Pharmacovigilance Programme and Its Future Perspectives: Indian Scenario

Abstract: Due to its ability to track drug interactions and their physiological effects on humans, pharmacovigilance is a vital component of the healthcare system. The ability to monitor and analyze medications for quality as well as identify and halt any unfavorable drug side effects makes pharmacovigilance a crucial component of modern technology. Drug safety data collection and coding, as well as case management reporting and submission, comprise case processing, which is the first step in pharmacovigilance. The Pharmacovigilance Programme of India was established in response to these advancements. India participates in the Uppsala Monitoring Centre system but contributes very little to the database itself. The objective of this research is to conduct a comprehensive analysis of the pharmacovigilance program in India and provide a succinct, current evaluation of the organization, taking into account its background and possible issues. The development of "A Pharmacovigilance Programme of India" mobile application was emphasized by the National Coordination Centre PvPI to India as a means of enhancing public health and encouraging prompt reporting of adverse drug reactions. With more and more cutting-edge veterinary medications entering the market, India needs a veterinary pharmacovigilance system. One of the most significant current responsibilities is demonstrating to the world that thousands of years-old Ayurveda Siddha Unani systems are safe and grounded in science.

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Publication Details

Journal
Applied Drug Research Clinical Trials and Regulatory Affairs
Published
2025-04-09
DOI
https://doi.org/10.2174/0126673371341986250228074620
Primary Topic
Pharmacovigilance and Adverse Drug Reactions
Type
article
Field-Weighted Citation Impact
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Pharmacovigilance Programme and Its Future Perspectives: Indian Scenario

Ashutosh Kumar, Shaveta Sharma, Annu Dagar
Applied Drug Research Clinical Trials and Regulatory Affairs
Pharmacovigilance and Adverse Drug Reactions
article

Pharmacovigilance Programme and Its Future Perspectives: Indian Scenario

Ashutosh Kumar, Shaveta Sharma, Annu Dagar
article en

Abstract

Abstract: Due to its ability to track drug interactions and their physiological effects on humans, pharmacovigilance is a vital component of the healthcare system. The ability to monitor and analyze medications for quality as well as identify and halt any unfavorable drug side effects makes pharmacovigilance a crucial component of modern technology. Drug safety data collection and coding, as well as case management reporting and submission, comprise case processing, which is the first step in pharmacovigilance. The Pharmacovigilance Programme of India was established in response to these advancements. India participates in the Uppsala Monitoring Centre system but contributes very little to the database itself. The objective of this research is to conduct a comprehensive analysis of the pharmacovigilance program in India and provide a succinct, current evaluation of the organization, taking into account its background and possible issues. The development of "A Pharmacovigilance Programme of India" mobile application was emphasized by the National Coordination Centre PvPI to India as a means of enhancing public health and encouraging prompt reporting of adverse drug reactions. With more and more cutting-edge veterinary medications entering the market, India needs a veterinary pharmacovigilance system. One of the most significant current responsibilities is demonstrating to the world that thousands of years-old Ayurveda Siddha Unani systems are safe and grounded in science.

Applied Drug Research Clinical Trials and Regulatory AffairsVol. 11
Chandigarh University (IN)
Openalex Percentile: Top 93%
Pharmacovigilance and Adverse Drug Reactions
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