LEGAL STATUS — verified 10 Aug 2026: DEA notices of intent to temporarily Schedule I concentrated 7-OH (above threshold) and related analogues are published; no temporary scheduling order located yet — recheck the Federal Register before counseling.

Clinician entry

Treat the exposure and the clinical state.

Not the word “kratom” on a package—and not a fixed number of hours on a clock. This is an emerging practice framework, not a nationally validated 7-OH guideline.

There is no universally validated dose-conversion formula, withdrawal clock, COWS threshold, or buprenorphine induction schedule specific to direct high-dose commercial 7-OH. Published series and cases are useful; they do not erase product heterogeneity.
Clinician triage flow for 7-OH exposure and disposition
Risk-stratify setting and pathway from exposure history and clinical state.

Ask now

Ask specifically about 7-OH, 7-hydroxy, hydroxie, kratom extract tablets, films, shots, gummies, capsules, powders, MGM-15, MGM-16, and pseudoindoxyl. Many patients deny “opioid use” because they bought the product at retail.

Document product/brand (photograph when possible), labeled mg/unit and units/day, route, redosing interval, duration, nocturnal/interdose withdrawal, last dose, coexposures, and likelihood of seeking illicit opioids if supply ends. Do not convert to morphine milligram equivalents—no validated 7-OH-to-MME conversion exists.

Severity beyond COWS

COWS remains useful for objective opioid-withdrawal findings but can under-read insomnia, dysphoria, GI distress, craving, and mixed-product symptoms. Assess hydration, autonomic burden, functional collapse, and evolving withdrawal for the chosen transition strategy.

Escalate the setting when

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Clinician contact

Use this site’s clinician materials first. For collegial case discussion, press, corrections, or educational talks: bharris@eusomniamd.com.

Patient care coordination: eusomniamd.com · (650) 308-4845 · office@eusomniamd.com