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Synthetic nootropics & research compounds

Phenibut

beta-phenyl-gamma-aminobutyric acid

Phenibut is a synthetic GABA analogue with GABA-B-related and alpha-2-delta calcium-channel evidence. It has older and regional medical-use literature, but no strong modern evidence for general nootropic performance. The better documented public record is safety-related: sedation and impairment, dependence and withdrawal, interaction risk, product-labeling concerns, and U.S. dietary-supplement regulatory issues.

RelaxationSleep SupportStress ResilienceMood SupportGabaergicSyntheticClinical Research
Updated June 2026/7 min read/12 citations
Prepared by the NootropicsIndex editorial team.Method: prioritize cited human research and official safety or regulatory sources; compare retailer-listed prices without endorsing products.Affiliate disclosure
01

What is it?

What phenibut is

1

Phenibut is a synthetic analogue of gamma-aminobutyric acid (GABA), commonly described as beta-phenyl-GABA. It is psychoactive and is not a routine dietary nutrient or low-risk wellness supplement.

High-risk profile4
Phenibut has a stronger public safety signal than most consumer nootropics. Sedation, impaired judgment, dependence, withdrawal, and interaction risk are central to the profile.

Evidence snapshot

6

The strongest public-facing conclusion is not that phenibut improves cognition. The more defensible summary is that older/regional medical-use literature exists, while modern evidence for general nootropic performance is limited and safety concerns are well documented.

02

Names, aliases and forms

Common NamePhenibut
Spelling VariantFenibut
AbbreviationsPhGABA; PGaba
Chemical Namesbeta-phenyl-gamma-aminobutyric acid; 4-amino-3-phenylbutanoic acid; beta-(aminomethyl)benzenepropanoic acid; beta-(aminomethyl)hydrocinnamic acid
Salt FormPhenibut HCl
Pharmaceutical NamesNoofen; Anvifen
03

Mechanisms of action

GABA-B-related pharmacology

6

Phenibut is structurally related to GABA and is commonly discussed in relation to GABA-B activity and central nervous system effects. This mechanistic framing helps explain sedation and dependence risk, but does not establish a cognitive-performance benefit.

Alpha-2-delta calcium-channel evidence

12

R-phenibut has been reported to bind the alpha-2-delta subunit of voltage-dependent calcium channels and to show gabapentin-like effects in preclinical models. This supports a more precise pharmacology description, but it remains mechanistic/preclinical evidence rather than a consumer benefit claim.

04

Potential effects and evidence map

Phenibut should not be presented as a well-established cognitive enhancer. Human evidence for performance, memory, motivation, or everyday nootropic use is limited or indirect. Safety is more clearly documented through poison-center surveillance, product-analysis studies, pharmacology reviews, and case literature for intoxication, dependence, and withdrawal.

Effect domainMagnitudeGrade
Calm / relaxation10
AcuteConfidence: Medium

Phenibut has been studied and used in older/regional contexts for calming effects, but the evidence base is limited and should not be generalized to unsupervised supplement use.

Note Do not convert regional therapeutic-use literature into broad consumer claims.

2/5
C
Sleep quality11
AcuteConfidence: Low

Sleep-related use appears in older/regional literature, but modern supplement-use evidence is limited and the same sedative effects create impairment risk.

Note Frame as studied context, not as a sleep recommendation.

1/5
C
Mood / wellbeing10
AcuteConfidence: Low

Mood or stress-related claims are not strongly established for consumer nootropic use; available human support is older, regional, and context-specific.

Note Keep wording cautious and avoid disease-treatment framing.

1/5
C
Social ease6
AcuteConfidence: Low

Anecdotal social-ease claims are common online, but reliable human evidence for this public-use claim is absent or too indirect.

Note Anecdotal popularity is not clinical evidence.

0/5
E
Focus / attention6
UnknownConfidence: Low

There is no reliable evidence signal that phenibut supports focus or attention in healthy consumers.

Note Do not infer attention benefits from GABA-related pharmacology.

0/5
E
Memory / learning10
UnknownConfidence: Low

Memory and learning claims are not supported by strong modern human evidence for consumer nootropic use.

Note Older nootropic terminology does not establish a current cognitive-performance claim.

0/5
E
05

Typical dosages and timing

Typical
250-750 mg/day
Not a recommendation
Lower bound
250 mg/day
Profile value
Upper bound
750 mg/day
Profile value
Reported range11250-750 mg/day

WHO ECDD review material discusses a 250-750 mg/day range in regulated or research/medical contexts. This field is retained for evidence context only and is not an over-the-counter dosing recommendation.

Supplement-use caution9Not established

Commercial product labels and online use patterns may not match clinical or reviewed contexts. Because dependence, withdrawal, and toxicity are documented, public copy should avoid optimization tips or escalation guidance.

06

Onset, duration and tolerance

Onset2-4 hours
Duration15-24 hours
Half-life5.3 hours
Limited timing data11

WHO ECDD material reports limited pharmacokinetic information, including an approximate 5.3-hour The time for blood levels to fall by half during the final elimination phase.Source, while oral onset around 2-4 hours and subjective duration around 15-24 hours are described as recreational-user reports. Treat timing fields as approximate context, not instructions for repeat use.

07

Safety, side effects and risk profile

Do not frame as routine supplement use2
Phenibut?s risk profile is high enough that public content should avoid casual wellness positioning, frequent-use advice, or language that normalizes unsupervised use.
Sedation / impairment4
Confidence: High

Sedation, lethargy, confusion, reduced consciousness, and coma are documented in poison-center and case literature.

Note This is one of the highest-priority public cautions.

4/5
B
Dependence / withdrawal risk7
Confidence: High

Repeated use can be associated with tolerance, dependence, and withdrawal; systematic reviews describe severe presentations including agitation, hallucinations, delirium, and seizures.

Note Withdrawal risk should remain prominent and not be diluted across repeated sections.

5/5
B
Interaction risk6
Confidence: High

Risk is elevated with alcohol and other CNS-active substances, including sedatives, anxiolytics, opioids, gabapentinoids, antipsychotics, anticonvulsants, and sleep aids.

Note Clinical management belongs with qualified professionals.

4/5
C
Legal / regulatory risk2
Confidence: High

The FDA states phenibut is not a dietary ingredient in the U.S.; products marketed as dietary supplements with phenibut are regulatory concerns.

Note Country-specific legal status still needs current local verification.

4/5
B
Overstimulation / insomnia8
Confidence: Medium

Agitation and insomnia are reported particularly in withdrawal or adverse-use contexts.

Note Do not frame phenibut as universally calming.

3/5
C
GI discomfort5
Confidence: Medium

Nausea and other gastrointestinal complaints appear in exposure and case literature.

Note GI effects are not the central risk, but should remain listed.

2/5
C
Headache / dizziness5
Confidence: Medium

Dizziness and neurologic symptoms are reported in poison-center and case literature.

Note Relevant for impairment-sensitive tasks.

2/5
C
Cardiovascular caution4
Confidence: Low

Tachycardia and blood-pressure related concerns appear in exposure reports, especially in adverse-use contexts.

Note Signal is less central than sedation and withdrawal, but clinically relevant.

2/5
C
Pregnancy / lactation caution6
Confidence: Medium

Pregnancy and lactation safety are not established; absence of data should be treated as a caution, not reassurance.

Note Keep as a conservative uncertainty flag.

4/5
E
Evidence uncertainty9
Confidence: High

The nootropic benefit evidence is weaker than the safety signal, and product quality/dose-labeling concerns add uncertainty for consumer products.

Note Public content should emphasize uncertainty rather than optimize for conversion.

4/5
C
U.S. poison centers4

CDC reported 1,320 phenibut exposure calls to U.S. poison centers during 2009-2019. Reported outcomes included drowsiness or lethargy, agitation, tachycardia, confusion, coma, major effects, and three deaths.

High-priority risk7

Repeated use can be associated with tolerance, dependence, and withdrawal. Review literature describes withdrawal presentations that may include agitation, insomnia, psychosis, delirium, hallucinations, and seizures.

Impairment4

Because sedation, confusion, and reduced consciousness are documented, phenibut should not be framed as compatible with driving, machinery operation, or other impairment-sensitive tasks.

08

Interactions and cautions

Highest concern6

Risk is most relevant with alcohol and other CNS depressants or CNS-active drugs, including sleep aids, benzodiazepines, opioids, gabapentinoids, antipsychotics, anticonvulsants, and anxiolytics.

Medication caution7

People using psychiatric, neurologic, pain, sleep, or seizure-related medications should not rely on public supplement content for phenibut decisions. Interaction and withdrawal management require qualified clinical guidance.

10

How it compares

Risk comparison6

Phenibut should not be grouped casually with lower-risk calming ingredients such as magnesium or L-theanine. Its psychoactive profile, withdrawal risk, and U.S. supplement-status issues make the comparison materially different.

11

Practical buying and quality notes

  • In the U.S., phenibut is not a lawful dietary ingredient for dietary supplements according to FDA. Public buying copy should emphasize regulatory caution rather than purchase encouragement.2
  • Products may list phenibut as a free amino acid or as a hydrochloride salt. Labels should identify the exact form and amount; do not assume equivalence when the form, assay, or purity testing is unclear.1
  • Published product-analysis work found phenibut quantities in supplements before and after FDA warnings, supporting a conservative approach to label accuracy and third-party testing claims.9
12

FAQ

Is phenibut a dietary supplement in the U.S.?

2

No. FDA states that phenibut does not meet the definition of a dietary ingredient under the FD&C Act, and products marketed as dietary supplements with phenibut as a dietary ingredient are considered misbranded.

What are the main safety concerns with phenibut?

4

The main concerns are sedation and impairment, confusion or reduced consciousness in adverse exposures, tolerance, dependence, withdrawal, and interactions with alcohol or other CNS-active substances.

Does phenibut have strong nootropic evidence?

6

No. Older/regional medical-use and pharmacology literature exists, but strong modern human evidence for general cognitive enhancement, focus, memory, or motivation in healthy consumers is not established.

Is the 250-750 mg/day range a recommendation?

11

No. The range is included as reported research or regulated-medical context only. It should not be read as advice to use phenibut, repeat doses, or combine it with other substances.

13

References

  1. PubChem. Phenibut (CID 14113). National Library of Medicine.
  2. U.S. Food and Drug Administration. Phenibut in Dietary Supplements.
  3. U.S. Food and Drug Administration. FDA Acts on Dietary Supplements Containing DMHA and Phenibut. Content current as of 2019-04-29.
  4. Graves JM, Dilley JA, Kubsad S, Liebelt E. Notes from the Field: Phenibut Exposures Reported to Poison Centers - United States, 2009-2019. MMWR Morb Mortal Wkly Rep. 2020;69(35):1227-1228.
  5. McCabe DJ, Bangh SA, Arens AM, Cole JB. Phenibut exposures and clinical effects reported to a regional poison center. Am J Emerg Med. 2019;37(11):2066-2071.
  6. Penzak SR, Bulloch M. Phenibut: Review and Pharmacologic Approaches to Treating Withdrawal. J Clin Pharmacol. 2024;64(6):652-671.
  7. Weleff J, Akiki M, Singh A, Baronia R, Deolia S, Nasur E, Hadan TF, Sharma P. Clinical Presentations and Treatment of Phenibut Toxicity, Withdrawal, and Use Disorder: A Systematic Literature Review. J Addict Med. 2023;17(4):407-417.
  8. Stewart C, et al. A Systematic Review of Phenibut Withdrawals. Cureus. 2024;16(9):e68775.
  9. Cohen PA, Avula B, Katragunta K, Travis JC, Khan I. Quantity of phenibut in dietary supplements before and after FDA warnings. Clin Toxicol (Phila). 2022;60(4):486-488.
  10. Lapin I. Phenibut (beta-phenyl-GABA): a tranquilizer and nootropic drug. CNS Drug Rev. 2001;7(4):471-481.
  11. World Health Organization Expert Committee on Drug Dependence. Phenibut: Critical Review Report. Forty-fourth meeting, 11-15 October 2021.
  12. Zvejniece L, Vavers E, Svalbe B, et al. R-phenibut binds to the alpha2-delta subunit of voltage-dependent calcium channels and exerts gabapentin-like anti-nociceptive effects. Pharmacol Biochem Behav. 2015;137:23-29.
Note

This page is informational and summarizes available evidence. It is not medical advice, a recommendation, or a substitute for guidance from a qualified clinician.