Organizer : NAVYUG VIDYABHAVAN TRUST’S
C. K. PITHAWALLA INSTITUTE OF PHARMACEUTICAL SCIENCE AND RESEARCH, SURAT In Collaboration with APTI (Gujarat State Branch) & Pharma Vision (Gujarat Chapter)
On “Pharmacovigilance-ADR”
About the Quiz Competition
- 4th National Pharmacovigilance Week-2024 “Building ADR Reporting Culture for Patient Safety”
- Date of Event: 25th September, 2024
- Link open Time: 10 am to 4:30 pm
- Certificates are Auto generated.
- If it is not received within 10 minuets by mail you can download your certificate on 27-09-2024 from College Website.
- Go on college website https://ckpipsr.ac.in/
- Go in news and announcement section
- Participation certificate of NATIONAL LEVEL ONLINE QUIZ ON “PHARMACOVIGILANCE-ADR” 25-09-2024.
- Download Certificate by searching your name.
- if any query kindly mail.
Apply Link
CO-ORDINATOR:
MS. KINJAL S. GAMIT, ASSISTANT PROFESSOR
CONVENOR:
DR. DHIREN P. SHAH, PRINCIPAL
Opposite Surat Airport, Behind DPS School, Near Malvan Mandir, Dumas Road, Surat-395007
ckpipsr
Mobile: 6355065636
Email: ckuijpsr@gmail.com
100% Correct Answers Available here
MedDRA includes all of the following except:
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0/5
a) Medical and surgical procedures
b) Patient demographic terms
c) Product quality issues
d) Toxicologic issues
Serious adverse event
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a) Result in death
b) Life threatening
c) Both a and b
d) None of the above
Who is responsible for WHO international drug monitoring Programme?
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a) Uppsala monitoring centre
b) WHO drug dictionary
c) PVPI
d) Contract research Organization
Which of the following is a predictable cause of most adverse drug reactions (ADRs)?
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5/5
a) Nonadherence
b) Allergic reactions
c) Dosage issues
d) Idiosyncratic causes
Which of the following database is maintained by UMC on behalf of World Health Organization?
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5/5
a) EudraVigilance
b) Motherisk
c) Vigibase
d) General Practice Research Database (GPRD)
The most commonly adopted method for reporting of ADR is
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a) Expedited reporting
b) Longitudinal electronic patient records
c) Spontaneous reporting
d) Suspected reporting
Indian Pharmacovigilance system is regulated by
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a) CDSCO
b) DRDO
c) IPC
d) USFDA
The science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems.
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a) Clinical research
b) Clinical data management
c) Pharmacovigilance
d) Project management
Pharmacovigilance programme of India was started by Govt of India on
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a) 14th July 2012
b) 14th July 2010
c) 10 June 2012
d) 10 July 2010
What is the first step in management of ADR?
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a) Dose reduction of drug causing ADR
b) Detection of ADR
c) Withdrawal of suspected drug
d) Treatment of ADR
CDSCO is located in __
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a) New Delhi
b) Chennai
c) Mumbai
d) Kolkata
Adverse event is due to –
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a) Life threatening
b) Due to drug/treatment
c) May or may not have casual relationship with treatment
d) None of above
Dose-related ADRs are a particular concern in which of the following circumstances?
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5/5
a) The patient has other known allergies.
b) The patient is also being treated with other drugs.
c) The drug is new on the market.
d) The drug has a narrow therapeutic index.
Which one of these is a genetically determined adverse drug reactions?
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5/5
a) Addiction
b) Teratogenecity
c) Carcinogenicity
d) Idiosyncracy
PV tools not used by UMC are
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a) VigiFlowTM
b) VigiSearchTM
c) VigiMineTM
d) VigiPassTM
Process of pharmacovigilance is-
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a) Case processing-signal management-risk management -submission to umc
b) Case processing-risk management -signal management-submission to umc
c) Submission to umc- case processing-signal management-risk management
d) Risk management- submission to umc- case processing-signal management
The objectives of PVPI includes
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a) Create national wide system for patient safety reporting
b) Patient counselling
c) Adverse drug reaction
d) Monitoring the Patients
Type B adverse reactions are
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a) Idiosyncratic
b) Dose independent
c) Dose dependent
d) Predictable
What is full form of MedDRA?
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a) Medical Dictionary for Regulatory Activities
b) Medical Directory for Regulatory Affairs
c) Medical Dictionary for Regulations and Actions
d) Medical Directory for Regulations of Affairs
Define Solicited reports
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a) Can occur in certain situations, such as after a direct healthcare professional communication (DHPC), a publication in the press or questioning of healthcare professionals by company representatives
b) An unsolicited communication to a company, regulatory authority, or other organization that describes an adverse drug reaction in a patient given one or more medicinal products and which does not derive from a study or any organized data collection scheme.
c) Part of the marketing authorisation of a medicinal product setting out the agreed position of the product as distilled during the course of the assessment process which includes the information described in Article 11 of Directive 2001/83/EC.
d) Those derived from organized data collection systems, which include clinical trials, registries, post-approval named patient use programs, other patient support and disease management programs, surveys of patients or healthcare providers, or information gathering on efficacy or patient