Biopharmaceuticals Breakthroughs and Beyond: Understanding and Mitigating Adverse Drug Reactions (ADRs)
Abstract
Biopharmaceuticals, while revolutionizing medicine, harbor potential for adverse reactions (ADRs)1,2,3. This presentation seeks to offer an exploration of adverse reactions (ADRs) linked to biopharmaceuticals. It will address the current scenario, emerging challenges, and essential pharmacovigilance strategies to enhance the safety of biopharmaceutical therapy.
Material :
This article is based on a comprehensive review of scientific literature published between 2017 and 2024. Relevant articles were identified in PubMed and Google Scholar using the keywords "biopharmaceuticals," "adverse reactions," "pharmacovigilance," and related terms. In addition to research papers, we reviewed case studies and reports from the World Health Organization (WHO) and the US Food and Drug Administration (FDA).
Methods :
This is a narrative review aimed at providing a comprehensive overview of the current understanding of ADRs associated with biopharmaceuticals. We critically assessed the identified literature, analyzed trends and patterns in ADR reporting, and incorporated case studies to illustrate the challenges and complexities involved.
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