Failing Public Health Again? Analytical Review of Depression and Suicidality From Finasteride
Mayer Brezis
The Journal of Clinical Psychiatry · 86(4):25nr158622025-09-22
Summary (paraphrased)
A narrative review by Mayer Brezis (Braun School of Public Health, Hadassah-Hebrew University) arguing that finasteride can cause depression, anxiety and suicidality, including after it is stopped, and analysing why recognition took two decades. Concerns appeared in studies from 2002; between 2017 and 2023, four analyses of adverse event reporting systems and four studies mining health records found a raised risk. Comparing the suicides reported to the FDA's adverse event system by 2024 (320) with the number he calculates would be expected over 30 years of use (19,320), the author argues for gross underreporting, and by an extrapolation he calls speculative estimates that over 20 years hundreds of thousands of users may have had depression and hundreds to thousands may have died by suicide. He attributes the delay to the manufacturer not running or publishing simple database pharmacovigilance studies and to regulators not requiring them, invokes the precautionary principle for a drug with a cosmetic indication, and concludes that regulators should require, and enforce, ongoing post-approval analytical studies.
Why it’s in the corpus
A single argument that pulls the finasteride depression and suicidality signals together and makes the case that regulators were slow; eight of its references are already in the library (among them DISC-013, LIT-049, LIT-010 and PFS-003). It is an analytical narrative review, not new data, and its harm estimates are the author's own extrapolations. Read alongside the FDA's 2022 response to the PFS Foundation petition (LIT-072) and the EMA's 2025 finasteride review (LIT-065).
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