Table 1.
Mechanism | Drug | Approved for obesity, either alone, or in combination | Favourable psychotropic effects | Unfavourable psychotropic effects | Euphoria or addiction |
---|---|---|---|---|---|
1. PREVENTING NUTRIENT ABSORPTION | |||||
Lipase inhibitor | Orlistat | Yes | No | No | |
2. HOMEOSTASIS: ENERGY AND CARBOHYDRATE BALANCE | |||||
Glucagon-like peptide-1 analog | Liraglutide | Yes | No | No | |
3. CENTRAL EFFECTS | |||||
Potentiating catecholamines (blocking reuptake, enhancing release) | Stimulants: Phentermine Dexamphetamine | Yes No | Improvements in executive functioning, mood elevation, increased vigor/activity | Anger/hostility, depression, paranoia, hyperlocomotion, psychosis | Yes |
Bupropion | Yes | Improvements in executive functioning | Hyperlocomotion psychosis | Yes | |
Tesofensine | No | Mood elevation, increased vigor/activity | Anger/hostility | ||
Selective serotonin 2C receptor agonist | Lorcaserin | Yes | Reduces impulsive behavior | Fatigue, depression, cognitive impairment | |
Cannibinoid type 1 receptor blocker | Rimonabant Taranabant | No No | Increased vigor/activity | Anger/hostility, anxiety, depression, suicide risk | |
Mu-opioid receptor antagonist | Naltrexone | Yes | Reduces craving | ||
Anticonvulsant: mechanism of action in obesity unclear | Topiramate | Yes | Mood improvement | Sedation, cognitive impairment, depression, aggression, psychosis |
The psychotropic effects may be managed by appropriate dosage adjustments.