Pharmacovigilance: the evolution of drug safety monitoring

被引:1
|
作者
Khan, Muhammad Akhtar Abbas [1 ,2 ]
Sara, Tehreem [2 ]
Babar, Zaheer-Ud-Din [3 ]
机构
[1] Hlth Serv Acad, Islamabad, Pakistan
[2] Drug Regulatory Author Pakistan, Islamabad, Pakistan
[3] Qatar Univ, Coll Pharm, Doha, Qatar
关键词
Adverse drug reactions; pharmacovigilance; medicines safety; public health; drug safety; monitoring;
D O I
10.1080/20523211.2024.2417399
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
The Pharmacovigilance system is aimed to promote and protect public health by ensuring the availability of essential medicines in the market and reducing the burden of ADRs. Pharmacovigilance is derived from two words; pharamakon rooted in the Greek word that means medicinal substance and vigilia rooted in the Latin word to keep watch. This concept evolved after Hannah Greener died in 1848 after having a tonsillectomy with chloroform. As a result of the Thalidomide tragedy, drug regulation in Europe has forever changed. From its earliest beginnings to its current state, pharmacovigilance has been shaped by several major milestones. The historical phases of pharmacovigilance can help us understand the value of pharmacovigilance and identify the challenges that lie ahead. Despite advancements in technology, it is imperative that we continue to strive for excellence in pharmacovigilance to ensure all individuals' safety and health. Through collaboration between the Council for International Organizations of Medical Sciences (CIOMS), World Health Organization (WHO), and the International Conference on Harmonization (ICH), Pharmacovigilance has evolved into a regulatory activity.
引用
收藏
页数:7
相关论文
共 50 条
  • [21] Utilizing drug-target-event relationships to unveil safety patterns in pharmacovigilance
    Hauser, Alexander Sebastian
    Kooistra, Albert Jelke
    Sverrisdottir, Eva
    Sessa, Maurizio
    EXPERT OPINION ON DRUG SAFETY, 2020, 19 (08) : 961 - 967
  • [22] Drug safety in Africa: a review of systems and resources for pharmacovigilance
    Ndagije, Helen Byomire
    Walusimbi, David
    Atuhaire, Joanita
    Ampaire, Sheila
    EXPERT OPINION ON DRUG SAFETY, 2023, 22 (10) : 891 - 895
  • [23] IMPROVING PEDIATRIC DRUG SAFETY: NEED FOR MORE EFFICIENT CLINICAL TRANSLATION OF PHARMACOVIGILANCE KNOWLEDGE
    Castro-Pastrana, Lucila I.
    Carleton, Bruce C.
    JOURNAL OF POPULATION THERAPEUTICS AND CLINICAL PHARMACOLOGY, 2011, 18 (01): : E77 - E88
  • [24] Safety Profile of Ibrutinib: An Analysis of the WHO Pharmacovigilance Database
    Allouchery, Marion
    Tomowiak, Cecile
    Lombard, Thomas
    Perault-Pochat, Marie-Christine
    Salvo, Francesco
    FRONTIERS IN PHARMACOLOGY, 2021, 12
  • [25] A Study on Drug Safety Monitoring Program in India
    Ahmad, A.
    Patel, Isha
    Sanyal, Sudeepa
    Balkrishnan, R.
    Mohanta, G. P.
    INDIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2014, 76 (05) : 379 - 386
  • [26] Diverse pharmacovigilance jurisdiction—The right way for global drug safety?
    Petra Zatovkaňuková
    Jiří Slíva
    European Journal of Clinical Pharmacology, 2024, 80 : 305 - 315
  • [27] Adverse Drug Reaction Monitoring at a Regional Pharmacovigilance Centre (BPKIHS)
    Rauniar, Gajendra Prasad
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2016, 25 : 453 - 453
  • [28] Big data, medicines safety and pharmacovigilance
    Rabia Hussain
    Journal of Pharmaceutical Policy and Practice, 14
  • [29] Big data, medicines safety and pharmacovigilance
    Hussain, Rabia
    JOURNAL OF PHARMACEUTICAL POLICY AND PRACTICE, 2021, 14 (01)
  • [30] The importance of drug–drug interactions as a cause of adverse drug reactions: a pharmacovigilance study of serotoninergic reuptake inhibitors in France
    Francois Montastruc
    Agnès Sommet
    Emmanuelle Bondon-Guitton
    Geneviève Durrieu
    Eric Bui
    Haleh Bagheri
    Maryse Lapeyre-Mestre
    Laurent Schmitt
    Jean-Louis Montastruc
    European Journal of Clinical Pharmacology, 2012, 68 : 767 - 775