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How long does Vyvanse stay in your system?

3 min read

In 2023, an estimated 6% of U.S. adults had a current ADHD diagnosis. For many, treatment involves stimulants like Vyvanse, leading to questions about how long does Vyvanse stay in your system for drug testing and metabolism purposes.

Quick Summary

Vyvanse is detectable in urine for up to 3 days, blood for up to 48 hours, saliva for up to 2 days, and hair for 90 days. Elimination time depends on dosage, metabolism, and test type.

Key Points

  • Prodrug Mechanism: Vyvanse (lisdexamfetamine) is inactive until the body metabolizes it into dextroamphetamine, the active stimulant.

  • Half-Life: The inactive prodrug has a half-life of under an hour, while the active metabolite (dextroamphetamine) has a half-life of about 10-12 hours.

  • Urine Detection: Vyvanse is most commonly tested via urine, where it is detectable for up to 3 days.

  • Longest Detection Window: Hair follicle tests offer the longest detection window, capable of identifying Vyvanse use for up to 90 days.

  • Key Influencing Factors: Elimination time is affected by dosage, kidney function, metabolic rate, and urinary pH.

  • Duration of Effects: The therapeutic effects of a single dose of Vyvanse can last for up to 14 hours in adults, providing all-day symptom coverage.

  • Comparison to Adderall: Unlike Adderall, Vyvanse is a prodrug with a slower onset and a lower potential for abuse due to its activation mechanism.

In This Article

Understanding Vyvanse and Its Purpose

Vyvanse, known generically as lisdexamfetamine dimesylate, is a Schedule II central nervous system (CNS) stimulant prescribed for ADHD in individuals over six and moderate to severe Binge Eating Disorder (BED) in adults. It functions by increasing levels of norepinephrine and dopamine in the brain, improving attention, focus, and impulse control. Due to its potential for abuse and dependence, it should only be used as directed by a healthcare provider.

The Pharmacology of Vyvanse: A Prodrug's Journey

Vyvanse is a unique prodrug, meaning it's inactive when taken and becomes active after being metabolized. Enzymes in red blood cells convert lisdexamfetamine into L-lysine and dextroamphetamine, the active component. This gradual conversion results in a smooth, long-lasting effect and potentially lower abuse risk compared to immediate-release stimulants. The active dextroamphetamine reaches peak levels around 3.5 to 4.4 hours after dosing, providing therapeutic effects that can last up to 14 hours in adults. The inactive lisdexamfetamine peaks around one hour after ingestion and has a short half-life.

Half-Life of Vyvanse and Its Metabolite

The half-life of a drug is the time it takes for half of it to be eliminated from the body. A substance is generally considered cleared after about five half-lives.

  • Lisdexamfetamine (inactive): Has a half-life of less than one hour.
  • Dextroamphetamine (active): Has a longer half-life of approximately 10 to 12 hours in adults.

Since tests primarily detect the active dextroamphetamine, Vyvanse can remain detectable in the system for about 2.5 to 3 days.

Vyvanse Detection Windows by Test Type

Detection times vary based on the type of drug test, which typically screens for amphetamines.

  • Urine Test: The most common test. Dextroamphetamine is detectable for up to 3 days.
  • Blood Test: Unconverted lisdexamfetamine may be present for up to 8 hours, while dextroamphetamine can be detected for up to 24-48 hours.
  • Saliva Test: Detectable for up to 2 days (48 hours).
  • Hair Follicle Test: Offers the longest detection window of up to 90 days. Detection is possible about a week after use as the drug incorporates into the hair shaft.

Factors Influencing Vyvanse Elimination Time

Individual factors impact how long Vyvanse remains detectable:

  • Dosage: Higher doses take longer to clear.
  • Frequency of Use: Regular use can prolong detection time due to accumulation.
  • Metabolism: Genetic variations in metabolism rates affect processing speed.
  • Organ Function: Impaired kidney or liver function slows excretion, as the drug is primarily cleared by the kidneys.
  • Age: Metabolic differences between children and adults influence elimination.
  • Body Composition: Body mass and fat can affect drug distribution and clearance.
  • Urinary pH: More acidic urine increases amphetamine excretion, while alkaline urine slows it down. Dietary factors and medications like Vitamin C or sodium bicarbonate can alter urine pH.

Comparison: Vyvanse vs. Adderall

Vyvanse and Adderall are both amphetamine-based ADHD treatments, but differ pharmacologically.

Feature Vyvanse Adderall (XR)
Active Ingredient(s) Lisdexamfetamine (converts to dextroamphetamine) Mixed amphetamine salts (d- and l-amphetamine)
Mechanism Prodrug; requires metabolic conversion Immediately active upon absorption
Onset of Action ~1.5 to 2 hours ~30 minutes to 1 hour
Duration of Effects 10–14 hours 10–12 hours
Active Half-Life ~10-12 hours (dextroamphetamine) ~10-13 hours
Abuse Potential Lower; prodrug design prevents rapid effect via non-oral routes Higher; can be crushed for faster effects

Conclusion

Understanding how long Vyvanse remains in the body involves recognizing its conversion from an inactive prodrug to active dextroamphetamine. While therapeutic effects last up to 14 hours, detection windows vary significantly by test type, ranging from up to 3 days in urine to 90 days in hair. Factors like dosage, metabolism, and kidney function also play a crucial role. Individuals taking Vyvanse should be aware of these variables, especially if drug testing is a possibility. Always consult a healthcare provider for personalized medical advice.

For official prescribing information, you can refer to resources from the FDA. [Link: https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/021977s050,208510s007lbl.pdf]

Frequently Asked Questions

Yes, standard drug panels that screen for amphetamines will detect the active metabolite of Vyvanse (dextroamphetamine), resulting in a positive test.

The therapeutic effects of Vyvanse typically last for up to 14 hours in adults and up to 13 hours in children, designed to provide symptom coverage throughout the day with a single morning dose.

Vyvanse has a dual half-life. The inactive ingredient, lisdexamfetamine, has a half-life of less than one hour. Its active metabolite, dextroamphetamine, has a much longer half-life of approximately 10 to 12 hours in adults.

Vyvanse's active metabolite can be detected in a urine test for up to 3 days after the last dose was taken.

While there is no guaranteed way to speed up elimination, some factors can influence the rate. Acidifying the urine by consuming things like ascorbic acid (Vitamin C) can increase amphetamine excretion. However, this should not be done without medical guidance. Staying well-hydrated may also help facilitate faster elimination through urine.

No. While both treat ADHD, Vyvanse is a prodrug (lisdexamfetamine) that the body converts to dextroamphetamine. Adderall is a combination of immediately active amphetamine salts. This gives Vyvanse a smoother onset and potentially lower abuse risk.

Taking Vyvanse with food can delay the time it takes to reach peak concentration by about an hour, but it does not significantly affect the overall amount of the drug absorbed or its half-life. Urinary pH, influenced by diet, has a more significant impact on excretion time.

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.