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Pharmacovigilance Quiz MCQs

The document is a pharmacovigilance quiz containing multiple choice questions (MCQs) related to the detection, assessment, and prevention of adverse drug reactions (ADRs). It covers topics such as the definition of pharmacovigilance, the responsibilities of healthcare professionals in reporting ADRs, and the history of the Pharmacovigilance Programme of India. The quiz is intended for students to test their knowledge in this field.

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freakins007
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1K views1 page

Pharmacovigilance Quiz MCQs

The document is a pharmacovigilance quiz containing multiple choice questions (MCQs) related to the detection, assessment, and prevention of adverse drug reactions (ADRs). It covers topics such as the definition of pharmacovigilance, the responsibilities of healthcare professionals in reporting ADRs, and the history of the Pharmacovigilance Programme of India. The quiz is intended for students to test their knowledge in this field.

Uploaded by

freakins007
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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Priyanshu Chandra

Name of Student ………………………………………………………


92
Roll No……………………………………………………………………..
03-02-2025
Date : ……………………………………………………………………….

Pharmacovigilance Quiz
Multiple Choice Questions (MCQs):

1. What is pharmacovigilance? 6. What should a Doctor/Pharmacist/Nurse do if


A. The study of pharmacokinetics and an ADR is suspected?
pharmacodynamics A. Discontinue the medication without
B. The process of discovering new drugs consulting anyone
C. The science of detecting, assessing, and B. Report the ADR to a pharmacovigilance
preventing adverse drug reactions centre
D. The study of drug interactions C. Ignore the ADR unless it is life-threatening
2. An adverse drug reaction (ADR) is defined as: D. Prescribe a different drug
A. An intentional overdose of a drug 7. What is the role of the nurse in
B. Any harmful and unintended response to a pharmacovigilance?
medication administered at normal doses A. Administering medication only
C. A beneficial side effect of a drug B. Monitoring and documenting adverse
D. A natural progression of the disease reactions, and reporting them
3. Who is responsible for reporting adverse drug C. Prescribing medications
reactions? D. None of the above
A. Only doctors 8. Pharmacovigilance Programme of India
B. Only pharmacists started in which year?
C. Only nurses A. 2015
D. All healthcare professionals, including B. 2010
doctors, nurses, and pharmacists C. 2008
4. The primary goal of pharmacovigilance is to: D. 2007
9. Suspected ADRs can be reported for
A. Promote the sale of safer medications
A. Allopathic Drugs
B. Prevent medication errors in hospitals
B. Homeopathic Medicines
C. Ensure the safety and well-being of patients C. Traditional Medicines
by monitoring drug safety D. All the Above
D. Evaluate the cost-effectiveness of 10. While filling ADR reporting form, which of the
medications following information is kept confidential
5. Which phase of a clinical trial primarily A. Patient’s & Reporter’s information
focuses on drug safety monitoring? B. Manufacturer Details
A. Phase I C. Adverse Drug Reactions
B. Phase II D. All the Above
C. Phase III
D. Phase IV (Post-marketing surveillance)

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