GROWTH OF PHARMACOVIGILANCE IN INDIA Dr Deven V Parmar MD Vice President – Global Clinical Research & Pharmacovigilance

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GROWTH OF PHARMACOVIGILANCE IN INDIA Dr Deven V Parmar MD Vice President – Global Clinical Research & Pharmacovigilance

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Benefits of developing pharmacovigilance in India

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Analyzing the current & future of PV In India

PHARMACOVIGILANCE IN INDIA 1986 ADR Monitoring System which contained 12 regional centers was proposed 1997 - India joined the World Health Organization (WHO) Adverse Drug Reaction Monitoring Program based in Uppsala, Sweden. -National Pharmacovigilance Centre (AIIMS, New Delhi) -WHO centre (KEM Hospital, Mumbai) -WHO centre (JLN Hospital, Aligarh Muslim University Unsuccessful attempt 01 Jan 2005 - the WHO-sponsored and World Bank-funded National Pharmacovigilance Program for India was made operational.

NATIONAL PHARMACOVIGILANCE PROGRAM ,[object Object],[object Object],[object Object],Hence from 1986 – Till Date, things have definitely changed for the better but at a very slow pace. the questions that arise are whether the strategy should be changed and if so, how? ?

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Asian J of Pharmaceutical & Clinical Research 2009;2(2): 10 - 14 ADVERSE DRUG REACTIONS REPORTING: ATTITUDES AND PERCEPTIONS OF MEDICAL PRACTITIONERS

Asian J of Pharmaceutical & Clinical Research 2009;2(2): 10 - 14

IJP 2008;40(1): S31- 34 From BJ Medical College, A’bad

Ground reality in ADR detection ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Courtesy : Dr YK Amdekar (IDMA PV Conf, 2009 Mumbai)

Where does fault lie? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Courtesy : Dr YK Amdekar (IDMA PV Conf, 2009 Mumbai)

Where does fault lie? ,[object Object],[object Object],Courtesy : Dr YK Amdekar (IDMA PV Conf, 2009 Mumbai)

Solutions to minimise ADRs ,[object Object],[object Object],[object Object],[object Object],Courtesy : Dr YK Amdekar (IDMA PV Conf, 2009 Mumbai)

Robust PV System in India ,[object Object],[object Object],[object Object],[object Object],Cont’d…

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Soliciting ADR reporting from private practitioners ,[object Object],[object Object],[object Object],[object Object],[object Object],Courtesy : Dr YK Amdekar (IDMA PV Conf, 2009 Mumbai)

FUTURE STRATEGIES AND PROPOSALS ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]

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Patient-centered pharmacovigilance represents a pivotal shift in the landscape of healthcare, emphasizing the active involvement of patients in the monitoring and reporting of adverse drug reactions. Unlike traditional pharmacovigilance, which primarily relies on healthcare professionals to identify and document adverse events, this approach recognizes patients as critical stakeholders in ensuring medication safety. By empowering patients to share their experiences, concerns, and observations regarding medication effects, whether positive or negative, healthcare systems can gain a comprehensive understanding of drug safety and efficacy in real-world settings. Patient-centered pharmacovigilance fosters a collaborative partnership between patients, healthcare providers, and regulatory agencies, promoting transparency, accountability, and ultimately, better patient outcomes. Through increased patient engagement and the utilization of patient-reported data, this approach enables healthcare systems to identify potential safety issues earlier, tailor treatment strategies to individual needs, and enhance overall drug safety surveillance efforts.

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