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4-Fluoromethamphetamine (4-FMA) is a stimulant drug related to methamphetamine and 4-fluoroamphetamine. It has been reported to be sold as a designer drug, but little is known about its pharmacology or toxicology. It was initially reported to be contained as an ingredient in some of the range of party pills sold internationally by the Israeli company Neorganics from around 2006 onwards, but this was later shown to be incorrect, and this ingredient was eventually identified as the closely related compound 2-fluoromethamphetamine.
4-Fluoromethamphetamine (4-FMA) is a stimulant drug related to methamphetamine and 4-fluoroamphetamine. It has been reported to be sold as a designer drug, but little is known about its pharmacology or toxicology. 2-Fluoromethamphetamine (2-FMA) is a stimulant drug of the amphetamine family which has been used as a designer drug. 2-FMA is purported to produce somewhat less euphoria than similar amphetamines, likely due to its main mechanism of action consisting of norepinephrine reuptake inhibition.
4-Fluoromethamphetamine (4-FMA) is a stimulant drug related to methamphetamine and 4-fluoroamphetamine. It has been reported to be sold as a designer drug, but little is known about it. It is purported that 2-FMA produces less euphoria than similar amphetamines, likely due to its main mechanism of action consisting of norepinephrine reuptake inhibition.
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4-Fluoromethamphetamine is a psychostimulant drug related to amphetamine sold online as a designer drug. This compound shares some empathogenic properties with amphetamine and partially substitutes for it in rats and mice.
4-Fluoromethamphetamine (4-FMA) belongs to a class of chemicals called substituted amphetamines. The pharmacology of 4-FMA, as with any other drug, is dependent on the dose and route of administration. The more commonly used routes are oral and intranasal. 4-FMA can be snorted or taken orally, with effects following in 15 minutes, peaking at 40 to 70 minutes, and lasting for up to 3–4 hours after oral administration. The effects last for approximately 4–6 hours after an oral dose.
FMA is a drug of the amphetamine family. It is known to display dopamine, serotonin, and norepinephrine reuptake inhibition.
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4-Fluoromethamphetamine (4-FMA) is a synthetic stimulant sold as a designer drug. It has been reported to be sold as a designer drug, but little is known about its pharmacology or toxicology.
2- Fluoromethamphetamine (2-FMA) is a stimulant drug of the amphetamine family which has been used as a designer drug. More specifically, 2-fluoroamphetamine is an alpha-methylated phenethylamine and fluorinated analog of methamphetamine. 2-FMA was first synthesized by G. Mann, B. Crespi, F. Eugster and Albert Hofmann in 1940s Germany. Still, its pharmacological activity was not studied until it was reexamined in the 1970s by a team at Boehringer Ingelheim, who also patented its use as a nasal decongestant under the brand name Fludrex.
