Last update Nov. 3, 2024

リスデキサンフェタミンメシル酸塩

Likely Compatibility

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

A prodrug that is metabolized directly in the intestine to dextroamphetamine. It is used to treat Attention Deficit Hyperactivity Disorder (ADHD) and Binge eating disorder. Dextroamfetamine is a sympathomimetic drug, central nervous system stimulant, whose action and uses are similar to amphetamine (see information) which is its dextro isomer. Oral administration.

Dextroamfetamine is excreted in breast milk, concentrating about 3 times more than in plasma. This concentration assumes a relative dose about 6% (Ilett, 2007)

In infants whose mothers were taking dexamfetamine as treatment for ADHD, levels ranging from undetectable to 14% of maternal plasma levels have been measured and no problems were observed in the clinical and developmental follow-up of these infants (Benassayag 2024, Ilett, 2007).

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)

Expert authors consider its therapeutic use compatible with breastfeeding. It is advisable to monitor the appearance of irritability, insomnia, poor feeding in the infant and developmental parameters (Benassayag 2024, Scoten 2024). It is contraindicated by some authors. (Ornoy 2018)

Its use as an illegal drug is totally discouraged. (Oei, 2012). 

To minimize the risk, after the last recreational use of amphetamine, it is advisable to wait 55 hours (5 T ½, which eliminates 97% of the substance) before resuming breastfeeding. In the meantime, to maintain production, milk should be expressed and discarded from the breast on a regular basis.


See below the information of these related products:

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

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

リスデキサンフェタミンメシル酸塩 is Lisdexamfetamine Mesilate in Japanese.

Is written in other languages:

リスデキサンフェタミンメシル酸塩 is also known as

Groups

リスデキサンフェタミンメシル酸塩 belongs to these groups or families:

Tradenames

Main tradenames from several countries containing リスデキサンフェタミンメシル酸塩 in its composition:

Pharmacokinetics

Variable Value Unit
Oral Bioavail. 96 %
Molecular weight 456 daltons
Protein Binding 16 - 20 %
VD 3.2 - 5.6 l/Kg
pKa 15.89 -
Tmax 3.5 - 4.7 hours
6.8 - 11 hours
M/P ratio 3.3 (2.2 - 4.8) -
Theoretical Dose 0.02 (0.01 - 0.04) mg/Kg/d
Relative Dose 5.7 (4 - 10.6) %

References

  1. Benassayag Kaduri N, Hazan A, De-Haan T, Kohn E, Berkovitch M, Berlin M. Amphetamine use for attention deficit hyperactive disorder during breastfeeding and children's neurodevelopmental outcomes: A pilot study. Psychiatry Res. 2024 Sep;339:116047. Consulted on Nov. 3, 2024 Abstract
  2. Scoten O, Tabi K, Paquette V, Carrion P, Ryan D, Radonjic NV, Whitham EA, Hippman C. Attention-deficit/hyperactivity disorder in pregnancy and the postpartum period. Am J Obstet Gynecol. 2024 Jul;231(1):19-35. Consulted on Nov. 3, 2024 Abstract Full text (link to original source)
  3. Ornoy A. Pharmacological Treatment of Attention Deficit Hyperactivity Disorder During Pregnancy and Lactation. Pharm Res. 2018 Abstract
  4. AEMPS. Lisdexanfetamina. Ficha técnica. 2016 Full text (in our servers)
  5. Öhman I, Wikner BN, Beck O, Sarman I. Narcolepsy Treated with Racemic Amphetamine during Pregnancy and Breastfeeding. J Hum Lact. 2015 Abstract
  6. Shire. Lisdexamfetamine. Drug Summary. 2013 Full text (in our servers)
  7. 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)
  8. 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
  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. Ilett KF, Hackett LP, Kristensen JH, Kohan R. Transfer of dexamphetamine into breast milk during treatment for attention deficit hyperactivity disorder. Br J Clin Pharmacol. 2007 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. 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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