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Buprenorphine/Naloxone

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Opioid agonist therapy (OAT); Partial μ-agonist + abuse-deterrent
Buprenorphine / Naloxone
Suboxone, Zubsolv, Bunavail, Cassipa
Buprenorphine/naloxone (most widely known as Suboxone) is one of the two pillars of medication-assisted treatment for opioid use disorder. The partial-agonist nature of buprenorphine gives it a ceiling effect on respiratory depression — far safer than full agonists like methadone. The naloxone is essentially inert SL; it exists as an injection deterrent. See Buprenorphine for the pharmacology of the active component.

Experience

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Problems

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Titration strategies

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Effects

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Pharmacokinetics

Absorption

Buprenorphine ~30% SL; naloxone negligible.

Distribution

Buprenorphine ~96% protein binding.

Metabolism

Buprenorphine: CYP3A4 → norbuprenorphine (active). Naloxone: hepatic glucuronidation.

Elimination

Fecal (buprenorphine and metabolites); renal (naloxone glucuronide).

Interactions

No interactions reported yet.

Pregnancy and lactation

Prefer buprenorphine monoproduct (Subutex) in pregnancy when possible — more pregnancy data.

Monitoring

Withdrawal scale (COWS) during induction; LFTs at baseline + periodically; toxicology screens per program.

Patient counseling

Precipitated withdrawal: do not induct until in moderate withdrawal (COWS ≥ 8–12). Hold under tongue until fully dissolved — do not chew or swallow. Combine with counseling and recovery support.

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Relevant Literature

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See also

Buprenorphine, Methadone, Naltrexone, Naloxone

References

Summary
Classes
Opioid agonist therapy (OAT); Partial μ-agonist + abuse-deterrent
Common uses
Opioid use disorder (OUD) maintenance0, Opioid withdrawal0
Pharmacy
Starting dose
Induction: 2/0.5 to 4/1 mg SL once in moderate withdrawal; titrate to 12–16/3–4 mg/d by day 2–3
Preparations
SL film or tablet, 2/0.5 to 12/3 mg per dose
US FDA Max
24/6 mg/d (most labels)
Pharmacology
Routes
Sublingual film or tablet (buccal for some)
Onset
30–60 min (SL)
Duration
24–36 h (driven by buprenorphine)
Half-life
24–42 h (buprenorphine); 1–2 h (naloxone)
Bioavailability
Buprenorphine ~30% SL; naloxone <10% SL (intentional — inactive sublingually, matters only if injected)
Pregnancy
Category C (buprenorphine-only formulations preferred in pregnancy)
Legal status
Schedule III in US; X-waiver no longer required (as of 2023)
Purported mechanism
Buprenorphine: high-affinity partial agonist at the μ-opioid receptor with ceiling effect on respiratory depression. Naloxone: abuse-deterrent — inactive SL but precipitates withdrawal if injected.