Opioid Antagonist · Addiction Pharmacotherapy
Naltrexone is a non-addictive medication used in addiction treatment.
It can reduce alcohol cravings and helps prevent opioid relapse by blocking opioid receptors. You MUST be opioid-free before starting or it can trigger sudden withdrawal. Don’t test the “block” with opioids—overdose risk goes up, especially near the end of the monthly injection or after stopping.
Reviewed by the HeyPsych Medical Review Board · Reviewed January 26, 2026
People don’t usually describe naltrexone as a “feeling” medication. It’s more like: you notice what doesn’t happen.
“I could drink, but it just didn’t hit the same.”
“The cravings got quieter—like the urge wasn’t running the show anymore.”
“I stopped chasing that “buzz,” because it wasn’t paying off.”
Choose a condition to see how it's used for it.
FDA-approved for
Also prescribed for (off-label)
FDA-approved use
Used to reduce cravings and cut down heavy-drinking days. It can be started even if the person is still drinking, as long as they’re not in dangerous withdrawal and there is no major reason they shouldn’t take it.
About Alcohol Use DisorderHow many people in 100 notice each one in clinical studies. Many early side effects fade within a few weeks.
About 33 in 100 people in studies
What helps
This is the classic early side effect. Taking oral naltrexone with food can help. It often fades after the first couple of weeks.
Choose what applies to you.
Naltrexone crosses the placenta. Data in pregnancy are limited.
It is not typically the preferred medication for opioid use disorder during pregnancy, and extended-release IM naltrexone is generally avoided in pregnant patients in many guideline-based approaches. If a patient is stable on naltrexone and becomes pregnant, the decision to continue vs transition should be individualized based on relapse risk and patient preference, with shared decision-making and close monitoring. Pregnancy testing is commonly recommended before initiation.
General information, not advice for your case. Talk it through with your prescriber or pharmacist.
Rapid onset (minutes), severe symptoms, sometimes requiring hospitalization.
Especially after stopping, missing doses, near the end of the injection interval, or attempting to override blockade.
Marked enzyme elevation, jaundice, systemic symptoms.
Abscess, cellulitis, hematoma, tissue necrosis; rare Nicolau syndrome.
Requires close monitoring and urgent intervention when present.
Evaluate for other causes and substance-related factors.
Thoughts of suicide? Call or text 988, any time.
Everything we know about Naltrexone (Vivitrol, ReVia), section by section.
14 chapters · about 15 min to read it all. Open any one.
Naltrexone starts blocking receptors quickly, but the real-life benefit (cravings and behavior) can take time to show up consistently.
Simple Explanation
Oral naltrexone is a daily pill that works best with strong routines or observed dosing when adherence is hard. Vivitrol is a monthly deep-IM injection that removes the daily decision but requires correct injection technique and long-range planning for surgeries or opioid pain needs.Common issues are nausea, headache, dizziness, insomnia/sleep disturbance, and injection-site reactions with Vivitrol. Most side effects are worst early and improve over time.
The main interaction story is simple: opioids and naltrexone do not mix. Beyond that, watch the liver and be smart about combination regimens.
With: Opioids (including partial agonists and opioid-containing products)
Risk: Blocks opioid effects and can precipitate severe withdrawal if opioids are in the body. Attempts to override blockade increase overdose and death risk.
Action: AVOID opioids while on naltrexone. Verify opioid-free status before starting. Make a pain plan before surgery or dental work.
With: Planned or emergency opioid pain management
Risk: Opioids may be ineffective; high-dose attempts can be dangerous. Pain control becomes complicated.
Action: Use non-opioid strategies when possible (regional anesthesia, non-opioid analgesics, general anesthesia strategies). If opioids are required, care should be under trained anesthesia/acute pain specialists.
With: Other hepatotoxic agents (including heavy alcohol use and frequent NSAID use)
Risk: Higher risk of liver enzyme elevation or hepatitis when the liver is already stressed.
Action: Check baseline liver tests and monitor periodically. Reassess if symptoms of liver injury appear.
With: Bupropion (when used in combination approaches for stimulant use disorder)
Risk: Combination can be activating for some patients (anxiety/insomnia). Bupropion also carries seizure risk in vulnerable patients.
Action: If using combination therapy, monitor sleep, anxiety, blood pressure, and seizure risk factors. Adjust timing and dosing to reduce activation.
Reduced risk of returning to heavy drinking (oral naltrexone 50 mg/day)
In psychiatry/addiction care, naltrexone is used for alcohol use disorder (to reduce cravings and heavy drinking) and opioid use disorder (to block opioid effects and reduce relapse risk after detox). It’s not a sedative and it’s not addictive.
Yes, many clinicians start it while someone is still drinking. You don’t have to be abstinent first for alcohol use disorder. The bigger issue is making sure you’re not using opioids—because opioids plus naltrexone can trigger sudden withdrawal.
Typically at least 7 to 10 days opioid-free (including tramadol). If you were on long-acting opioids like methadone or buprenorphine, some people need up to 14 days. When there’s any doubt, a supervised start and/or naloxone challenge can help confirm you’re truly opioid-free.
You may feel little to nothing because the receptors are blocked. The dangerous part is people trying to override the block by taking larger doses—that can cause overdose and death, especially as the medication wears off or after stopping when tolerance is lower.
It’s not really about “stronger.” Vivitrol is long-acting and removes the daily pill decision, which can be a huge advantage. Oral naltrexone works well when adherence is strong. The best choice is usually the one you can realistically stick with.
Nausea is the classic one, especially early. Headache, dizziness, sleep problems, and anxiety/restlessness can happen too. With Vivitrol, injection-site reactions are common—anything severe, worsening, or associated with fever, drainage, or skin breakdown needs urgent evaluation.
It can. Depression and suicidal thoughts have been reported, including postmarketing reports. If mood gets darker, you feel hopeless, or you have suicidal thoughts, treat it like a real emergency and reach out immediately.
It can raise liver enzymes, usually mildly and sometimes transiently. Rarely, more serious hepatitis-type injury has been reported. That’s why baseline and periodic liver tests are standard, and why clinicians avoid starting it during acute hepatitis or liver failure.
Plan ahead. If opioid pain meds might be needed, oral naltrexone is typically stopped at least 72 hours before elective surgery. With Vivitrol, you generally need about 30 days after the last injection for opioid responsiveness to return. Always tell surgeons, dentists, and ER clinicians you’re on naltrexone.
No taper is required. But stopping changes your risk profile—especially in opioid use disorder—because tolerance drops and overdose risk can rise if relapse occurs. If you stop, you should also have a clear relapse prevention plan and naloxone access if opioids are part of your history.
Sometimes off-label, usually as part of combination treatment in specialty addiction care (often paired with bupropion). It’s not a guaranteed fix, but it may provide modest benefit for some people when combined with therapy and structured support.
This treatment information is for educational purposes only. Treatment decisions should be made in consultation with qualified healthcare professionals based on individual circumstances, symptoms, and medical history. Do not attempt treatment without professional guidance.
Thinking about Naltrexone (Vivitrol, ReVia)? A prescriber can tell you if it fits.
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