Real-World Data on Severe Cutaneous Adverse Reactions to Drugs

<b>Background/Objectives</b>: Cutaneous adverse drug reactions (CADRs) represent the most common manifestations of drug-induced allergy, with most unfavorable clinical outcomes seen in severe cutaneous adverse reactions (SCARs). To manage SCARs immediate cessation of the offending drug is needed; therefore, it is crucial to identify the list of medications associated with SCARs in real-world clinical practice. The objective of this study was to evaluate the structure of drugs associated with SCARs and to analyze drug-induced SCAR signals by calculating the reporting odds ratio (ROR) and proportional reporting ratio (PRR) based on spontaneous reports extracted from the Russian national pharmacovigilance database. <b>Methods</b>: A retrospective, descriptive pharmacoepidemiological analysis of spontaneous reports (SRs) registered in the pharmacovigilance database from 1 April 2019 to 31 March 2025. <b>Results</b>: A total of 7011 SRs with SCARs were finally revealed, with 907 identified drug triggers. The most frequently reported were antibacterial drugs for systemic use (22.8%), antineoplastic agents (17.8%), and antiepileptics (6.0%). The top five drugs involved in SCARs were dupilumab (2.14%, <i>n</i> = 244), piperacillin and beta-lactamase inhibitor (2.0%, <i>n</i> = 227), pembrolizumab (1.98%, <i>n</i> = 225), levofloxacin (1.95%, <i>n</i> = 222), and linagliptin (1.93%, <i>n</i> = 220). The strongest signals were detected for linagliptin (PRR = 15.37, 95% CI: 13.54-17.44; ROR = 17.24, 95% CI: 14.95-19.88), followed by clindamycin (PRR = 12.44, 95% CI: 10.89-14.21; ROR = 13.62, 95% CI: 11.77-15.77) and by piperacillin and beta-lactamase inhibitor (PRR = 10.02, 95% CI: 8.86-11.43; ROR = 10.81, 95% CI: 9.42-12.40). <b>Conclusions</b>: Pharmacovigilance databases facilitate the identification of diverse phenotypes of SCARs and the list of culprit drugs. The accumulated data serve as a valuable tool to enhance clinical practice outcomes and strengthen overall healthcare monitoring.

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Publication Details

Journal
Pharmaceuticals
Published
2025-12-22
DOI
https://doi.org/10.3390/ph19010021
Primary Topic
Drug-Induced Adverse Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Real-World Data on Severe Cutaneous Adverse Reactions to Drugs

Sergey Kensarinovich Zyryanov, Alexander Yudin, Irina Asetskaya, Elizaveta Terehina et al.
Pharmaceuticals
Drug-Induced Adverse Reactions
article

Real-World Data on Severe Cutaneous Adverse Reactions to Drugs

Sergey Kensarinovich Zyryanov, Alexander Yudin, Irina Asetskaya, Elizaveta Terehina, Vitaly Polivanov, Olga Butranova
article en

Abstract

<b>Background/Objectives</b>: Cutaneous adverse drug reactions (CADRs) represent the most common manifestations of drug-induced allergy, with most unfavorable clinical outcomes seen in severe cutaneous adverse reactions (SCARs). To manage SCARs immediate cessation of the offending drug is needed; therefore, it is crucial to identify the list of medications associated with SCARs in real-world clinical practice. The objective of this study was to evaluate the structure of drugs associated with SCARs and to analyze drug-induced SCAR signals by calculating the reporting odds ratio (ROR) and proportional reporting ratio (PRR) based on spontaneous reports extracted from the Russian national pharmacovigilance database. <b>Methods</b>: A retrospective, descriptive pharmacoepidemiological analysis of spontaneous reports (SRs) registered in the pharmacovigilance database from 1 April 2019 to 31 March 2025. <b>Results</b>: A total of 7011 SRs with SCARs were finally revealed, with 907 identified drug triggers. The most frequently reported were antibacterial drugs for systemic use (22.8%), antineoplastic agents (17.8%), and antiepileptics (6.0%). The top five drugs involved in SCARs were dupilumab (2.14%, <i>n</i> = 244), piperacillin and beta-lactamase inhibitor (2.0%, <i>n</i> = 227), pembrolizumab (1.98%, <i>n</i> = 225), levofloxacin (1.95%, <i>n</i> = 222), and linagliptin (1.93%, <i>n</i> = 220). The strongest signals were detected for linagliptin (PRR = 15.37, 95% CI: 13.54-17.44; ROR = 17.24, 95% CI: 14.95-19.88), followed by clindamycin (PRR = 12.44, 95% CI: 10.89-14.21; ROR = 13.62, 95% CI: 11.77-15.77) and by piperacillin and beta-lactamase inhibitor (PRR = 10.02, 95% CI: 8.86-11.43; ROR = 10.81, 95% CI: 9.42-12.40). <b>Conclusions</b>: Pharmacovigilance databases facilitate the identification of diverse phenotypes of SCARs and the list of culprit drugs. The accumulated data serve as a valuable tool to enhance clinical practice outcomes and strengthen overall healthcare monitoring.

PharmaceuticalsVol. 19(1)
Peoples' Friendship University of Russia (RU), Pirogov Russian National Research Medical University (RU), City Clinical Hospital No. 2 (RU), Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing (RU)
RUDN University
Good health and well-being
Openalex Percentile: Top 31%
Drug-Induced Adverse Reactions
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