Kratom: The Opioid Supplement Hiding in Plain Sight
Kratom is a Southeast Asian plant sold in the US as a “botanical supplement” for energy, mood, and opioid withdrawal, but its main alkaloids — mitragynine and 7-hydroxymitragynine — act on the same mu-opioid receptors as opioid drugs, with 7-HMG binding more tightly than morphine in lab studies. The effects follow a classic opioid dose curve (pain relief, then euphoria and sedation, then breathing suppression), physical dependence builds within weeks, and withdrawal mirrors opioid withdrawal; US poison centers logged 3,484 kratom calls from 2014–2019 and the CDC has linked it to dozens of deaths, most involving other drugs. Because it is sold as a supplement, it skips FDA approval entirely, so potency varies widely, contamination is possible, and there are no dosing standards. For someone already dependent on opioids it may be less harmful than illicit fentanyl, but that is a clinical decision for a doctor with a withdrawal plan, not a gas-station purchase. Since 26 August 2026, mitragynine pseudoindoxyl (MGPI) and the synthetic derivatives MGM-15 and MGM-16 have been temporarily in Schedule I. A 14 October 2026 DEA notice of intent would also schedule concentrated 7-hydroxymitragynine and MGPI above set thresholds; plain botanical kratom is outside that proposal, and the order will not be issued before 13 November 2026.
Kratom (Mitragyna speciosa) is a Southeast Asian plant whose ground leaves are sold in the United States as a "botanical supplement." You will find it in capsules, powders, and shots at gas stations, convenience stores, smoke shops, and online. The marketing pitches it for energy, mood, and opioid withdrawal. What is usually missing from the label: kratom's two main alkaloids, mitragynine and 7-hydroxymitragynine, act on the same brain receptors as opioid drugs.
The Pharmacology
7-hydroxymitragynine (7-HMG) binds mu-opioid receptors with greater affinity than morphine in laboratory studies, and rats will self-administer it like an opioid. The effects you feel are dose-dependent in the same pattern as a classic opioid: pain relief at low doses, euphoria and sedation at higher doses, and breathing suppression at toxic doses. The DEA proposed Schedule I status for mitragynine and 7-hydroxymitragynine in 2016 and withdrew that proposal after public comment. The withdrawal was not a finding that the alkaloids are safe.
Concentrated 7-OH, 2026
On 26 August 2026 the DEA temporarily placed mitragynine pseudoindoxyl (MGPI) and two synthetic 7-hydroxymitragynine derivatives, MGM-15 and MGM-16, in Schedule I. The 14 October 2026 notice cites that order as 91 FR 54948 and says it stays in effect until 26 August 2028, or until a replacement order is published. The FDA describes the same 26 August action (Hiding in Plain Sight: 7-OH Products).
On 14 October 2026 the DEA published a notice of intent to issue a further temporary Schedule I order for 7-hydroxymitragynine and MGPI (91 FR 65370; Federal Register, 14 October 2026). It follows an HHS letter dated 8 October 2026, which HHS announced on 9 October (HHS, 9 October 2026). The proposal covers either substance, or the two combined, when the amount is above a threshold: more than 1 mg per gram in a solid, or more than 1 mg per millilitre in a liquid, or when the mass of mitragynine divided by the mass of 7-OH, of MGPI, or of both is less than 100. The notice says that line is meant to reach concentrated or enhanced products and not natural botanical kratom, in which 7-OH is a minor or trace alkaloid (under 2 percent of total alkaloids, or a trace). The temporary order will not be issued before 13 November 2026. Neither HHS nor the DEA has found amounts below the threshold to be safe.
HHS, describing FDA’s scientific review, says preclinical studies find 7-OH about two to nine times as potent as morphine, depending on the study. The Federal Register notice says 7-OH has opioid activity comparable to morphine, including tolerance, dependence, and respiratory depression, and that preclinical data show MGPI produces an analgesic effect more potent than morphine. This page stays at Tier 4. A plain-leaf exclusion is not a reason to treat a concentrated 7-OH product as a supplement.
Dependence and Withdrawal
Physical dependence builds with regular use, often within a few weeks. Withdrawal — documented in hundreds of case reports and multiple observational studies — includes muscle aches, insomnia, anxiety, irritability, sweating, nausea, and cravings. The pattern looks like opioid withdrawal, though usually milder. The FDA has received thousands of adverse event reports tied to kratom, and the CDC has linked kratom to dozens of overdose deaths, most involving other drugs. Even when kratom alone is hard to isolate as the cause, the signal is real.
Poison Center Trends
U.S. poison centers logged 3,484 kratom-related calls between 2014 and 2019, with the rate climbing each year, according to American Association of Poison Control Centers (AAPCC) data. Reports include seizures, liver injury, and dozens of deaths in older adults whose cases involved drug interactions. Drug-induced liver injury cases tied to kratom have been published in hepatology journals on multiple continents.
Who Uses Kratom
Kratom has a real user community: people managing chronic pain, tapering off prescription opioids, and recreational users. Some users say it helps. For someone already dependent on opioids, kratom may be less harmful than illicit fentanyl. But that is a medical decision — one that belongs in a clinic with a doctor and a withdrawal plan, not in the checkout line at a gas station.
The Regulatory Gap
Because kratom is sold as a supplement rather than a drug, it skips the FDA approval process. Products vary widely in potency, can be contaminated, and have no required dosing standards. The American Kratom Association has lobbied to keep kratom unscheduled. Several states have passed a Kratom Consumer Protection Act that requires labeling and basic purity standards — a small step toward harm reduction, but it does not resolve the bigger safety questions.
Reviewed against 10 peer-reviewed and regulatory sources
- Veltri C, Grundmann O. "Current perspectives on the impact of kratom use." Substance Abuse and Rehabilitation, 2019. PMID: 31308789.
- Hemby SE, et al. "Abuse liability and therapeutic potential of the Mitragyna speciosa (kratom) alkaloids mitragynine and 7-hydroxymitragynine." Addiction Biology, 2018. PMID: 29949228. DOI: 10.1111/adb.12639.
- Graves JM, et al. "Kratom exposures among older adults reported to U.S. poison centers, 2014–2019." Journal of the American Geriatrics Society, 2021. PMID: 34143890. DOI: 10.1111/jgs.17326.
- Olsen EO, et al. "Notes from the field: unintentional drug overdose deaths with kratom detected — 27 states, July 2016–December 2017." MMWR (CDC), 2019. PMID: 30973850.
- FDA. "FDA and Kratom." US Food and Drug Administration. Updated 2024. https://www.fda.gov/news-events/public-health-focus/fda-and-kratom
- DEA. "Withdrawal of Notice of Intent to Temporarily Place Mitragynine and 7-Hydroxymitragynine into Schedule I." Federal Register, 2016.
- DEA. "Schedules of Controlled Substances: Temporary Placement of 7-Hydroxymitragynine and Mitragynine Pseudoindoxyl Above a Specified Threshold in Schedule I." Federal Register, 14 October 2026;91 FR 65370. Full text. Cites the 26 August 2026 temporary order for MGPI, MGM-15, and MGM-16 (91 FR 54948).
- U.S. Department of Health and Human Services. "HHS Recommends Science-Based Thresholds to Target Dangerous Enhanced Kratom Products." 9 October 2026. HHS press release.
- FDA. "Hiding in Plain Sight: 7-OH Products." Updated 2026. FDA.
- Henningfield JE, et al. "Risk of death associated with kratom use compared to opioids." Preventive Medicine, 2019. PMID: 31647958.