Exam Details
Subject | clinical research and regulatory affairs | |
Paper | ||
Exam / Course | m.pharm | |
Department | ||
Organization | Gujarat Technological University | |
Position | ||
Exam Date | January, 2019 | |
City, State | gujarat, ahmedabad |
Question Paper
Seat No.: Enrolment
GUJARAT TECHNOLOGICAL UNIVERSITY
M.PHARM SEMESTER EXAMINATION -WINTER 2018
Subject Code: MCP103T Date: 05/01/2019
Subject Name: Clinical Toxicology Pharmacovigilance
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
Role of clinical pharmacist in reporting, evaluation, and management of ADR
06
Explain in detail the clinical symptoms and management of acute poisoning of
Salicylates.
05
Explain in detail carbamate poisoning.
05
Q.2
Write a note on the general principles in the management of heavy metals poisoning.
06
Write the signs and symptoms and treatment of opioid dependence.
05
Discuss the need for medicine information services.
05
Q.3
Write a note on gut decontamination.
06
Write a brief note on toxicokinetics.
05
Discuss the factors and approaches to be considered for the evaluation of causality assessment.
05
Q.4
Write the clinical manifestations and management of chronic mercury poisoning.
06
Discuss symptoms, and management of food poisoning.
05
Mention the clinical symptoms and specific antidote for pyrethroids poisoning.
05
Q.5
Explain in detail about the general principles involved in the management of poisoning.
06
Clinical symptoms and management of radiations poisoning.
05
Discuss the toxicity of benzodiazepines and its treatment.
05
Q. 6
What are the symptoms, signs, and treatment of Organophosphorus compound poisoning?
06
Clinical features of acute methanol poisoning and its treatment.
05
Discuss various methods and importance of elimination enhancement in the treatment of poisoning.
05
Q.7
Write the requirements for establishment of drug information center.
06
Discuss organization and functions of poison information centre.
05
List down the signs and symptoms to detect poisoning cases with examples.
05
GUJARAT TECHNOLOGICAL UNIVERSITY
M.PHARM SEMESTER EXAMINATION -WINTER 2018
Subject Code: MCP103T Date: 05/01/2019
Subject Name: Clinical Toxicology Pharmacovigilance
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
Role of clinical pharmacist in reporting, evaluation, and management of ADR
06
Explain in detail the clinical symptoms and management of acute poisoning of
Salicylates.
05
Explain in detail carbamate poisoning.
05
Q.2
Write a note on the general principles in the management of heavy metals poisoning.
06
Write the signs and symptoms and treatment of opioid dependence.
05
Discuss the need for medicine information services.
05
Q.3
Write a note on gut decontamination.
06
Write a brief note on toxicokinetics.
05
Discuss the factors and approaches to be considered for the evaluation of causality assessment.
05
Q.4
Write the clinical manifestations and management of chronic mercury poisoning.
06
Discuss symptoms, and management of food poisoning.
05
Mention the clinical symptoms and specific antidote for pyrethroids poisoning.
05
Q.5
Explain in detail about the general principles involved in the management of poisoning.
06
Clinical symptoms and management of radiations poisoning.
05
Discuss the toxicity of benzodiazepines and its treatment.
05
Q. 6
What are the symptoms, signs, and treatment of Organophosphorus compound poisoning?
06
Clinical features of acute methanol poisoning and its treatment.
05
Discuss various methods and importance of elimination enhancement in the treatment of poisoning.
05
Q.7
Write the requirements for establishment of drug information center.
06
Discuss organization and functions of poison information centre.
05
List down the signs and symptoms to detect poisoning cases with examples.
05
Other Question Papers
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