- Everything You Need to Know About Breast Density, From the Experts
- First Doses of Mpox Vaccine Reach Africa, But Many More Are Needed
- Seeing Through: Scientists Use Food Dye to Render Mouse Skin Transparent
- Gun Deaths to Children and Teens Have Risen in Almost All States
- Too Much Light at Night Linked to Higher Alzheimer’s Risk
- Almost 1 in 4 U.S. Adults Under 40 Have High Blood Pressure
- Exposure to PFAS ‘Forever Chemicals’ in Pregnancy Could Boost Long-Term Obesity Risk
- Cuffs on At-Home Blood Pressure Monitors Don’t Fit Some Patients
- Brain’s Wiring May Trigger Depression in Some People
- Saltwater Drops in Nose Could Shorten Kids’ Colds
Brintellix Approved for Major Depressive Disorder
![](https://ladylively.com/wp-content/uploads/2013/08/drugs10-300x336.jpg)
TUESDAY, Oct. 1Brintellix (vortioxetine) has been approved by the U.S. Food and Drug Administration to treat adults with major depressive disorder, often referred to as depression.
The disorder may have symptoms including lack of interest in usual activities, weight or appetite changes, sleep problems, feelings of guilt or worthlessness, lack of concentration and thoughts of suicide.
In seven clinical studies, Brintellix proved effective in treating depression and in preventing future episodes, the FDA said in a news release. The most common side effects observed included nausea, constipation and vomiting.
Brintellix has a boxed label warning that antidepressants can raise the risk of suicidal thoughts among some users, especially among children, adolescents and adults aged 18 to 24. Doctors should carefully monitor users of Brintellix and similar drugs, especially during initial treatment, the FDA advised.
Brintellix is marketed by Takeda Pharmaceuticals and Lunbeck, both based in Deerfield, Ill.
More information
The U.S. National Institute of Mental Health has more about depression.
Source: HealthDay
Copyright © 2024 HealthDay. All rights reserved.