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diazepam
Diazepam_structure.svg
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Diazepam
Systematic (IUPAC) name
7-chloro-1-methyl-
5-phenyl-1,3-dihydro-2H-
1,4-benzodiazepin-2-one
Identifiers
CAS number 439-14-5
ATC code N05 BA01 N05BA17
PubChem 3016
DrugBank APRD00642
Chemical data
Formula C16 H13 Cl N2 O 
Mol. mass 284.7 g/mol
Pharmacokinetic data
Bioavailability 93%
Metabolism Hepatic
Half life 20-100 hours
Excretion Renal
Therapeutic considerations
Pregnancy cat.

C(AU) D(US)

Legal status

Prescription Only (S4)(AU) Schedule IV(CA) Schedule IV(US) Schedule IV (International)

Routes Oral, IM, IV, suppository

Diazepam (IPA: [daɪˈæzəˌpæm]), marketed under brand names Valium, Stesolid, Diazemuls, Seduxen, Bosaurin, Diapam, Antenex, Ducene, Apozepam and Pax (South Africa))[1] is a drug which is a benzodiazepine derivative. It possesses anxiolytic, anticonvulsant, sedative, skeletal muscle relaxant and amnestic properties. This makes it a useful drug for treating anxiety, insomnia, seizures, alcohol withdrawal, and muscle spasms. It is also used before certain medical procedures (such as endoscopies) to reduce tension and anxiety, and in some surgical procedures to induce amnesia.[2][3]

Diazepam is a core medicine in the World Health Organization's "Essential Drugs List", which is a list of minimum medical needs for a basic health care system.[4] Diazepam is used to treat a wide range of conditions and is one of the most frequently prescribed benzodiazepines.

Benzodiazepine

Diazepam is a benzodiazepine that binds to a specific subunit on the GABAA receptor at a site that is distinct from the endogenous GABA molecule.[5][6]The GABAA receptor is an inhibitory channel which, when activated, decreases neurologic activity.

Due to the role of diazepam as a positive allosteric modulator of GABA, when it binds to benzodiazepine receptors it causes inhibitory effects. This arises from the hyperpolarization of the post- synaptic membrane, due to the control exerted over negative chloride ions by GABAA receptors.[5][7]

Diazepam appears to act on areas of the limbic system, thalamus and hypothalamus, inducing anxiolytic effects. Its actions are due to the enhancement of GABA activity.[2][5]this drug is not a narcotic

History

Diazepam was the second benzodiazepine to be invented by Leo Sternbach of Hoffmann-La Roche, and was approved for use in 1963. It is five times more potent than its predecessor, chlordiazepoxide, which it quickly surpassed in terms of sales. After this initial success, other pharmaceutical companies began to introduce other benzodiazepine derivatives.[8]

The benzodiazepines gained popularity among medical professionals as an improvement upon barbiturates, which have a comparatively narrow therapeutic index, and are far more sedating at therapeutic doses. The benzodiazepines are also far less dangerous; death rarely results from diazepam overdose, except in cases where it is consumed with large amounts of other depressants (such as alcohol or other sedatives).[9]

Diazepam was the top-selling pharmaceutical in the United States from 1969 to 1982, with peak sales in 1978 of 2.3 billion pills.[8] In 1966, The Rolling Stones released the song "Mother's Little Helper," which is about a mother needing the "little yellow pill" to get through the day.[10]

While psychiatrists continue to prescribe diazepam for the short-term relief of anxiety, neurology has taken the lead in prescribing diazepam for the palliative treatment of certain types of epilepsy and spastic activity, e.g., forms of paresis. It is also the first line of defense for a rare disorder called stiff-person syndrome.[11]

Diazepam is also found in nature. Several plants, such as potato and wheat, contain trace amounts of naturally occurring diazepam and other benzodiazepines.[12]

Pharmacokinetics

Diazepam can be administered orally, intravenously, intramuscularly, or as a suppository.[13]

When diazepam is administered orally, it is rapidly absorbed and has a fast onset of action. The onset of action is 1-5 minutes for IV administration and 15-30 minutes for IM administration. The duration of the diazepam's main pharmacological effects is 15 minutes to 1 hour for both routes of administration.[14]

Peak plasma levels are achieved 30 minutes to 2 hours after oral administration. When diazepam is administered as an intramuscular injection, absorption is slow, erratic and incomplete.[1][15]

Diazepam is highly lipid-soluble, and is widely distributed throughout the body after administration. It easily crosses both the blood-brain barrier and the placenta, and is excreted into breast milk. After absorption, diazepam is redistributed into muscle and adipose tissue. Continual daily doses of diazepam will quickly build up to a high concentration in the body (mainly in adipose tissue), which will be far in excess of the actual dose for any given day.[13][15]

Diazepam is metabolised in the liver via the cytochrome P450 enzyme system. It has a biphasic half-life of 1-2 and 2-5 days, and has several pharmacologically active metabolites. The main active metabolite of diazepam is desmethyldiazepam (also known as nordazepam or nordiazepam). Diazepam's other active metabolites include temazepam and oxazepam. These metabolites are conjugated with glucuronide, and are excreted primarily in the urine. Because of these active metabolites, the serum values of diazepam alone are not useful in predicting the effects of the drug.[1][15]

Diazepam has a half-life (t1/2α) of 20-50 hours, and desmethyldiazepam has a half-life of 30-200 hours.[15]

Most of the drug is metabolised; very little diazepam is excreted unchanged.[13]

In humans, the protein binding of diazepam is around 98.5%.[1]

Indications

Diazepam is mainly used to treat anxiety, insomnia, and symptoms of acute alcohol or opiate withdrawal. It is also used as a premedication for inducing sedation, anxiolysis or amnesia prior to certain medical procedures (e.g. endoscopy).[1]

Diazepam is rarely used as a primary drug for the long-term treatment of epilepsy. This is due to the fact that tolerance to the anticonvulsant effects of diazepam usually develops within 6 to 12 months of treatment, effectively rendering it useless for this purpose.[13]

Diazepam has a broad spectrum of indications (most of which are off-label), including:

  • Treatment of the symptoms of alcohol and opiate withdrawal[1]
  • Treatment of tetanus, together with other measures of intensive-treatment[16]
  • Adjunctive treatment of painful muscle conditions[11]
  • Adjunctive treatment of spastic muscular paresis (para-/tetraplegia) caused by cerebral or spinal cord conditions such as stroke, multiple sclerosis, spinal cord injury (long-term treatment is coupled with other rehabilitative measures)[11]
  • Pre-/postoperative sedation, anxiolysis and/or amnesia (e.g. before endoscopic or surgical procedures)[11]

Veterinary uses

  • Diazepam is used as a short term sedative and anxiolytic for cats and dogs. It is also used for short-term treatment of seizures in dogs and short-term and long-term treatment of seizures in cats. For emergent treatment of seizures, the typical dose is 0.5 mg/kg intravenously or 1-2 mg/kg per rectum of the injectable solution.[19]
  • Diazepam is also used as a muscle relaxant for horses, to be given intravenously, the usual dose is 0.02 - 0.1 mg/kg in conjunction with or just after induction of general anesthesia.

Dosage

Dosages should be determined on an individual basis, depending upon the condition to be treated, the severity of symptoms, the body weight of the patient, and any comorbid conditions the patient may have.[13]

Typical dosages for healthy adults range from 2mg per dose to 30mg per dose, depending on such factors as body weight and condition being treated. For the elderly or people with liver disorders, initial dose is at the low end of the range, with the dose being increased as required.[7]

Availability

 

Diazepam is supplied in the following forms:

  • For oral administration:
    • Tablets - 2mg, 5mg, 10mg[7]. Generic versions available.
    • Capsules, time-release - 15mg (marketed by Roche as Valrelease®)[15]
    • Liquid solution - 1mg/ml in 500ml containers and unit-dose (5mg & 10mg); 5mg/ml in 30 ml dropper bottle (marketed by Roxane as Diazepam Intensol®)[15]
  • For parenteral administration:
    • Solution for IV/IM injection - 5mg/ml. 2ml ampoules and syringes; 1ml, 2ml, 10ml vials; 2 ml Tel-E-Ject; also contains 40% propylene glycol, 10% ethyl alcohol, 5% sodium benzoate and benzoic acid as buffers, and 1.5% benzyl alcohol as a preservative.[20][15]
  • For rectal administration:
  • For inhalation administration:This method uses heating diazepam to form a vapor later producing an aerosol. This allows the drug to be passed through an inhalation route during an inhalation therapy.Provided in doses 2mg-20mg either in a single inhalation or multiple small inhalations [22]

Side effects

Diazepam has a range of side effects which are common to most benzodiazepines. Most common side effects include:

Rare paradoxical side effects can include: nervousness, irritability, insomnia, muscle cramps, and in extreme cases, rage, and violence.[23][24][25] If these side effects are present, diazepam treatment should be immediately terminated.

Up to 30% of individuals treated on a long-term basis develop a form of dependence known as "low-dose-dependence." These patients do not develop a tolerance, and do not need increasingly large doses to experience the euphoric side effects of the drug. [citation needed]

Diazepam may impair the ability to drive vehicles or operate machinery. The impairment is worsened by consumption of alcohol, because both act as central nervous system depressants.[7]

During the course of therapy, tolerance to the sedative effects usually develops, but not to the anxiolytic and myorelaxant effects.[26]

Patients with severe attacks of apnea during sleep may suffer respiratory depression (hypoventilation) leading to respiratory arrest and death.

Organic changes such as leukopenia[27] and liver-damage of the cholostatic type with or without jaundice (icterus) have been observed in a few cases. [citation needed]

Interactions

If diazepam is to be administered concomitantly with other drugs, attention should be paid to the possible pharmacological interactions. Particular care should be taken with drugs that enhance the effects of diazepam, such as barbiturates, phenothiazines, narcotics and antidepressants.[7]

Diazepam does not increase or decrease hepatic enzyme activity, and does not alter the metabolism of other compounds. There is no evidence that would suggest diazepam alters its own metabolism with chronic administration.[13]

Agents which have an effect on hepatic cytochrome P450 pathways or conjugation can alter the rate of diazepam metabolism. These interactions would be expected to be most significant with long-term diazepam therapy, and their clinical significance is variable.[13]

  • Oral contraceptives ("the pill") significantly decrease the elimination of desmethyldiazepam, a major metabolite of diazepam.[29]
  • Cisapride may enhance the absorption, and therefore the sedative activity, of diazepam.[30]
  • Smoking tobacco can enhance the elimination of diazepam and decrease its action.[28]
  • Foods that acidify the urine can lead to faster absorption and elimination of diazepam, reducing drug levels and activity.[28]
  • Foods that alkalinize the urine can lead to slower absorption and elimination of diazepam, increasing drug levels and activity.[13]
  • There are conflicting reports as to whether food in general has any effects on the absorption and activity of orally administered diazepam.[28]

Contraindications

Use of diazepam should be avoided, when possible, in individuals with the following conditions:

Special caution needed

  • Pediatric patients
    • Less than 18 years of age - Treatment usually not indicated, except treatment of epilepsy, and pre-/postoperative treatment. The smallest possible effective dose should be used for this group of patients.[29]
    • Under 6 months of age - Safety and effectiveness have not been established; diazepam should not be given to individuals in this age group.[7][29]
  • Elderly and very ill patients - Possibility that apnea and/or cardiac arrest may occur. Concomitant use of other central nervous system depressants increases this risk. The smallest possible effective dose should be used for this group of patients..[7][29][32]
  • I.V. or I.M. injections in hypotensive individuals or those in shock should be administered carefully and vital signs should be monitored.[32]

Patients at a high risk for abuse and dependence

Diazepam can lead to


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