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Paracetamol orodispersible tablets: a risk for severe poisoning in children?

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Abstract

Purpose

Childhood paracetamol (acetaminophen) ingestion with subsequent risk of hepatotoxicity is a major medical problem. The aim of this study was to investigate the risk of high-dose ingestion of orodispersible, fast-disintegrating paracetamol tablets in children.

Methods

A retrospective single-center case study of all accidental selfadministrations of solid or orodispersible 500-mg paracetamol tablets occurring in children ≤ 6 years, reported to the Swiss Toxicological Information Centre between June 2003 and August 2009.

Results

We found 187 cases with ingestion of solid 500-mg paracetamol tablets and 16 cases with ingestion of orodispersible 500-mg tablets. The mean ingested dose in the orodispersible-tablet group was 59% higher than in the solid-tablet group (p = 0.085). Administration of activated charcoal and/or N-acetylcysteine because of ingestion of a potentially hepatotoxic paracetamol dose ( ≥ 150 mg/kg body weight) was recommended in 32 patients (17.1%) in the solid-tablet group and in five (31%) in the orodispersible-tablet group.

Conclusions

Orodispersible paracetamol formulations may represent an important risk factor for severe paracetamol poisoning in children. Over-the-counter availability may contribute to increasing the use of this galenic formulation and eventually the number of poisonings in children.

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Acknowledgements

This work was supported entirely by the internal resources of the Swiss Toxicological Information Centre

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Correspondence to Alessandro Ceschi.

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Ceschi, A., Hofer, K.E., Rauber-Lüthy, C. et al. Paracetamol orodispersible tablets: a risk for severe poisoning in children?. Eur J Clin Pharmacol 67, 97–99 (2011). https://doi.org/10.1007/s00228-010-0943-x

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  • DOI: https://doi.org/10.1007/s00228-010-0943-x

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