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Download DNB 2017 Dec PHARMA PHARMA Paper I Question Paper

Download Diplomate in National Board (DNB) 2017 Dec PHARMA PHARMA Paper I Previous Question Papers

This post was last modified on 17 April 2020

DNB 2017 Dec Previous Question Papers-(Diplomate of National Board) Under NBE


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DECEMBER 2017

PHARMACOLOGY

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PAPER-I

PHARMA/D/17/34/

Time: 3 hours

Max. Marks: 100

Attempt all questions in order.

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Each question carries 10 marks.

Read the question carefully and answer to the point neatly and legibly.

Do not leave any blank pages between two answers.

Indicate the question number correctly for the answer in the margin space

Answer all the parts of a single question together.

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Start the answer to a question on a fresh page or leave adequate space between two answers.

Draw table/diagrams/flowcharts wherever appropriate.

Write short notes on:

  1. a) Write the in-vitro and animal toxicity tests required for new drug development. (5+5)

    b) What are preclinical evaluation methods for potential antiepileptic new chemical entity?

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  2. a) What are the ethical and regulatory issues in use of animals in biomedical research? (5+5)

    b) Composition and functions of Institutional Ethics Committee for research in human subjects.

  3. a) Methods of Pharmacovigilance with their advantages and limitations (5+5)

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    b) Pharmacogenomics interlink-with pharmacovigilance, giving examples.

  4. a) What are the inclusion and exclusion criteria of papers in meta analysis? What is the advantage of meta analysis? (5+5)

    b) What are the methods and implications of drug utilization studies?

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  6. a) Difference between partial agonist and inverse agonist giving suitable examples. (4+6)

    b) Define median lethal dose and median effective dose and their importance in Therapeutics.

  7. a) Define bioavailability and how it is determined. Give suitable examples. (5+5)

    b) What is the difference between pharmaceutical equivalent and therapeutic equivalent? Give suitable equivalence.

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  8. a) Role of Placebo in clinical trials. (5+5)

    b) Mention advantages and disadvantages of fixed dose combination.

  9. a) Principles and steps in preparing National List of Essential Medicine (NLEM) (5+5)

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    b) Potential uses of NLEM in rational therapeutics.

  10. a) Define plasma half life of a drug and its clinical significance with suitable examples. (5+5)

    b) Nanotechnology in drug delivery system.

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  12. a) Define drug dependence and its mechanisms. (5+5)

    b) Principles of treatment of drug dependence with suitable examples.

POSSESSION/USE OF CELL PHONES OR ANY SUCH ELECTRONIC GADGETS IS NOT PERMITTED INSIDE THE EXAMINATION HALL.

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