How do I transition a patient from Kratom (7-hydroxymitragynine) to Suboxone (buprenorphine/naloxone)?

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Last updated: January 7, 2026View editorial policy

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Transitioning from Kratom (7-OH) to Suboxone

Buprenorphine/naloxone is an effective treatment for kratom dependence and can be safely initiated as early as 8 hours after last kratom use, with induction doses typically ranging from 4-16 mg and maintenance doses of 8-16 mg daily. 1, 2

Timing of Induction

  • Begin buprenorphine/naloxone induction 8 hours after the patient's last kratom dose 2
  • Unlike traditional opioid induction, precipitated withdrawal appears less problematic with kratom due to the partial agonist properties of its alkaloids (mitragynine and 7-hydroxymitragynine) 3
  • Patients may present with opioid-like withdrawal symptoms including myalgias, chills, nausea/vomiting, and anxiety that respond well to buprenorphine 4, 5

Induction Dosing Strategy

Start with 4-8 mg of buprenorphine/naloxone on day one, observing the patient's response 1:

  • Most patients (18 of 28 in the largest case series) required induction doses between 8-16 mg 1
  • A minority (9 of 28 patients) responded adequately to lower induction doses of 1-6 mg 1
  • One patient required 20 mg for adequate symptom control 1
  • There is no correlation between the patient's daily kratom dose and the required buprenorphine stabilization dose, so titrate based on withdrawal symptoms rather than attempting dose conversion 1

Maintenance Dosing

Stabilize patients on 8-16 mg daily of buprenorphine/naloxone 1, 6:

  • The majority of patients (23 of 28) stabilized on maintenance doses between 8-16 mg daily 1
  • For patients with persistent withdrawal symptoms or co-occurring chronic pain, consider divided dosing (every 6-8 hours) or doses up to 24 mg daily 2, 6
  • Single daily dosing of 16 mg is appropriate for most patients with opioid use disorder maintenance 6

Special Considerations for Kratom Patients

Monitor for prolonged withdrawal symptoms that may persist despite adequate buprenorphine dosing 2:

  • Some kratom-dependent patients report continued withdrawal symptoms even on therapeutic buprenorphine doses, likely due to kratom's effects on adrenergic, serotonergic, and dopaminergic pathways beyond opioid receptors 3
  • Higher doses (up to 24 mg daily) or divided dosing may be necessary for these patients 2

Screen for polysubstance use, which is common in kratom users 2:

  • Patients with concurrent substance use disorders may require higher buprenorphine doses and more intensive levels of care 2
  • Many kratom users have histories of prescription opioid dependence and may be using kratom as self-treatment for opioid withdrawal 4, 5

Monitoring and Follow-up

Utilize urine drug screening for kratom alkaloids (mitragynine) to monitor treatment response 1, 2:

  • In the largest case series, 68% of patients had negative mitragynine tests at 4 weeks, increasing to 82% at both 8 and 12 weeks 1
  • Facilities treating kratom dependence should have kratom-specific testing available, as standard opioid screens will not detect kratom alkaloids 2

Expect good retention rates with buprenorphine maintenance 1:

  • 20 of 28 patients (71%) remained in treatment, with average duration of 11 months and range of 5-22 months 1
  • This retention rate is comparable to traditional opioid use disorder treatment 1

Common Pitfalls to Avoid

  • Do not attempt to calculate equianalgesic conversions from kratom to buprenorphine—no reliable conversion exists, and stabilization doses do not correlate with kratom intake 1
  • Do not use mixed agonist-antagonist opioids, as these should never be combined with opioid agonist therapy and could precipitate withdrawal 7
  • Do not assume standard 24-hour waiting periods are necessary—kratom's pharmacology allows for earlier induction at 8 hours 2
  • Do not overlook the need for higher or divided doses in patients with persistent symptoms, as kratom affects multiple neurotransmitter systems beyond opioid receptors 2, 3

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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