Quiz Competition. Title: Know The Drug & Know The ADR

Uppsala Monitoring Centre (UMC) UMC was established in Uppsala, ________ in the year_______ as the World Health Organization (WHO) Collaborating Centre for International Drug Monitoring

• Swedan,1979

• Switzerland, 1978

• Swedan, 1978

• Switzerland, 1979

Who is the Canadian-American pharmacologist and physician was a reviewer for the U.S. Food and Drug Administration (FDA), she refused to authorize thalidomide for market because she had concerns about the lack of evidence regarding the drug's safety.

• Darrell R. Abernethy

• Frances Oldham Kelsey

• Charles Antzelevitch

• Margaret Georgia Kelly

The Pharmacovigilance Program of India (PvPI) was launched with a broad objective to safeguard the health of _____billion people of India

• 2.0

• 2.5

• 1.27

• 1.29

In which year, PvPI- Indian Pharmacopoeia Commission (IPC), in Ghaziabad, India, became a WHO Collaborating Centre?

• 2017

• 2011

• 2016

• 1978

With which three Collaborating centers the WHO Pharmacovigilance team works?

• Pharmacovigilance roche, Uppsala Monitoring centre, Pharmacovigilance Program of India

• Uppsala Monitoring centre, Pharmacovigilance Program of India, Global Pharmacovigilance

• Pharmacovigilance roche, Uppsala Monitoring centre, Global Pharmacovigilance

• Uppsala Monitoring centre, Centre Anti poison et de Pharmacovigilance du Maroc, Pharmacovigilance Program of India

What are the various causality assessment categories?

• certain, possible, probable/likely, unlikely, conditional, and unassessable

• certain, possible, probable/likely, conditional, unlikely, and unassessable

• certain, probable/likely, possible, unlikely, conditional, and unassessable

• certain, possible, probable/likely, unlikely, unassessable, and conditional

SUSAR: What does that mean?

• Suspected Unwanted Serious Adverse Reaction

• Suspected Unexpected Serious Adverse Reaction

• Serious Unexpected Suspected Adverse Reaction

• Serious Unwanted Suspected Adverse Reaction

Volume 9A brings together general guidance on the requirements, procedures, roles and activities in the field of

• pharmacovigilance

• Marketing Authorisation Holders

• Competent Authorities of medicinal products

• All the above

What is the Minimum Criterion Required For A Valid Case?

• An identifiable patient

• A suspect product

• An identifiable reporter

• An adverse drug event

Explain the Hierarchy In Meddra?

• System Organ Class (SOC)

• High Level Term (HLT)

• High Level Group Term (HLGT)

• Lower Level Term (LLT)