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A Firstranker's choice
DECEMBER 2017
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PHARMACOLOGYPAPER-IV
PHARMA/D/17/34/IV
Time: 3 hours
Max. Marks: 100
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Attempt all questions in order.
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
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Answer all the parts of a single question together.Start the question to a question on a fresh page or leave adequate space between two answers.
Draw table/diagrams/flowcharts wherever appropriate.
Write short notes on:
- a) Mention ethical issues in biomedical research on human subjects. (5+5)
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b) What are the regulatory requirements for conduct of clinical trial in India? (5+5) - Application of Biotechnology in Medicine (5+5)
- Orphan drug (4+6)
- Monoclonal antibodies in therapeutics (5+5)
- Role of TNF-alpha blockers in rheumatoid arthritis (5+5)
- Enumerate teratogenic-drugs (6+4)
- Role of GnRH in infertility (4+6)
- Current status of malaria and dengue vaccine. (5+5)
- a) Antibiotic stewardship programme.
b) Why and where therapeutic drug monitoring is required?--- Content provided by FirstRanker.com ---
Mention its usefulness, limitations in patient management giving example. - a) Define protocol violation and protocol deviation. Give examples. (5+5)
b) Composition and responsibilities of Human Ethics Committee.
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Characteristics of various phases of clinical trials
Microdosing
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Off label use of drugs with examples.
Medication errors, types and role of pharmacologist to control in hospital
Recent advances in drug treatment of HIV infection
Signal detection in medicine safety
POSSESSION/USE OF CELL PHONES OR ANY SUCH ELECTRONIC GADGETS IS NOT PERMITTED INSIDE THE EXAMINATION HALL
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This download link is referred from the post: DNB 2017 Dec Previous Question Papers-(Diplomate of National Board) Under NBE
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