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Contrave

2.11
A weight management aid that works on the brain to help reduce food cravings and control appetite.


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

Alternative/Local Brand
Mysimba
Active Ingredient(s)
Naltrexone, Bupropion
Primary Category
Weight Management
Therapeutic Class
Anti-obesity preparations
Pharmacological Class
Opioid antagonist and aminoketone antidepressant combination
Indications
Weight management in adults with obesity, Overweight with weight-related complications
Contraindications
Uncontrolled high blood pressure, Seizure disorders, Eating disorders (Bulimia/Anorexia), Opioid withdrawal
Minor Side Effects
Nausea, Dry mouth, Headache
Moderate Side Effects
Constipation, Dizziness, Insomnia, Anxiety
Serious Side Effects
Seizures, Suicidal thoughts, Severe allergic reactions, Glaucoma
Dosage Forms
Prolonged-release tablet
Administration Route
Oral
Mechanism of Action
This drug combines two medicines that target the reward system and hunger centres in the brain to reduce appetite and food cravings, helping people stick to a reduced-calorie diet.
Prescription Status
Rx
Patient Summary
A weight management aid that works on the brain to help reduce food cravings and control appetite.
Onset Time
Variable; weight loss usually seen within weeks
Duration
12-24 hours per dose
Storage Instructions
Store below 25°C.
Drug Interactions
Opioids, Alcohol, MAO inhibitors, Theophylline, Steroids
Age Restrictions
Only for adults aged 18 and over.
Pregnancy Use
Contraindicated in pregnancy.
Alternative Drugs
Orlistat, Liraglutide (Saxenda), Semaglutide (Wegovy)

Contrave: Generic Medication Overview

Contrave is a prescription pill that combines two active ingredients-naltrexone (8 mg) and bupropion (90 mg). It belongs to the therapeutic categories of addiction & quit-smoking and weight-loss management. In Hong Kong, Contrave is classified as a prescription medication and is regulated by the Department of Health, with its approval aligned with standards used by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). The product is marketed in a single tablet strength of 8 mg/90 mg.

How Contrave Works in the Body

Contrave targets two neural pathways that influence appetite and reward:

  • Naltrexone is an opioid-receptor antagonist. By blocking the μ-opioid receptors in the brain’s reward centers, it reduces the pleasure associated with eating, especially high-calorie foods.
  • Bupropion is a norepinephrine-dopamine reuptake inhibitor (NDRI). It increases the activity of these neurotransmitters in the hypothalamus, which helps to suppress hunger and boost energy expenditure.

Together, the combination dampens cravings while promoting satiety. The onset of effect typically begins within a few days, with maximal weight-loss benefit observed after several weeks of consistent use. Both ingredients are absorbed well from the gastrointestinal tract, and bupropion is metabolized primarily by the CYP2B6 enzyme, while naltrexone undergoes hepatic metabolism via glucuronidation.

Conditions Treated by Contrave

Contrave is officially approved for chronic weight management in adults who meet one of the following criteria:

  • Body-mass index (BMI) ≥ 30 kg/m² (obesity)
  • BMI ≥ 27 kg/m² (overweight) with at least one weight-related comorbidity such as hypertension, type 2 diabetes, or dyslipidaemia.

The medication is intended to be used alongside a reduced-calorie diet and increased physical activity. While both naltrexone and bupropion have individual approvals for addiction-related indications (naltrexone for alcohol dependence, bupropion for smoking cessation), Contrave itself is not approved for smoking cessation or alcohol-use disorder in Hong Kong.

Evidence-Based Off-Label Uses

  • Alcohol-Use Disorder: Small clinical studies have explored the combination for reducing alcohol cravings, but evidence is limited and the use remains off-label.
  • Smoking Cessation: Bupropion alone is an established smoking-cessation aid; adding naltrexone has been investigated in research settings, yet Contrave is not approved for this purpose.

Off-label use requires close medical supervision and individualized risk assessment.

Evaluating Contrave for Your Health Profile

Ideal Candidates

  • Adults with BMI ≥ 30 kg/m² or BMI ≥ 27 kg/m² plus a relevant comorbidity.
  • Individuals who have not achieved satisfactory weight loss through diet and exercise alone.
  • Patients without a history of seizure disorders, uncontrolled hypertension, or active opioid therapy.

Absolute Contraindications

  • Allergy to naltrexone, bupropion, or any tablet excipients.
  • Current use of opioid analgesics, opioid dependence, or recent opioid discontinuation (within 7 days).
  • Current or past diagnosis of seizure disorder, eating disorders (e.g., bulimia, anorexia nervosa), or uncontrolled hypertension.
  • Pregnancy or breastfeeding (both ingredients cross the placenta and are present in breast milk).

Relative Contraindications & Special Populations

  • Renal or hepatic impairment: Dose adjustments may be required; clinicians should assess kidney and liver function before initiating therapy.
  • Elderly patients: Start at the lowest tolerated dose and monitor for blood pressure changes.
  • Patients on monoamine-oxidase inhibitors (MAOIs): Bupropion can increase the risk of hypertensive reactions; a wash-out period of at least 14 days is recommended.

If you fall into any of these categories, discuss alternative weight-management strategies with your healthcare provider.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Nausea, constipation, or dry mouth (often mild and transient).
  • Insomnia or abnormal dreams (related to bupropion’s stimulant effect).
  • Headache or dizziness (generally resolves within a few weeks).

Serious Adverse Events

  • Seizures: Bupropion lowers the seizure threshold; the risk rises with higher doses or pre-existing risk factors.
  • Hypertensive crisis: May occur when bupropion is combined with MAOIs or certain sympathomimetic agents.
  • Suicidal thoughts: Bupropion carries a boxed warning for increased suicidal ideation in younger adults; monitor mood changes closely.

Drug Interactions

  • Major: Concurrent use with MAOIs, other opioid antagonists, or medications that also lower seizure threshold (e.g., tramadol, certain antipsychotics).
  • Moderate: CYP2B6 inhibitors (e.g., clopidogrel) can increase bupropion levels; dose adjustment may be needed.
  • Food and Lifestyle Interactions: Alcohol can enhance the central nervous system effects of bupropion and increase seizure risk; limit intake while on Contrave. Caffeine may exacerbate insomnia.

Patients should provide a complete medication list-including over-the-counter drugs, supplements, and herbal products-to their prescriber.

How to Take Contrave

  • Standard dosing schedule:

  • Week 1: One tablet daily.

  • Week 2: Two tablets daily (one in the morning, one in the evening).

  • Week 3 onward: Three tablets daily (morning, midday, evening).

  • Administration tips: Swallow each tablet whole with a full glass of water. The medication can be taken with or without food, but taking it with food may reduce nausea.

  • Missed dose: If you miss a dose, take the missed tablet as soon as you remember, unless it is close to the next scheduled dose. Do not double up.

  • Overdose: Symptoms may include seizures, rapid heart rate, high blood pressure, or severe nausea. Seek emergency medical care; supportive care and activated charcoal are typical first-line measures.

  • Discontinuation: Abrupt cessation is permissible, but a gradual taper may reduce the likelihood of rebound weight gain. Discuss tapering with your prescriber.

Monitoring and Follow-Up

  • Baseline assessments: Weight, BMI, blood pressure, heart rate, and a review of psychiatric history.
  • Routine monitoring:
  • Weight & BMI: Every 2-4 weeks during the initial phase, then quarterly.
  • Blood pressure: At each follow-up visit, especially during dose escalation.
  • Mental health: Screen for mood changes or suicidal ideation at each encounter.

If any adverse reaction or inadequate weight loss (less than 5 % of baseline weight after 12 weeks) occurs, your clinician may reassess the treatment plan.

Storage and Handling

  • Keep the tablets in their original container, tightly closed.
  • Store at room temperature (15 °C-30 °C), away from excess moisture and direct sunlight.
  • Do not use the medication after the printed expiration date.
  • Dispose of unused tablets according to local pharmacy take-back programs or household hazardous waste guidelines.

Medication-Specific Glossary

Naltrexone
An opioid-receptor antagonist that blocks the rewarding effects of substances that act on μ-opioid receptors, thereby dampening cravings.
Bupropion
A norepinephrine-dopamine reuptake inhibitor that raises levels of these neurotransmitters in the brain, aiding appetite control and mood regulation.
Seizure Threshold
The level of neuronal excitability at which a seizure can be triggered; bupropion lowers this threshold.
Monoamine Oxidase Inhibitor (MAOI)
A class of antidepressants that inhibit the enzyme monoamine oxidase, increasing levels of serotonin, norepinephrine, and dopamine; combining MAOIs with bupropion can raise blood pressure dramatically.
Boxed Warning
The FDA’s most prominent safety alert, highlighting serious or life-threatening risks associated with a medication.

Medical Disclaimer

This article provides educational information about Contrave 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.

Contrave FAQ

Can Contrave be used without a diet or exercise plan?

Contrave is intended to complement a reduced-calorie diet and regular physical activity. Using the medication alone typically yields modest weight loss, whereas combined lifestyle changes enhance effectiveness.

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

Most patients notice a gradual reduction in weight within the first 12 weeks; clinically significant loss (≥ 5 % of baseline weight) is often observed after 6 months of consistent use.

Is Contrave safe for people with a history of depression?

Bupropion has antidepressant properties, but it can also cause mood swings or suicidal thoughts, especially in younger adults. Close monitoring by a healthcare professional is essential.

What should I do if I experience a seizure while on Contrave?

Seek emergency medical care immediately. Inform the medical team that you are taking bupropion, as it may influence treatment decisions.

Can I drink alcohol while taking Contrave?

Alcohol may increase the risk of seizures and exacerbate side effects such as dizziness and nausea. Limit alcohol intake and discuss any consumption with your prescriber.

Will Contrave affect my blood sugar if I have diabetes?

Contrave does not directly raise blood glucose, and weight loss can improve glycaemic control. However, monitor blood sugar regularly and inform your diabetes care team of any medication changes.

Are there any known drug-test interferences with Contrave?

Bupropion and its metabolites can be detected in urine drug screens, potentially leading to a positive result for stimulants. Notify testing agencies of your prescription if relevant.

How does Contrave differ from other weight-loss drugs like orlistat?

Contrave acts centrally on appetite and reward pathways, while orlistat works peripherally by inhibiting fat absorption in the gut. The mechanisms, side-effect profiles, and dosing regimens are distinct.

Can I travel with Contrave on an international flight?

Yes, but keep the medication in its original packaging with the prescription label, and carry a copy of the prescription. Check the destination country’s import regulations for prescription drugs.

What should I do if I miss an entire week’s dose during the titration phase?

Contact your prescriber before restarting. Typically, you would repeat the missed week’s dosing schedule rather than jumping ahead, to minimise side-effect risk.

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