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    Pseudoephedrine molecular structure

    Pseudoephedrine Stats & Data

    pseudoephrine
    NPS DataHub
    MW165.24
    FormulaC10H15NO
    CAS90-82-4
    IUPAC(1S,2S)-2-methylamino-1-phenylpropan-1-ol
    SMILESCNC(C)C(O)c1ccccc1
    InChIKeyKWGRBVOPPLSCSI-WCBMZHEXSA-N
    Phenethylamines; 2020/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2021/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2022/1. Von 2-Phenethylamin abgeleitete Verbindungen
    Psychoactive Class Stimulant

    Pharmacology

    DrugBank
    State Solid

    Description

    Pseudoephedrine is structurally related to ephedrine but exerts a weaker effect on the sympathetic nervous system. Both drugs naturally occur in in ephedra plant which have a history of use in traditional Eastern medicine and were first researched in the west in 1889. The decongestant effect of pseudoephedrine was described in dogs in 1927.

    Mechanism of Action

    Pseudoephedrine acts mainly as an agonist of alpha adrenergic receptors and less strongly as an agonist of beta adrenergic receptors. This agonism of adrenergic receptors produces vasoconstriction which is used as a decongestant and as a treatment of priapism. Pseudoephedrine is also an inhibitor of norepinephrine, dopamine, and serotonin transporters. The sympathomimetic effects of pseudoephedrine include an increase in mean arterial pressure, heart rate, and chronotropic response of the right atria. Pseudoephedrine is also a partial agonist of the anococcygeal muscle. Pseudoephedrine also inhibits NF-kappa-B, NFAT, and AP-1.

    Pharmacodynamics

    Pseudoephedrine causes vasoconstriction which leads to a decongestant effect. It has a short duration of action unless formulated as an extended release product. Patients should be counselled regarding the risk of central nervous system stimulation.

    Metabolism

    Pseudoephedrine is <1% N-demethylated to an inactive metabolite. The majority of pseudoephedrine is eliminated unmetabolized in the urine.

    Absorption

    A 240mg oral dose of pseudoephedrine reaches a Cmax of 246.3±10.5ng/mL fed and 272.5±13.4ng/mL fasted, with a Tmax of 6.60±1.38h fed and 11.87±0.72h fasted, with an AUC of 6862.0±334.1ng\*h/mL fed and 7535.1±333.0ng\*h/mL fasted.

    Toxicity

    The oral LD50 of pseudoephedrine is 2206mg/kg in rats and 726mg/kg in mice. Patients experiencing an overdose of pseudoephedrine may present with giddiness, headache, nausea, vomiting, sweating, thirst, tachycardia, precordial pain, palpitations, difficulty urinating, muscle weakness, muscle tension, anxiety, restlessness, insomnia, toxic psychosis, cardiac arrhythmias, circulatory collapse, convulsions, coma, and respiratory failure. Treat overdose with symptomatic and supportive treatment including removal of unabsorbed drug.

    Indication

    Pseudoephedrine is a sympathomimetic amine used for its decongestant activity.

    Half-life

    The mean elimination half life of pseudoephedrine is 6.0h.

    Protein Binding

    -pseudoephedrine is 6.6±0.4% bound to human serum albumin and 22.5±3.2% protein bound in serum. +pseudoephedrine is 6.7±1.2% protein bound to human serum albumin and 25.4±3.9% protein bound in human serum.

    Elimination

    55-75% of an oral dose is detected in the urine as unchanged pseudoephedrine.

    Volume of Distribution

    The apparent volume of distribution of pseudoephedrin is 2.6-3.3L/kg.

    Clearance

    A 60mg oral dose of pseudoephedrine has a clearance of 5.9±1.7mL/min/kg.

    Effect Profile

    Curated + 21 Reports
    Stimulant 8.5

    Strong stimulation, euphoria, anxiety/jitters, and focus

    Stimulation / Energy×3
    107.1
    Euphoria / Mood Lift×2
    106.4
    Focus / Productivity×2
    92.9
    Anxiety / Jitters×1
    1010
    Catalog Erowid

    Tolerance & Pharmacokinetics

    drugs.wiki

    Tolerance Decay

    Full tolerance 1d Half tolerance 10d Baseline ~18d

    Experience Report Analysis

    Erowid
    21 Reports
    2000–2024 Date Range
    5 With Age Data
    20 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid

    Effects aggregated from 21 experience reports (21 Erowid)

    21 Reports
    20 Effects Detected
    7 Positive
    7 Adverse
    6 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 7

    Euphoria 42.9% 70%
    Stimulation 42.9% 70%
    Body High 23.8% 70%
    Music Enhancement 19.0% 70%
    Color Enhancement 14.3% 70%
    Focus Enhancement 14.3% 70%
    Tactile Enhancement 14.3% 70%

    Adverse Effects 7

    Anxiety 61.9% 70%
    Confusion 33.3% 70%
    Increased Heart Rate 23.8% 70%
    Sweating 19.0% 70%
    Headache 19.0% 70%
    Memory Suppression 19.0% 70%
    Nausea 14.3% 70%

    Dose-Response Correlation

    How effect frequency changes across dose levels

    View data table
    Effect Heavy (n=10)
    Euphoria 70.0%
    Anxiety 60.0%
    Stimulation 60.0%
    Sedation 30.0%
    Sweating 30.0%
    Increased Heart Rate 30.0%
    Headache 30.0%
    Body High 30.0%
    Confusion 20.0%
    Nausea 20.0%
    Visual Distortions 20.0%
    Focus Enhancement 20.0%
    Auditory Effects 20.0%
    Memory Suppression 20.0%

    Dose–Effect Mapping

    Experience Reports

    How reported effects shift across dose tiers, based on 21 experience reports.

    Limited tier coverage — most reports fall within the Heavy range. Effects at other dose levels may not be represented.

    Oral dose range: 120.0–300.0 mg (median 180.0 mg)
    Effect Heavy (n=10)
    euphoria
    70%
    anxiety
    60%
    stimulation
    60%
    sedation
    30%
    sweating
    30%
    increased heart rate
    30%
    headache
    30%
    body high
    30%
    confusion
    20%
    nausea
    20%
    visual distortions
    20%
    focus enhancement
    20%
    auditory effects
    20%
    memory suppression
    20%

    Dosage Distribution

    Dose distribution from experience reports

    Median: 180.0 mg IQR: 120.0–300.0 mg n=10

    Real-World Dose Distribution

    62K Doses

    From 42 individual dose entries

    Oral (n=36)

    Median: 120.0mg 25th: 120.0mg 75th: 127.5mg 90th: 220.0mg
    mg/kg median: 2.076 mg/kg 75th: 3.282

    Common Combinations

    Most co-occurring substances in experience reports

    Form / Preparation

    Most common forms and preparations reported

    Body-Weight Dosing

    Dose relative to body weight from reports with weight data

    Median: 3.0 mg/kg IQR: 1.961–3.78 mg/kg n=10

    Redose Patterns

    Redosing behavior across 16 reports

    12.5% Redosed
    1.2 Avg Doses
    53m Median Interval
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