Table 1. Anti-obesity drugs approved, rejected, withdrawn or revised by the FDA.
| Drug | Company | Mechanism of action | Comments |
|---|---|---|---|
| Anti-obesity drugs presently on the market | |||
| Orlistat | Roche, GSK | Pancreatic lipase inhibitor | Approved for long-term use in 1999 |
| Phentermine | Not available | Adrenaline reuptake inhibitor | Schedule IV drug, approved for short-term use |
| Diethylpropion | Not available | Norepinephrine/dopamine releasing stimulator | Schedule IV drug, approved for short-term use |
| Benzphetamine | Pharmacia | Norepinephrine/dopamine releasing stimulator | Schedule III drug, approved for short-term use |
| Phendimetrazine | Not available | Norepinephrine/dopamine releasing stimulator | Schedule III drug, approved for short-term use |
| Anti-obesity drugs that await for decisions | |||
| Contrave | Orexigen | Bupropion+naltrexone | The FDA requested data on long-term cardiovascular risk assessment in 2011 |
| Qnexa | Vivus | Phentermine+topiramate | The FDA requested data on teratogenic potential in 2010 |
| Anti-obesity drugs rejected by the FDA | |||
| Rimonabant | Sanofi-Aventis | CB1R antagonist | Not approved in the USA due to its psychiatric sideeffects and withdrawn from the European market in 2009 for increased risk of serious psychiatric disorders |
| Lorcaserin | Arena Pharma | Selective 5-HT2C receptor agonist | Not approved due to concerns over carcinogenicity observed in rats in 2010 |
| Anti-obesity drugs withdrawn from the market | |||
| Fenfluramine and dexfenfluramine | Wyeth-Ayerst | 5-HT2B receptor agonist | Withdrawn after reports of valvular heart damage and primary pulmonary hypertension in 1997 |
| Phenylpropanolamine | Not available | Norepinephrine/dopamine releasing stimulator | Withdrawn for increased risk of hemorrhagic stroke in 2000 |
| Sibutramine | Abbott | NA/5-HT reuptake blocker | Withdrawn for increased risk of cardiovascular events in 2010 |
5-HT, 5-hydroxytryptamine; NA, noradrenaline; CB1R, cannabinoid 1 receptor; FDA, Food and Drug Administration; GSK, GlaxoSmithKline.