Literature DB >> 30222390

Regulatory Definitions and Good Pharmacovigilance Practices in Social Media: Challenges and Recommendations.

Paulami Naik1,2, Thomas Umrath3, John van Stekelenborg4, Regina Ruben5,2, Nasiba Abdul-Karim6, Robert Boland7, Michael Ibara8,2, Jethro Ekuta4, Dana Washburn9, Stella Stergiopoulos1.   

Abstract

Social media presents new challenges to the biopharmaceutical industry for conducting pharmacovigilance activities. The authors reviewed worldwide regulatory guidance documents related to monitoring of adverse events posted on social media sites and identified gaps in current regulatory definitions for pharmacovigilance. Points to consider for addressing these gaps are made to offer standards for industry consideration and a potential framework for guidance from global health authorities.

Keywords:  adverse events on social media; drug safety; pharmacovigilance; regulatory harmonization; social media monitoring

Year:  2015        PMID: 30222390     DOI: 10.1177/2168479015587362

Source DB:  PubMed          Journal:  Ther Innov Regul Sci        ISSN: 2168-4790            Impact factor:   1.778


  1 in total

1.  Combining Social Media and FDA Adverse Event Reporting System to Detect Adverse Drug Reactions.

Authors:  Ying Li; Antonio Jimeno Yepes; Cao Xiao
Journal:  Drug Saf       Date:  2020-09       Impact factor: 5.606

  1 in total

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