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Antidepressant Use in Children, Adolescents, and Adults

The Food and Drug Administration (FDA) requests a Warning Statement

in the labeling for certain antidepressants to encourage close

observation of adult and pediatric patients treated with these agents

for worsening depression or the emergence of suicidality. The drugs

that are the focus of this new Warning Statement include: Prozac

(fluoxetine); Zoloft (sertraline); Paxil (paroxetine); Luvox

(fluvoxamine); Celexa (citalopram); Lexapro (escitalopram); Wellbutrin

(bupropion); Effexor (venlafaxine); Serzone (nefazodone); and Remeron

(mirtazapine).

Public

Health Advisory (issued 3/22/2004)

FDA

Talk Paper (issued 3/22/2004)

Background

Information on the Suicidality Classification Project (issued

3/22/2004)

Questions

and Answers on Antidepressant Use in Children, Adolescents and Adults

(issued 3/22/2004)

February 2, 2004, joint meeting of the Psychopharmacologic

Advisory Committee and the Pediatric Subcommittee of the Anti-Infective

Drugs Advisory.

Notice of Meeting

 or

[PDF]

Amendment of Notice [html] or [PDF]

Briefing Information

Presentation Slides

Meeting Transcript [html]

or [PDF]

or [Word]

Concordance Index

Pediatric

Drug Development Web page

PDF files, marked with an icon , require the free Adobe Acrobat Reader.

Back

to Top Back

to Drug Information

Date created: March 22, 2004

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