qsymia
qsymia: developed by 1 company · 1 FDA decision.
qsymia evidence translation
What we can confirm
1 FDA record
What it means
What to watch
Prepared research question
How could qsymia → VVUS affect its developer, and what evidence supports the link?
Traceable citations · Unknowns marked
See linked entities and source evidence1 indications · 0 study sponsors
Related indications
Study sponsors
No additional listed-company sponsor is linked.
Development Pipeline (1)
| Company | Phase |
|---|---|
| VIVUS INC (VVUS) Chronic weight management | Approved |
FDA Decisions1 records
Frequently asked questions
Who is developing qsymia?
qsymia is being developed by VIVUS INC.
What is qsymia's latest FDA decision?
The most recent tracked FDA decision for qsymia is Approval for 1 INDICATIONS AND USAGE QSYMIA is indicated in combination with a reduced-calorie diet and increased physical activity to reduce excess body weight and maintain weight reduction long term in: Adults and pediatric patients aged 12 years and older with obesity Adults with overweight in the presence of at least one weight-related comorbid condition QSYMIA is a combination of phentermine, a sympathomimetic amine anorectic, and topiramate, indicated in combination with a reduced-calorie diet and incr, dated July 17, 2012.