Alternative
Phenibut
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Phenibut
, Phenibut Toxicity, Anvifen, Fenibut, Noofen
See Also
Herbal Medicine
Background
Categorized as a dietary supplement (and relatively unregulated in U.S.)
Marketed to consumers in U.S. for anxiety, relaxation, and sleep
Increased poison control related cases 2010-2019 (see MMWR reference below)
Developed in Soviet Union in 1960s as an
Anxiolytic
and sleep aid
Mechanism
Similar to
Baclofen
in structure and activity
GABA
Agonist
(primarily
GABA
-B)
Sedation
Hypothermia
Beta-Phenylethylamine
Antagonist
Anxiolysis
Dopamine
increase
Sedation
Dystonic Reaction
Pharmacokinetics
Onset: 2-4 hours after oral dose
Half-Life
: 5.3 Hours
Urinary excretion: 65%
Dosing
Typical: 250 mg orally once to three times daily
Adverse Effects
Standard Doses
Nausea
and
Vomiting
Sedation
Irritability or
Agitation
Dizziness
Headache
Adverse Effects
Toxicity (high dose or prolonged use)
Agitated Delirium
Seizure
s
Respiratory depression
Aspiration
Agitated Withdrawal (prolonged use)
Labs
Toxicity
See
Unknown Ingestion
Altered Level of Consiousness
Bedside
Glucose
Consider coningestion
Acetaminophen
Level
Alcohol
Level
Urine Drug Screen
May result in
Methamphetamine
False Positive
Management
Toxicity
See
Unknown Ingestion
Consider
Activated Charcoal
if intake within 1 hour of ingestion (in alert patient)
Supportive Care
Endotracheal Intubation
and sedation if unprotected airway
Benzodiazepine
s for
Agitation
or withdrawal
Phenobarbital
or
Baclofen
may also be used for withdrawal symptoms
Baclofen
is a derivative of Phenibut
Disposition
May discharge home if asymptomatic at 4 hours after ingestion
Resources
Phenibut (Wikipedia)
https://en.wikipedia.org/wiki/Phenibut
References
Tomaszewski (2020) Crit Dec Emerg Med 34(1): 32
Graves (2020) MMWR Morb Mortal Wkly Rep 69:1227-8 [PubMed]
https://www.cdc.gov/mmwr/volumes/69/wr/mm6935a5.htm
Winter (2001) CNS Drug Rev 7(4):471-81 [PubMed]
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