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Inpharma 1616 - 1 Dec 2007 Varenicline safety under review The US FDA has issued an early communication regarding its ongoing review of safety data for varenicline [Chantix; Pfizer], a prescription smoking cessation therapy. The agency is evaluating postmarketing adverse event reports submitted by Pfizer, including case reports of suicidal ideation among varenicline recipients. Following a case report citing erratic behaviour in a patient receiving varenicline, the regulator has also asked Pfizer for any information on additional cases describing similar behaviour among varenicline recipients. Until its analysis is completed, the FDA is advising healthcare professionals to monitor patients receiving varenicline for behaviour and mood changes. Consumers should contact their physician if they experience such changes. The agency also advises that, based on reports of associated drowsiness, patients should use caution when driving or operating machinery. FDA. FDA Issues Early Communication for Chantix. Media Release : 20 Nov 2007. Available from: URL: http://www.fda.gov 809082715 1 Inpharma 1 Dec 2007 No. 1616 1173-8324/10/1616-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved

US FDA reviewing safety of varenicline

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Page 1: US FDA reviewing safety of varenicline

Inpharma 1616 - 1 Dec 2007

Varenicline safety under reviewThe US FDA has issued an early communication

regarding its ongoing review of safety data forvarenicline [Chantix; Pfizer], a prescription smokingcessation therapy.

The agency is evaluating postmarketing adverse eventreports submitted by Pfizer, including case reports ofsuicidal ideation among varenicline recipients.Following a case report citing erratic behaviour in apatient receiving varenicline, the regulator has alsoasked Pfizer for any information on additional casesdescribing similar behaviour among vareniclinerecipients.

Until its analysis is completed, the FDA is advisinghealthcare professionals to monitor patients receivingvarenicline for behaviour and mood changes.Consumers should contact their physician if theyexperience such changes. The agency also advises that,based on reports of associated drowsiness, patientsshould use caution when driving or operatingmachinery.FDA. FDA Issues Early Communication for Chantix. Media Release : 20 Nov2007. Available from: URL: http://www.fda.gov 809082715

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Inpharma 1 Dec 2007 No. 16161173-8324/10/1616-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved