What is the difference between Suboxone (buprenorphine/naloxone) and Subutex (buprenorphine)?

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Last updated: August 13, 2025View editorial policy

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Difference Between Suboxone and Subutex

The main difference between Suboxone and Subutex is that Suboxone contains both buprenorphine and naloxone, while Subutex contains only buprenorphine; Suboxone is generally preferred for most patients due to its reduced potential for misuse. 1

Key Differences

Active Ingredients

  • Subutex: Contains only buprenorphine, a partial opioid agonist
  • Suboxone: Contains buprenorphine plus naloxone, an opioid antagonist 2

Abuse Deterrent Properties

  • Suboxone includes naloxone specifically to discourage intravenous misuse. If injected, the naloxone component can precipitate withdrawal symptoms, making it less likely to be abused 3
  • Subutex lacks this abuse-deterrent feature, making it potentially more susceptible to misuse via injection 2

Clinical Applications

Pregnancy

  • Subutex (buprenorphine alone) is recommended for pregnant women according to the American College of Obstetricians and Gynecologists 1
  • This recommendation exists because of theoretical risks to the fetus if withdrawal is precipitated by the naloxone component, though limited data do not support this theoretical concern 4

General Treatment

  • Suboxone is the preferred formulation for most non-pregnant patients due to its safety features that prevent misuse 1
  • Both medications are equally effective in treating opioid use disorder when used as prescribed 2

Clinical Considerations

Dosing and Administration

  • Both medications are administered sublingually
  • Typical target dose is 16 mg daily (range 4-24 mg based on individual response) 1
  • Median disintegration time is similar for both formulations (6-12 minutes) 5

Bioequivalence

  • Studies have shown that Suboxone formulations are bioequivalent to equivalent doses of Subutex 5
  • When switching from Subutex to Suboxone, most patients can be maintained at the same dose, though some patients on higher doses (>22 mg) may require dose adjustments 6

Side Effects

  • When patients are switched from Subutex to Suboxone, approximately 50% report adverse events during the first 4 weeks, decreasing to 26.6% at four months 6
  • Despite these adverse events, discontinuation rates due to side effects are relatively low 6

Practical Implications

Prescribing Considerations

  • Both medications can be prescribed in office-based settings under DATA 2000 regulations 2
  • Patients who would not accept treatment in traditional opiate-maintenance clinics may find office-based buprenorphine treatment more acceptable 2

Risk Management

  • Multiple drug-drug interactions with either formulation can result in QT-interval prolongation, serotonin syndrome, paralytic ileus, reduced analgesic effect, or precipitation of withdrawal symptoms 4
  • Concomitant use of buprenorphine (either formulation) with QT-prolonging agents is contraindicated 4

Special Populations

  • For perioperative management, the prescribed daily dose of buprenorphine (either formulation), indication for treatment, risk of relapse, and expected level of postsurgical pain should guide decision-making 4

Common Pitfalls to Avoid

  1. Incorrect switching: When transferring patients from Subutex to Suboxone, careful planning and discussion should occur to minimize adverse events 6

  2. Overlooking pregnancy status: Using Suboxone instead of Subutex in pregnant women, though recent evidence suggests this theoretical concern may be unfounded 4

  3. Inadequate monitoring: Failing to monitor for side effects, cravings, and withdrawal symptoms, especially when switching between formulations 6

  4. Ignoring potential for misuse: Despite Suboxone's abuse-deterrent properties, both medications still have some potential for misuse and should be prescribed with appropriate monitoring 2

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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