Exam Details

Subject clinical pharmacy practice
Paper
Exam / Course m.pharm
Department
Organization Gujarat Technological University
Position
Exam Date May, 2018
City, State gujarat, ahmedabad


Question Paper

Seat No.: Enrolment No.
GUJARAT TECHNOLOGICAL UNIVERSITY
M. Pharm. SEMESTER I EXAMINATION SUMMER 2018
Subject Code: 910106 Date: 05/05/2018
Subject Name: Clinical Pharmacy Practice
TIME: 02:30PM TO 05:30PM Total Marks: 80
Instructions:
1. Attempt any five questions.
2. Make suitable assumptions wherever necessary.
3. Figures to the right indicate full marks.
Q.1

Discuss the reasons and dangers of self medication
06

Enumerate different types of medication errors and the possible reasons for the errors.
05

Discuss goals and objectives for clinical pharmacist on ward rounds.
05
Q.2

What is medication adherence. Discuss the role of pharmacist in improving medication adherence.
06

Highlight the dangers of Irrational drug use with suitable examples.
05

What is the role of pharmacist in ADR monitoring?
05
Q.3

Enlist the methods for causality assessment for ADR. Discuss anyone in detail.
06

Write a note on essential drug list.
05

Write in brief about pharmaceutical care.
05
Q.4

Explain in brief the different types pharmacoeconomic evaluations.
06

Discuss direct and indirect cost.
05

Distinguish between adverse drug events and adverse drug reactions, giving examples.
05
Q.5

Explain pharmacodynamic and pharmacokinetic drug interactions with suitable examples (atleast two examples each).
06

Discuss various lab tests used for assessment of anemia.
05

Classify ADR according to Rawlins and Thomson and discuss its limitations.
05
Q. 6

Give the normal range and significance of the following: (any three)
1. HbA1C 2. TSH 3. FEV1 4. SGOT
06

Write in brief about drug induced diseases with suitable examples.
05

Discuss the role and responsibilities of a clinical pharmacist.
05
Q.7

Discuss reasons for medication non-adherence. How will you assess medication adherence.
06

Discuss the communication skills needed by a clinical pharmacist
05

Write in brief about drug therapy monitoring.
05



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Subjects

  • advanced medicinal chemistry
  • advanced organic chemistry-i
  • advanced organic chemistry-ii
  • advanced pharmacology ii
  • advanced pharmacology-i
  • advances in drug delivery system
  • advances in pharmacology
  • applied pharmacotherapeutics - ii
  • applied pharmacotherapeutics-i
  • audits and regulatory compliance
  • biological evaluations & clinical research
  • cellular and molecular pharmacology
  • clinical and hospital pharmacy
  • clinical pharmacy practice
  • clinical research and pharmacy practice
  • clinical research and regulatory affairs
  • clinical research regulations
  • cosmetic and cosmeceuticals
  • documentation and regulatory writing
  • drug design and discovery
  • drug regulation and regulatory authority
  • experimental design and patents
  • global regulatory requirements
  • gmp, glp and validation
  • good manufacturing and good laboratory practice
  • good manufacturing practice and process validation
  • good regulatory practices
  • hazards and safety management
  • industrial pharmacy practice
  • modern analytical techniques
  • modern pharmaceutical analysis
  • novel drug delivery system part-i
  • novel drug delivery system-ii
  • pharm. management -ii
  • pharmaceutical analysis ii
  • pharmaceutical and cosmetic analysis
  • pharmaceutical formulation and development
  • pharmaceutical formulation development and biopharmceutics
  • pharmaceutical manufacturing technology
  • pharmaceutical production management & technology
  • pharmaceutical regulatory affairs
  • pharmacological and toxicological screening methods-i
  • pharmacological and toxicological screening methods-ii
  • pharmacometrics and methods of biological evaluation of drugs
  • pharmacotherapeutics
  • principles of biopharmaceutics& pharmacokinetics
  • product development and technology transfer
  • quality control & quality assurance
  • quality control and quality assurance
  • quality management system
  • regulatory affairs - i
  • regulatory affairs and new drug applications
  • regulatory aspects of hebbal and biologicals
  • research methodology
  • validation and product development