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Dextromoramide

This article is a stubmissing:
Subjective Effects
Interactions
Legality
Dextromoramide molecule structureDextromoramide molecule structure
Chemical Class

Dextromoramide is an opioid analgesic1, classified as a depressant and habit-forming substance. It emerged from research into related compounds and is the right-handed isomer of moramide. It is approximately three times more potent than morphine but shorter acting. Reports describe unusual, rapid tolerance behavior, and its habit-forming properties present dependence risk.

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold~2.5 mg
Light2.5-5 mg
Moderate5-7.5 mg
Strong7.5-10 mg
Heavy10+ mg

Dextromoramide is reported to have unpredictable effects and an unusually rapid tolerance development, which may complicate accurate dosing.

Duration

After Effects1-12 hours

Subjective Effects

Subjective Effects not written up yet

Reagent Testing

Expected colorimetric results for common reagent tests. Colors show reaction change over 1–2 minutes.

Marquis(MQ)
No reaction
No reaction
Mecke(ME)
No reaction
No reaction
Froe(FR)
No reaction
No reaction
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Pharmacology

Pharmacodynamics

Dextromoramide is a powerful opioid analgesic, reported to be approximately three times more potent than morphine. It has a shorter action than morphine2, while tolerance to its analgesic effects was reported to develop relatively slowly compared with most other short-acting opioids.

Pharmacokinetics

In nine surgical patients given a single oral dose with an anticholinergic, dextromoramide was rapidly absorbed from the gastrointestinal tract3. Taken orally, it is also reported to have a fast onset and high bioavailability, with oral dosing producing almost as much effect as injection. In five patients given oral dextromoramide with an anticholinergic, plasma concentrations declined after the peak with first-phase half-lives of 0.4–1.6 hours and terminal half-lives of 6.3–21.8 hours3. In the nine-patient oral-dose study, apparent volume of distribution values ranged from 0.6 to 2.4 L/kg3. In nine surgical patients given a single oral dose with an anticholinergic, peak plasma levels were usually reached within 0.5–4.0 hours after dosing3. In five of these patients, plasma concentrations declined after the peak in a biphasic pattern, with first-phase half-lives of 0.4–1.6 hours and terminal half-lives of 6.3–21.8 hours3. In the remaining patients, no clear-cut biphasic pattern was observed; half-lives calculated between 4 and 10 hours after administration ranged from 1.5 to 4.7 hours3. Less than 0.06% of the dose is excreted unchanged in urine within 8 hours3.

Metabolitesnone documented yet

Interactions

Interactions not written up yet

An unlisted combination is an unknown one, not a safe one. Check a dedicated combination chart before mixing.

Check TripSit

Tolerance

Tolerance timelines are rules of thumb, not exact schedules, and vary widely between individuals and use patterns.

Full Tolerance
Tolerance is reported to develop with strange and rapid behavior, while tolerance to analgesic effects is described as developing relatively slowly compared with most other short-acting opioids.

Harm Potential

Addiction & Dependence

Psychological

High

Described as highly addictive with significant abuse potential. The substance was reportedly not returned to market in part due to concerns about its addictive properties as an oral painkiller.

Physical

High

Dependence liability is similar to morphine, though the withdrawal syndrome is reportedly less severe than morphine withdrawal.

History & Culture

Discovery and development

Dextromoramide was discovered and patented in 1956 by Paul Janssen at Janssen Pharmaceuticals. Janssen was also associated with the development of several other notable medicines, including fentanyl and haloperidol.

Legality

Legality not written up yet

Article Status

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