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Amphetamine Facts

Stimulant; Substituted amphetamine; Dopamine releasing agent

Description

Amphetamine — also known as speed — is a synthetic stimulant of the phenethylamine class. It is the structural parent of methamphetamine and MDMA. It works by reversing dopamine and norepinephrine transporters,[1] flooding the synapse with these neurotransmitters and driving its characteristic stimulation.[2]

Subjective effects include euphoria, increased energy, heightened focus, appetite suppression, and talkativeness. The experience has a driven, physically activating clarity — a steady stimulation that channels into sustained productivity or social confidence depending on context.

Psychological dependence liability is high, and cardiovascular toxicity — elevated heart rate, blood pressure, and heart damage with chronic heavy use[3] — is the primary organ risk. Tolerance to euphoria develops fast while the drive to use intensifies, creating escalating compulsion with diminishing reward.[4]

Dose and durationby route · individual sensitivity varies

Oral(mg)
Threshold< 5 mgLight5 – 15 mgCommon15 – 30 mgStrong30 – 50 mgHeavy50+ mg

Starts in 15 – 30 minLasts 4 – 8 hoursAfter-effects 6 – 24 hours

Body and dependence

Acute toxicity
Low
Chronic toxicity
Moderate
Physical dependence
Low
Psychological dependence
High
Withdrawal
Moderate
Compulsive redosing
High

Tolerance

Builds
Rapid
Fully resets after
14 days
Carries over to
methamphetamine; cocaine; methylphenidate; other dopaminergic stimulants

Effectslikely at a common dose

Perception
Dreaming suppression; +6 possible
Body
Physical fatigue; Wakefulness; Insomnia; Stimulation; Appetite suppression; Pupil dilation; +22 possible, including Dehydration sensation, Vasoconstriction, Abnormal heartbeat
Thinking
Cognitive euphoria; Focus enhancement; Thought acceleration; +19 possible, including Compulsive redosing urge, Cognitive dysphoria
Feeling
Euphoria; +8 possible, including Depression, Dysphoria, Anxiety
Self
none likely · 8 possible, including Craving, Ego inflation
Awareness
Sustained attention (vicara); +1 possible

Who shouldn't take it

Absolute
Structural heart disease; Psychotic disorders; Pregnancy; MAOI co-administration
Relative
Hypertension; Seizure disorders; Bipolar disorder; Hyperthyroidism; Glaucoma

Combinations61 recorded

Lethal (3)
Ibogaine; MAOIs; Tramadol
Dangerous (33)
Anticholinergics; Atypical antipsychotics; Benzodiazepines, Barbiturates; Caffeine; Dopamine agonists; Ephedrine, Pseudoephedrine; Local anesthetics; MDMA, Amphetamines; MDMA, MDA; NDRIs (Wellbutrin); NRIs; Opioids; Psychedelics; SNRIs; SSRIs; Stimulants; 5-HTP, Tryptophan; Alpha-2 adrenergic receptor antagonist; Antihistamines; Antipsychotics; Buspirone; Clonidine, Guanfacine; DXM; GHB, Baclofen; and 9 more, see full page
Caution (22)
See full page: psychedex.org/substances/amphetamine
Not graded (3)
Not listed never means safe.

Seek help immediately if

  • Chest pain; racing, pounding, or irregular heartbeat
  • Very high body temperature; heavy sweating; hot, flushed skin
  • Severe agitation, paranoia, panic, or confusion
  • Severe headache; muscle rigidity or twitching
  • Seizures
  • Signs of stroke — face drooping, one-sided weakness, slurred speech
  • Difficulty breathing; collapse or unconsciousness

What to do

  1. Call emergency services for chest pain, overheating, seizure, or unresponsiveness
  2. Move them to a cool, quiet place and reduce stimulation
  3. Cool the body — remove excess clothing, apply cool damp cloths, fan them
  4. Keep them calm; reassure — panic worsens the cardiovascular strain
  5. If seizing, protect from injury (don't restrain); recovery position afterward
  6. Monitor breathing and be ready to give rescue breaths / CPR

Most stimulant overdoses settle with cooling, a calm environment, and time. The medical danger is hyperthermia, cardiac events (arrhythmia, heart attack, stroke), and seizures — get help immediately if any appear.

988 Suicide & Crisis LifelineFireside Project: 62-FIRESIDE

Version r1 · Not medical advice

References

  1. [1]
    ^Rothman RB, Baumann MH, Dersch CM, Romero DV, Rice KC, Carroll FI, Partilla JS (2001) Amphetamine-type central nervous system stimulants release norepinephrine more potently than they release dopamine and serotonin — Synapse PMID:11071707
  2. [2]
    ^Jones SR, Gainetdinov RR, Wightman RM, Caron MG (1998) Mechanisms of Amphetamine Action Revealed in Mice Lacking the Dopamine Transporter — Journal of Neuroscience doi:10.1523/jneurosci.18-06-01979.1998
  3. [3]
    ^O'Connor AD, Rusyniak DE, Bruno A (2005) Cerebrovascular and cardiovascular complications of alcohol and sympathomimetic drug abuse — Medical Clinics of North America PMID:16105252
  4. [4]
    ^Berridge KC, Robinson TE (2016) Liking, wanting, and the incentive-sensitization theory of addiction — American Psychologist PMID:27977239
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