Citation noticeOur citation system is being overhauled
References and citation markers may currently be incomplete, mismatched, or incorrect. This system is being rebuilt and reviewed before the full site launch.
3-FPM
3-FPM is a stimulant and a fluorinated derivative of phenmetrazine.1 3-FPM appeared on the drug market in 2014.1 Users often describe its stimulation as relatively subtle, with less nervousness, insomnia, and euphoria than other stimulants. It is classified as habit-forming, and some anecdotal reports describe serious nervous system reactions in people who use it.
Dosage & Duration
Dosage
Doses are population estimates that vary widely between individuals.
Duration
Subjective Effects
Legacy content. A statistically backed ontology from Mindstate Design Labs is coming soon.
Effects vary widely by individual, dose, and context.
Physical
The physical effects of 3-FPM can be broken down into several components which progressively intensify proportional to dosage.
Cognitive
The cognitive effects of 3-FPM can be broken down into several components which progressively intensify proportional to dosage. It contains a large number of typical stimulant cognitive effects. Although negative side effects are usually mild at low to moderate doses, they become increasingly likely to manifest themselves with higher amounts or extended usage. This particularly holds true during the offset of the experience.
Pharmacology
Pharmacodynamics
3-FPM primarily releases norepinephrine and dopamine by reversing their transporters, moving these neurotransmitters from inside cells into the extracellular space. It has negligible efficacy as a serotonin releaser. In HEK293 cells, it also inhibits dopamine and norepinephrine uptake,2 with substantially weaker inhibition of serotonin uptake.3
Pharmacokinetics
3-FPM undergoes N-oxidation, hydroxylation of its aromatic ring followed by O-methylation, and hydroxylation and oxidation of its alkyl portion.4 Breakdown of the ethyl bridge produces a metabolite with both O- and N-dealkylation.4 These transformations can occur in combination, followed by glucuronidation or sulfation.4
Tolerance
Tolerance timelines are rules of thumb, not exact schedules, and vary widely between individuals and use patterns.
All dopaminergic stimulants
Harm Potential
Addiction & Dependence
Psychological
ModerateChronic 3-FPM use is moderately addictive, with high abuse potential and psychological dependence in some users; cravings and withdrawal effects may follow abrupt cessation once addiction develops. Repeated redosing and escalating consumption despite diminishing reward have also been reported.
Toxicity
The toxic dose of 3-FPM is unknown.
Several users have reported severe flu-like symptoms during the comedown from 3-FPM, including muscle and joint pain, fever, chills, and headaches, sometimes accompanied by migraine auras; systemic inflammation is a proposed explanation, with causality uncertain.
History & Culture
3-FPM was developed as an analogue of phenmetrazine6, which was used clinically as an appetite suppressant in Europe in the…
Legality
International
3-FPM is not named in the INCB lists of narcotic drugs under the 1961 Convention or psychotropic substances under the 1971 Convention. It is also not named in the precursor tables of the 1988 Convention.
By Country
References
Source Pages
Citations
Further Reading
Article Status
Step 1 · Automated synthesisAn autonomous workflow built by Josie Kins compiled this article's foundation from information published across the web.
- Step 2 · First-pass reviewPending
Not yet reviewed: this article is pending editorial review by Lyrea.
- Step 3 · Citation reviewPending
No one has reviewed this article's citations yet. That second pass checks each claim against the source it cites.
Suggest an edit
Spotted a mistake, an outdated claim, or something missing from the 3-FPM article? Send the editors a private note. Feedback lands in a moderation queue and is never shown on the site.
Wish to give generalised feedback? You can do so here.