Piracetam (Nootropil) - 800 mg x 60 capsules

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Quick Overview

Piracetam users report a range of cognitive, mood, social and physical benefits with regular usage.  The most commonly reported benefit of this supplement is an improvement in the areas of learning and memory.

√ Improves Memory

√ Increases Learning

√ Enhances Focus

You will find Piracetam to be an effective brain supplement in the areas of perception, concentration and overall cognition.

References, Research & Articles:

Clinical Efficacy of Piracetam in Cognitive Impairment

Improved Mitochondrial Function in Brain Aging with Piracetam

Suggested Use: As a dietary supplement take 1 capsule 3 times daily or as directed by your health care professional.

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Piracetam is a nootropic (a term which comes from a Greek word meaning acting on the mind.) that is commonly reported to be a stimulant to the Central Nervous System and a booster of intelligence with no known toxicity or addictive properties. People who have used the product often describe the sensation as waking up the brain.

Piracetam enhances memory and cognitive performance, it slows down the aging process on the brain, increases blood flow and oxygen into the brain, aids in the recovery after a stroke and improves Alzheimer's, Down syndrome, senile dementia and dyslexia. Piracetam a derivative of GABA, is one of the few racetams which can inhibit brain damage caused by a variety of factors including a lack of oxygen to the brain and even excessive alcohol consumption.




In 1964 Dr Corneliu Giurgea led the Belgian pharmaceutical company UCB to first synthesize Piracetam and it was he who first coined the phrase or term Nootropic drug - a substance which enhances mental performance. Nootropil was the first brand name of Piracetam and was launched clinically in the early 1970's.

Dr Giurgea felt that nootropics should have some of the following characteristics:

Memory and learning enhancement; In conditions which usually disrupt learning behaviors or memories like hypoxia (oxygen starved brain) they should enhance this resistance; Brain protection against various physical or chemical injuries; The lack of the usual effects common to other psychotropic drugs like sedation; Have very few side effects and extremely low toxicity. Over the last 4 decades and mainly in Europe, Piracetam has been used experimentally or clinically to treat a wide range of diseases and conditions, some of which are covered below.

Piracetam has been used successfully to treat alcoholism and alcohol withdrawal syndrome. It has brought improvement, or slowed deterioration in senile dementia and Alzheimer's disease and after a stroke improved recovery from speech impairment. For those suffering with decreased brain blood flow or cerebral ischaemia, Piracetam has restored some limb function, speech and a state of consciousness. For elderly psychiatric patients with cerebral impairment Piracetam improved IQ, alertness and co-operation.

With Piracetam dyslexic children have better reading comprehension, accuracy of reading, writing, spelling and an increased memory and verbal learning.

For those experiencing middle-aged forgetfulness to the elderly suffering from age related memory impairment Piracetam has improved mental performance, memory and recall. Piracetam reversed the typical EEG slowing associated with normal human aging whilst at the same time increasing vigilance, attention and memory.

Following head injuries, comatose or post-concussional patients had a reduction in the severity of major symptoms and an improved state of consciousness with Piracetam.

It has been used successfully to treat motion sickness and vertigo.

With severe muscle spasms (Myoclonus) or vasospasm's in the hands or feet (Raynaud's syndrome) Piracetam has proved to be one the best products for treatment.

Both clinically and experimentally Piracetam has been used to inhibit sickle cell anemia.

Piracetam has improved Parkinson's disease, and can work synergistically with standard L-dopa treatment.

One of the major key points to note with Piracetam is its amazing lack of toxicity. Clinical toxicity studies have failed to find a lethal dose (LD50) of Piracetam and one conclusion stated that Piracetam is virtually non-toxic and is therefore considered to be one of the safest products ever developed.

Piracetam has repeatedly demonstrated its ability to prevent or reverse the toxic action of an array of chemicals and conditions. It was discovered that after one year feeding alcohol to rats the formation of lipofuscin (an age-related waste pigment) in brain cells was significantly increased. After high doses of Piracetam were given to the alcohol-fed rats their lipofuscin levels significantly reduced.

Clinical Trials

In a clinical experiment lasting 3 weeks, rats were given Hexachlorophene (HCP), a toxic chemical that induces edema, membrane damage and increases the sodium whilst decreasing the potassium levels in brain cells. The HCP seriously disrupted the rats' ability to navigate a horizontal ladder without frequently falling off the rungs. After the introduction of Piracetam the fall rate reduced by 75%. Piracetam was also found to increase the survival rate of rats subjected to severe hypoxia (low oxygen levels in the brain) and also proved to reverse the induced amnesia and learning problems plus speeded up the post hypoxic recovery time. In humans, when a single 2400mg dose of Piracetam was administered and tested in an environment equal to 5300m./17,000 ft. altitude, eye movement reflexes were enhanced and the breathing rate and choice reaction time were reduced.

Neuroscientists in the 1980's discovered that brain cholinergic neural networks are intimately involved in memory and learning. They also discovered that the structure and function of the cholinergic nerves degenerate in brain aging and in dementias such as Alzheimer's, impairing both the ability of memory and of learning.

During this same period evidence began to show that Piracetam works in part through a multimodal cholinergic activity. When combining Piracetam with either lecithin or choline studies in both aged rats and humans proved to radically enhance learning ability in both plus significant improvement in memory in Alzheimer's patients. Yet giving choline or lecithin alone provided little or no benefit, while Piracetam alone at least provided some benefit.

Research has also shown that Piracetam increases high-affinity choline uptake (HACU), a process which forms acetylcholine (ACh) through the cholinergic nerve endings. In another rat experiment using a drug which blocks ACH receptors learning was prevented and glucose utilization was reduced. But when pre-treated with Piracetam learning was normal as was the glucose-energy metabolism.

In normal aging humans a decline occurs in the cortex acetylcholine receptors. The same happens in aged mice with receptors becoming inactive but with oral treatment of a high dose of Piracetam the activity of the ACh cortex nerves were partially restored.

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ACh and Glutamate (GLU) are two of the most central activating neurotransmitters facilitating alertness, focus, attention, memory and learning. As Piracetam improves memory and mental performance its effects on ACh/GLU neurotransmission must be presumed. Another interesting point to note is that although Piracetam is usually reported to have little to no side effects, on the rare occasion side effects including anxiety, insomnia, agitation, irritability and tremor are identical to the symptoms of excessive ACh/GLU neuroactivity.

Piracetam has shown in the numerous animal and human studies that it has a diverse range of neurological and psychological effects but it is not considered to be a direct activator or inhibitor of the synaptic action of most neurotransmitters. Findings indicated that Piracetam and other similar nootropics in fact enhance neuronal excitability [electrical activity] within specific neuronal pathways exerting their effect in the cell membrane of all excitable cells. Therefore the result of their action is an increase in general neuronal sensitivity towards stimulation thus optimizing the functional state of the brain.

Various studies have found that Piracetam enhances brain energy levels especially under deficit conditions. ATP is Energy and it is essential to the brain's very survival. The brain uses 15-20% of the body's total ATP production. Created out of glucose and oxygen brain cells have to produce all their own ATP. Studies of cerebral blood flow, oxygen uptake and glucose utilization have shown that brain carbohydrate metabolism is impaired in a variety of dementias and that the degree in the reduction of brain carbohydrate metabolism correlates to the severity of the dementia. A 1987 study concluded that with Piracetam there was a 22% increase in whole brain glucose metabolism.

In humans and animals the cerebral cortex is divided into two hemispheres - the left and right. Generally the left hemisphere (which controls the right side of the body) is the dominant hemisphere tending to be logical, analytical, linguistic and sequential in its information processing, while the right will be intuitive, picture-oriented and simultaneous in its information processing. Most favour one side over the other with the dominant hemisphere showing more electrical activity and even though the two sides are linked by nerve fibres, it seems that they are separated. Part of the definition of a nootropic is to facilitate inter cerebral information transfer between the two hemispheres and research has shown Piracetam to do so.

Side Effects

Even at long term high doses Piracetam is regularly recognized as being devoid of negative side effects. In a study on 225 dyslexic children it was noted that piracetam was well tolerated, with no serious adverse clinical or laboratory effects reported. There are so many clinical studies which share and draw the same conclusion, Piracetam is incredibly well tolerated and without side effects.

Yet symptoms such as anxiety, insomnia, irritability, headache, agitation, nervousness and tremor (as noted above in the section on glutamate) can occur for some who are unusually sensitive to Piracetam. Reduce dosage to alleviate this over stimulation or taking magnesium supplements (300-500mg/day) can reduce neural activity. Those highly sensitive to caffeine or MSG should be cautious as should anyone taking other nootropics such as centrophenoxine, idebenone, vinpocetine or deprenyl as the overall synergistic effect could lead to over stimulation. To enhance the brain energising effects of Piracetam taking B complex vitamins, choline, NADH, lipoic acid, CoQ10 or idebenone and magnesium could prove to be beneficial.

Consult with your medical professional before taking.

In clinical literature dosages of Piracetam vary but generally it is taken 3-4 times daily because of it relatively short half life. 1.6 gm, 3 times daily, or 1.2 gm 3-4 times daily is a fairly typical dosage, but for some a noticeable improvement in memory and cognition was gained from just 1.2 gm twice daily.


1. P. Berga et al (1986) "Synergistic interactions between Piracetam and [Hydergine] in some aninnal models of cerebral hypoxia and ischaemia" Arzneim Forsch/ Drug Res 36, 1314-20.

2. R.J. Branconnier et al (1983) "The therapeutic efficacy of Pramiracetam in Alzheimer’s disease- preliminary observations" Psychopharmacol Bull 19,726-30.

3. O. Buresova, J. Bures "Piracetam induced facilitation of interhemispheric transfer of visual information in rats" Psychopharmacologia (Berlinr) 46,93-102.

4. H.R. Chaudhry et al (1992) "Clinical use of Piracetam in epileptic patients" Curr Ther Res 52, 355-60.

5. W. Deberdt (1994) "Interaction between psychological and pharmacological treatment in cognitive impairment" Life Sci 55, 2057-66.

6. S.J.Dimond (1976) "Drugs to improve learning in man" in the neuropsychology of learning disorders, R. Knight, D. Bakker, eds., 367-79. Univ. Park Baltimore.

7. S.J. Dimond, E. Brouwers (1976) "Increase in the power of human memory in normal man through the use of drugs" Psychopharmacol 49, 307-09.

8. S.J. Dimond et al (1979) "Some effects of Piracetam on chronic schizophrenia" Psychopharmacol 64,341-48.

9. S.H. Ferris et al (1982) "Combination Choline/ Piracetam treatment of senile dementia" Psychopharm Bull 18, 94-98.

10. S. Giaquinto (1986) "EEG changes induced by Oxiracetam on Diazepam-Medicated volunteers" Clin. Neuropharmacol 9, S79-S84.

11. C. Giurgea, F. Moyersoons (1970) "Differential pharmacological reactivity of three types of cortical evoked potentials" Arch Int. Pharmacodyn Ther. 188,401-04.

12. C. Giurgea, M. Salama (1977) "Nootropic drugs" Prog. Neuro-Pharmac. 1.235-47.

13. A. Goutiaev, A. Senning (1994) "Piracetam and other structurally related nootropics" Brian Res. Rev. 19, 180-222.

14. T. Itil et al (1983) "Pramiracetam, a new nootropic, a controlled quantitative pharmaco-EEG study" Psychopharm. Bull. 19, 708-16.

15. T. Itil et al (1986) "CNS pharmacology and clinical therapeutic effects of Oxiracetam" Clin. Neuropharmacol. 9, S70-S72.

16. G. Maina et al (1989) "Oxiracetam in the treatment of degenerative and multi infarct dementia" Neuropsychobiol. 21. 141

17. P. Mindus et al (1976) "Piracetam-induced improvement of mental performance" Acta Psychiat Scand 54, 150-60. 

18. A. Moglia et al (1986) "Activity of Oxiracetam in patients with organic brain syndrome" Clin. Neuropharmac 9, S73-S78.

19. C. Mondadori et al (1992) "Elevated corticosteroid levels block the memory improving effects of nootropics" Psychopharmac. 108, 1 1-'

20. F. Moyersoons, C. Giurgea (1974) "Protective effect of Piracetam in experimental barbiturate intoxication: EEG and behavioural studies Arch. Int. Pharmacodyn Ther 210. 38-48.

21. S. Okuyama, H. Aihara (1988) "Action of nootropic drugs on transcollosal responses of rats" Neuropharmac. 27. 67-72.

22. L. Parnetti et al (1985) "Haemorheological pattern in initial mental deterioration; Results of a long term study using Piracetam and Pefylline" Arch Gerontol. Geriatr4, 141-55.

23. G. Pepeu. G. Spignoli (1990) "Neurochemical actions of nootropic drugs" in Advances in Neurology V51; Alzheimer’s disease. R. Wu ed. 247-52, Raven Press.

24. B. Saletu et al (1985) "Oxiracetam in the organic brain syndrome of late life" Neuropsychobiol 13, 44-52.

25. K. Schaffler, W. Klausnitzer (1988) "Antihypoxidotic effects of Piracetam using psychophsiological measures in healthy volunteers" Ar Forsch. Drug Res. 38, 288-91.

26. M. Tacconi, R. Wurtman (1986) "Piracetam: physiological disposition and mechanism of action" in Advances in Neurology V43; Myocio Fahn, ed. 675-685, Raven Press.

27. P. Wester (1987) "Magnesium" Am. J. Clin. Nutr. 45, 1305-12.

28. C. Wilsher et al (1987) "Piracetam and dyslexia-.effects on reading tests" J. Clin. Psychopharmac. 7, 230-37.

Additional Information


Piracetam (800 mg x 60 capsules)

SKU Piracetam-001

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Customer Reviews

Good for students and those who need to get a lot done in tight deadlines
I am in college and take piracetam (and adrafinil) every now and then when I need a study boost or extra concentration and memory for an exam. I have found that piracetam makes me more articulate and think more creatively - it is great to get over a writer's block. I took it before an interview one time and felt like I did really well, the talking just came more natural. Review by Maureen
Piracetam is great but then I get nervous that it was not FDA approved. Review by Gloria, Florida

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