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    Propoxyphene molecular structure

    Propoxyphene Stats & Data

    Psychoactive Class Opioid / Depressant

    Pharmacology

    DrugBank
    Half-life 12.0 hours Metabolism Hepatic

    Mechanism of Action

    Propoxyphene acts as a weak agonist at OP1, OP2, and OP3 opiate receptors within the central nervous system (CNS). Propoxyphene primarily affects OP3 receptors, which are coupled with G-protein receptors and function as modulators, both positive and negative, of synaptic transmission via G-proteins that activate effector proteins. Binding of the opiate stimulates the exchange of GTP for GDP on the G-protein complex. As the effector system is adenylate cyclase and cAMP located at the inner surfac

    Tolerance & Pharmacokinetics

    drugs.wiki

    Tolerance Decay

    Full tolerance 1d Half tolerance 21d Baseline ~35d

    Experience Report Analysis

    Erowid
    13 Reports
    1999–2021 Date Range
    1 With Age Data
    9 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid

    Effects aggregated from 13 experience reports (13 Erowid)

    13 Reports
    9 Effects Detected
    7 Positive
    1 Adverse
    1 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 7

    Euphoria 53.8% 70%
    Sedation 46.2% 70%
    Music Enhancement 30.8% 70%
    Tactile Enhancement 30.8% 70%
    Empathy 23.1% 70%
    Stimulation 23.1% 70%
    Anxiety Suppression 23.1% 70%

    Adverse Effects 1

    Nausea 23.1% 70%

    Real-World Dose Distribution

    62K Doses

    From 36 individual dose entries

    Oral (n=21)

    Median: 162.5mg 25th: 100.0mg 75th: 300.0mg 90th: 400.0mg
    mg/kg median: 2.051 mg/kg 75th: 3.779

    Form / Preparation

    Most common forms and preparations reported

    Redose Patterns

    Redosing behavior across 12 reports

    16.7% Redosed
    1.2 Avg Doses
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