Buy Bupropion + Naltrexone
Bupropion + Naltrexone

2.11
This combination therapy is indicated for weight management in patients with secondary risk factors. It requires medical supervision as it influences neurotransmitters associated with reward and appetite. Patients must avoid abrupt discontinuation and monitor for mood shifts or neurological symptoms while on therapy.


Ingredients
Availability
In Stock
Delivery
Airmail (14-21 days) | EMS trackable (5-9 days)
Product is shipped in a fully discreet envelope with no content disclosure, including all required documentation inside

Product Sheet

Active Ingredient(s)
Bupropion, Naltrexone
Reference Brand
Bupropion + Naltrexone
Manufacturer
Takeda
Product Form
Tablet
Regulatory Classification
Rx
Primary Category
Weight Loss, Addiction Recovery
Product Category
Appetite suppressant
Pharmacological Class
Aminoketone and opioid antagonist
Clinical Indications
Weight management
Manufacturer Description
This combination therapy is indicated for weight management in patients with secondary risk factors. It requires medical supervision as it influences neurotransmitters associated with reward and appetite. Patients must avoid abrupt discontinuation and monitor for mood shifts or neurological symptoms while on therapy.
Mechanism of Action
Combines two agents to affect the brain's reward system. Bupropion acts as a dopamine and norepinephrine reuptake inhibitor to curb appetite, while naltrexone blocks opioid receptors to reduce cravings, collectively assisting with weight management.
Route of Administration
Oral
Onset Time
Initial weeks
Duration
24 hours
Contraindications
Uncontrolled high blood pressure, Seizure disorders, Eating disorders
Severe Adverse Events
Seizures, Suicidal ideation, Severe allergic reaction
Common Side Effects
Nausea, Constipation, Dizziness
Uncommon Side Effects
Insomnia, Dry mouth, Anxiety
Drug Interactions
MAO inhibitors, Opioids
Pregnancy Safety Warnings
Not recommended during pregnancy.
Age Restrictions
Adults only
Storage Guidelines
Store at room temperature below 25°C.
Related Products
Liraglutide, Orlistat

Bupropion + Naltrexone FAQ

What is the difference between this combination pill and taking bupropion and naltrexone separately?

The fixed-dose tablet delivers a low dose of bupropion (8 mg) together with a higher dose of naltrexone (90 mg) in a single capsule, simplifying the regimen and ensuring consistent drug ratios that have been studied for weight-loss efficacy.

Can I take this medication if I have a history of high blood pressure?

Patients with uncontrolled hypertension should avoid the combination. Those with well-managed blood pressure may be prescribed the drug after careful assessment and regular monitoring.

Will this medication affect my ability to pass a drug test for employment?

Bupropion and naltrexone are not typically screened for in standard workplace drug tests. However, any unexpected results should be discussed with the testing authority, providing a prescription note if needed.

Is it safe to travel internationally with this prescription?

Yes, provided you carry a valid prescription, the original pharmacy labeling, and declare the medication at customs if required by Hong Kong or the destination country's regulations.

How long does it take to see weight-loss results?

Clinical studies show that noticeable weight reduction often begins within the first 8-12 weeks, but individual results vary and depend on adherence to diet and exercise recommendations.

Can I drink alcohol while on this medication?

Moderate alcohol consumption is permissible, but excessive intake may increase seizure risk and diminish the medication’s effectiveness. Discuss your drinking habits with your prescriber.

What should I do if I experience severe insomnia?

Take the tablet early in the morning and avoid late-day dosing. If insomnia persists, contact your healthcare provider for possible dose adjustment or alternative therapy.

Are there any inactive ingredients that might cause allergies?

Common fillers include lactose, microcrystalline cellulose, and magnesium stearate. If you have known sensitivities, verify the excipient list with your pharmacist.

Does this medication interact with birth-control pills?

No clinically significant interaction has been identified between the combination and hormonal contraceptives; however, always inform your clinician of all concurrent medications.

Will my insurance cover this medication in Hong Kong?

Coverage depends on individual health plans and the prescribed indication. Check with your insurer or hospital pharmacy for reimbursement details.

Bupropion + Naltrexone: What Is This Medication?

Bupropion + Naltrexone is a fixed-dose combination pill that contains two active ingredients: bupropion and naltrexone. The tablet is marketed for adults seeking weight-loss support and is also relevant to the management of addiction-related conditions such as smoking cessation. In Hong Kong, the product is classified as a prescription medication and must be prescribed by a qualified healthcare professional.

  • Active ingredients: bupropion (8 mg) + naltrexone (90 mg) per tablet
  • Formulation: oral pill
  • Strength available: 8 mg / 90 mg (single tablet)
  • Regulatory body: Hong Kong Department of Health (HKDoH)

The combination leverages the distinct mechanisms of each component to address appetite regulation and reward pathways that underpin overeating and substance use.

How Bupropion + Naltrexone Works in the Body

Bupropion is a norepinephrine-dopamine reuptake inhibitor (NDRI). By blocking the reabsorption of these neurotransmitters, it increases their levels in synaptic clefts, which can reduce cravings and improve mood. Naltrexone is an opioid receptor antagonist; it blocks µ-opioid receptors that are involved in the brain’s reward circuitry. When combined, the two agents produce a synergistic effect:

  • Bupropion stimulates the release of pro-appetitive neuropeptides (e.g., PYY) and dampens appetite-stimulating signals.
  • Naltrexone curtails the reward response that often drives binge eating and nicotine use.

Together, they help to diminish both the physiological drive to eat and the psychological reinforcement that sustains unhealthy eating or smoking habits. Onset of action is typically within the first week, with peak therapeutic effects observed after several weeks of consistent dosing.

Conditions Treated by Bupropion + Naltrexone

Approved Medical Uses

In Hong Kong, the combination is approved for chronic weight management in adults with a body mass index (BMI) ≥ 30 kg/m², or ≥ 27 kg/m² with at least one weight-related comorbidity (e.g., hypertension, dyslipidaemia, type 2 diabetes). The medication is intended as an adjunct to a reduced-calorie diet and increased physical activity.

  • Primary indication: Long-term obesity treatment under medical supervision.
  • Secondary benefit: The bupropion component is individually approved for smoking cessation; clinicians may consider the combination for patients who have concurrent weight-management and smoking-cessation goals, though this latter use is not an official indication.

Off-Label and Investigational Applications

  • Smoking cessation adjunct: Small clinical studies have explored the combination as a dual-purpose therapy for patients who wish to quit smoking while losing weight. This use is off-label and not approved by the HKDoH.
  • Disclaimer: Off-label use requires careful medical supervision, assessment of risks, and monitoring for adverse effects.

Other off-label investigations (e.g., alcohol-use disorder) exist, but evidence remains limited. Healthcare providers should evaluate the risk-benefit profile for each individual.

Who Should (Not) Use Bupropion + Naltrexone?

Ideal Patient Profile

  • Adults (≥ 18 years) with a BMI meeting the approved criteria.
  • Individuals motivated to adopt lifestyle changes (diet, exercise).
  • Patients without uncontrolled psychiatric conditions or severe cardiovascular disease.

Absolute Contraindications

  • Known hypersensitivity to bupropion, naltrexone, or any tablet excipients.
  • Current or prior diagnosis of bulimia nervosa or anorexia nervosa (risk of seizure).
  • Severe uncontrolled hypertension (SBP > 180 mmHg or DBP > 110 mmHg).
  • Concurrent use of monoamine oxidase inhibitors (MAOIs) or any medication that lowers seizure threshold.
  • Pregnancy (first trimester) and breastfeeding without explicit medical justification.

Relative Contraindications & Special Populations

  • History of seizure disorder - use only if benefits outweigh risks.
  • Renal or hepatic impairment - dose adjustments may be needed; close monitoring required.
  • Elderly - start at the lowest effective dose; monitor for blood pressure changes.
  • Psychiatric conditions (e.g., bipolar disorder) - evaluate for potential mood destabilisation.

If any of these conditions apply, a thorough assessment by a prescriber is essential before initiating therapy.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Dry mouth - often transient; stay hydrated.
  • Nausea or upset stomach - may improve after several days.
  • Insomnia - take the tablet early in the day to minimise sleep disturbance.
  • Headache - usually mild and self-limiting.

Serious Adverse Events

  • Seizures - risk increased in patients with eating disorders or on high-dose bupropion.
  • Elevated blood pressure - monitor weekly during titration; seek medical attention for severe hypertension.
  • Hepatotoxicity - rare; watch for jaundice or unexplained fatigue.
  • Allergic reactions - rash, pruritus, or swelling require immediate medical evaluation.

Drug Interactions

  • Major interactions:
  • MAO inhibitors - concurrent use can precipitate hypertensive crises.
  • CYP2B6 substrates (e.g., efavirenz, cyclophosphamide) - bupropion may increase their plasma levels.
  • Moderate interactions:
  • Opioid analgesics - naltrexone blocks opioid effects; patients using prescribed opioids may experience reduced analgesia.
  • Antidepressants (SSRIs, SNRIs) - monitor for additive serotonergic effects.

Patients should disclose all prescription, over-the-counter, and herbal products before starting therapy.

Food and Lifestyle Interactions

  • Alcohol: Moderate consumption is acceptable, but excessive intake may heighten seizure risk.
  • Caffeine: No direct interaction, but excess caffeine may exacerbate insomnia.
  • Driving/Machinery: Most patients are not impaired; however, dizziness can occur, especially at treatment initiation.

How to Take Bupropion + Naltrexone

  • Formulation: Each tablet delivers 8 mg bupropion and 90 mg naltrexone.
  • Standard dosing protocol (HKDoH-approved):
  • Week 1: One tablet taken once daily in the morning.
  • Weeks 2-3: Increase to two tablets daily (one in the morning, one in the early afternoon).
  • Maximum: Two tablets per day (total 16 mg/180 mg).
  • Administration tips:
  • Swallow the tablet whole with a full glass of water.
  • Take with or without food; consistency each day aids tolerability.
  • Do not split, crush, or chew the tablet.
  • Missed dose: Take the missed tablet as soon as remembered, unless it is close to the next scheduled dose; do not double-dose.
  • Overdose: Symptoms may include seizures, rapid heart rate, severe hypertension, or loss of consciousness. Seek emergency medical care immediately; supportive measures and, if indicated, intravenous benzodiazepines are used for seizure control.
  • Discontinuation: Gradual tapering is advised for patients on the maximum dose to reduce the risk of withdrawal-related mood changes.

Dosing must be individualized by a prescriber based on blood pressure, seizure risk, and overall treatment response.

Monitoring and Follow-Up

  • Blood pressure: Check weekly during dose escalation, then every 1-2 months once stable.
  • Weight and BMI: Document baseline weight and monitor weekly for the first month, then monthly.
  • Liver function tests (LFTs): Baseline and periodic testing if pre-existing hepatic disease.
  • Psychiatric assessment: Evaluate mood and any suicidal ideation, especially in the first few weeks.
  • Seizure surveillance: Promptly report any episodes of loss of consciousness or convulsions.

Regular follow-up visits enable dose adjustments, reinforcement of lifestyle changes, and early detection of adverse events.

Storage and Handling

  • Store at room temperature (15-30 °C), protected from moisture and direct sunlight.
  • Keep the bottle tightly closed and out of reach of children.
  • Do not use the medication after the printed expiration date.
  • Dispose of unused tablets according to local pharmaceutical waste guidelines or return them to a pharmacy for safe disposal.

Medication-Specific Glossary

Monoamine transporter inhibition
The process by which bupropion blocks reuptake of norepinephrine and dopamine, increasing their extracellular concentrations.
Opioid receptor antagonism
Naltrexone’s ability to bind to µ-opioid receptors without activating them, thereby blocking the rewarding effects of endogenous and exogenous opioids.
Therapeutic window
The dosage range in which a medication provides clinical benefit with an acceptable safety profile; for this combination, the window is defined by the 8 mg/90 mg tablet up to a maximum of two tablets daily.
QT prolongation
A lengthening of the heart’s electrical repolarisation interval, which can increase the risk of arrhythmias; bupropion may modestly affect QT interval in susceptible individuals.

Medical Disclaimer

This article provides educational information about Bupropion + Naltrexone and is not a substitute for professional medical advice. Treatment decisions, including use for unapproved indications, must be made under the guidance of a qualified healthcare provider. The content is intended for informational purposes and does not constitute medical recommendations. Always consult a physician before starting, stopping, or changing any medication regimen.

Categories