Are all the examinees ready for the licensed pharmacist exam? This article "Examination Questions and Answers 1 of Pharmaceutical Affairs Management and Regulations for Licensed Pharmacists in 217", let's take a look. Believe that as long as you have enough strength, you will not be afraid of anything!
217 "Pharmaceutical Affairs Management and Regulations" test questions and answers 1
1. The Chinese herbal medicines that are strictly prohibited from trading in the professional market of Chinese herbal medicines are
A. Poria
B. Paeonia lactiflora
C. Glycyrrhiza uralensis
D. Angelica sinensis
E. Codonopsis pilosula
Correct answer: C < p. > B. Cortex Phellodendri
C. Cortex Eucommiae
D. Cortex Magnolia Officinalis
E. Scutellariae Radix
Correct answer: E
3. About the implementation of "The Chinese People * * * The calculation of the validity period of drugs stipulated in the notice on matters related to the 1995 edition of the Chinese Pharmacopoeia
A. From the date of drug storage
B. From the date of drug storage
C. From the date of drug production
D. From the date of drug delivery
E. From the date of drug inspection report
Correct answer: C
. The State Council's institutional reform programme, China * * * Central Committee and the State Council decided to set up the
A. State Drug Administration
B. State Drug Administration
C. State Drug Quality Supervision Bureau
D. National Medical Products Administration
E. State Drug Administration
Correct answer: D
5. People's Republic of China * * * The definition of inferior drugs in the Drug Administration Law of the People's Republic of China is
A. The names of ingredients contained in drugs are not in conformity with the statutory drug standards
B. The contents of pharmaceutical ingredients are not in conformity with the statutory drug standards
C. The products produced without the approval number are
D. The products are contaminated and cannot be used for medicine
E. The products are deteriorated and cannot be used for medicine
Correct answer: b < Measures for the Implementation of the Drug Administration Law of the People's Republic of China, Medical institutions preparing preparations must have corresponding
A. Drug testing room
B. Toxicology room
C. Animal room
D. Measurement room
E. Sample storage room
Correct answer: A
7. Retail pharmaceutical stores can supply and allocate psychotropic drugs with legal prescriptions
A. Toxic drugs
E. Narcotic drug preparation
Correct answer: D
8. The Company Law of the People's Republic of China stipulates that you may not serve as a director, supervisor, The manager's name is
A. Director of the enterprise
B. Secretary of the enterprise
C. National civil servant
D. Legal representative of shareholders with limited capacity for civil conduct
E. Guardian of shareholders without capacity for civil conduct
Correct answer: C
9. The department that has the right to re-examine the inspection results of imported drug inspection reports is
. . China Customs
C. China Import and Export Commodity Inspection Bureau
D. China Institute for the Control of Pharmaceutical and Biological Products
E. Port Institute for Drug Control
Correct answer: D
1. According to the "Standards for the Quality Management of Pharmaceutical Commodities", Quality management institutions established by large and medium-sized pharmaceutical trading enterprises
A. Directly led by the deputy manager in charge of quality of the enterprise
B. Directly led by the deputy manager in charge of operation of the enterprise
C. Directly led by the person in charge appointed by the enterprise manager
D. Directly led by the enterprise manager
E. Directly led by the chief engineer of the enterprise
Correct answer: D
According to the Patent Law of the People's Republic of China, what can be granted patent right is
A. Scientific discovery
B. Rules and methods of intellectual activities
C. Production methods of animal and plant varieties
D. Diagnosis and treatment methods of diseases
E. Substances obtained by nuclear transformation
Correct answer: C
12. The new drug that changes the traditional oral decoction of Chinese medicine into injection belongs to
A. Western medicine II
B. Chinese medicine II
C. Western medicine III
D. Chinese medicine III
E. Chinese medicine IV
Correct answer: B
13. The drug produced on January 22, 1989 has a validity period of three years. Its expiration date is
A. January 22, 1992
B. January 21, 1992
C. January 23, 1992
D. January 3, 1993
E. December 3, 1992
Correct answer: b <
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correct answer to the management autonomy stipulated by laws and regulations: D
15. The "Quality Management Standard for Pharmaceutical Commodities" requires that medical commodity keepers should
a. be responsible for providing accurate inspection data
b. scientifically store commodities according to their different natural attributes
c. carefully select products that meet the requirements
d. Do a good job in analyzing market demand and inventory structure
. Handling
Correct answer: B
16. The characteristics of drug quality do not include
A. Effectiveness
B. Safety
C. Practicality
D. Homogeneity
E. Stability
Correct answer: C
17. Basic principles of the responsibilities of licensed pharmacists. Ensure the safety and effectiveness of people's drug use
B. Take the lead in implementing medical regulations
C. Constantly update knowledge, Maintain a high professional level
D. Evaluate the efficacy of drugs
E. Put forward suggestions on handling violations
Correct answer: A
18. Adverse drug reactions generally refer to
A. Harmful reactions caused by intentional overdose and wrong medication
B. Harmful reactions caused by unintentional overdose and wrong medication. Harmful reactions that have nothing to do with the purpose of treatment under dosage < P > D. Normal usage, Predictable related reaction under dosage
E. Chronic poisoning reaction caused by long-term drug use
Correct answer: C
19. "Drug for detoxification" refers to drugs that control and eliminate the symptoms and signs of acute withdrawal of drug addicts who abuse which of the following types of drugs
A. Cannabis
B. Opioids
C. Ephedrine
D. Correct answer: B
2. The statutory body that organizes the formulation and revision of national drug standards is
A. Drug Certification Committee
B. China Institute for the Control of Pharmaceutical Biological Products
C. National Pharmacopoeia Committee
D. Drug Evaluation Center
E. Drug Evaluation Center
Correct answer: C.