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Atlanta, Georgia | Naltrexone Treatment Guide

Naltrexone Treatment for Atlanta Residents: Oral Naltrexone vs Vivitrol vs Long-Acting Naltrexone Implant

DeBinge opioid transition: When travelling to DeBinge in The Bahamas for OLANI treatment, there is no requirement to complete a separate opioid-free waiting window before arrival. DeBinge uses a medically supervised 4-to-5-day buprenorphine transition. Buprenorphine is introduced to bridge the patient away from full-agonist opioids, stabilised and tapered over the first several days, and the O’Neil Long-Acting Naltrexone Implant is typically inserted around day 4 or 5 while buprenorphine is still being tapered. The planned overlap continues as buprenorphine clears and the implant gradually releases naltrexone. This pathway is clinician-supervised because mistimed naltrexone exposure can precipitate withdrawal.

Based on DeBinge’s clinical experience in The Bahamas since 2018, the implant typically provides its strongest craving and relapse-prevention support on average 9 months, while clinically meaningful opioid-receptor blockade may persist for longer, in some patients up to about 15 months. This longer blockade may continue to reduce opioid effects and overdose risk.

Ongoing recovery: The implant is not a cure. The DeBinge programme includes a full year of professional counselling after implantation to address the behavioural and psychological side of addiction.

If you live in Atlanta and are researching naltrexone for alcohol or opioid recovery, one of the first things you may discover is that “naltrexone treatment” can mean several different things. There are tablets taken regularly, extended-release injections such as Vivitrol, and longer-acting implant formulations used in certain settings outside the United States.

The medication is the same in principle, but the way it is delivered can substantially change adherence, treatment duration, preparation, follow-up and what happens if you decide to stop treatment.

Important: This guide is educational. It does not determine whether naltrexone, Vivitrol, an implant, or any other medication is appropriate for you. That requires an individual medical assessment.
In this guide

Understanding Your Options Before Choosing a Treatment Path

The Atlanta treatment landscape

Why Atlanta Patients Are Researching Naltrexone

People throughout Atlanta, Buckhead, Midtown, Sandy Springs, Marietta, Decatur, Alpharetta, Roswell and the wider Metro Atlanta area already have access to established hospitals, addiction physicians, outpatient programs, counseling and medication-based treatment. Local services may be exactly the right choice for many patients.

The questions often become more specific after someone has already learned the basics. A person may know that naltrexone exists but still want to understand why one patient takes a tablet, another receives a monthly Vivitrol injection, and another investigates a longer-acting implant outside the United States.

This distinction matters because treatment is not simply about selecting a drug. It is also about how reliably medication will remain active, how the patient will manage appointments, what medical preparation is required and what recovery support will continue after the medication is started.

01

Medication

Understand what naltrexone does and what it cannot do.

02

Delivery

Compare daily oral dosing, approximately monthly injection and longer sustained release.

03

Recovery

Plan counseling, support, mental-health care and relapse prevention around the medication.

Atlanta and Georgia residents who want to understand how an international treatment option could fit into this wider picture can review the main guide to addiction treatment options for Atlanta residents.

The basic science

What Does Naltrexone Actually Do?

Naltrexone is an opioid antagonist. Rather than activating opioid receptors, it occupies them and blocks or substantially reduces the effects of opioids such as heroin and many prescription opioid medications while adequate medication levels are present.

This is fundamentally different from methadone and buprenorphine, which interact with opioid receptors as agonist or partial agonist medications. Naltrexone does not produce an opioid high and is not itself an opioid.

For opioid use disorder, the blockade can reduce the rewarding effects a person would otherwise experience if opioids were taken. Naltrexone may also reduce opioid craving in some patients. However, the blockade should never be deliberately tested by taking progressively larger amounts of opioids. Attempting to overpower naltrexone can result in serious or fatal overdose.1

For alcohol use disorder, the mechanism is more complex. Naltrexone’s interaction with the endogenous opioid system can reduce some of alcohol’s reinforcing or rewarding effects and can help some people reduce heavy drinking or maintain abstinence as part of a broader treatment plan.2

Naltrexone does not erase addiction. It does not automatically change stress responses, relationships, learned habits, trauma, social environments or the reasons substance use became established. This is why medical guidance describes medication as one component of comprehensive treatment rather than a replacement for counseling and behavioral recovery work.
Option one

Oral Naltrexone: Regular Dosing With More Day-to-Day Responsibility

Oral naltrexone is supplied as a tablet and is commonly prescribed on a regular schedule, often daily. It has established uses in alcohol dependence and opioid blockade, with the exact treatment plan determined by the prescribing clinician.3

The major practical advantage of a tablet is flexibility. A doctor can prescribe it without a procedure, adherence can be reviewed frequently, and treatment can be changed or stopped when clinically appropriate.

The disadvantage is closely connected to the same flexibility: the medication only works when it is actually taken as prescribed. Someone must remember the dose and remain willing to take it on days when motivation is low, cravings increase or the idea of returning to substance use becomes stronger.

Potential practical advantages

  • No injection or implantation procedure.
  • Allows relatively straightforward medication adjustment.
  • Can fit well for someone with reliable medication routines.
  • Widely familiar to U.S. prescribers.

Questions to consider

  • Will doses realistically be taken consistently?
  • Who will monitor side effects and progress?
  • What happens if medication is repeatedly missed?
  • What counseling and recovery support accompany it?

Adherence has historically been an important limitation of oral naltrexone, particularly in opioid-use treatment. A medication cannot maintain receptor blockade during periods when it is not being taken. This adherence problem is one reason longer-acting formulations were developed.

Option two

Vivitrol: Extended-Release Injectable Naltrexone

Vivitrol is an extended-release intramuscular formulation of naltrexone. It is generally administered once every four weeks by a healthcare professional and is FDA-approved in the United States for alcohol dependence and prevention of relapse to opioid dependence following opioid detoxification.

Because medication is released over an extended period, a patient does not have to decide each morning whether to take a tablet. This can address one major adherence challenge associated with oral treatment.

One monthly injection does not eliminate the need for follow-up

A longer dosing interval can reduce daily medication decisions, but patients still need scheduled injections, clinical review and a plan for counseling, behavioral change and recovery support. Missing the next injection can create a gap in medication coverage.

The opioid-free period before starting Vivitrol is critical

A patient who is physically dependent on opioids cannot simply receive Vivitrol immediately. Giving naltrexone while opioids remain in the body can abruptly displace opioids from receptors and precipitate withdrawal.

The FDA prescribing information for extended-release injectable naltrexone recommends an opioid-free interval before treatment; this describes standard U.S. injectable-naltrexone initiation and is not the DeBinge OLANI transition protocol. At DeBinge, opioid-dependent patients are transitioned under medical supervision using buprenorphine, which is stabilised and tapered over the first several days. The O’Neil Long-Acting Naltrexone Implant is typically inserted around day 4 or 5 while buprenorphine is still being tapered, followed by a planned overlap through days 5–7 as buprenorphine clears and the implant gradually releases naltrexone. Timing is individualized because mistimed naltrexone can precipitate withdrawal.1

SAMHSA similarly emphasizes that extended-release injectable naltrexone should be used as part of comprehensive treatment that includes behavioral healthcare and appropriate medical evaluation.4

Option three

What Is a Long-Acting Naltrexone Implant?

A naltrexone implant is a sustained-release formulation designed to be placed beneath the skin and release naltrexone over a longer period than an oral tablet or monthly injection. The exact duration, dose, formulation and clinical evidence vary between implant products, so the phrase “naltrexone implant” should not be treated as though it describes one standardized medication.

The practical concept is straightforward: instead of requiring a patient to take a tablet each day or return for another injection approximately every month, an implant is intended to maintain naltrexone exposure for a longer period.

Research has investigated implant formulations lasting for months, and randomized and observational research has explored whether sustained delivery can address adherence problems seen with oral naltrexone.5 However, evidence varies by formulation, study population and product, and findings from one implant cannot automatically be applied to every other implant.

Regulatory distinction for U.S. readers

Naltrexone implant products are not FDA-approved in the United States. Oral naltrexone and extended-release injectable naltrexone are established U.S. formulations, while implant products remain investigational in the U.S. regulatory context. Current U.S. clinical research continues to evaluate implant formulations.6

DeBinge treatment involving a long-acting naltrexone implant takes place in Nassau, The Bahamas. DeBinge does not operate an implant clinic in Atlanta or elsewhere in Georgia.

For Atlanta residents investigating this route, the question should therefore be broader than “Does the implant last longer?” A careful discussion should include the specific formulation, clinical evidence, regulatory status, preparation requirements, procedure, adverse effects, monitoring, expected duration, pain-management implications and recovery support after returning home.

The DeBinge treatment pathway for Atlanta residents explains how assessment, preparation, treatment in Nassau and continuing recovery in Georgia are intended to connect.

Side-by-side comparison

Oral Naltrexone vs Vivitrol vs Long-Acting Implant

Feature Oral naltrexone Vivitrol / XR injection Long-acting implant
How it is given Tablet taken according to the prescribed schedule. Intramuscular injection administered by a healthcare professional. Implant placed under the skin according to the specific product and procedure.
Typical dosing interval Often daily. Approximately every four weeks. Potentially months, depending on the specific formulation.
Daily adherence requirement High. The patient must continue taking tablets as prescribed. No daily tablet during the active injection period. No daily tablet while the implant is providing medication exposure.
U.S. regulatory position Oral naltrexone is an established FDA-regulated prescription formulation. FDA-approved for specified alcohol and opioid-dependence indications. Naltrexone implants are not FDA-approved in the United States.
Opioid preparation Requires an adequate opioid-free period where opioid dependence is relevant. Requires an adequate opioid-free period to avoid precipitated withdrawal. Also requires appropriate assessment and opioid-free preparation.
Main adherence issue Remembering and choosing to take medication consistently. Returning on schedule for subsequent injections. Daily adherence is reduced, but procedural, medical and longer-term planning become especially important.
Recovery support Still needed. Still needed. Still needed.
Longer-acting does not automatically mean better for every patient. Duration can solve one problem, such as repeatedly remembering medication, while creating different considerations around medical screening, procedures, adverse effects, pain treatment and follow-up. Treatment selection should be individualized.
A practical difference that matters

Adherence: Why the Length of Treatment Delivery Matters

One of the most important differences between formulations is not the molecular action of naltrexone but how often a patient has to make another decision to continue it.

With oral treatment, that decision may occur every day. With Vivitrol, it generally occurs when the next monthly appointment is due. A longer-acting implant can extend the time before another dosing decision is required.

This matters because motivation is not perfectly stable during recovery. Someone may be committed to treatment today but experience a high-risk period months later after relationship problems, work stress, isolation, exposure to old contacts or renewed cravings.

Reducing the number of opportunities to discontinue medication impulsively can be clinically relevant for some patients. At the same time, longer medication exposure means the decision before treatment deserves more careful consideration.

Daily

More flexibility, but more repeated decisions about adherence.

Monthly

Fewer medication decisions, with scheduled repeat appointments.

Longer acting

Potentially fewer dosing decisions, with greater importance placed on appropriate selection before treatment.

Opioid safety

What Happens if Someone Tries to Use Opioids While Naltrexone Is Active?

When adequate naltrexone levels are present, opioid receptors are blocked. A person taking heroin, fentanyl or another opioid may therefore experience substantially less of the expected opioid effect.

That does not mean opioids become safe.

Never try to overpower the blockade

Naltrexone’s blockade is competitive and can potentially be overcome with sufficiently high opioid concentrations. Attempting to defeat it by taking increasingly large amounts can lead to life-threatening opioid poisoning and fatal respiratory depression.

A person should also make sure healthcare professionals know about naltrexone treatment if emergency pain management, surgery or another situation involving opioid analgesics arises. Pain management while opioid receptors are blocked can require specialist planning.

Someone receiving naltrexone should discuss naloxone access and overdose preparation with a clinician, particularly where there is any possibility of opioid exposure.

An often misunderstood risk

Opioid Tolerance Can Fall During Treatment

Naltrexone does not preserve a person’s previous opioid tolerance. After a period without opioids, the body may become more sensitive to amounts that were previously tolerated.

This creates particular risk when medication exposure declines, a Vivitrol dosing interval ends, treatment is discontinued or a person returns to opioid use after a prolonged period of abstinence.

The FDA warns that patients can be vulnerable to potentially fatal overdose after Vivitrol treatment because reduced tolerance means a previously used dose may now be dangerous.1

Blockade is not the same as permanent overdose protection

Naltrexone should never be described as making opioid use safe. Overdose risk remains relevant during treatment, when someone tries to overcome receptor blockade, and after medication levels fall. Recovery planning should include overdose education and access to naloxone where opioid exposure is possible.

Alcohol use disorder

How Naltrexone Is Used in Alcohol Treatment

Naltrexone is also used in the treatment of alcohol use disorder. Oral naltrexone and extended-release injectable naltrexone are among the FDA-approved medication options for AUD in the United States.2

The treatment goal is not to create sickness when alcohol is consumed. That is a different pharmacological strategy associated with disulfiram. Naltrexone instead influences reward-related pathways and can help some patients reduce drinking, heavy-drinking risk or craving.

Results vary. Some people respond substantially; others obtain less benefit. A clinician should consider drinking pattern, treatment goals, other medications, physical health, liver-related considerations, possible opioid use and the wider recovery plan.

Naltrexone is not an alcohol-detox medication. If a person has developed physical alcohol dependence, suddenly stopping alcohol can cause dangerous withdrawal, including seizures or delirium in severe cases. Withdrawal risk should be assessed medically before treatment or international travel.

This distinction is especially important for Atlanta residents considering treatment in Nassau. Travel should follow clinical preparation rather than become the reason someone abruptly stops alcohol or opioids without an appropriate plan.

Before treatment

Who May Need a Different Plan or Further Medical Assessment?

Naltrexone is not appropriate in every situation. A clinician needs enough information to identify contraindications, risks and alternative treatment options.

Opioid-related factors

Current opioid use, physical opioid dependence, acute opioid withdrawal, treatment with methadone or buprenorphine, opioid-containing medication or anticipated opioid pain treatment can significantly affect whether and when naltrexone can be used.

Medical factors

Liver health, other medications, previous reactions to naltrexone, pregnancy-related considerations, upcoming procedures and significant physical or psychiatric conditions should be discussed with a qualified clinician.

Medical screening should answer more than one question

  • What substances are currently being used?
  • When was the last opioid exposure?
  • Is physical dependence present?
  • Is withdrawal likely to require medical management?
  • Are methadone, buprenorphine, opioid pain medications or other relevant drugs being taken?
  • What happened during previous treatment attempts?
  • Are there liver or other medical concerns requiring review?
  • What mental-health treatment or support is needed?
  • What will happen after medication treatment begins?

No online article or quiz can safely determine those answers for an individual patient.

Beyond medication

Why Naltrexone Alone Does Not Constitute Recovery

A medication can change the biological consequences of taking a substance. It cannot automatically rebuild daily life.

Someone may still return home to the same relationship problems, financial pressures, social circle, loneliness, work stress, insomnia, anxiety, depression, trauma reminders or environments previously associated with substance use.

This is why SAMHSA describes naltrexone as one part of a comprehensive treatment plan that includes counseling and other behavioral-health treatment.4

Counseling

Work on triggers, behavior, coping skills, relationships and patterns associated with substance use.

Support

Build appropriate family, peer, clinical and community support instead of relying on medication alone.

Relapse planning

Know what to do if cravings increase, appointments are missed or substance use resumes.

The objective is not to expect medication to do the psychological and behavioral work. A more realistic model is to use medication, when appropriate, as one layer of protection while the person develops the skills and structure needed for longer-term recovery.

For Georgia residents

How Treatment Planning Can Work From Atlanta to Nassau

Atlanta residents researching an implant need to understand an important geographical distinction: DeBinge does not operate a medical clinic in Atlanta. Treatment involving the implant takes place in Nassau, The Bahamas.

The practical pathway should therefore begin before a flight is booked.

STEP 01

Atlanta

Research options and discuss your substance-use and treatment history.

STEP 02

Preparation

Determine what medical assessment, detoxification or other preparation is required.

STEP 03

Nassau

Travel only after the clinical pathway and timing have been established.

STEP 04

Return home

Continue counseling, follow-up and relapse-prevention work in Georgia.

Atlanta’s air connections can make Nassau accessible, but convenient travel does not determine medical readiness. A person experiencing potentially serious alcohol withdrawal, uncontrolled opioid withdrawal, overdose symptoms, seizures, loss of consciousness or another medical emergency needs appropriate local medical care rather than an international flight.

Before making travel arrangements, review the full addiction recovery programme for people travelling from Atlanta and discuss whether the proposed treatment pathway is clinically relevant to your circumstances.

The part that begins after treatment

Returning to Atlanta With an Ongoing Recovery Plan

A treatment trip should have a return plan built into it. The neighborhoods, jobs, relationships and routines waiting in Georgia will still be there when the medical stage ends.

Before returning to Atlanta, a patient should know who will provide ongoing counseling, whether local medical follow-up is necessary, who can be contacted if cravings or substance use return and how overdose risk will be handled where opioids may be involved.

Your clinical plan

Identify an appropriate doctor, therapist or addiction professional where ongoing local care is needed. Make sure relevant providers know about naltrexone treatment, particularly before surgery or opioid pain treatment.

Your everyday plan

Build structure around sleep, work, family responsibilities, counseling, supportive relationships, physical activity and situations that have historically increased the risk of substance use.

For some people, the most valuable question is not only “How long will the medication last?” but “What am I going to build while that medication is active?”

Before deciding

Questions to Ask a Doctor About Naltrexone Treatment

About suitability

  • Why are you considering naltrexone in my case?
  • What other evidence-based treatment options should I compare?
  • Do I need to be opioid-free before treatment, and for how long?
  • How will you determine whether I am ready to start?
  • Are any of my medications incompatible with naltrexone?

About the formulation

  • How long is this specific formulation expected to remain active?
  • What evidence supports this specific product?
  • What is its regulatory status?
  • What adverse effects or procedure-related risks should I understand?
  • What happens if I need opioid pain medication?

About recovery

  • What counseling should continue alongside medication?
  • How will cravings and relapse risk be monitored?
  • What should my family or support network know?
  • Should I have naloxone available?

About stopping

  • What happens when medication exposure ends?
  • How does reduced opioid tolerance affect overdose risk?
  • What follow-up should occur before and after treatment ends?
  • What is the plan if I return to substance use?
Personal treatment discussion

Which Naltrexone Treatment Questions Should You Discuss With a Doctor?

This short educational assessment can help you identify subjects worth raising during a medical consultation. It does not diagnose addiction, assess medical suitability or recommend tablets, Vivitrol or an implant.

Your answers are processed inside this page and are not submitted to DeBinge by this quiz.

Question 1 of 9
Your treatment goal

1. Which substance is the main reason you are researching naltrexone?

Opioid preparation

2. Is recent opioid use or opioid medication potentially relevant to you?

Medication adherence

3. How confident are you that you could remember and continue a daily medication?

Previous treatment

4. Have you previously used naltrexone or another addiction medication?

Alcohol goals

5. If alcohol is involved, what would you most want to discuss with a clinician?

Medical safety

6. Are surgery, chronic pain, liver problems or other significant medical issues relevant?

Recovery support

7. What support would be available after medication treatment begins?

Follow-up

8. How realistic would regular follow-up appointments be for you?

Atlanta and travel planning

9. If treatment outside Georgia were considered, what would you most need to clarify?

Your discussion guide

Your Results

Based on your answers, these subjects may deserve additional attention when you speak with a qualified clinician. They are discussion priorities only, not a medical assessment or recommendation for a particular formulation.

Whatever your result

A clinician still needs to review your actual substance use, medical history, medication list, physical dependence, withdrawal risk and treatment goals before determining whether any form of naltrexone is appropriate.

Putting the comparison into context

There Is No Universal “Best” Form of Naltrexone

Oral naltrexone may fit someone who can follow a medication routine and values flexibility. Extended-release injectable naltrexone may reduce daily adherence demands but requires repeat appointments. An implant may extend medication exposure further, but brings different procedural, regulatory and medical considerations and is not FDA-approved in the United States.

The right discussion therefore starts with the patient rather than the product.

What substance is involved? Is physical dependence present? How has previous treatment gone? What is likely to happen during a difficult month? What support exists at home? Would the person continue a daily tablet? Would monthly appointments be realistic? Is international treatment being considered for a clinically sensible reason?

Those questions are more useful than assuming that the formulation lasting longest must automatically be the most appropriate.

Atlanta → Nassau

Learn How the DeBinge Treatment Pathway Works for Atlanta Residents

If you are comparing naltrexone options and want to understand how assessment, preparation, treatment in Nassau and recovery planning after returning to Georgia may fit together, review the dedicated Atlanta information page.

You can also discuss your history and questions with the DeBinge team before deciding whether a full clinical assessment is appropriate. A consultation is intended to help you understand the pathway, not to guarantee that an implant or another treatment will be suitable.

Explore the Atlanta Treatment Pathway
Frequently asked questions

Naltrexone Treatment for Atlanta Residents: FAQ

1. Is naltrexone the same as Vivitrol?

Naltrexone is the active medication. Vivitrol is a specific extended-release injectable formulation of naltrexone that is generally administered every four weeks. Naltrexone is also available in oral form, while longer-acting implant formulations have been developed and studied separately.

2. Is a naltrexone implant FDA-approved in the United States?

No. Naltrexone implant products are not FDA-approved in the United States. Implant formulations have been used or studied in other jurisdictions and remain the subject of clinical research. DeBinge treatment involving an implant takes place in Nassau, The Bahamas, not in Atlanta.

3. Is Vivitrol available in Atlanta?

Yes. Atlanta has healthcare providers and addiction-treatment services that use extended-release injectable naltrexone where clinically appropriate. Patients interested specifically in Vivitrol can discuss local treatment with a qualified Georgia healthcare professional.

4. Why can’t someone start naltrexone immediately after using opioids?

Naltrexone blocks opioid receptors. If a physically opioid-dependent person receives it while opioids are still active in the body, it can precipitate abrupt and potentially severe withdrawal. Appropriate opioid-free preparation and medical assessment are therefore essential.

5. How long must someone be opioid-free before Vivitrol?

The FDA prescribing information recommends at least 7 to 10 opioid-free days for people previously dependent on short-acting opioids. People transitioning from methadone or buprenorphine may remain vulnerable to precipitated withdrawal for as long as two weeks. Individual circumstances vary, and a clinician should determine readiness.

6. Does naltrexone completely prevent opioid overdose?

No. It should never be presented as a guarantee against overdose. Attempting to overcome receptor blockade with large amounts of opioids can be fatal. Overdose risk can also increase after naltrexone exposure declines or treatment ends because opioid tolerance may have fallen.

7. Does naltrexone stop alcohol withdrawal?

No. Naltrexone is not a medication for treating acute alcohol withdrawal. A person who may be physically dependent on alcohol should obtain appropriate medical advice before suddenly stopping drinking because severe withdrawal can be dangerous.

8. Can naltrexone help someone drink less alcohol?

For some people with alcohol use disorder, naltrexone can reduce alcohol’s reinforcing effects and may help reduce heavy drinking or support abstinence. Response differs between individuals, so treatment goals and effectiveness should be reviewed with the prescribing clinician.

9. Is a longer-lasting formulation automatically better?

No. Longer duration can reduce the burden of remembering medication, but treatment selection also depends on medical history, side effects, treatment goals, the evidence for the specific formulation, regulatory status, need for future pain treatment, follow-up and patient preference.

10. Does DeBinge have a clinic in Atlanta?

No. DeBinge does not operate a treatment clinic in Atlanta or Georgia. Atlanta residents can begin consultation and planning from home, while DeBinge treatment involving its implant pathway takes place in Nassau, The Bahamas.

11. What happens when I return to Atlanta after treatment?

Recovery planning should continue in Georgia. Depending on individual needs, this can include counseling, local medical care, family or peer support, structured routines, trigger management, mental-health treatment and an overdose-safety plan where opioid exposure remains possible.

12. Should I choose oral naltrexone, Vivitrol or an implant?

An article cannot safely make that decision for you. A qualified clinician should review your substance use, physical dependence, previous treatment, medical history, current medications, ability to adhere to treatment, recovery environment and personal goals before discussing which options may be appropriate.

Evidence and further reading

Clinical Sources Used in This Guide

1. U.S. Food and Drug Administration — Vivitrol Prescribing Information
Safety information covering opioid-free preparation, precipitated withdrawal, receptor blockade and vulnerability to opioid overdose.
Review the FDA prescribing information
2. National Institute on Alcohol Abuse and Alcoholism — Understanding Alcohol Use Disorder
U.S. government information covering evidence-based AUD treatment and FDA-approved medication options including oral and extended-release injectable naltrexone.
Read NIAAA guidance
3. DailyMed — Naltrexone Hydrochloride Tablets
Current U.S. prescribing information covering indications, contraindications, opioid blockade, precipitated withdrawal and other safety information.
Review DailyMed prescribing information
4. SAMHSA — Naltrexone
Current Substance Abuse and Mental Health Services Administration information on oral and extended-release naltrexone and its place within comprehensive addiction treatment.
Read SAMHSA’s naltrexone guidance
5. Hulse et al. — Randomized Controlled Trial of Oral or Implant Naltrexone
Peer-reviewed randomized research comparing oral naltrexone with a specific sustained-release implant formulation in people with heroin dependence. Results apply to the studied formulation and should not be generalized to every implant product.
View the study on PubMed
6. ClinicalTrials.gov — Long-Acting Naltrexone Implant Research
Current U.S. research illustrating the investigational status and continuing evaluation of implantable extended-release naltrexone formulations.
View the clinical trial record
7. Peer-Reviewed Review — Naltrexone Implant for Opioid Use Disorder
Review of implant research, pharmacology, adherence considerations and the distinction between implant research and FDA-approved U.S. formulations.
Read the full review on PubMed Central

Medical and emergency information

This article provides general educational information and does not replace medical assessment, diagnosis or treatment. Naltrexone is not appropriate for everyone. Do not stop opioids, methadone, buprenorphine, alcohol or prescribed medication in preparation for treatment without appropriate medical guidance.

If someone is unconscious, having difficulty breathing, experiencing a suspected overdose, seizure, severe confusion or another medical emergency in the United States, call 911. Where opioid overdose is suspected, administer naloxone if available and follow emergency-dispatch instructions.

Medical Review

Prepared for Medical Review by Dr Fergus Law, BSc, MBChB, FRCPsych

Dr Fergus Law is a Consultant Psychiatrist specialising in substance misuse and addiction psychiatry. His clinical experience supports the medical review of DeBinge educational content relating to addiction treatment, opioid dependence, relapse prevention and medication-based approaches.

Review status: Pending clinical approval

View Dr Fergus Law’s Clinical & Scientific Profile →

This article is intended for education and does not replace individualized medical assessment, diagnosis or treatment from a qualified healthcare professional.

Categories: Education & Resources, Atlanta, Treatment Options
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