Is the safety of finasteride correlated with its route of administration: Topical versus oral? A pharmacovigilance study with data from the United States food and drug administration Aadverse event reporting system

bracu.type.groupResearch Publications
datacite.rightsOpen Access
dc.contributor.authorGupta A.K.
dc.contributor.authorTalukder, Mesbah
dc.contributor.authorKeene S.A.
dc.contributor.authorBamimore M.A.
dc.contributor.departmentSchool of Pharmacy
dc.date.accessioned2026-09-21T12:12:26Z
dc.date.available2026-09-21T12:12:26Z
dc.date.issued2026-01-01
dc.description.abstractThe United States Food and Drug Administration (FDA) approved oral finasteride for androgenetic alopecia. In 2022, approximately 2.6 million U.S. men used it for hair loss and prostate conditions. Post-finasteride syndrome (PFS), proposed in 2012, involves persistent sexual and neuropsychiatric adverse events (AEs) after cessation. These AEs are controversial and often lack assessment of contributing risk factors. We analyzed FDA Adverse Event Reporting System (FAERS) data to explore finasteride's administration route and PFS-like AEs. Using the information component (IC) method for disproportionality analyses, we assessed signals for 13 PFS-related AEs with topical and oral finasteride and dutasteride across two periods: 2006–2011 (pre-PFS reporting) and 2019–2024 (post-PFS reporting). These periods reflect times before and after formal PFS reporting in 2012. Eight analyses per AE were conducted based on agent, route, and era. Fewer signals for PFS-like AEs were detected with topical finasteride compared to oral finasteride in both eras. No signals were found for topical dutasteride, possibly because its use is very limited. Many reported AEs, such as erectile dysfunction and depression, may be influenced by age, stress, or comorbidities. Signals for PFS-like AEs were detected with topical finasteride, but were less frequent than with oral finasteride. The high prevalence of these AEs in the general population and the influence of confounding factors, such as psychological stress or nocebo effects, combined with the lack of genotyping, hormonal assessments, or family history data in most reports, suggest caution in attributing causality to finasteride. Topical finasteride may pose a lower risk, but robust evidence is needed to clarify its safety profile. © 2025 The Author(s). International Journal of Dermatology published by Wiley Periodicals LLC on behalf of the International Society of Dermatology.
dc.description.versionPublished
dc.format.extent108-118
dc.identifier.citationGupta, A.K., Talukder, M., Keene, S.A. and Bamimore, M.A. (2026), Is the Safety of Finasteride Correlated With Its Route of Administration: Topical Versus Oral? A Pharmacovigilance Study With Data From the United States Food and Drug Administration Adverse Event Reporting System. Int J Dermatol, 65: 108-118. https://doi.org/10.1111/ijd.17957
dc.identifier.doi10.1111/ijd.17957
dc.identifier.issn00119059
dc.identifier.other2-s2.0-105010964883
dc.identifier.urihttps://hdl.handle.net/10361/30121
dc.language.isoen_US
dc.publisherJohn Wiley and Sons Inc
dc.relation.hasversion10.1111/ijd.17957
dc.relation.ispartofInternational Journal of Dermatology
dc.relation.ispartofseriesInternational Journal of Dermatology
dc.relation.journalInternational Journal of Dermatology
dc.relation.urihttps://onlinelibrary.wiley.com/doi/10.1111/ijd.17957
dc.rightstrue
dc.subjectAdverse event
dc.subjectConfounding factors
dc.subjectDisproportionality analysis
dc.subjectPharmacovigilance
dc.subjectPost-finasteride Syndrome
dc.subjectTopical finasteride
dc.subject.lcshUnited States. Food and Drug Administration.
dc.subject.lcshPharmacoepidemiology.
dc.titleIs the safety of finasteride correlated with its route of administration: Topical versus oral? A pharmacovigilance study with data from the United States food and drug administration Aadverse event reporting system
dc.typeJournal
oaire.citation.issue1
oaire.citation.volume65
person.affiliation.nameMediprobe Research Inc.
person.affiliation.nameMediprobe Research Inc.
person.affiliation.namePhysician’s Hair Institute
person.affiliation.nameMediprobe Research Inc.
person.identifier.orcid0000-0002-8664-7723
person.identifier.orcid0000-0003-0691-640X
person.identifier.orcid0000-0002-5610-375X
person.identifier.scopus-author-id35476368700
person.identifier.scopus-author-id57226303680
person.identifier.scopus-author-id6701523429
person.identifier.scopus-author-id55935506600

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