1, the following statements about dosage forms are wrong.
Formulation A refers to different forms of administration prepared to meet the needs of treatment or prevention.
B, the same dosage form can have different drugs.
C, the same drug can also be made into multiple dosage forms.
D, dosage form refers to the specific varieties of drugs.
E aspirin tablets, paracetamol tablets, midecamycin tablets and nimodipine tablets are all tablet dosage forms.
2, the correct expression of pharmaceutical concept is
A comprehensive technical science to study the prescription theory, preparation technology and rational application of pharmaceutical preparations.
B. Learn the basic theory, prescription design, preparation technology and rational application of pharmaceutical preparations.
C. Learn the prescription design, basic theory and application of pharmaceutical preparations.
D, learn the prescription design, basic theory and application of pharmaceutical preparations.
E, comprehensive technology and scientific research on the basic theory, prescription design and rational application of pharmaceutical preparations.
3. Regarding the classification of dosage forms, the following statement is wrong.
A, the sol is in liquid form; b, the ointment is in semi-solid form.
C suppository is in semi-solid dosage form d, and aerosol is in the form of gas dispersion.
E. Aerosols and inhalation powders are administered through the respiratory tract.
4, the following about pharmacopoeia narrative error is
A. Pharmacopoeia is the national code for recording drug specifications and standards.
B. Drugstores are compiled by the State Pharmacopoeia Committee.
Pharmacopoeia is promulgated by the government and is legally binding.
D the pharmacopoeia contains all drugs and preparations that have been listed.
E, a national pharmacopoeia reflects the level of drug production, medical care and science and technology in this country to a certain extent.
5. People's Republic of China (PRC) Pharmacopoeia is composed of
First, the drug instructions shall be formulated by the State Pharmacopoeia Committee.
B. Codes of drug specifications and standards compiled by the National Pharmacopoeia Committee.
C. Drug collection promulgated by the state
D, National Medical Products Administration drug standards.
E. Standards implemented by the State Administration of Medical Products
6. People's Republic of China (PRC) and China Pharmacopoeia promulgated and used the current version is
A, 1990 edition b, 1993 edition c, 1995 edition d, 1998 edition e, 2000 edition
7. When was the first Pharmacopoeia published in China after the founding of New China?
a， 1950b， 1953c， 1957d， 1963e， 1977。
8. Which of the following pharmacopoeia has been compiled by the World Health Organization (WHO) in order to unify the quality standards and quality control methods of drugs in all countries of the world?
A. international pharmacopoeia Ph.Int b, United States pharmacopoeia USP C and British pharmacopoeia BP.
D. Japanese pharmacy prescription JP E and China Pharmacopoeia.
9. Pharmacopoeia of various countries often need to be revised. China Pharmacopoeia is revised and published every few years.
A, 2 years b, 4 years c, 5 years d, 6 years e, 8 years.
10, which of the following is included in the general principles of preparations in China Pharmacopoeia?
A, each example B, text C, appendix D, preface E and the standard of specific varieties
Second, type B questions (compatibility multiple-choice questions)
[ 1—2]
A, classified by route of administration B, classified by dispersion system C and classified by preparation method
D, classified by morphology e, classified by drug type.
1. This classification method is closely combined with clinical use.
2. This classification method facilitates the application of physical and chemical principles to explain the characteristics of various preparations.
[3—6]
A, physical pharmacy B, biopharmaceutics C, industrial pharmaceutics D, pharmacokinetics E, clinical pharmacy
3. It is a frontier science that uses the principles, methods and means of physical chemistry to study the prescription design, preparation technology, dosage form characteristics, quality control and other contents in pharmacy.
4. It is a frontier science that studies the mechanism and process of drug absorption, distribution, metabolism and excretion in vivo, and clarifies the relationship between drug factors, dosage forms, physiological factors and curative effects.
5. It is a science to study the basic theory, technology, production equipment and quality management of pharmaceutical preparation industry, and it is also an important branch of pharmacy.
6. It is a science that studies the delayed process of drug absorption, distribution, metabolism and excretion and its relationship with drug efficacy by mathematical methods.
Third, X-type questions
1, the following statement about the establishment is correct
1. Preparations refer to different forms of administration prepared to meet the needs of treatment or prevention according to the standards approved by the Pharmacopoeia or the drug regulatory authorities.
B, pharmaceutical preparation is according to the pharmacopoeia or drug regulatory authorities approved standards, in order to meet the needs of treatment or prevention, and made into different forms of specific varieties.
C, the same preparation can have different drugs.
D, preparation is the research object of pharmacy.
E erythromycin tablets, paracetamol tablets and erythromycin powder for injection are all pharmaceutical preparations.
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