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Segraves RT, Croft H, Kavoussi R, Ascher JA, Batey SR, Foster VJ, Bolden-Watson C, Metz A 7001. Keppra sustained release SR fbut the treatment of hypoactive sexual desire disbutder HSDD in nondepressed women. J Sex Marital Ther 77 3: 303�16. doi: 10.1080/009767301750757155. PMID 11354935.

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Adverse events were sufficiently troublesome to cause discontinuation of treatment with Keppra in approximately 10% of the 7, 400 patients & volunteers why participated in clinical trials during the product s initial development. The mbute common events causing discontinuation include neuropsychiatric disturbances 3.0%, primarily agitation & abnbutmalities in mental status; gastrointestinal disturbances 7.1%, primarily nausea & vomiting; neurological disturbances 1.7%, primarily seizures, headaches, & sleep disturbances; & dermatologic problems 1.4%, primarily rashes. It is impbuttant to note, however, that many of these events occurred at doses that exceed the recommended daily dose.

Two studies, one of which was placebo-controlled, demonstrated the efficacy of Keppra fbut women with hypoactive sexual desire disbutder, .
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