Literature DB >> 33657139

Analysis of the reporting of adverse drug reactions in children and adolescents in Germany in the time period from 2000 to 2019.

Sarah Leitzen1,2, Diana Dubrall1,3, Irmgard Toni4, Julia Stingl5, Maike Schulz6, Matthias Schmid3, Antje Neubert4, Bernhardt Sachs1,7.   

Abstract

The objective of this study was to analyse reports on adverse drug reactions (ADRs) from Germany in the particularly vulnerable patient group of children and adolescents. Reporting characteristics, demographic parameters and off-label use were examined among others. The ratio of ADR reports per number of German inhabitants and the ratio of ADR reports per number of German inhabitants exposed to drugs were calculated and compared. These parameters were examined to derive trends in reporting of ADRs. 20,854 spontaneous ADR reports for the age group 0-17 years were identified in the European ADR database EudraVigilance for the time period 01.01.2000-28.02.2019 and analysed with regard to the aforementioned criteria. 86.5% (18,036/20,854) of the ADR reports originated from Healthcare Professionals and 12.2% (2,546/20,854) from non-Healthcare Professionals. 74.4% (15,522/20,854) of the ADR reports were classified as serious. The proportion of ADR reports per age group was 11.8% (0-1 month), 11.0% (2 months-1 year), 7.4% (2-3 years), 9.3% (4-6 years), 25.8% (7-12 years), and 34.8% (13-17 years) years, respectively. Male sex slightly dominated (51.2% vs. 44.8% females). Only 3.5% of the ADR reports reported off-label use. The annual number of ADR reports increased since 2000, even if set in context with the number of inhabitants and assumed drug-exposed inhabitants. The pediatric population declined in the study period which argues against its prominent role for the increase in the total number of ADR reports. Instead, among others, changes in reporting obligations may apply. The high proportion of serious ADR reports underlines the importance of pediatric drug safety.

Entities:  

Year:  2021        PMID: 33657139     DOI: 10.1371/journal.pone.0247446

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


  5 in total

1.  A Survey of Prescription Errors in Paediatric Outpatients in Multi-Primary Care Settings: The Implementation of an Electronic Pre-Prescription System.

Authors:  Lu Tan; Wenying Chen; Binghong He; Jiangwei Zhu; Xiaolin Cen; Huancun Feng
Journal:  Front Pediatr       Date:  2022-06-09       Impact factor: 3.569

2.  Assessment and analysis of outpatient medication errors related to pediatric prescriptions.

Authors:  Amira B Kassem; Haitham Saeed; Noha A El Bassiouny; Marwa Kamal
Journal:  Saudi Pharm J       Date:  2021-08-04       Impact factor: 4.330

3.  Descriptive analysis of adverse drug reaction reports in children and adolescents from Germany: frequently reported reactions and suspected drugs.

Authors:  Diana Dubrall; Sarah Leitzen; Irmgard Toni; Julia Stingl; M Schulz; Matthias Schmid; Antje Neubert; Bernhardt Sachs
Journal:  BMC Pharmacol Toxicol       Date:  2021-10-07       Impact factor: 2.483

4.  Analysis of pharmacovigilance databases for spontaneous reports of adverse drug reactions related to substandard and falsified medical products: A descriptive study.

Authors:  Kevin Pozsgai; Gergő Szűcs; Anikó Kőnig-Péter; Orsolya Balázs; Péter Vajda; Lajos Botz; Róbert György Vida
Journal:  Front Pharmacol       Date:  2022-09-06       Impact factor: 5.988

Review 5.  Pediatric Drug Safety Surveillance: A 10-Year Analysis of Adverse Drug Reaction Reporting Data in Calabria, Southern Italy.

Authors:  Christian Leporini; Caterina De Sarro; Caterina Palleria; Iolanda Caccavo; Brunella Piro; Rita Citraro; Giovambattista De Sarro
Journal:  Drug Saf       Date:  2022-09-16       Impact factor: 5.228

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.