Assessment of Reye’s syndrome profile with data from the US Food and Drug Administration Adverse Event Reporting System and the Japanese Adverse Drug Event Report databases using the disproportionality analysis

Author:

Matsumoto Kiyoka1,Hasegawa Shiori12,Nakao Satoshi13,Shimada Kazuyo1,Mukai Ririka1,Tanaka Mizuki1,Satake Riko1,Yoshida Yu1,Goto Fumiya1,Inoue Misaki1,Ikesue Hiroaki2,Iguchi Kazuhiro4,Hashida Tohru2,Nakamura Mitsuhiro1ORCID

Affiliation:

1. Laboratory of Drug Informatics, Gifu Pharmaceutical University, Gifu, Japan

2. Department of Pharmacy, Kobe City Medical Center General Hospital, Hyogo, Japan

3. Department of Pharmacy, Kyusyu University Hospital, Fukuoka, Japan

4. Laboratory of Community Pharmacy, Gifu Pharmaceutical University, Gifu, Japan

Abstract

Objectives: Reye’s syndrome is a rare and potentially fatal illness that is defined as encephalopathy accompanied by liver failure. The aim of this study was to assess Reye’s syndrome profiles by analyzing data from the spontaneous reporting system database. Methods: We analyzed reports of Reye’s syndrome using the US Food and Drug Administration Adverse Event Reporting System and the Japanese Adverse Drug Event Report databases. The reporting odds ratio and proportional reporting rate were used to detect the pharmacovigilance signal. Results: The US Food and Drug Administration Adverse Event Reporting System contains 12,201,620 reports from January 2004 to June 2020, of which 186 are on Reye’s syndrome. The Japanese Adverse Drug Event Report contains 646,779 reports from April 2004 to September 2020, of which 30 are on Reye’s syndrome. In the US Food and Drug Administration Adverse Event Reporting System database, the reporting odds ratios (95% confidence interval, number of cases) of aspirin, diclofenac, ibuprofen, acetaminophen, and valproate sodium were 404.6 (302.6–541.0, n = 80), 15.1 (6.7–34.1, n = 6), 26.2 (16.1–42.6, n = 18), 10.7 (5.5–20.9, n = 9), and 47.1 (26.2–84.6, n = 12), respectively. In the Japanese Adverse Drug Event Report database, the reporting odds ratios (95% confidence interval, number of cases) of aspirin, diclofenac, ibuprofen, loxoprofen, acetaminophen, and valproate sodium were 14.1 (5.4–36.8, n = 5), 51.7 (22.2–120.5, n = 7), 135.0 (40.8–446.2, n = 3), 17.6 (6.7–46.0, n = 5), 24.0 (9.2–62.6, n = 5), and 13.8 (3.3–57.9, n = 2), respectively. The reported number of female patients aged 30–39 years was the highest in the Japanese Adverse Drug Event Report. Conclusion: Although the frequency of the occurrence of Reye’s syndrome is low, the possible risk of the disease occurring in adult females should be considered.

Funder

Japan Society for the Promotion of Science

Publisher

SAGE Publications

Subject

General Medicine

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