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High-risk compound

Surface here is educational only; do not use without medical supervision. Our editorial verdict is SKIP-FOR-NOW — current cost / risk / redundancy puts it below the line.

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Mydayis

Emerging

SKIP-FOR-NOW for users in this archetype with HIGH confidence.

Aliases (5)
Mixed amphetamine salts (three-bead XR) · MAS three-bead · dextroamphetamine saccharate + amphetamine aspartate + dextroamphetamine sulfate + amphetamine sulfate (triple-pulse) · SHP-465 · Adderall XR-XR
TYPICAL DOSE
FDA-approved adolescent (13-17): Same dose rang…
Once daily AM
ROUTE
Oral (tablet)
Oral
CYCLE
ADHD clinical practice often runs continuous daily
As prescribed
STORAGE
Room temp; original container
Room temp

Overview

What is Mydayis?

Mydayis is a triple-bead extended-release formulation of mixed amphetamine salts (same active ingredient as Adderall) approved by the FDA in 2017 for ADHD in adults and adolescents (≥13). Its three-stage release profile delivers up to 16 hours of coverage from a single morning dose.

Key Benefits

Provides longest-acting amphetamine ADHD treatment available, improving sustained attention, working memory, executive function, and impulse control across the full waking day. Single morning dosing eliminates the afternoon "crash" or need for booster doses common with shorter-acting stimulants.

Mechanism of Action

Mixed dextroamphetamine and levoamphetamine salts release in three sequential pulses, blocking dopamine and norepinephrine reuptake transporters (DAT/NET) and reversing them to drive monoamine efflux into the synapse, increasing prefrontal catecholamine signaling that underlies attentional control.

Pharmacokinetics

·
PeakHalf-life
Approximate curve — visual aid only, not data-precise PK
Brand options3 known
MAS three-beadSHP-465Adderall XR-XR

StatusSchedule II (US DEA) | Schedule II (Canada CDSA, equivalent products limited) | WADA-banned in-competition (S6 stimulant)

Peptide Interactions

MAOIs
Avoid

(hypertensive crisis — absolute contraindication)

Selegiline >10 mg
Avoid

(loses MAO-B selectivity)

Other stimulants
Avoid

(methylphenidate, modafinil, high-dose caffeine — cumulative CV load)

MDMA, methamphetamine, cocaine
Avoid

(severe NT system overload, neurotoxicity, cardiac event risk)

SSRIs
Avoid

(especially fluoxetine, paroxetine — strong CYP2D6 inhibitors raise amphetamine exposure)

Tramadol, dextromethorphan
Avoid

(serotonin syndrome)

Yohimbine, ephedrine, high-dose synephrine
Avoid

(sympathomimetic stacking)

Acidifying agents
Avoid

(high-dose vit C, ammonium chloride — accelerate renal clearance, blunt effect unpredictably)

Alkalinizing agents
Avoid

(bicarbonate, antacids — slow renal clearance, prolong/intensify unpredictably — *especially problematic with three-bead delivery* because PPI/antacid use ca…

Quality Indicators

Pharmacy-dispensed, intact packaging

Prescription tablets in original sealed packaging from a licensed pharmacy.

!

Generic vs branded

Generics are usually fine but bioavailability can vary slightly; track if you switch.

Unbranded blister or counterfeit risk

Counterfeit pharmaceuticals are a known issue; verify pharmacy and lot if buying internationally.

What to Expect

  • Day 1
    PK-driven acute peak per administration. Verify dose tolerated.
  • Week 1
    Steady-state reached for most daily-dosed pharma.
  • Week 2-4
    Therapeutic effect established; titration window if needed.
  • Long-term
    Periodic monitoring per drug class (labs, BP, ECG as applicable).

Side Effects & Safety 9

Side Effects

  1. 1Insomnia ~25% (the differentiator from other MAS — directly attributable to 16-hr duration)
  2. 2Reduced appetite — extended into evening hours (worse than IR/XR for athletes)
  3. 3Dry mouth, increased thirst
  4. 4Headache — first 1-2 weeks
  5. 5Increased HR + BP — sustained throughout 14-16 hour window
  6. 6Anxiety / nervousness
  7. 7Bruxism / jaw clenching
  8. 8All Adderall-class less-common effects apply: palpitations, dizziness, weight loss, GI symptoms, reduced libido, ED, tremor, sweating, restlessness, dependence patterns
  9. 9Mood drop in late evening as third bead clears — some users report a "5 PM dip" before the bead 3 effect kicks in fully

When to Stop

  • Cardiomyopathy / heart failure with chronic use — same case-report literature as Adderall; cumulative daily catecholamine load is *higher* per day on Mydayis than on Adderall IR (longer AUC), so the chronic CV risk is at least as high
  • Sudden cardiac death — same FDA black-box class warning
  • Stroke / MI, psychosis, mania switch, serotonin syndrome (with MAOIs/SSRIs/MDMA/tramadol), stimulant use disorder, withdrawal syndrome on discontinuation
  • First 2 weeks: Sleep onset disruption (the differentiator), cardiovascular adjustment, anxiety, appetite
  • Weeks 4-12: Tolerance development; insomnia rarely resolves with continued use unlike some other side effects
  • Year 1+: Same cardiovascular structural concerns as Adderall, plus cumulative sleep debt from chronic 16-hr daily exposure

References

Mydayis FDA prescribing information (2017, updated 2023)

accessdata.fda.gov · 2017

official PK, three-bead delivery system, indications, side effects, age restriction (13+).

View Study

Wigal et al. 2017 — SHP-465 mixed amphetamine salts XR adult ADHD pivotal trial (J Clin Psychopharmacol)

pubmed.ncbi.nlm.nih.gov · 2017

adult RCT efficacy data.

View Study

Wigal et al. 2018 — Adolescent SHP-465 study

pubmed.ncbi.nlm.nih.gov · 2018

13-17 age group efficacy + safety.

View Study

Mydayis Wikipedia 2026

en.wikipedia.org · 2026

composition, brand history, PK overview.

View Study

Roberts et al. 2020 — Pharmaceutical cognitive enhancement meta-analysis

pubmed.ncbi.nlm.nih.gov · 2020

d-amphetamine showed no overall significant cognitive enhancement effect in healthy adults; applies directly to Mydayis as same molecule.

View Study
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