Role and Responsibilities of Various Stakeholders in Pharmacovigilance (PV)

Title:Role and Responsibilities of Various Stakeholders in Pharmacovigilance (PV)

Volume: 19

Author(s): Pinki Phougat, Meenu Beniwal, Garima Kapoor, Navidha Aggarwal, Aanchal Kumari, Rashmi Sharma, Hitesh Chopra, Rohit Sharma and Mohammad Amjad Kamal*

Affiliation:

• Enzymoics, 7 Peterlee place, Hebersham, NSW 2770; Novel Global Community Educational Foundation, Australia
• Institutes for Systems Genetics, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, China
• King Fahd Medical Research Center, King Abdulaziz University, Saudi Arabia
• Department of Pharmacy, Faculty of Allied Health Sciences, Daffodil International University, Bangladesh

Abstract: In this review paper, we have analyzed the potential and issues associated with Pharmacovigilance (PV). The analysis is divided into four sections: background, stakeholders, data sources, and medicinal chemistry. Each section discusses the current state, the future trends, and the best practices of Pharmacovigilance (PV). The main purpose, methods, results, and implications of our analysis are summarized.

Background: Pharmacovigilance (PV) is the science and practice of monitoring, evaluating, understanding, and preventing adverse drug reactions. Pharmacovigilance (PV) was established by the World Health Organization in response to the thalidomide tragedy of 1961. The main purpose of Pharmacovigilance (PV) is to ensure the safety and efficacy of drugs in clinical practice.

Stakeholders: Pharmacovigilance (PV) involves various stakeholders, such as patients, pharmacists, pharmaceutical companies, healthcare professionals, and regulatory authorities. Each stakeholder has a different role and responsibility in reporting, processing, analyzing, and communicating information about adverse drug reactions. Patient engagement is a key factor for enhancing Pharmacovigilance (PV) practices.

Data Sources: Pharmacovigilance (PV) relies on data from various sources, such as clinical trials, spontaneous reports, electronic medical records, biomedical literature, and patient-reported data in online health forums. These data sources can provide valuable insights into the real-world use and safety of drugs, as well as the preferences and needs of patients. However, these data sources also pose challenges in terms of quality, validity, reliability, and accessibility.

Medicinal Chemistry: Medicinal chemistry is the branch of chemistry that deals with the design, synthesis, and evaluation of new drugs and their biological effects. Medicinal chemistry can enhance Pharmacovigilance (PV) practices by finding new therapeutic indications for existing drugs or compounds that have already been tested for safety and efficacy. Medicinal chemistry also requires careful design and evaluation of covalent inhibitors, bi-substrate inhibitors, stabilizers of protein non-effective conformations, and hydrophobic pocket modifiers to ensure their safety and efficacy.

Implications: Pharmacovigilance (PV) is a dynamic and evolving discipline that requires collaboration, regulation, education, and innovation to improve patient safety and care. This review aims to provide a comprehensive overview of the potential and issues associated with Pharmacovigilance (PV) practices.

Cite this article as:

Phougat Pinki, Beniwal Meenu, Kapoor Garima, Aggarwal Navidha, Kumari Aanchal, Sharma Rashmi, Chopra Hitesh, Sharma Rohit and Kamal Amjad Mohammad*, Role and Responsibilities of Various Stakeholders in Pharmacovigilance (PV), Current Drug Safety 2024; 19 () . https://dx.doi.org/10.2174/0115748863277574240125045459