Last update July 7, 2023

(R,S)-α-Methylphenethylamine

Likely Compatibility

Fairly safe. Mild or unlikely adverse effects. Compatible under certain circumstances. Follow-up recommended. Read Commentary.

A sympathomimetic drug and central nervous system stimulant, it has a similar action and uses to its isomer dextroamphetamine. It is used in the treatment of narcolepsy (Wise 2007) and Attention Deficit Hyperactivity Disorder (ADHD), and is also used as an illegal drug. (Oei 2012; Bartu 2009). Oral administration.

It is excreted in breast milk, concentrating between 2 and 8 times more than in plasma (FDA 2017, Steiner 1984). This concentration, although it could be significant (Bartu 2009), assumes a relative dose between 2% (Öhman 2015) and 13.8%. (FDA 2017)

In infants whose mothers were taking amphetamine as narcolepsy treatment, low plasma levels (Öhman 2015) and urine (Steiner 1984) were measured and no problems were observed in the clinical follow-up of these infants. (Öhman 2015, Steiner 1984)

There is little information on the impact of amphetamine abuse on the development and health of infants (Oei 2012, Wise 2007, Moretti 2000), but it is known that they are more exposed to social problems, domestic violence, and lower breastfeeding rates. (Oei 2010)

There is controversy over the possibly mild negative effect of amphetamine on prolactin (Petraglia 1987, DeLeo 1983), but milk production in mothers who took it therapeutically was not affected. (Öhman 2015)

During breastfeeding, the therapeutic use (narcolepsy, ADHD) of amphetamine can be assessed, using the lowest possible effective dose and monitoring the occurrence of irritability, insomnia, lack of appetite and weight loss. Some authors contraindicate it. (Ornoy 2018)

Its use as a drug of abuse is totally discouraged. (Oei, 2012)

To minimize the risk, after the last recreational use of amphetamine, it is advisable to wait 56 hours (5 T½, which eliminates 97% of the substance) before breastfeeding again. For other authors, it is enough to wait 48 hours (Bartu, 2009). Meanwhile, express and discard milk regularly.


See below the information of these related products:

  • Dexamfetamine Sulfate (Fairly safe. Mild or unlikely adverse effects. Compatible under certain circumstances. Follow-up recommended. Read Commentary.)
  • Lisdexamfetamine Mesilate (Fairly safe. Mild or unlikely adverse effects. Compatible under certain circumstances. Follow-up recommended. Read Commentary.)
  • Narcolepsy. Narkolepsy. (Fairly safe. Mild or unlikely adverse effects. Compatible under certain circumstances. Follow-up recommended. Read Commentary.)

Alternatives

  • Dexamfetamine Sulfate (Fairly safe. Mild or unlikely adverse effects. Compatible under certain circumstances. Follow-up recommended. Read Commentary.)
  • Fluoxetine Hydrochloride (Fairly safe. Mild or unlikely adverse effects. Compatible under certain circumstances. Follow-up recommended. Read Commentary.)
  • Methylphenidate (Safe substance and/or breastfeeding is the best option.)
  • Sodium Oxybate (Fairly safe. Mild or unlikely adverse effects. Compatible under certain circumstances. Follow-up recommended. Read Commentary.)

Suggestions made at e-lactancia are done by APILAM team of health professionals, and are based on updated scientific publications. It is not intended to replace the relationship you have with your doctor but to compound it. The pharmaceutical industry contraindicates breastfeeding, mistakenly and without scientific reasons, in most of the drug data sheets.

Jose Maria Paricio, Founder & President of APILAM/e-Lactancia

Your contribution is essential for this service to continue to exist. We need the generosity of people like you who believe in the benefits of breastfeeding.

Thank you for helping to protect and promote breastfeeding.

José María Paricio, founder of e-lactancia.

Other names

(R,S)-α-Methylphenethylamine is Amfetamine in Chemical name.

Is written in other languages:

(R,S)-α-Methylphenethylamine is also known as

Groups

(R,S)-α-Methylphenethylamine belongs to these groups or families:

Tradenames

Main tradenames from several countries containing (R,S)-α-Methylphenethylamine in its composition:

  • Adderall™. Contains other elements than (R,S)-α-Methylphenethylamine in its composition
  • Adzenys
  • Dyanavel
  • Evekeo
  • MAS-ER™. Contains other elements than (R,S)-α-Methylphenethylamine in its composition

Pharmacokinetics

Variable Value Unit
Oral Bioavail. 96 %
Molecular weight 135 daltons
Protein Binding 15 - 40 %
VD 4 (3 - 5) l/Kg
pKa ≈ 10 -
Tmax 4 (2 - 8) hours
10 - 11 hours
M/P ratio 2 - 8 -
Theoretical Dose 0.02 (0.01 - 0.04) mg/Kg/d
Relative Dose 2 - 14 %

References

  1. Ornoy A. Pharmacological Treatment of Attention Deficit Hyperactivity Disorder During Pregnancy and Lactation. Pharm Res. 2018 Abstract
  2. FDA. Amphetamine. Drug Summary. 2017 Full text (in our servers)
  3. Vallersnes OM, Dines AM, Wood DM, Yates C, Heyerdahl F, Hovda KE, Giraudon I; Euro-DEN Research Group., Dargan PI. Psychosis associated with acute recreational drug toxicity: a European case series. BMC Psychiatry. 2016 Aug 18;16:293. Abstract Full text (link to original source)
  4. Öhman I, Wikner BN, Beck O, Sarman I. Narcolepsy Treated with Racemic Amphetamine during Pregnancy and Breastfeeding. J Hum Lact. 2015 Abstract
  5. Carvalho M, Carmo H, Costa VM, Capela JP, Pontes H, Remião F, Carvalho F, Bastos Mde L. Toxicity of amphetamines: an update. Arch Toxicol. 2012 Aug;86(8):1167-231. Abstract
  6. Oei JL, Kingsbury A, Dhawan A, Burns L, Feller JM, Clews S, Falconer J, Abdel-Latif ME. Amphetamines, the pregnant woman and her children: a review. J Perinatol. 2012 Oct;32(10):737-47. Abstract Full text (link to original source) Full text (in our servers)
  7. Oei J, Abdel-Latif ME, Clark R, Craig F, Lui K. Short-term outcomes of mothers and infants exposed to antenatal amphetamines. Arch Dis Child Fetal Neonatal Ed. 2010 Jan;95(1):F36-41. Abstract
  8. Bartu A, Dusci LJ, Ilett KF. Transfer of methylamphetamine and amphetamine into breast milk following recreational use of methylamphetamine. Br J Clin Pharmacol. 2009 Apr;67(4):455-9. Abstract Full text (link to original source) Full text (in our servers)
  9. Wise MS, Arand DL, Auger RR, Brooks SN, Watson NF; American Academy of Sleep Medicine. Treatment of narcolepsy and other hypersomnias of central origin. Sleep. 2007 Abstract Full text (link to original source) Full text (in our servers)
  10. de la Torre R, Farré M, Navarro M, Pacifici R, Zuccaro P, Pichini S. Clinical pharmacokinetics of amfetamine and related substances: monitoring in conventional and non-conventional matrices. Clin Pharmacokinet. 2004;43(3):157-85. Review. Abstract
  11. Moretti ME, Lee A, Ito S. Which drugs are contraindicated during breastfeeding? Practice guidelines. Can Fam Physician. 2000 Sep;46:1753-7. Review. Abstract Full text (link to original source) Full text (in our servers)
  12. Petraglia F, De Leo V, Sardelli S, Mazzullo G, Gioffrè WR, Genazzani AR, D'Antona N. Prolactin changes after administration of agonist and antagonist dopaminergic drugs in puerperal women. Gynecol Obstet Invest. 1987;23(2):103-9. Abstract
  13. Steiner E, Villén T, Hallberg M, Rane A. Amphetamine secretion in breast milk. Eur J Clin Pharmacol. 1984 Abstract
  14. DeLeo V, Cella SG, Camanni F, Genazzani AR, Müller EE. Prolactin lowering effect of amphetamine in normoprolactinemic subjects and in physiological and pathological hyperprolactinemia. Horm Metab Res. 1983 Sep;15(9):439-43. Abstract

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