Abstract
The highly selective α1A-adrenergic receptor antagonist silodosin rapidly improves the signs and symptoms of benign prostatic hyperplasia (BPH). Oral silodosin is generally well tolerated in men with BPH, with a favourable cardiovascular tolerability profile. Abnormal ejaculation is the most commonly reported adverse effect associated with silodosin therapy; however, only 3.9% of patients discontinued treatment due to this event.
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Acknowledgements and Disclosure
This review was updated from Drugs 2011; 71 (7): 897–907[1] and was reviewed by S. Gravas, Department of Urology, University Hospital of Larissa, Larissa, Greece; R. Janknegt, Department of Clinical Pharmacy and Toxicology, Maasland Ziekenhuis, Sittard, the Netherlands; T. Schneider, Praxisklinik Urologie Rhein-Ruhr, Mülheim, Germany.
The preparation of these articles was not supported by any external funding. During the peer review process, the manufacturer of the agent under review was offered an opportunity to comment on the articles. Changes resulting from comments received were made by the authors on the basis of scientific and editorial merit.
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Keating, G.M., Curran, M.P. Silodosin: a guide to its use in benign prostatic hyperplasia. Drugs Ther Perspect 28, 1–4 (2012). https://doi.org/10.2165/11606250-000000000-00000
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DOI: https://doi.org/10.2165/11606250-000000000-00000