Your personalized stack
Built from your goals & the supplement evidence library. You can edit doses & timing.
CaffeineHighMorning or pre-workout • Caffeine anhydrous • Caffeine acutely improves multiple performance outcomes; common effective range is ~3–6 mg/kg in many studies, with high inter-individual variability.200mg
Impairs sleep onset and deep sleep if consumed within 8–10 hours of bedtime
Tolerance develops within 1–2 weeks of daily use, reducing efficacy
Withdrawal: headache and fatigue on cessation after sustained daily use
Elevated heart rate, anxiety, jitteriness — individual sensitivity varies widely
Context: doses >400mg
Caffeine significantly improves reaction time (g=0.28) & accuracy (g=0.27) on attention tasks; dose ≥200 mg shows larger effects.
Strong evidence that 3–6 mg/kg caffeine improves endurance, strength, & power; benefits consistent but moderated by genetics & habituation.
Caffeine prolongs sleep latency, reduces total sleep time & efficiency; clinically meaningful disruption occurs with 400 mg within 8–12 h of bedtime.
Beta-AlanineModerateEvening • Beta-alanine • Chronic beta-alanine supplementation increases muscle carnosine & can improve performance, commonly using multi-gram daily dosing over weeks.3200mg
Significant overall effect size (ES = 0.18, 95% CI 0.08–0.28); greatest benefit for exercise in 1–10 min duration window.
4–6 g/day for ≥4 weeks significantly augments muscle carnosine (intracellular pH buffer) & improves exercise lasting 1–4 min; no benefit for efforts <60 s.
50mg
Vitamin D at 700–800 IU/day reduced hip fracture risk by 26% (RR 0.74) & any nonvertebral fracture by 23% (RR 0.77); no significant benefit was observed at 400 IU/day.
Vitamin D supplementation reduced risk of acute respiratory tract infection (adjusted OR 0.88, 95% CI 0.81–0.96); greatest benefit in those with baseline deficiency (<25 nmol/L) & those receiving daily or weekly dosing rather than bolus doses.
Vitamin D insufficiency is prevalent among athletes, particularly indoor athletes & those in northern latitudes in winter. Insufficiency is associated with reduced muscle strength, power, & endurance; supplementation of 2,000–6,000 IU/day recommended to maintain 25(OH)D >40 ng/mL.
Creatine MonohydrateModerateEvening • Creatine monohydrate • Creatine monohydrate is safe & effective for improving performance & lean mass at commonly used doses.5500mg
Water retention of 1–2 kg in the first week (intramuscular, not fat)
GI discomfort — bloating and cramping; spread loading doses across the day
Context: loading phase >10g/day
Non-responders (~25–30%) see minimal benefit regardless of dose
Oral creatine may improve short-term memory & intelligence/reasoning in healthy individuals; effect on other cognitive domains unclear.
Consistent improvements in strength, power, & training volume; safe for long-term use (up to 30 g/day for 5 years studied). Loading optional; maintenance commonly 3–5 g/day.
Support ingredientsHelpful add-ons, secondary support, and the rest of the stack.2 more
Evening • Triglyceride fish oil • Improves triglycerides & other risk markers; outcomes depend on baseline risk & dose.2000mg
Fishy aftertaste/burps — take with food or use enteric-coated softgels
Mild anticoagulant effect — caution pre-surgery or with blood thinners
Context: doses >3g EPA+DHA/day
High-dose omega-3 (≥2 g EPA+DHA/day) consistently reduces fasting triglycerides by 15–30% in adults with elevated baseline levels.
Omega-3 PUFA supplementation produced a statistically significant reduction in DOMS (MD −0.93, 95% CI −1.44 to −0.42; p=0.0004) across 12 RCTs, though the effect size fell below the minimal clinically important difference of 1.4 on a 10-point VAS. Low-quality evidence overall.
Omega-3 supplementation associated with reductions in cardiovascular events; benefit most consistent at higher EPA+DHA doses (≥2 g/day) & in high-risk populations.
Evening • Lyophilized powder • Retatrutide produced large, dose-dependent mean body-weight reductions over 48 weeks versus placebo; GI adverse effects were common & dose-related.12mg
Retatrutide produced substantial mean body-weight reductions over 48 weeks (up to ~24% at highest dose), with larger losses at higher doses; GI adverse effects were common & dose-related.
The TRIUMPH phase 3 program (4 trials, >5800 participants) evaluates once-weekly subcutaneous retatrutide vs. placebo for weight management & obesity-related complications (OSA, OA, CVD). No primary efficacy results published as of early 2026; design & rationale published in 2025.
Pre-check is rule-based, not medical advice. Consult a healthcare professional for personalised guidance.
Interaction analysis is based on peer-reviewed pharmacology. PMID links go to PubMed. Not medical advice.
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My Sample Stack
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