substances of Class I: Medical institutions shall apply for seal cards to the municipal health administrative departments with districts (hereinafter referred to as municipal health administrative departments) and submit the following materials (detailed materials are omitted here).
Best multiple-choice questions: the questions are in the front and the options are in the back. There are five alternative answers, A, B, C, D and E, of which only one is the best answer, and the rest are interference answers. Candidates must choose the answer that best fits the meaning of the question among the five options.
24. according to the regulations on the administration of pharmaceutical affairs in medical institutions, the main responsibilities of pharmacists in medical institutions do not include
A. Publicize the knowledge of rational drug use to the public
B. Engaged in the research and development of new pediatric drugs
C, prepare tumor intravenous chemotherapy drugs.
D. Carry out pharmaceutical rounds and discuss the medical treatment of critically ill patients.
E, combined with clinical drug treatment practice, to carry out clinical application research of pharmacy.
Correct answer: b
Analysis of the answer: Article 36 of the Regulations on the Administration of Pharmaceutical Affairs in Medical Institutions: Responsibilities of pharmacists in medical institutions: ① Responsible for drug procurement and supply, prescription or medication order review, drug dispensing, intravenous centralized drug use and hospital preparations, and guiding nurses in wards (districts) to obtain, use and manage drugs. ② Participate in clinical drug treatment, design and implement individualized drug treatment plan, carry out pharmaceutical rounds, and provide pharmaceutical professional technical services for patients. (3) Participate in ward rounds, consultations, case discussions and medical treatment of difficult and critical patients, cooperate with doctors in drug selection, put forward clinical drug treatment opinions or adjustment suggestions, and jointly take charge of drug treatment with doctors. ④ Monitor the clinical application of antibacterial drugs, carry out prescription review and extraordinary early warning, and promote rational drug use. ⑤ Carry out drug quality monitoring, collect, sort out and report serious adverse drug reactions and drug damage. ⑥ Master the drug information related to clinical drug use, provide drug use information and pharmaceutical consulting services, and publicize the knowledge of rational drug use to the public. ⑦ To study the clinical application of pharmacy in combination with clinical drug treatment practice; To carry out drug utilization evaluation and clinical application research; Participate in clinical trials of new drugs and monitor the safety and effectiveness of new drugs after listing. ⑧ Other professional and technical work related to hospital pharmacy. Option b is not in this range, so choose B.
25. According to the Administrative Measures for Clinical Application of Antibacterials, there are few clinical data on the effectiveness and safety of an antibacterial drug. When drugs are used in clinical practice, they should be
A. management according to unlimited usage level
B. Management according to the restricted use level
C. Management according to special use level
D. it is forbidden to be listed in the supply catalogue of medical institutions.
E. it is forbidden to be listed in the provincial classified management catalogue of antibacterial drugs.
Correct answer: C.
Analysis of the answer: Article 6 of the Measures for the Administration of Clinical Application of Antibacterials: (3) Special-use antibiotics refer to antibiotics with one of the following circumstances: ① Antibacterials with obvious or serious adverse reactions that are not suitable for random use; ② Use should be strictly controlled to prevent bacteria from producing drug-resistant antibiotics too quickly; ③ Antibacterials with less clinical data on effectiveness and safety; 4 expensive antibacterial drugs.
26. According to the "Measures for Drug Supervision and Administration of Medical Institutions (Trial)", medical institutions shall submit an annual self-inspection report on drug quality management to the local drug supervision and administration department, which does not include.
A. Implementation of drug quality management system
B. Changes in preparations in medical institutions
C. Clinical pharmacists participate in the implementation of clinical drug therapy
D accept the supervision and inspection of the drug supervision and administration department and the implementation of rectification.
E. opinions and suggestions on drug supervision and administration departments
Correct answer: C.
Article 5 of the Measures for Drug Supervision and Administration of Medical Institutions (for Trial Implementation): (1) A medical institution shall submit an annual self-inspection report on drug quality management to the local drug supervision and administration department, which shall include the following contents: ① the implementation of the drug quality management system; ② Changes of preparations in medical institutions; (3) accept the supervision and inspection of the drug supervision and administration department and the implementation of rectification; (4) put forward opinions and suggestions to the drug supervision and administration department. The self-inspection report shall be submitted before 65438+February 3 1 this year.
Best multiple-choice questions: the questions are in the front and the options are in the back. There are five alternative answers, A, B, C, D and E, of which only one is the best answer, and the rest are interference answers. Candidates must choose the answer that best fits the meaning of the question among the five options.
27. According to the Measures for the Administration of Preparation Registration in Medical Institutions, if you provide false documents, application materials, samples or apply for approval documents by other deceptive means, if you have obtained the approval documents, your approval documents shall be revoked.
If the application is not accepted within one year, a fine of 1 10,000 yuan but not more than 30,000 yuan shall be imposed.
B if the application is not accepted within two years, a fine of not less than 10,000 yuan but not more than 30,000 yuan shall be imposed.
C will not accept the application within three years and impose a fine of not less than 10,000 yuan but not more than 30,000 yuan.
D the application will not be accepted within four years, and a fine of not less than 10,000 yuan but not more than 30,000 yuan will be imposed.
E if the application is not accepted within five years, a fine of not less than 10,000 yuan but not more than 30,000 yuan shall be imposed.
Correct answer: e
Analysis of the answer: Article 41 of the Measures for the Administration of Preparation Registration in Medical Institutions: If false certification documents, application materials, samples or other fraudulent means are provided to apply for approval certification documents, the (food) drug supervision and administration departments of provinces, autonomous regions and municipalities directly under the Central Government will not accept the application, give a warning to the applicant, and will not accept the application within one year; If the approval certificate has been obtained, the approval certificate will be revoked, the application will not be accepted within five years, and a fine of 1 10,000 yuan but not more than 30,000 yuan will be imposed.
28. According to the Standards for the Examination and Publication of Drug Advertisements, what should not appear in drug advertisements is
A. the name of the pharmaceutical manufacturer is indicated on the drug advertisement.
B: The TV station broadcasts drug advertisements to improve sexual function at six in the morning.
C. there is a promise in the drug advertisement to be responsible for the invalid claim.
Prescription drug advertisements have the warning that this advertisement is for medical and pharmaceutical professionals only.
E. indicate the name of non-prescription drugs in the advertisements of commercial activities in the name of non-prescription drugs.
Correct answer: C.
Article 12 of the Standards for the Examination and Publication of Drug Advertisements: Drug advertisements shall publicize and guide the rational use of drugs, and shall not directly or indirectly encourage the random and excessive purchase and use of drugs, and shall not contain the following contents: (1) It contains unscientific expressions or inappropriate expressions, causing unnecessary worries and fears of the public about their health status and diseases, or misleading the public to suffer from a certain disease or aggravate their illness without using the drug; (two) drugs containing free treatment, free gifts, sales with prizes, and taking drugs as gifts or prizes; (3) Containing "household necessities" or similar contents; (4) It contains such guarantee contents as "invalid refund" and "insurance by insurance company"; (5) Including comprehensive evaluation contents such as appraisal, ranking, recommendation, designation, selection and award-winning. Option C belongs to the content of "(4)", so it is the correct option for this question.
29. The contents of drug advertisements must be based on
A. subject to the license
The instructions approved by the drug supervision and administration department of the State Council shall prevail.
C. The approval shall prevail.
D. the content of the advertisement design shall prevail.
E. the new drug application materials shall prevail.
Correct answer: b
Article 15 of the Advertising Law of People's Republic of China (PRC): The contents of drug advertisements must be based on the instructions approved by the health administrative department of the State Council or the health administrative departments of provinces, autonomous regions and municipalities directly under the Central Government.
A. fixed-term imprisonment of not more than three years or criminal detention, and fined B. fixed-term imprisonment of not less than three years 10 year, and fined C. death penalty D. public surveillance E. life imprisonment.
Compatibility multiple-choice questions: It is a set of questions (2 to 5) * * A set of five alternative answers, A, B, C, D and E, with the options in front and the questions in the back. There is only one correct answer to every question. Each option can be selected once, repeated or not. Candidates only need to choose the best answer to each question.
30 production and sale of counterfeit drugs, punishable by
Fixed-term imprisonment of not more than three years or criminal detention and a fine.
B more than 3 years 10 years, with a fine.
C. Death penalty with a fine
D. control
E. Life imprisonment
Correct answer: a
Analysis of the answer: (1) Crime of producing and selling counterfeit drugs: ① Whoever produces or sells counterfeit drugs enough to seriously endanger human health shall be sentenced to fixed-term imprisonment of not more than three years or criminal detention and fined. (2) Whoever produces or sells counterfeit drugs and causes serious harm to human health shall be sentenced to fixed-term imprisonment of not less than 3 years/kloc-0 and not more than 0 years, and shall also be fined. (3) Whoever produces or sells counterfeit drugs, causing death or especially serious harm to human health, shall be sentenced to fixed-term imprisonment of not less than 10, life imprisonment or death, and shall also be fined or confiscated. (2) Crime of producing and selling inferior drugs: ① Whoever produces and sells inferior drugs and causes serious harm to human health shall be sentenced to fixed-term imprisonment of not less than 3 years 10 years and fined. (2) Whoever produces or sells inferior drugs and causes serious harm to human health, especially if the consequences are serious, shall be sentenced to fixed-term imprisonment of not less than 10 or life imprisonment, and shall also be fined or confiscated. So choose ABC. The test center has high probability compatibility multiple-choice questions. It is recommended that candidates be arrested three times for producing and selling counterfeit drugs, and 30 serious counterfeit drugs; "If you are too heavy, you will never die; If you are overweight, you will not die. " Formulas are easier to remember.
3 1. Whoever produces or sells counterfeit drugs and causes serious harm to human health or has other serious circumstances shall be punished.
Fixed-term imprisonment of not more than three years or criminal detention and a fine.
B more than 3 years 10 years, with a fine.
C. Death penalty with a fine
D. control
E. Life imprisonment
Correct answer: b
Analysis of the answer: (1) Crime of producing and selling counterfeit drugs: ① Whoever produces or sells counterfeit drugs enough to seriously endanger human health shall be sentenced to fixed-term imprisonment of not more than three years or criminal detention and fined. (2) Whoever produces or sells counterfeit drugs and causes serious harm to human health shall be sentenced to fixed-term imprisonment of not less than 3 years/kloc-0 and not more than 0 years, and shall also be fined. (3) Whoever produces or sells counterfeit drugs, causing death or especially serious harm to human health, shall be sentenced to fixed-term imprisonment of not less than 10, life imprisonment or death, and shall also be fined or confiscated. (2) Crime of producing and selling inferior drugs: ① Whoever produces and sells inferior drugs and causes serious harm to human health shall be sentenced to fixed-term imprisonment of not less than 3 years 10 years and fined. (2) Whoever produces or sells inferior drugs and causes serious harm to human health, especially if the consequences are serious, shall be sentenced to fixed-term imprisonment of not less than 10 or life imprisonment, and shall also be fined or confiscated. So choose ABC. The test center has high probability compatibility multiple-choice questions. It is recommended that candidates be arrested three times for producing and selling counterfeit drugs, and 30 serious counterfeit drugs; "If you are too heavy, you will never die; If you are overweight, you will not die. " Formulas are easier to remember.
32. Whoever produces or sells counterfeit drugs and causes death or has other particularly serious circumstances shall be punished.
Fixed-term imprisonment of not more than three years or criminal detention and a fine.
B more than 3 years 10 years, with a fine.
C. Death penalty with a fine
D. control
E. Life imprisonment
Correct answer: C.
Analysis of the answer: (1) Crime of producing and selling counterfeit drugs: ① Whoever produces or sells counterfeit drugs enough to seriously endanger human health shall be sentenced to fixed-term imprisonment of not more than three years or criminal detention and fined. (2) Whoever produces or sells counterfeit drugs and causes serious harm to human health shall be sentenced to fixed-term imprisonment of not less than 3 years/kloc-0 and not more than 0 years, and shall also be fined. (3) Whoever produces or sells counterfeit drugs, causing death or especially serious harm to human health, shall be sentenced to fixed-term imprisonment of not less than 10, life imprisonment or death, and shall also be fined or confiscated. (2) Crime of producing and selling inferior drugs: ① Whoever produces and sells inferior drugs and causes serious harm to human health shall be sentenced to fixed-term imprisonment of not less than 3 years 10 years and fined. (2) Whoever produces or sells inferior drugs and causes serious harm to human health, especially if the consequences are serious, shall be sentenced to fixed-term imprisonment of not less than 10 or life imprisonment, and shall also be fined or confiscated. So choose ABC. The test center has high probability compatibility multiple-choice questions. It is suggested that candidates be arrested three times for producing and selling counterfeit drugs, and 30 serious counterfeit drugs; "If you are too heavy, you will never die; If you are overweight, you will not die. " Formulas are easier to remember.
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