Postmarketing Surveillance of Suicidal Adverse Events with Pediatric Use of Antidepressants
Author:
Affiliation:
1. Division of Drug Risk Evaluation, Office of Drug Safety, U.S. Food and Drug Administration, Rockville, Maryland.
Publisher
Mary Ann Liebert Inc
Subject
Pharmacology (medical),Psychiatry and Mental health,Pediatrics, Perinatology, and Child Health
Link
http://www.liebertpub.com/doi/pdf/10.1089/cap.2006.16.33
Reference5 articles.
1. Adverse drug event monitoring at the food and drug administration
2. Adverse Event Reporting with Selective Serotonin-Reuptake Inhibitors
3. Emergence of Self-Destructive Phenomena in Children and Adolescents during Fluoxetine Treatment
4. Pemoline Hepatotoxicity and Postmarketing Surveillance
5. Emergence of intense suicidal preoccupation during fluoxetine treatment
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5. Postmarketing surveillance of serious adverse events associated with the use of rofecoxib from 1999–2002;Current Medical Research and Opinion;2009-05-14
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