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Nootropic

Piracetam

Also called 2-Oxo-1-pyrrolidineacetamide, Nootropil, Pyracetam

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Common dose · Oral2–3 g PW
Onset30–90 minutes PW
Total4–8 hours PW

Dosage

When sources disagree, both rows are shown as published. Nothing is averaged or merged.

Oral

SourceThresholdLightCommonStrongHeavy
PsychonautWiki0.25–0.5 g PW0.5–2 g PW2–3 g PW3–5 g PW5 g+ PW
TripSit––1200–4800 mg TS––

Note: Doses are normally split up to be taken 3x a day. TS

TripSit dose text

TripSit's factsheet also states its doses as text.

Common: 1200-4800mg | Note: Doses are normally split up to be taken 3x a day. TS

What dose are you on? (self-reported, unverified)
Read this first. These numbers come from anonymous visitors typing in a box. Nobody checks them. People misjudge, mistype, troll, or take untested products of unknown strength. They are not a dose guide and never override the sourced table above. They exist only so the sourced ranges can be compared with what people say they take. If you are deciding what to take, use the sourced table, start low, and read the risks section.
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Duration

Route · sourceOnsetCome-upPeakOffsetTotalAfter-effects
Oral · PsychonautWiki30–90 minutes PW–––4–8 hours PW–

TripSit factsheet

Onset
15-35 minutes TS
Duration
3-6 hours TS
Aftereffects
1-6 hours TS

Mixing

Acute combinations: what happens when these are taken close together. Entries backed by a medical journal or agency are listed first.

Backed by medical journals

Awaiting sourcePeer-reviewed reports on acute combinations, from PubMed and the journals the harm reduction sites cite.

Risks and toxicity

Adverse effects, although rare and of short duration are limited to anxiety, insomnia, drowsiness, headaches and agitation. It may be safe for up to 18 months in humans at doses of 3.2g daily with one year-long study in ambulatory patients with Alzheimer's using 8g daily reporting no side effects. However, a possibility for adverse drug-drug interactions persists for piracetam due to it interacting with blood in an anti-clotting manner. Therefore, caution should be taken when pairing piracetam with pharmaceutical blood thinning agents such as Warfarin or potent nutraceutical options and individuals prone to brain hemorrhaging are discouraged from using piracetam.[5] PW

Patients with renal insufficiency should also not use piracetam. PW

No fatal overdoses associated with piracetam use have been reported as of 2016. In animal models (rodents, dogs, and marmoset), an LD₅₀ failed to be established at the dosage of 8-10g/kg. PW

Regardless, it is strongly recommended that one use harm reduction practices when using this substance. PW

Lethal dosage

The median lethal dosage (LD50) of piracetam has not been officially published as it has low abuse potential, but the typical dosage is two grams once to three times a day. PW

Dependence and abuse potential

The chronic use of piracetam can be considered as not addictive with a low potential for abuse. It does not seem to be capable of causing psychological dependence among certain users. PW

Tolerance to many of the effects of piracetam develops with prolonged and repeated use. This results in users having to administer increasingly large doses to achieve the same effects. After that, it takes about 3 - 7 days for the tolerance to be reduced to half and 1 - 2 weeks to be back at baseline (in the absence of further consumption). Piracetam may presents cross-tolerance with all racetam nootropics, meaning that after the consumption of piracetam certain nootropics such as aniracetam and pramiracetam may have a reduced effect. PW

Dangerous interactions

Piracetam showed nonselective MAO activity in a rat study. Piracetam and MAOIs are a potentially dangerous combination. It is likely that MAOIs could increase the effects of piracetam unpredictably. Taking this chemical while on prescription MAOIs is strongly discouraged.[6][7] PW

Median lethal dose (LD50) in animals

Quoted from PubChem's Non-Human Toxicity Values, which come from the Hazardous Substances Data Bank (HSDB). PubChem describes them as: “Quantitative non-human toxicity values (e.g., lethal dose) for this compound. The data shown here are mostly for lab animals (e.g., rat, mouse, guinea pig, and rabbit).” and defines the “LD50 (median lethal dose, the estimated amount of a chemical expected to kill 50% of test animals in a single dose)”. PC

LD50 (as the source gives it)Reference
LD50 Mouse oral 26 g/kg PCMedicines.org.uk; Nootropil 800mg & 1200mg Tablets and Solution. (UCB Pharma Limited; August 2005) electronic Medicines Compendium. Datapharm Communications. Available from, as of July 31, 2007: https://emc.medicines.org.uk/ (via HSDB record 7529)

Testing

Awaiting sourceReagent reactions and test kit guidance from a harm reduction testing service.

Effects

Awaiting sourceSubjective and physical effects from PsychonautWiki or TripSit.

Overview

Piracetam (2-oxo-1-pyrrolidine acetamide) is a nootropic substance of the racetam class. It is a derivative of GABA. PW

A racetam nootropic claimed by many to have cognitive benefits however this has never been strongly supported in healthy individuals. Prescribed in the UK as a treatment for myoclonus. Potentially an ampakine. One of the first popular 'nootropics.' TS

Piracetam is a drug that has efficacy in cognitive disorders, vertigo, cortical myoclonus, dyslexia, and sickle cell anemia; sources differ on its usefulness for dementia. Piracetam is sold as a medication in many European countries. Piracetam in the United States is not approved for general use.[1–4] WP

Piracetam is in the racetams group, with chemical name 2-oxo-1-pyrrolidine acetamide. It is a cyclic derivative of the neurotransmitter GABA and shares the same 2-oxo-pyrrolidone base structure with pyroglutamic acid. Related drugs include the anticonvulsants levetiracetam and brivaracetam, and the putative nootropics aniracetam and phenylpiracetam.[2] WP

History

History

Piracetam was first made some time between the 1950s and 1964 by Corneliu E. Giurgea. There are reports of it being used for epilepsy in the 1950s.[8][9] WP

Pharmacology

Awaiting sourcePharmacology from Wikipedia and the journal papers it cites.

Chemistry

Formula
C6H10N2O2 PC
CAS number
7491-74-9 PC
Molar mass (g/mol)
142.16 PC
IUPAC name (computed by PubChem)
2-(2-oxopyrrolidin-1-yl)acetamide PC
SMILES
C1CC(=O)N(C1)CC(=O)N PC
InChIKey
GMZVRMREEHBGGF-UHFFFAOYSA-N PC
PubChem CID
4843

User reports

Erowid erowid.org

Listings

Erowid Experience Vault listing

Link as published on TripSit's factsheet.

Top stories
Awaiting sourceShort summaries of the most-read reports, each linked, saying only what the report says.

Bluelight bluelight.org

Listings
Awaiting sourceTrip report threads and this substance's discussion forum.
Top stories
Awaiting sourceShort summaries of the most-read reports, each linked, saying only what the report says.

Reddit reddit.com

Listings
Awaiting sourceTrip report posts and the relevant subreddits.
Top stories
Awaiting sourceShort summaries of the most-read reports, each linked, saying only what the report says.

Pop culture

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References

  1. Other Nootropil Tablets 1200 mg. 2017-02-15
  2. Journal / agency Winblad B. Piracetam: a review of pharmacological properties and clinical uses. CNS Drug Reviews. 2005. doi:10.1111/j.1527-3458.2005.tb00268.x · PMID 16007238 · PMC6741724
  3. Journal / agency Flicker L, Grimley Evans G. Piracetam for dementia or cognitive impairment. The Cochrane Database of Systematic Reviews. 2001. doi:10.1002/14651858.CD001011 · PMID 11405971 · PMC12016011
  4. Journal / agency Cohen PA, Zakharevich I, Gerona R. Presence of Piracetam in Cognitive Enhancement Dietary Supplements. JAMA Internal Medicine. March 2020. doi:10.1001/jamainternmed.2019.5507 · PMID 31764936 · PMC6902196
  5. Journal / agency Fedi, M., Reutens, D., Dubeau, F., Andermann, E., D’Agostino, D., Andermann, F. Long-term efficacy and safety of piracetam in the treatment of progressive myoclonus epilepsy. Archives of Neurology. May 2001. doi:10.1001/archneur.58.5.781
  6. Journal / agency Stancheva, S. L., Alova, L. G. Effect of centrophenoxine, piracetam and aniracetam on the monoamine oxidase activity in different brain structures of rats. Farmakologiia I Toksikologiia. June 1988
  7. Journal / agency Trabucchi, M., Govoni, S., Battaini, F. Changes in the interaction between CNS cholinergic and dopaminergic neurons induced by L-alpha-glycerylphosphorylcholine, a cholinomimetic drug. Il Farmaco; Edizione Scientifica. April 1986
  8. Other Li JJ, Corey EJ. Drug Discovery: Practices, Processes, and Perspectives. 2013
  9. Other Schmidt D, Shorvon S. The End of Epilepsy?: A History of the Modern Era of Epilepsy Research 1860-2010. 2016
  10. Other Anlage 1 AMVV - Einzelnorm
  11. Other Medew J. Call for testing on 'smart drugs'. 1 October 2009
  12. Harm reduction site Erowid Piracetam Vault: Legal Status
  13. Harm reduction site Piracetam
  14. Other Bellamy J. FDA proposes ban on curcumin and other naturopathic favorites in compounded drugs. 26 September 2019
  15. Other Parallel import (PI) licences granted in June 2015
  16. Other Nootropil Tablets 800 mg
  17. Other UCB's piracetam approved in Japan. 1999-11-25
  18. Other Fulltext
  19. Other Data file for medicines?
  20. Other Guidance Document on the Import Requirements for Health Products under the Food and Drugs Act and its Regulations (GUI-0084). 1 June 2010

Text and values on this page are quoted from PsychonautWiki (CC BY-SA 4.0), Wikipedia (CC BY-SA 4.0), TripSit factsheets, PubChem (public domain). Each value links to the exact revision it came from.