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DOI 10.1038/s41443-022-00568-2

Медицинская библиотека · International journal of impotence research · 2022

Are finasteride-related penile curvature/Peyronie's disease Adverse Event Reports worthy of further clinical investigation? Disproportionality analysis based on both the Food and Drug Administration (FDA) and the European Medicines Agency (EMA) pharmacovigilance databases.

Schifano Nicolò, Capogrosso Paolo, Boeri Luca, Fallara Giuseppe, Chiappini Stefania, Rewhorn Matthew, Cakir Omer Onur, Harvey Hannah, Castiglione Fabio, Alnajjar Hussain M, Muneer Asif, Deho' Federico, Schifano Fabrizio, Montorsi Francesco, Salonia Andrea

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Аннотация

A limited number of studies have described patients on finasteride showing findings which were consistent with Peyronie's disease (PD). We aimed to detect a pharmacovigilance signal of possible association between finasteride and PD-related clinical features. The Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) database was queried to identify the ten drugs which were associated the most with the adverse drug reactions (ADRs) recorded as "penile curvature" and/or "Peyronie's disease". A similar analysis, including the same drugs, was carried out for the EMA (European Medicines Agency) EudraVigilance (EV) database. Descriptive data have been analyzed, and Proportional Reporting Ratios (PRRs) have been computed against the other nine drugs of the database. Overall, 860 reports of "penile curvature" and/or "Peyronie's disease", were identified in the FAERS database, 214 of which (24.9%) were associated with finasteride. Most reports (56.9%) were submitted by healthcare professionals. Where a treatment-indication was stated, the vast majority of reports (176/210; 83.8%) were associated with androgenetic alopecia. The outcome of most ADRs was "serious" (82.2%), with 96 ADRs resulting in levels of permanent disability. For 97/214 individual cases, penile curvature/PD reports were not part of a syndromic cluster suggestive of post-finasteride syndrome (PFS). The PRR resulted 6.6 (95% CI: 5.6-7.8) and 11.8 (95% CI: 9.08-15.33), respectively, in the FAERS and in the EV databases. Notwithstanding the related limitations and biasing factors of pharmacovigilance studies based on spontaneous reporting, the PRR values here identified should be interpreted as strong signals of disproportionality. These findings, per se, are however not useful to confirm any causal association. Clinical studies are needed to investigate on the possible role for finasteride in causing PD-related clinical features, an hypothesis which remains highly speculative due to the very questionable quality of present data.

Для цитирования: Schifano Nicolò, Capogrosso Paolo, Boeri Luca, Fallara Giuseppe, Chiappini Stefania, Rewhorn Matthew, Cakir Omer Onur, Harvey Hannah, Castiglione Fabio, Alnajjar Hussain M, Muneer Asif, Deho' Federico, Schifano Fabrizio, Montorsi Francesco, Salonia Andrea. Are finasteride-related penile curvature/Peyronie's disease Adverse Event Reports worthy of further clinical investigation? Disproportionality analysis based on both the Food and Drug Administration (FDA) and the European Medicines Agency (EMA) pharmacovigilance databases.. International journal of impotence research. 2022. DOI: 10.1038/s41443-022-00568-2.

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