| Subject: | FDA Advises of Changes to Prescribing Information for Paxil Tablets and Oral Suspension and Paxil CR Controlled-Release Tablets |
| Category: | Food and Drug Administration (FDA)
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| Published: | Tue, 16 May 2006 - 10:00 am |
| Audience: Neuropsychiatric and other healthcare professionals
GlaxoSmithKline (GSK) and FDA notified healthcare professionals of changes to the Clinical Worsening and Suicide Risk subsection of the WARNINGS section in the prescribing Information for Paxil and Paxil CR. These labeling changes relate to adult patients, particularly those who are younger adults.
A recent meta-analysis conducted of suicidal behavior and ideation in placebo-controlled clinical trials of paroxetine in adult... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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