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Also: creatine mono · N-carbamimidoyl-N-methylglycine monohydrate · creatin
Four separate measurements, never averaged. Independent evidence counts only studies with no sponsor attached. Methodology version v2.0-2026-10 · how we grade evidence
Claimed to increase muscle strength, power, lean or fat-free mass and high-intensity exercise capacity, and marketed increasingly for cognition, bone health and healthy ageing. The strength and body-composition claims are among the best-evidenced in this cluster: hundreds of randomised trials, pooled in the largest synthesis to date across 143 studies, and two authorised health claims in the European Union — one for physical performance in successive bursts of short-term high-intensity exercise, one for the effect of resistance training on muscle strength in adults over 55.
The effects are real and small. The pooled figures are +0.86 kg body mass, +0.82 kg fat-free mass and −0.28% body fat, with no heterogeneity at all across studies — the authors’ own word for this is a "small effect". Part of the fat-free-mass gain is water rather than contractile tissue: NIH ODS notes creatine often causes weight gain from water retention, and when the outcome is measured as direct regional muscle thickness instead of whole-body mass the pooled estimate crosses zero.
Safety knowledge is established, with hundreds of trials from 7 to 52 weeks plus multi-year follow-up noted by NIH ODS, and no hepatotoxicity signal. No tolerable upper intake level has been set. The frequently-asserted absence of renal harm could not be verified from a dedicated safety meta-analysis and is recorded here as unverified rather than confirmed.
At a glance
Expands intramuscular phosphocreatine stores, which buffers ATP resynthesis during short maximal efforts; secondary mechanisms proposed are cell volumisation and effects on protein synthesis. Both the phosphocreatine-loading step and the downstream performance and body-composition effects are demonstrated in human randomised trials, which is why this is one of the few compounds here whose mechanism is confirmed in humans rather than inferred from cell or animal work.
Dated determinations, each flagged for whether it is final and whether it covers safety only. A safety review is not an efficacy finding, and most reporting in this category conflates the two.
The US dietary supplement framework means the compound reaches the market without pre-market review of either efficacy or safety. No FDA warning or enforcement action against creatine was located in this pass.
NIH ODS fact sheet, page last modified 12 October 2026. Documented effects are weight gain from water retention plus anecdotal nausea, diarrhoea, muscle cramps, heat intolerance, reduced range of motion and muscle stiffness. No hepatotoxicity signal. The frequently-asserted absence of renal harm could not be verified from a dedicated renal-safety meta-analysis and is not asserted here. A safety statement says nothing about whether a compound works.
Commission Implementing Regulation (EU) 2017/672 of 7 April 2017, published 8 April 2017 and in force 28 April 2017, conditioned on a daily intake of 3 g of creatine in adults over 55 engaged in regular resistance training. Unusual for a sports supplement: an authorised efficacy claim aimed at older adults.
In the Annex of authorised claims under Regulation (EU) 432/2012, usable only where the food provides a daily intake of 3 g of creatine and only for foods targeting adults performing high-intensity exercise. Underlying assessment EFSA Journal 2011;9(7):2303; consolidated entries 739, 1520–1534, 1922–1924. This is a claim about efficacy, not safety — and creatine is one of only two compounds in this cluster to hold two of them.
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