Exam Details
Subject | pharmacotherapeutics | |
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- II EXAMINATION SUMMER 2017
Subject Code: 2920203 Date: 31/05/2017
Subject Name: Pharmacotherapeutics
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 clinical manifestation, diagnosis and therapeutic management of Depression.
06
Suggest a suitable therapeutic plan for the clinical management of hypothyroidism.
05
Discuss various mechanisms responsible for cardiac arrhythmias.
05
Q.2
Briefly explain the pharmacotherapy and diagnostic test used for Angina pectoris.
06
Write a short note on Insomnia.
05
Write a brief account on Adrenocortical dysfunction.
05
Q.3
Describe risk factors, diagnosis and treatment of COPD.
06
Discuss the management of hypertension.
05
Write a short note on Infertility in males.
05
Q.4
Briefly describe the pathophysiology and pharmacotherapy of Atherosclerosis.
06
Describe the pathophysiology and pharmacotherapy of Migraine.
05
Discuss etiopathogenesis and treatment of inflammatory bowel disease.
05
Q.5
Discuss etiology, diagnosis, and management of acute renal failure.
06
Discuss management of epilepsy in general.
05
Explain the pathophysiology and management of glaucoma.
05
Q. 6
Write symptoms, laboratory findings, complications of hepatitis.
06
Explain the role of H. pylori in Peptic Ulcer disease and also give therapeutic plan for its treatment.
05
Classify spasticity, and discuss the etiology of spasticity.
05
Q.7
Discuss risk factors, pathophysiology and management of Bronchial asthma.
06
Discuss etiology and treatment of Parkinson's disease.
05
Write a note on Sickle cell anaemia.
05
GUJARAT TECHNOLOGICAL UNIVERSITY
M. PHARM. SEMESTER- II EXAMINATION SUMMER 2017
Subject Code: 2920203 Date: 31/05/2017
Subject Name: Pharmacotherapeutics
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 clinical manifestation, diagnosis and therapeutic management of Depression.
06
Suggest a suitable therapeutic plan for the clinical management of hypothyroidism.
05
Discuss various mechanisms responsible for cardiac arrhythmias.
05
Q.2
Briefly explain the pharmacotherapy and diagnostic test used for Angina pectoris.
06
Write a short note on Insomnia.
05
Write a brief account on Adrenocortical dysfunction.
05
Q.3
Describe risk factors, diagnosis and treatment of COPD.
06
Discuss the management of hypertension.
05
Write a short note on Infertility in males.
05
Q.4
Briefly describe the pathophysiology and pharmacotherapy of Atherosclerosis.
06
Describe the pathophysiology and pharmacotherapy of Migraine.
05
Discuss etiopathogenesis and treatment of inflammatory bowel disease.
05
Q.5
Discuss etiology, diagnosis, and management of acute renal failure.
06
Discuss management of epilepsy in general.
05
Explain the pathophysiology and management of glaucoma.
05
Q. 6
Write symptoms, laboratory findings, complications of hepatitis.
06
Explain the role of H. pylori in Peptic Ulcer disease and also give therapeutic plan for its treatment.
05
Classify spasticity, and discuss the etiology of spasticity.
05
Q.7
Discuss risk factors, pathophysiology and management of Bronchial asthma.
06
Discuss etiology and treatment of Parkinson's disease.
05
Write a note on Sickle cell anaemia.
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