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   » » Wiki: Phenobarbital
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Phenobarbital, also known as phenobarbitone or phenobarb, sold under the brand name Luminal among others, is a of the type. It is recommended by the World Health Organization (WHO) for the treatment of certain types of in developing countries. In the developed world, it is commonly used to treat in , while other medications are generally used in older children and adults. It is also used for veterinary purposes.

(2025). 9780813812496, Iowa State Press.

It may be administered by slow intravenous infusion (IV infusion), (IM), or orally (swallowed by mouth). Subcutaneous administration is not recommended. The IV or IM (injectable forms) may be used to treat status epilepticus if other drugs fail to achieve satisfactory results. Phenobarbital is occasionally used to treat , , and benzodiazepine withdrawal (as well as withdrawal from certain other drugs in specific circumstances), and prior to surgery as an and to induce . It usually begins working within five minutes when used intravenously and half an hour when administered orally. Its effects last for between four hours and two days.

(2025). 9780323054720, Mosby/Elsevier. .

Potentially serious side effects include a decreased level of consciousness and respiratory depression. There is potential for both and following long-term use. It may also increase the risk of .

It is pregnancy category D in Australia, meaning that it may cause harm when taken during pregnancy. If used during it may result in drowsiness in the baby. Phenobarbital works by increasing the activity of the inhibitory .

Phenobarbital was discovered in 1912 and is the oldest still commonly used anti-seizure medication.

(2025). 9781455702787, Elsevier/Saunders.
(2025). 9780781757775, Wolters Kluwer Health/Lippincott Williams & Wilkins. .
It is on the World Health Organization's List of Essential Medicines.


Medical uses
Phenobarbital is used in the treatment of all types of , except .British National Formulary 51 It is no less effective at seizure control than , but phenobarbital is not as well tolerated. Phenobarbital may provide a clinical advantage over for treating . Carbamazepine may provide a clinical advantage over phenobarbital for generalized onset tonic-clonic seizures.

The first-line drugs for treatment of status epilepticus are , such as , , , or . If these fail, then may be used, with phenobarbital being an alternative in the US (favored in infants), but used only third-line in the UK.

(2025). 9780853696766, BMJ Publishing.
Failing that, the only treatment is in . The World Health Organization (WHO) gives phenobarbital a first-line recommendation in the developing world and it is commonly used there.
(2025). 9781444316674, Wiley-Blackwell.

Phenobarbital is the first-line choice for the treatment of .

(2025). 9780853696766, BMJ Publishing.
(2001). 9781888799309, Demos Medical Publishing.
Concerns that neonatal seizures in themselves could be harmful make most physicians treat them aggressively. No reliable evidence, though, supports this approach.

Phenobarbital is sometimes used for alcohol detoxification and benzodiazepine detoxification for its and anti-convulsant properties. The benzodiazepines (Librium) and (Serax) have largely replaced phenobarbital for detoxification.

Phenobarbital is useful for and .

(2025). 9780781765879, Lippincott Williams & Wilkins. .


Other uses
Phenobarbital properties can effectively reduce tremors and seizures associated with abrupt withdrawal from benzodiazepines.

Phenobarbital is occasionally prescribed in low doses to aid in the conjugation of in people with Crigler–Najjar syndrome, type II,

(2015). 9780071802154, Mc Graw Hill.
or in people with Gilbert's syndrome. In infants suspected of neonatal , phenobarbital is used in preparation for a 99mTc-IDA hepatobiliary (HIDA; hepatobiliary 99mTc- imino diacetic acid) study that differentiates atresia from or .

In massive doses, phenobarbital is prescribed to terminally ill people to allow them to end their life through physician-assisted suicide.

Like other barbiturates, phenobarbital can be used recreationally, but this is reported to be relatively infrequent.

The synthesis of a photoswitchable analog (DASA-barbital) and phenobarbital has been described for use as a research compound in photopharmacology.


Side effects
Sedation and hypnosis are the principal side effects (occasionally, they are also the intended effects) of phenobarbital. Central nervous system effects, such as dizziness, nystagmus and , are also common. In elderly patients, it may cause excitement and confusion, while in children, it may result in paradoxical hyperactivity.

Phenobarbital is a cytochrome P450 hepatic enzyme inducer. It binds transcription factor receptors that activate cytochrome P450 transcription, thereby increasing its amount and thus its activity. Caution is to be used with children. Among anti-convulsant drugs, behavioural disturbances occur most frequently with and phenobarbital.


Contraindications
Acute intermittent porphyria, hypersensitivity to any barbiturate, prior dependence on barbiturates, severe respiratory insufficiency (as with chronic obstructive pulmonary disease), severe , pregnancy, and breastfeeding are contraindications for phenobarbital use.


Overdose
Phenobarbital causes a depression of the body's systems, mainly the central and peripheral nervous systems. Thus, the main characteristic of phenobarbital overdose is a "slowing" of bodily functions, including decreased (even ), , , , and (in massive overdoses). Overdose may also lead to and acute renal failure as a result of shock and can result in death.

The electroencephalogram (EEG) of a person with phenobarbital overdose may show a marked decrease in electrical activity, to the point of mimicking . This is due to profound depression of the central nervous system and is usually reversible.

Treatment of phenobarbital overdose is , and mainly consists of the maintenance of patency (through endotracheal intubation and mechanical ventilation), correction of bradycardia and hypotension (with intravenous fluids and , if necessary), and removal of as much drug as possible from the body. In very large overdoses, multi-dose activated charcoal is a mainstay of treatment as the drug undergoes enterohepatic recirculation. Urine alkalization (achieved with sodium bicarbonate) enhances renal excretion. is effective in removing phenobarbital from the body and may reduce its half-life by up to 90%. No specific antidote for barbiturate poisoning is available.


Mechanism of action
Phenobarbital acts as an allosteric modulator which extends the amount of time the chloride ion channel is open by interacting with subunits. Through this action, phenobarbital increases the flow of ions into the neuron which decreases the excitability of the post-synaptic neuron. Hyperpolarizing this post-synaptic membrane leads to a decrease in the general excitatory aspects of the post-synaptic neuron. By making it harder to the neuron, the threshold for the action potential of the post-synaptic neuron will be increased.

Direct blockade of glutamatergic and are also believed to contribute to the hypnotic/anticonvulsant effect that is observed with phenobarbital.

(2025). 9780444626196, Elsevier.


Pharmacokinetics
Phenobarbital has an oral of about 90%. Peak plasma concentrations (Cmax) are reached eight to 12 hours after oral administration. It is one of the longest-acting barbiturates available – it remains in the body for a very long time (half-life of two to seven days) and has very low protein binding (20 to 45%). Phenobarbital is metabolized by the liver, mainly through and and induces many of the cytochrome P450 system. Cytochrome P450 2B6 (CYP2B6) is specifically induced by phenobarbital via the CAR/RXR . It is excreted primarily by the .
(2025). 9780323393072, Elsevier.


History
The first barbiturate drug, , was synthesized in 1902 by German chemists and Joseph von Mering and was first marketed as Veronal by . By 1904, several related drugs, including phenobarbital, had been synthesized by Fischer. Phenobarbital was brought to market in 1912 by the drug company as the brand Luminal. It remained a commonly prescribed sedative and hypnotic until the introduction of in the 1960s.
(2005). 9780471899792, John Wiley and Sons.

Phenobarbital's soporific, sedative and hypnotic properties were well known in 1912, but it was not yet known to be an effective anti-convulsant. The young doctor gave it to his epilepsy patients as a and discovered their seizures were susceptible to the drug. Hauptmann performed a careful study of his patients over an extended period. Most of these patients were using the only effective drug then available, bromide, which had terrible side effects and limited efficacy. On phenobarbital, their epilepsy was much improved: The worst patients had fewer and lighter seizures and some patients became seizure-free. In addition, they improved physically and mentally as bromides were removed from their regimen. Patients who had been institutionalised due to the severity of their epilepsy were able to leave and, in some cases, resume employment. Hauptmann dismissed concerns that its effectiveness in stalling seizures could lead to patients developing a build-up that needed to be "discharged". As he expected, withdrawal of the drug led to an increase in seizure frequency – it was not a cure. The drug was quickly adopted as the first widely effective anti-convulsant, though World War I delayed its introduction in the U.S.

(1993). 9781850703914, Taylor & Francis.

In 1939, a German family asked to have their disabled son killed; the five-month-old boy was given a lethal dose of Luminal after Hitler sent his own doctor to examine him. A few days later 15 psychiatrists were summoned to Hitler's Chancellery and directed to commence a clandestine program of involuntary euthanasia.

In 1940, at a clinic in , Germany, around 50 intellectually disabled children were injected with Luminal and killed that way. A plaque was erected in their memory in 1988 in the local hospital at Feuchtwanger Strasse 38, although a newer plaque does not mention that patients were killed using barbiturates on site. Luminal was used in the Nazi children's euthanasia program until at least 1943.

Phenobarbital was used to treat neonatal jaundice by increasing liver metabolism and thus lowering levels. In the 1950s, was discovered, and became the standard treatment.

Phenobarbital was used for over 25 years as in the treatment of .

(2001). 9781888799309, Demos Medical Publishing.
Although an effective treatment in preventing recurrent febrile seizures, it had no positive effect on patient outcome or risk of developing epilepsy. The treatment of simple febrile seizures with anticonvulsant prophylaxis is no longer recommended.


Society and culture

Names
Phenobarbital is the International Nonproprietary Name (INN) and phenobarbitone is the British Approved Name (BAN).


Synthesis
drugs are obtained via condensation reactions between a derivative of and in the presence of a strong base.
(1996). 9780582462366, Longman Science & Technical. .
The synthesis of phenobarbital uses this common approach as well but differs in the way in which this derivative is obtained. The reason for this difference is because do not typically undergo nucleophilic substitution in Malonic ester synthesis in the same way as or do.
(2025). 9780471007265, John Wiley & Sons, Inc.. .
To overcome this lack of chemical reactivity two dominant synthetic approaches using as a starting material have been developed:

The first of these methods consists of a of benzyl cyanide, giving phenylacetic acid ethyl ester. Subsequently, this ester undergoes cross Claisen condensation using , giving diethyl ester of phenyloxobutandioic acid. Upon heating this intermediate easily loses , yielding diethyl phenylmalonate. Malonic ester synthesis using leads to the formation of α-phenyl-α-ethylmalonic ester. Finally, a condensation reaction with gives phenobarbital.

The second approach utilizes diethyl carbonate in the presence of a strong base to give α-phenylcyanoacetic ester. Alkylation of this ester using ethyl bromide proceeds via a intermediate to give the α-phenyl-α-ethylcyanoacetic ester. This product is then further converted into the 4-iminoderivative upon condensation with urea. Finally acidic of the resulting product gives phenobarbital.

A new synthetic route based on diethyl 2-ethyl-2-phenylmalonate and urea has been described.


Regulation
The level of regulation includes Schedule IV non-narcotic (depressant) ( 2285) in the United States under the Controlled Substances Act 1970—but along with a few other barbiturates and at least one , and , , or at low concentrations, it also has exempt prescription and had at least one exempt OTC combination drug now more tightly regulated for its content. pp 12 printed PDF 23.I.2016 The phenobarbitone/phenobarbital exists in subtherapeutic doses which add up to an effective dose to counter the overstimulation and possible seizures from a deliberate overdose in ephedrine tablets for , which are now regulated at the federal and state level as: a restricted OTC medicine and/or watched precursor, uncontrolled but watched/restricted prescription drug & watched precursor, a Schedule II, III, IV, or V prescription-only controlled substance & watched precursor, or a Schedule V (which also has possible regulations at the county/parish, town, city, or district as well aside from the fact that the pharmacist can also choose not to sell it, and photo ID and signing a register is required) exempt Non-Narcotic restricted/watched OTC medicine. page 1,7, 12, accessed 23.I.2016


Selected overdoses
A mysterious woman, known as the , was found dead in , Norway, on 29 November 1970. Her death was caused by some combination of burns, phenobarbital, and poisoning; many theories about her death have been posited, and it is believed that she may have been a .

British veterinarian Donald Sinclair, better known as the character Siegfried Farnon in the "All Creatures Great and Small" book series by , committed suicide at the age of 84 by injecting himself with an overdose of phenobarbital. Activist also committed suicide by consuming phenobarbital, combined with alcohol, on 12 April 1989; the residue of around 150 pills was found in his body at autopsy.

Thirty-nine members of the Heaven's Gate UFO cult committed mass suicide in March 1997 by drinking a lethal dose of phenobarbital and vodka "and then lay down to die" hoping to enter an alien spacecraft.


Veterinary uses
Phenobarbital is one of the first-line drugs of choice to treat epilepsy in , as well as .

It is also used to treat feline hyperesthesia syndrome in cats when anti-obsessional therapies prove ineffective.

It may also be used to treat seizures in when treatment has failed or is contraindicated.

(2005). 9780911910506, John Wiley & Sons.

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