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Post-Finasteride Syndrome Foundation : ウィキペディア英語版 | Post-Finasteride Syndrome Foundation
The Post-Finasteride Syndrome Foundation is a nonprofit organization based in the United States that "coined the phrase 'post finasteride syndrome' (PFS), which they say is characterised by sexual, neurological, hormonal and psychological side effects that can persist in men who have taken finasteride for hair loss or an enlarged prostate."〔 This term has gained attention in the media. The foundation's mission is to fund medical research and raise public awareness of the syndrome. ==History==
The PFS Foundation was established in July 2012, and in February 2013 was granted retroactive 501(c)(3) status by the U.S. Internal Revenue Service.〔(【引用サイトリンク】url=http://www.pfsfoundation.org/news/the-post-finasteride-syndrome-foundation-is-granted-nonprofit-status-by-the-irs-as-a-public-charity/ )〕 Founding board members include John Santmann, CEO, Rosemary McGeady, general counsel, and Matthew Weintraub vice president. The foundation is headquartered in Somerset, New Jersey.
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Post-Finasteride Syndrome Foundation」の詳細全文を読む
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