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Фенобарбитал

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Фенобарбитал

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Medically reviewed

Marina Burgos

Last updated on 10/01/2026

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

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Overview of Фенобарбитал

What is Phenobarbital? (Что такое Фенобарбитал?)

Quick Facts

Property Description
Active Ingredient Phenobarbital (Фенобарбитал)
Form Oral tablet, Elixir (solution), Injection solution
Pharmacological Class Barbiturate, Anticonvulsant (Antiepileptic)
Origin Synthetic (Barbituric acid derivative)
General Purpose CNS stabilization, Sedation, Seizure control

Phenobarbital (Фенобарбитал) is a synthetic medicinal agent belonging to the chemical class of barbituric acid derivatives and pharmacologically classified as a barbiturate. The active substance is 5-ethyl-5-phenylbarbituric acid with the molecular formula C12H12N2O3. The drug is classified as an anticonvulsant (antiepileptic), which is reflected in its ATC code N03AA02. Phenobarbital is utilized for the long-term control of seizure disorders, providing seizure control.

Its action is described as a non-selective central nervous system (CNS) depressant. As a long-acting barbiturate, Phenobarbital stabilizes nerve cells and raises the excitability threshold in the brain, preventing uncontrolled bursts of activity. The drug has an extended duration of action, with a half-life ranging from 53 to 118 hours.

Phenobarbital is available in several pharmaceutical forms, including tablets for oral administration, elixir (solution), and solution for injection. Phenobarbital is used to reduce CNS hyperexcitability and instability. Thus, this medication helps provide a calmer and more stable state of the nervous system, which is critical for conditions requiring constant control of excitability.

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What side effects are possible with Фенобарбитал?

Possible side effects and safety information

The safety profile of Phenobarbital is officially documented based on its classification as a non-selective CNS depressant. Adverse reactions are grouped by physiological systems and frequency categories as defined in regulatory documents. CNS effects are categorized as Common and are most often observed during the initial phase of treatment or following dose increases, and they often decrease with continued use.

System-Organ Class Common Adverse Reactions (Examples) Serious Adverse Reactions (Rare)
Nervous System Drowsiness, Sedation, Ataxia, Nystagmus Severe Withdrawal Syndrome
Dermatological Skin rashes Stevens-Johnson Syndrome (SJS), Toxic Epidermal Necrolysis (TEN)
Blood/Skeletal Megaloblastic Anemia, Osteomalacia (Long-Term Use)
Hepatobiliary Liver function abnormalities Severe Hepatotoxicity

Serious adverse reactions, though Rare, include severe cutaneous events (SJS/TEN) and specific hematological effects like megaloblastic anemia, which is associated with long-term exposure. The medicine is officially documented to carry a risk of physical and psychological dependence, and regulatory texts stipulate that treatment must not be stopped abruptly to prevent severe withdrawal symptoms.

Specific population safety notes are included in official labeling. Children and older adults are documented to have an increased risk of paradoxical reactions, such as excitement or hyperactivity. Phenobarbital is formally contraindicated in individuals with severe hepatic impairment, severe respiratory depression, or acute intermittent porphyria.

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Overdose and Emergency Response

Overdose Manifestations

A Phenobarbital overdose is officially documented as causing profound central nervous system (CNS) depression, escalating from initial signs like drowsiness, slurred speech, and loss of coordination (ataxia) to severe manifestations, including stupor and coma. Respiratory depression is a major and early concern, often leading to slow or shallow breathing and the risk of apnea. The most severe documented outcomes involve life-threatening physiological collapse, including significant hypotension, shock syndrome, and circulatory collapse. Failure to rapidly address these effects may lead to respiratory complications, acute renal failure, and death.

Required Emergency Action

Official regulatory guidance requires that all suspected cases of overdose must result in immediately seeking medical attention. Emergency services must be contacted if the affected person cannot be awakened or exhibits severe signs, particularly breathing difficulties. Management is defined as symptomatic and supportive therapy, as no specific antidote is known. Officially described procedures may include measures to remove the ingested substance, such as gastric lavage, along with maintaining essential functions like blood pressure and respiratory exchange. Advanced procedures, including dialysis, may be required in severe cases to enhance elimination. Regulatory information also notes that accidental ingestion is particularly hazardous for children, and elderly patients face heightened risk due to diminished clearance.

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Therapeutic Uses of Фенобарбитал

Phenobarbital (Фенобарбитал) is an established therapeutic agent that contributes to symptomatic management within the neurological and physiological domains. The primary therapeutic use of the drug is for its anticonvulsant properties. It is commonly used for managing symptoms of increased neurological or muscular activity associated with various types of epilepsy. This is relevant in conditions characterized by periods of heightened symptoms linked to acute changes.

Beyond its role as an anti-seizure agent, phenobarbital is applied across domains where additional symptomatic support is needed due to its supportive sedative effect. It is commonly used to help with symptoms related to heightened physiological activity, such as may assist with easing anxiety or supporting comfort to aid rest. Indications include the use as an anticonvulsant, a sedative to help with easing anxiety, and in managing withdrawal symptoms in patients dependent on other barbiturate medications. Overall, it provides support that helps ease the overall symptom burden and assists with maintaining functional stability during symptomatic periods.

Quick Fact: Supports easing Symptoms that interfere with daily functioning

The goal of management is supportive relief during difficult episodes. It is also relevant for managing withdrawal symptoms in patients who are dependent on other barbiturate medications.

Regulatory References

  1. NIH MedlinePlus Drug Information
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Eligibility and Restrictions for Use

Who can and cannot use Phenobarbital (Фенобарбитал)?

This section outlines the official population eligibility rules for Phenobarbital based on regulatory documentation, detailing who is permitted or restricted from using the medicine.

Contraindications and Prohibited Populations

Phenobarbital is strictly contraindicated for patients with a known hypersensitivity to barbiturates and those diagnosed with acute intermittent porphyria. It must also not be used in patients with severe respiratory depression or marked impairment of liver function.

Eligibility by Age and Condition

Category Official Regulatory Status
Pediatric Use Established, including neonates and infants for certain conditions, but requires specific monitoring.
Older Adults Requires caution and often a reduced dosage due to increased sensitivity and risk of confusion.
Renal Impairment Use requires caution; potential dose reduction may be needed.
Severe Hepatic Impairment Contraindicated (prohibited use).

Pregnancy and Lactation Status

Use during pregnancy is classified as Category D by the FDA, indicating evidence of risk to the fetus, but potential benefits may warrant use in severe cases. The medicine is not recommended for individuals who are breastfeeding as it is excreted into breast milk and may cause sedation in the infant.

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What should I know about interactions with other medicines?

Interactions with other medicines and products

Phenobarbital's interaction profile is significantly defined by its ability to act as a potent inducer of hepatic microsomal enzymes, including the cytochrome P450 system. This induction accelerates the metabolism and therefore decreases the plasma concentration and clinical efficacy of many co-administered medicines.

Key Pharmacokinetic Interactions (Enzyme Induction)

Affected Drug Category Interaction Mechanism Practical Implication
Oral Anticoagulants (e.g., warfarin) Increased metabolism, decreasing anticoagulant effect. Requires close monitoring of INR and dose adjustment.
Corticosteroids (e.g., prednisone) Increased metabolism, decreasing therapeutic effect. Requires higher corticosteroid doses to maintain efficacy.
Hormonal Contraceptives Increased metabolism, potentially rendering contraception ineffective. Requires use of an alternate, non-hormonal birth control method.
Other Drugs (e.g., doxycycline, voriconazole, tricyclic antidepressants) Increased metabolism, decreasing therapeutic drug levels. Requires dose increase or therapeutic substitution.

Pharmacodynamic and Other Interactions

Co-administration with other Central Nervous System (CNS) depressants (including alcohol, opioids, and other sedatives) results in an additive CNS depressant effect, increasing the risk of respiratory depression and deep sedation. Furthermore, drugs such as valproic acid can inhibit Phenobarbital's metabolism, leading to increased Phenobarbital plasma levels and potential toxicity, requiring careful plasma level monitoring. Concomitant use with agents that prolong the QT interval may increase the risk of serious cardiac arrhythmias.

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Mechanism of Action

Mechanism of Action: Phenobarbital Pharmacodynamics

Enhancement of GABA Inhibition and Neuronal Hyperpolarization

Phenobarbital operates as a positive allosteric modulator of the GABA A-receptor, the primary inhibitory ion channel in the central nervous system. Binding to the receptor prolongs the duration of the chloride channel's open state, facilitating a sustained influx of negatively charged chloride ( Cl^-) ions, which causes hyperpolarization of the neuronal membrane. This action raises the threshold required for the cell to fire an action potential, promoting stabilization of the membrane potential and suppression of high-frequency neuronal discharge.

Dual Action: Suppression of Excitatory Signals

In addition to amplifying inhibition, Phenobarbital exerts nonselective CNS depression by influencing excitatory systems. The compound inhibits the presynaptic release of excitatory neurotransmitters, such as glutamate, and also acts to block certain postsynaptic glutamatergic receptors (AMPA/Kainate types). This dualistic mechanism—combining enhanced inhibition with direct suppression of excitation—culminates in generalized CNS depression, which limits the propagation of synchronized or excessive neuronal signaling.

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Dosage and Administration Information

Phenobarbital administration is established across oral, intravenous (IV), and intramuscular (IM) routes, corresponding to its dosage forms, which include tablets, elixir, and injection solution. The method of use is defined by the clinical context. For sustained maintenance, the medicine is typically taken orally in adults at a dose ranging from 60 mg to 200 mg daily, often administered as a single dose at bedtime or split into two or three divided doses.

In acute, emergent situations, the intravenous route is employed. The protocol involves a loading dose of 15 mg/kg to 20 mg/kg, which must be administered slowly. Standard protocols for administration specify that the IV infusion rate in adults not exceed 60 mg per minute. The injection solution requires dilution before delivery and is restricted from use via the subcutaneous or intra-arterial routes.

Dose modifications are required for certain populations. Pediatric dosing is weight-based, typically falling within the range of 3 mg/kg to 8 mg/kg per day. Furthermore, a reduced initial dose is specified for older adults or patients with hepatic impairment. When discontinuing long-term use, established protocols require the dose to be slowly withdrawn (tapered) to avoid abrupt cessation effects. Short-term uses, such as for sedation, are generally limited to periods of two weeks or less.

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Recent Clinical Evidence

Phenobarbital: Recent Clinical Evidence

Phenobarbital is an anticonvulsant and sedative that has been used for over a century. While newer agents are often preferred for certain conditions, recent clinical evidence continues to support Phenobarbital's role in specific therapeutic areas, particularly in the management of seizures.

Efficacy in Epilepsy Management

Studies have investigated Phenobarbital's effectiveness in controlling tonic-clonic seizures and focal seizures. Research confirms its efficacy in reducing seizure frequency in both adults and children, although potential cognitive side effects may influence its use in pediatric populations. For specific types of epilepsy, such as neonatal seizures, Phenobarbital remains a first-line treatment option supported by clinical practice guidelines.


Therapeutic Use in Neonates

Clinical evidence consistently supports the use of Phenobarbital for the initial treatment of seizures in newborns. Its ability to cross the blood-brain barrier effectively and its established dosing guidelines make it a standard choice in neonatal intensive care. Research continues to monitor long-term neurodevelopmental outcomes associated with its use in this vulnerable population.


Research into Other Applications

While its primary use is for seizures, research has also explored Phenobarbital for the management of unconjugated hyperbilirubinemia in newborns, an application leveraging its ability to induce liver enzymes that process bilirubin. For treating anxiety and insomnia, its use has significantly declined due to the availability of newer agents with better safety profiles, limiting recent clinical investigation in these areas.

Key Studies & References

  1. Phenobarbital: Still Has a Role in Epilepsy Treatment (Journal of Child Neurology, 1999)
  2. Epilepsies in children, young people and adults (NICE Guideline NG217)
  3. Guidelines and consensus-based recommendations: Special report from the ILAE Task Force on Neonatal Seizures (PubMed)
  4. Neonatal Seizure Treatment Care Guideline (CHOC Clinical Guideline)
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Frequently Asked Questions (FAQ)

Common questions about Фенобарбитал (FAQ)

Q: How quickly does the effect of Фенобарбитал usually begin?

According to official prescribing information, for intravenous use, the onset of effect is documented as approximately five minutes. For oral use as a sedative, the effect is generally observable within an hour. The onset time is dependent on the route of administration.

Q: How long does the effect of one dose of Фенобарбитал last?

The medicine is classified as a long-acting barbiturate with a very long half-life. Official information indicates that for sedative doses, the effects typically last more than six hours.

Q: Is Фенобарбитал the same type of medicine as benzodiazepines?

No. Phenobarbital belongs to the barbiturate pharmacological class, while medicines such as diazepam belong to the benzodiazepine class. Both are classified as central nervous system depressants, but they are defined as distinct chemical groups.

Q: What kind of liver function changes are sometimes linked to Фенобарбитал use?

Official documents list liver function abnormalities and, rarely, severe hepatotoxicity. Hepatotoxicity is described as severe liver injury. Phenobarbital is a potent inducer of liver enzymes (cytochrome P450), which can affect the liver's function in processing substances.

Q: Does Фенобарбитал affect sleep patterns besides causing drowsiness?

The medicine is a substance that causes general central nervous system depression. Official documentation lists drowsiness and sedation as common nervous system effects, reflecting the drug's fundamental purpose to promote CNS stabilization.

Q: What does official information say about using alcohol with Фенобарбитал?

Official prescribing information strongly advises against consuming alcohol while taking this medicine. Combining alcohol with Фенобарбитал can result in an additive CNS depressant effect that increases the risk of serious side effects, such as respiratory depression.

Q: Does Фенобарбитал affect the way I metabolize vitamin D?

Official information indicates that the medicine is known to induce liver enzymes, which can interfere with the normal metabolism of vitamin D. This mechanism is associated with the long-term risk of conditions like osteomalacia (softening of the bones).

Q: Does Фенобарбитал interact with herbal supplements like St. John's Wort?

Official sources state that St. John's Wort may cause a harmful interaction with Фенобарбитал. This includes potentially increasing sensitivity to the sun, which can add to the risk of skin rash or sunburn already associated with the medicine.

Q: Is Фенобарбитал considered a strong sedative?

Official prescribing information describes the medicine as a nonselective central nervous system (CNS) depressant. The medicine is classified as a potent agent, which in overdosage is associated with effects ranging from sedation to deep coma.

Q: Can Фенобарбитал affect my driving ability?

Official prescribing information states that the medicine may impair the mental and physical abilities required for performing potentially hazardous tasks. These tasks include driving or operating machinery.

Q: Is it normal to feel very drowsy when first starting Фенобарбитал?

Official documentation classifies drowsiness and sedation as common adverse reactions. These effects are most often observed during the initial phase of treatment or following dose increases.

Q: Can taking Фенобарбитал make other medications less effective?

Official product information confirms that Phenobarbital is a potent inducer of liver enzymes, which can accelerate the metabolism of many co-administered medicines. This action can lead to a decrease in the plasma concentration and clinical efficacy of those other medicines.

Q: Does Фенобарбитал interact with commonly used over-the-counter pain relievers?

Official documents indicate a potential interaction with acetaminophen (a common ingredient in OTC pain relievers). Phenobarbital may alter the effects of acetaminophen and increase the risk of serious side effects that affect the liver.

Q: What is meant by 'therapeutic drug monitoring' for Фенобарбитал?

Therapeutic drug monitoring (TDM) is a process of measuring the amount of the medicine in the blood to determine if the concentration is within the desired therapeutic range. The goal of TDM is to determine if the medicine's concentration is within the desired range to support effectiveness while avoiding unsafe levels.

Q: Does Фенобарбитал have a risk of causing confusion, especially in older people?

Confusion is listed as a potential adverse reaction. Official labeling requires caution for older adults, noting they have an increased sensitivity and risk of side effects, including confusion.

Q: How long after stopping Фенобарбитал does it stay in the system?

Phenobarbital has a very long half-life, which can range from approximately 53 to 118 hours. A medicine's clearance from the body is generally calculated to take a period equal to about four to five half-lives.

Q: Is there evidence that Фенобарбитал can worsen depression?

Official prescribing information and regulatory warnings state that monitoring is necessary for notable changes in behavior. This includes the emergence or worsening of depression, anxiety, and/or suicidal thoughts or behavior.

Q: Can I take multivitamins or supplements while using Фенобарбитал?

Phenobarbital can affect the metabolism of certain nutrients and supplements, such as Vitamin D, Folic Acid, and Vitamin K. Official information states that co-administration with other substances must be assessed to prevent increased side effects or reduced effectiveness.

Q: Can Фенобарбитал cause skin rashes or other allergic reactions?

The safety profile includes skin rashes as a common side effect. Rare, but serious, reactions such as severe allergic reactions (e.g., DRESS) and severe skin reactions like Stevens-Johnson Syndrome (SJS) are also documented in official labeling.

Q: Does the body build up a tolerance to the effects of Фенобарбитал over time?

Official information states that both tolerance and physical dependence can develop, particularly after prolonged use. Tolerance means the body adapts to the drug's presence, leading to a reduced effectiveness over time.

Q: Can emotional changes be a side effect of Фенобарбитал?

The adverse reaction profile includes various nervous system effects such as anxiety, agitation, nervousness, and psychiatric disturbances. Official documentation advises monitoring for changes in mood or mental health, including worsening depression.

Q: Is Фенобарбитал known to cause problems with memory?

Cognitive issues, including difficulty with memory, concentration, and processing delays, are described in the regulatory literature as potential adverse effects.

Q: What is the risk of overdose associated with Фенобарбитал?

Overdose with this medicine is associated with serious effects due to profound central nervous system depression. Documented signs include extreme drowsiness that progresses to deep coma, slowed or absent breathing, and dangerously low blood pressure (shock).

Q: Is there a recommended maximum duration of use for Фенобарбитал?

For its main use in seizure control, the medicine is typically used as long as required. However, for short-term uses, such as sedation, the duration is generally limited to a period of two weeks or less.

Q: How often do people need blood tests when they are on Фенобарбитал?

Blood tests are a required part of measuring the medicine's concentration in the blood, a process called Therapeutic Drug Monitoring. Tests are typically done when first starting the medicine (after a few weeks) and then periodically (e.g., every 6–12 months) to monitor long-term effects on the liver.

Q: What is the typical timeframe for seeing the full benefit of Фенобарбитал?

The full benefit of the medicine is typically observed after the drug has reached a stable concentration in the body, known as the steady state. Official guidance suggests that plasma concentrations are generally stable after two to three weeks of consistent use.

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How should Фенобарбитал be stored and disposed of?

Storage and Disposal of Phenobarbital

Official regulatory guidelines mandate specific conditions for the storage and disposal of Phenobarbital.

Storage Conditions

Requirement Specification
Temperature Store at Controlled Room Temperature, 20 C to 25 C (68 F to 77 F). Do not store above 25 C.
Protection The product must be protected from light and moisture.
Container Store in the original, tightly closed, light-resistant container.
Child Safety Keep out of the sight and reach of children; the container must have a child-resistant closure.

Disposal Instructions

Phenobarbital is classified as a Schedule IV controlled substance. Unused or expired medication must be disposed of in accordance with Federal, State, and local regulations. Disposal should prioritize using an authorized drug take-back program. If a take-back option is unavailable, the medicine should be mixed with an undesirable substance, placed in a sealed container, and then discarded with household trash. All identifying information must be removed from the original packaging before disposal.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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