Exam Details
Subject | clinical and hospital pharmacy | |
Paper | ||
Exam / Course | m.pharm | |
Department | ||
Organization | Gujarat Technological University | |
Position | ||
Exam Date | May, 2017 | |
City, State | gujarat, ahmedabad |
Question Paper
Seat No.: Enrolment No.
GUJARAT TECHNOLOGICAL UNIVERSITY
M. Pharm -SEMESTER-I EXAMINATION -SUMMER 2017
Subject Code: 910206 Date: 01/05/2017
Subject Name: CLINICAL AND HOSPITAL PHARMACY
Time: 10:30 AM to 01:30 PM 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
Explain the outcomes and applications of pharmacoepidemiology.
06
Brief about drug dosing in the elderly and obese patients.
05
Enumerate floor stock method.
05
Q.2
Briefly explain the meta-analysis usage in pharmacoepidemiology.
06
Explain the conversion of IV dosing system to oral dosing system.
05
Write brief about the process of TDM.
05
Q.3
Define hospital pharmacy. Explain the organizational structure and budget implementation in hospital pharmacy.
06
Write the clinical symptom and management of lead and copper.
05
Explain the dosage adjustment in renal impairment patient.
05
Q.4
What mean by PTC. Explain the structure and functions of PTC.
06
Discuss- Organophosphorus compound poisoning.
05
Brief about pharmacokinetic drug interactions
05
Q.5
Briefly explain the role of cohort studies in drug usage studies.
06
Differentiate attributed and relative risk.
05
Explain the role of antidotes and its applications in poison treatment.
05
Q. 6
Briefly explain the methods of inventory control and its applications.
06
Write brief in controlled substances distribution.
05
Brief about food poisoning.
05
Q.7
Define TDM. Explain the kinetic variability's and uses of TDM.
06
Define hospital formulary. Explain the components of hospital formulary.
05
Discuss-Toxicokinetics.
05
GUJARAT TECHNOLOGICAL UNIVERSITY
M. Pharm -SEMESTER-I EXAMINATION -SUMMER 2017
Subject Code: 910206 Date: 01/05/2017
Subject Name: CLINICAL AND HOSPITAL PHARMACY
Time: 10:30 AM to 01:30 PM 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
Explain the outcomes and applications of pharmacoepidemiology.
06
Brief about drug dosing in the elderly and obese patients.
05
Enumerate floor stock method.
05
Q.2
Briefly explain the meta-analysis usage in pharmacoepidemiology.
06
Explain the conversion of IV dosing system to oral dosing system.
05
Write brief about the process of TDM.
05
Q.3
Define hospital pharmacy. Explain the organizational structure and budget implementation in hospital pharmacy.
06
Write the clinical symptom and management of lead and copper.
05
Explain the dosage adjustment in renal impairment patient.
05
Q.4
What mean by PTC. Explain the structure and functions of PTC.
06
Discuss- Organophosphorus compound poisoning.
05
Brief about pharmacokinetic drug interactions
05
Q.5
Briefly explain the role of cohort studies in drug usage studies.
06
Differentiate attributed and relative risk.
05
Explain the role of antidotes and its applications in poison treatment.
05
Q. 6
Briefly explain the methods of inventory control and its applications.
06
Write brief in controlled substances distribution.
05
Brief about food poisoning.
05
Q.7
Define TDM. Explain the kinetic variability's and uses of TDM.
06
Define hospital formulary. Explain the components of hospital formulary.
05
Discuss-Toxicokinetics.
05
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