Diazepam
7-chloro-1,3-dihydro-1-methyl-5-phenyl-2H-1,4-benzodiazepin-2-one
Empiric formula	C16H13ClN2O
Molecular weight	284.7
Bioavailability	?
Metabolism	Liver
Elimination half life	biphasic 1-2d/2-5d
Excretion	Urine
ATC code	N05BA01
Pregnancy category	D (USA) C (Aus)

Diazepam, brand names: Valium, Seduxen, in Europe Apozepam, is a 1,4-benzodiazepine derivative, which possesses anxiolytic, anticonvulsant, sedative and skeletal muscle relaxant properties. Diazepam is used to treat anxiety and tension and muscle spasms. It is also used as a sedative premedication and to treat alcohol withdrawal symptoms.

Mode of action

Diazepam affects mainly the central nervous system. It binds in to specific benzodiazepine-receptors, which are part of the GABA-receptors. When diazepam binds to this receptor, it causes an increase in the inhibitory effects on GABA. The effect of diazepam does not last long, partly because it is fairly quickly redistributed into tissues and fat depots, and partly because of the adaptation of benzodiazepine receptors.

Pharmacokinetics

Diazepam can be administered orally, as an injection (i.v. and i.m.), or as a suppository. When taken orally, diazepam is rapidly absorbed. Absorption is much slower and more erratic when diazepam is given as an intramuscular injection. Diazepam is highly lipid-soluble and therefore crosses the blood-brain barrier easily. Diazepam is metabolised in the liver, and it has a biphasic half-life. The first phase half-life (t½α) is 24-48 hours, and its main active metabolite, desmethyldiazepam, has a half-life of 2-5 days. Diazepam's other active metabolites include, among others, temazepam and oxazepam. Diazepam and its metabolites are excreted into the urine.

Side effects

Diazepam has few side effects. It increases the sedating effects of alcohol and hypnotics. It can paradoxically cause agitation. As with all benzodiazepines, diazepam can cause an addiction when used for a long time, especially when the doses are large.

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