Adverse drug reactions

Min-Kyung Cho; Dong Yoon Kang; Hye-Ryun Kang

doi:10.5124/jkma.2019.62.9.472

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Cho, Kang, and Kang: Adverse drug reactions

Focused Issue of This Month

Adverse Drug and Medical Device Reactions

Journal of the Korean Medical Association 2019; 62(9): 472-479.

Published online: 19 September 2019

DOI: https://doi.org/10.5124/jkma.2019.62.9.472

Adverse drug reactions

Min-Kyung Cho, MD¹

, Dong Yoon Kang, MD¹

, Hye-Ryun Kang, MD^1,^2,³

¹Drug Safety Center, Seoul National University Hospital, Korea.

²Institute of Allergy and Clinical Immunology, Seoul National University Medical Research Center, Korea.

³Division of Allergy and Clinical Immunology, Seoul National University Hospital, Seoul, Korea.

Corresponding author: Hye-Ryun Kang. helenmed@snu.ac.kr

Received 19 June 2019 Accepted 29 July 2019

Korean Medical Association

(open-access):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

There are no drugs without the risk of potential adverse reactions. All pharmacologically active substances can cause adverse drug reactions (ADRs). This paper aims at introducing recent trends in pharmacosurveillance systems for ADRs, which can be broadly classified into type A and B reactions. Since type A reactions are associated with drug pharmacology, they are usually dose-dependent and predictable. Whereas, type B reactions occur in some susceptible individuals, regardless of the pharmacological action of drug. Drug hypersensitivity reactions are typical examples of type B reactions and are subclassified according to the underlying pathomechanism. Recent advancements in pharmacogenomics have enlightened the understanding of individual differences in drug efficacy and susceptibility to ADRs. Therefore, expectations for safe personalized medicines are higher than ever before. However, premarketing clinical trials are too small and too short to uncover rare but serious ADRs and detect long-standing ADRs. In the past, post-marketing surveillance systems mainly focused on passive ADR monitoring systems, based on spontaneous reports. Recently, the importance of active pharmacovigilance systems, which use big data, is growing with recent advancements in medical informatics. Thus, regarding ADRs, suspecting and detecting the causative drug using causality assessment based on data science may contribute to decrease suffering induced by ADRs.

Keywords: Drug-related side effects and adverse reactions, Pharmacovigilance, Adverse drug reaction reporting systems, Pharmacogenetics, Big data

Figures and Tables

Table 1

Classification of adverse drug reactions

Adapted from Edwards IR et al. Lancet 2000;356:1255-1259 [6].

SSRI, serotonin-selective reuptake inhibitor.

Table 2

Classification of drug hypersensitivity reactions

Adapted from Weiss ME et al. Clin Allergy 1988;18:515-540 [8].

SJS, Steven-Johnson syndrome; TEN, toxic epidermal necrosis; AGEP, acute generalized exanthematous pustulosis; DRESS, drug reaction with eosinophilia and systemic symptoms; DiHS, drug-induced hypersensitivity syndrome.

Table 3

World Health Organization-Uppsala Monitoring Center causality categories

Adapted from Edwards IR et al. Lancet 2000;356:1255-1259 [6].

Notes

^{Conflict of Interest} No potential conflict of interest relevant to this article was reported.

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ORCID iDs

Min-Kyung Cho
https://orcid.org/0000-0001-9453-3366

Dong Yoon Kang
https://orcid.org/0000-0003-4283-2633

Hye-Ryun Kang
https://orcid.org/0000-0002-2317-4201

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