FDA panel rejects testosterone patch for women on safety grounds

BMJ 2004; 329 doi: (Published 09 December 2004) Cite this as: BMJ 2004;329:1363
  1. Ray Moynihan
  1. Washington, DC

A panel of advisers to the US Food and Drug Administration last week unanimously rejected an experimental testosterone patch as a treatment for women with sexual difficulties.

Procter & Gamble, global manufacturer of household products, wants to market the patch to women who have become menopausal after ovarian surgery, are currently taking oestrogen, and are said to have a controversial condition—“hypoactive sexual desire disorder.”

The FDA had granted Procter & Gamble a fast track review of the testosterone patch, but the committee's unanimous …

View Full Text

Log in

Log in through your institution


* For online subscription