Adverse events of alpelisib: A postmarketing study of the World Health Organization pharmacovigilance database
- PMID: 34786743
- DOI: 10.1111/bcp.15143
Adverse events of alpelisib: A postmarketing study of the World Health Organization pharmacovigilance database
Abstract
Aims: To explore and describe the adverse reaction signals in the safety reporting for alpelisib.
Methods: We performed a disproportionality analysis of the World Health Organization's VigiBase pharmacovigilance database from 1 January 2019 to 30 June 2021. Disproportionality analysis by information components (ICs) were used to evaluate the potential association between adverse events (AEs) and alpelisib.
Results: A total of 33 327 reports were extracted, 5695 of them were chosen with alpelisib as the suspected drug. After combining the same ID, 687 cases remained. The 45-64-years group had the most cases (n = 203, 29.55%). There were 129 Preferred Terms with significant signals. Hyperglycaemia (IC025 = 6.74), breast cancer metastatic (IC025 = 5.85) and metastases to liver (IC025 = 4.70) were the AEs with the strongest signal. AEs with the most cases were hyperglycaemia (n = 595), rash (n = 535) and diarrhoea (n = 475).
Conclusion: We established a comprehensive list of AEs potentially associated with alpelisib. AEs with the most significant signals were hyperglycaemia, breast cancer metastatic, metastases to liver. The AEs with the most cases were hyperglycaemia, rash, diarrhoea, blood glucose increase and nausea.
Keywords: VigiBase; adverse events; alpelisib; disproportionality analysis.
© 2021 British Pharmacological Society.
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