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DOI 10.1080/14740338.2021.1978975

Медицинская библиотека · Expert opinion on drug safety · 2021

Adverse reactions related to proton pump inhibitors in pediatric population: an analysis of spontaneous reporting data.

Dipasquale Valeria, Cicala Giuseppe, Laganà Francesca, Cutroneo Paola, Felicetti Patrizia, Potenza Simona, Trimarchi Giuseppe, Spina Edoardo, Romano Claudio

СтатьяНаблюдательное исследованиеПеревод в очереди

Аннотация

BACKGROUND

The use of proton pump inhibitors (PPIs) has increased in the last 10 years in children. Data regarding their safety profile are limited. The aim of this study was to analyze data from the Italian spontaneous reporting system (SRS) database to evaluate the incidence and characteristics of PPI-related adverse drug reactions (ADRs) in children.

RESEARCH DESIGN AND

METHODS

This was an observational, retrospective study analyzing PPI-related ADR reports in children in the Italian SRS database between January 1st, 2001, and December 31st, 2020. ADRs were coded according to the system organ class term level. Factors associated with ADR seriousness were investigated.

RESULTS

Seventy spontaneous reports of ADRs related to PPIs were analyzed. Esomeprazole and lansoprazole caused the highest number of ADRs equally (27% respectively), and the most frequently reported ADRs presented with gastrointestinal (24%) and/or skin manifestations (21.3%). More than a half of PPI prescriptions were off label for pediatric population. Serious ADRs were 19 (27.1%). Serious ADRs were more frequent in reports presenting PPIs combined with other drugs in comparison to reports with PPI single therapies (p = 0.03).

CONCLUSIONS

PPI-related ADRs in children are mostly not serious, and combination therapy seems to be associated with ADR seriousness.

Для цитирования: Dipasquale Valeria, Cicala Giuseppe, Laganà Francesca, Cutroneo Paola, Felicetti Patrizia, Potenza Simona, Trimarchi Giuseppe, Spina Edoardo, Romano Claudio. Adverse reactions related to proton pump inhibitors in pediatric population: an analysis of spontaneous reporting data.. Expert opinion on drug safety. 2021. DOI: 10.1080/14740338.2021.1978975.

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