FDA Information
Nortriptyline was approved as an antidepressant by the FDA in 1964.
On October 15th 2004, the FDA directed manufacturers of all antidepressants to include a Black Box warning, expanded warning statements, and clinical trial results detailing the increased risk of suicidality in children and adolescents. A Patient Medication Guide (MedGuide) will also accompany all prescriptions for antidepressants.
Additionally, the FDA is currently assessing the risk of suicidality in adults taking antidepressants and a final report is expected by mid-to-late 2006.
Why is this medication prescribed?
Dosage and using this medicine
What special precautions should I follow?
What should I do if I forget a dose?
What side effects can this medication cause?