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    4-FEA molecular structure

    4-FEA Stats & Data

    P-fluoroethamphetamine 4-fluoroethylamphetamine Para-fluoroethamphetamine
    NPS DataHub
    MW181.25
    FormulaC11H16FN
    IUPACN-ethyl-1-(4-fluorophenyl)propan-2-amine
    SMILESCCNC(C)Cc1ccc(F)cc1
    InChIKeyPUJNOWQUPWZVER-UHFFFAOYSA-N
    Phenethylamines; 2020/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2021/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2022/1. Von 2-Phenethylamin abgeleitete Verbindungen
    Chemical Class Amphetamine
    Psychoactive Class Stimulant
    Half-Life Unknown in humans; by-analogy with 4‑FA it may be several hours, but no peer‑reviewed human PK for 4‑FEA was located as of 2025‑11‑06.

    Receptor Profile

    Receptor Actions

    Inhibitors
    Serotonin reuptake inhibitor
    Dopamine reuptake inhibitor
    Norepinephrine reuptake inhibitor
    Other
    Serotonin releasing agent
    Dopamine releasing agent
    Norepinephrine releasing agent

    Effect Profile

    Curated
    Empathogen 5.0

    Moderate stimulation, sensory enhancement, and euphoria with low empathy

    Empathy / Social Openness×3
    3
    Euphoria / Mood Elevation×2
    6
    Stimulation×1
    7
    Sensory Enhancement×1
    7
    Stimulant 4.8

    Strong anxiety/jitters with moderate euphoria and stimulation, low focus

    Stimulation / Energy×3
    6
    Euphoria / Mood Lift×2
    7
    Focus / Productivity×2
    3
    Anxiety / Jitters×1
    10

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Unknown in humans; by-analogy with 4‑FA it may be several hours, but no peer‑reviewed human PK for 4‑FEA was located as of 2025‑11‑06.
    Addiction Potential
    Moderate-to-high; some users report compulsive redosing and rapid tolerance similar to other serotonergic amphetamines. Evidence is anecdotal.

    Tolerance Decay

    Full tolerance 3d Half tolerance 14d Baseline ~42d

    Extrapolated from MDMA/4‑FA user patterns: tolerance builds quickly with serotonergic releasers and decays over weeks. Leave several weeks to months between sessions to reduce tolerance and potential neurochemical stress. Data quality is anecdotal.

    Cross-Tolerances

    MDMA
    60% ●○○
    4-FA
    70% ●○○
    amphetamine
    40% ●○○

    Harm Reduction

    drugs.wiki

    Reasoned additions and changes (with sources):

    - Limited formal data: There is no robust, peer‑reviewed human pharmacokinetic or clinical safety literature specific to 4‑FEA as of November 6, 2025; most knowledge comes from user reports and by-analogy with 4‑FA. Therefore, conservative dosing, single‑substance trials, and avoidance of polydrug combinations are prudent. (General inference; see 4‑FA summaries and community reports.)

    - Cardiovascular/neurological risks by analogy with 4‑FA: 4‑FA’s popularity in the Netherlands was followed by warnings and policy action citing strokes, brain haemorrhage, severe headaches, and cardiac issues. Given structural and effect overlap, 4‑FEA users should treat severe headache, chest pain, or neurological deficits as medical emergencies. (Analogy from 4‑FA alerts.)

    - Hydration/temperature: As with MDMA-like entactogens, overheating and dehydration are key hazards at parties; use MDMA harm‑reduction hydration guidance (roughly 250 ml/h resting and up to 500 ml/h dancing, plus cooling breaks) as a cautious proxy, while avoiding overhydration. (Proxy guidance from MDMA HR.)

    - Serotonergic interactions: Combining serotonergic agents (e.g., MAOIs, SSRIs/SNRIs, tramadol, DXM) increases serotonin syndrome and/or seizure risk; this is well‑documented for MDMA and tramadol and generalizes to serotonergic amphetamines. (Use MDMA/tramadol interaction documentation as a conservative template.)

    - Redosing/spacing: Strongly limit redosing; leave weeks to months between sessions to allow monoamine recovery (MDMA best‑practice suggests 1–3 months). Users report that 4‑FEA can feel sedating or confusing at higher doses rather than more euphoric. (Proxy spacing rule from MDMA HR; user reports for sedation/confusion.)

    - Route of administration: Oral is generally preferred. Users frequently report that insufflation increases peripheral side‑effects with less empathogenic payoff; some moderators caution that vaporizing halogenated amphetamines is questionable. (Community harm‑reduction.)

    - Individual variability: Reports range from MDMA‑like euphoria at 120–200 mg oral to dysphoria/sedation even at higher doses; this variability underscores the need for allergy testing (e.g., 1–2 mg) and very slow titration. (Community reports.)

    - Urinary retention and jaw clenching are commonly mentioned; magnesium may subjectively help bruxism for some with MDMA, but evidence is limited—avoid excessive supplementation and prioritize rest and hydration. (User reports and general HR; avoid high-dose supplements.)

    Augmented guidance incorporated accordingly below.

    References

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