Naltrexone-Bupropion (Contrave) vs. Levitricram for Weight Loss
Naltrexone-bupropion (Contrave) is FDA-approved for weight loss with an average weight reduction of 3-6% of total body weight, while "Levitricram" is not a recognized medication for weight management. 1
Mechanism of Action and Efficacy
Naltrexone-Bupropion (Contrave)
- Mechanism: Bupropion stimulates hypothalamic proopiomelanocortin neurons while naltrexone blocks opioid-mediated autoinhibition, reducing food cue reactivity and improving eating control 1
- Efficacy:
- Produces moderate weight loss of approximately 3-6% compared to placebo (1%) at 56 weeks 1
- Mean percentage total body weight loss (TBWL) of 3.01% according to American Gastroenterological Association (AGA) guidelines 1
- Clinical trials showed significant weight loss with 32/360 mg/d dosing compared to placebo 1, 2
Levitricram
- Not an FDA-approved medication for weight loss
- No evidence in medical literature supporting its existence as a weight loss medication
- The term may be a confusion or misspelling of another medication
Administration and Dosing
Naltrexone-Bupropion (Contrave)
- Starting dose: Gradual titration over 4 weeks to minimize gastrointestinal side effects 3
- Maintenance dose: Naltrexone SR/bupropion SR 32/360 mg daily (usually divided as two tablets twice daily) 1, 3
- Administration: Oral tablets taken with food to reduce gastrointestinal side effects
Side Effects and Safety Profile
Naltrexone-Bupropion (Contrave)
- Common side effects: Nausea (most common), constipation, headache, dizziness, insomnia, dry mouth, vomiting 1, 3, 2
- Serious concerns:
- Increased treatment discontinuation due to adverse events (RR 2.39) compared to placebo 1
- Neuropsychiatric effects including risk of depression and suicidal ideation 4
- Modest increase in blood pressure and heart rate 4, 2
- Contraindicated with opioid use, seizure disorders, uncontrolled hypertension, and during pregnancy 3
- Should not be used within 14 days of MAOIs 1, 3
Monitoring and Follow-up
Naltrexone-Bupropion
- Efficacy assessment: If less than 5% weight loss after 12 weeks at maintenance dose, discontinue treatment 3
- Discontinuation: Gradual tapering recommended to minimize withdrawal symptoms 3
- Weeks 1-2: Reduce to 1 tablet twice daily
- Weeks 3-4: Reduce to 1 tablet daily
- Week 5: Complete discontinuation
- Monitoring: Regular assessment of blood pressure, heart rate, and mood changes 3
Comparative Efficacy with Other Weight Loss Medications
Naltrexone-bupropion produces less weight loss than newer medications:
- Less effective than semaglutide (10.76% TBWL) 1
- Less effective than liraglutide (4.81% TBWL) 1
- Less effective than phentermine-topiramate (8.45% TBWL) 1
- More effective than orlistat (2.8-4.8% weight loss) 1
Special Considerations
Potential Benefits Beyond Weight Loss
- May be particularly beneficial for patients with:
Contraindications
- Absolute contraindications include:
- Concurrent opioid use
- Seizure disorders
- Uncontrolled hypertension
- Use of MAOIs within 14 days
- Pregnancy 3
Clinical Decision Algorithm
Patient Selection:
- BMI ≥30 kg/m² or BMI ≥27 kg/m² with weight-related comorbidities
- No contraindications (seizure disorders, uncontrolled hypertension, opioid use)
- Consider for patients with comorbid depression or alcohol use disorder
Treatment Initiation:
- Start with gradual dose titration over 4 weeks
- Combine with comprehensive lifestyle intervention
Monitoring:
- Assess efficacy and safety monthly for first 3 months
- Continue only if ≥5% weight loss achieved at 12 weeks
- Monitor blood pressure, heart rate, and mood regularly
Discontinuation:
- If <5% weight loss after 12 weeks at full dose
- If intolerable side effects develop
- Use gradual tapering schedule when discontinuing
In conclusion, naltrexone-bupropion (Contrave) is a moderately effective FDA-approved medication for weight loss with specific benefits for certain patient populations, while Levitricram is not a recognized weight loss medication.