Guest guest Posted December 22, 2003 Report Share Posted December 22, 2003 Hi all, I got this in the mail and thought I'd pass it along. Courage FDA MedWatch - Permax (pergolide mesylate) associated with fallin g asleep without warning >MedWatch - The FDA Safety Information and Adverse Event Reporting Program > >FDA and Lilly modified the WARNINGS and PRECAUTIONS sections to inform >healthcare professionals of the possibility of patients falling asleep while >performing daily activities, including operation of motor vehicles, while >receiving treatment with Permax, a dopamine agonist, indicated as adjunctive >treatment to levodopa/carbidopa in the management of the signs and symptoms >of Parkinson's disease. Many patients who have fallen asleep have perceived >no warning of somnolence. Healthcare professionals should be alerted to the >potentially serious risks associated with these events and should carefully >evaluate their patients for the presence of somnolence. > >Read the MedWatch 2003 safety summary, including links to the " Dear >Healthcare Professional " letter and revised label, at: > >http://www.fda.gov/medwatch/SAFETY/2003/safety03.htm#permax2 > >-------- > >Thank you for using MedWatch as a trusted source for timely safety information on drugs and other medical products regulated by the U.S. Food and Drug Administration. If you find this e-mail notification helpful, please consider telling colleagues and friends about MedWatch. They can learn more about us and subscribe/unsubscribe to the e-list at the MedWatch homepage, http://www.fda.gov/medwatch or by going directly to http://list.nih.gov/cgi-bin/wa?SUBED1=medwatch & A=1 > >This is an automated message delivery system -- replying to this message will not reach MedWatch staff. If you have comments or questions about MedWatch or this e-mail, please contact us through our comments & feedback web page, http://www.fda.gov/medwatch/feedback.htm Quote Link to comment Share on other sites More sharing options...
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