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General prescriptions
Brand names
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Reviewed 2026-10-04

Oxymorphone

A strong opioid pain medicine in immediate- and extended-release tablets for severe pain when other treatments are inadequate.

psilodex.org/m/oxymorphone · data v2026.10.05

Clinical contraindication
None listed
No label contraindication covering psilocybin was found. This is not a finding that the combination has been shown to be without risk.
Psilocybin evidence
No psilocybin data
Half-life
9–11 h
Approximate, in adults. Source under Interaction below.
Named in state rules?
Cite asPsilodex, “Oxymorphone”, v2026.10.05. psilodex.org/m/oxymorphone

Clinical data and state rules are separate facts. Both are shown; neither is a decision.

What it is used for

FDA status

FDA-approved

Availability

Generic only in US

FDA-approved for
  • Acute pain severe enough to require an opioid when other treatments are inadequate (immediate-release)
  • Severe, persistent pain needing an opioid that other options cannot treat (extended-release)
Sources [1][2]
Other safety

Boxed warning: addiction, abuse and misuse; life-threatening respiratory depression; and profound sedation, respiratory depression, coma and death when combined with benzodiazepines or other CNS depressants, including alcohol.

About the medication itself, separate from any interaction with psilocybin.

Sources [1]

01 Interaction with psilocybin

ND

Its sedation and nausea may add to psilocybin's effects; slowed breathing is its own risk. Stopping it suddenly after regular use can cause withdrawal.

Detail Oxymorphone is a full mu-opioid agonist (a strong opioid). Its sedation and nausea may add to psilocybin's effects. Respiratory depression (slowed breathing) is an opioid risk that rises with other CNS depressants (sedating drugs); psilocybin does not depress breathing. Opioid labels report serotonin syndrome when opioids are combined with serotonergic (serotonin-boosting) drugs; there are no psilocybin data. Also, labels report severe hypotension (low blood pressure), including on standing, and more frequent seizures in seizure disorders. Stopping it suddenly can cause withdrawal.

Human data with psilocybin
No psilocybin data; based on how it works and its label
Half-life
9–11 h (oral, immediate-release) (FDA label, checked 2026-10-04)
Evidence types on this record
No psilocybin dataNo psilocybin data: no human data with psilocybin or another classic psychedelic; the text draws on the medication's own pharmacology and its label or reference facts

02 Pharmacology relevant to psilocybin

6 listed · counted on reports
Sedating or CNS depressant
Slows the central nervous system: drowsiness, slower reactions and impaired coordination, and slowed breathing at high doses. Effects add with other sedating substances. Sources [1]
Withdrawal or rebound if stopped abruptly
Stopping suddenly can cause withdrawal or a rebound of symptoms. Sources [1]
Lowers blood pressure or causes orthostasis
Lowers blood pressure, or causes a drop on standing (orthostasis) that can bring dizziness or fainting. Sources [1]
Opioid
Activates opioid receptors, causing pain relief, sedation and slowed breathing at higher doses. Psilocybin does not slow breathing, but stopping an opioid suddenly can cause withdrawal. Sources [1]
Lowers seizure threshold or carries seizure risk
Makes a seizure more likely, or has been linked to seizures. Sources [1]
Serotonergic
Increases serotonin activity, for example by blocking its reuptake or releasing it. Psilocybin acts on serotonin receptors, so effects can add together. With antidepressant use, the psilocybin response can be weaker. Sources [1]

03 State rules

Plain-language summary · official text governs
CO4 CCR 755-1
Not namedCondition rules (3)

No provision names this medication or its class.

Colorado · checked 2026-10-04
OROAR 333-333
Not named

No provision names this medication or its class.

Oregon · checked 2026-10-04
NM7.35.3 NMAC (proposed)
Pending

New Mexico's clinical rules (proposed 7.35.3 NMAC) are not final. No provision naming this medication has been found.

New Mexico · checked 2026-10-04

04 Conditions to ask about

Screening items in state rules

This medication is usually taken for a condition. State rules screen for some conditions directly, so the medication is a prompt to ask about them. Confirm with the participant; never assume a condition from the medication.

  • Chronic pain
    • CO 2.5(A)(2) · Clinical Facilitator licensees
    • CO 6.16(F)(2)(a) · Facilitators without a clinical facilitator license
    • CO 6.16(F)(1) · All licensees

05 Sources

2
  1. Oxymorphone Hydrochloride Tablets (Aurolife) · FDA label (DailyMed) — Opioid: 12.1 "Oxymorphone is a full opioid agonist and is relatively selective for the mu-opioid receptor" | Sedating or CNS depressant: Boxed Warning "Concomitant use of opioids with benzodiazepines or other central nervous system (CNS) depressants, including alcohol, may result in profound sedation, respiratory depression, coma, and death." | Serotonergic: 7 Drug Interactions "The concomitant use of opioids with other drugs that affect the serotonergic neurotransmitter system has resulted in serotonin syndrome." | Lowers blood pressure or causes orthostasis: 5.10 "Oxymorphone Hydrochloride Tablets may cause severe hypotension including orthostatic hypotension and syncope in ambulatory patients." | Lowers seizure threshold or carries seizure risk: 5.13 "may increase the frequency of seizures in patients with seizure disorders" | Withdrawal or rebound if stopped abruptly: 5.14 "Do not rapidly reduce or abruptly discontinue oxymorphone hydrochloride tablets in a patient physically dependent on opioids." | 12.3 "half-life ranges from approximately 9-11 hours after a single oral dose (5-40 mg)"
  2. Oxymorphone Hydrochloride Extended-Release Tablets (Amneal) · FDA label (DailyMed) — Indications: "management of severe and persistent pain that requires an opioid analgesic and that cannot be adequately treated with alternative options, including immediate-release opioids"

Record history

  • v2026.10.02First published.
  • 2026-10-04Last reviewed against its sources.

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Before you startTerms 2026-10-01

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