THIOPENTAL Powder for solution for injection Ref.[8346] Active ingredients: Thiopental

Source: Medicines & Healthcare Products Regulatory Agency (GB)  Revision Year: 2018  Publisher: PANPHARMA, Z.I. du Clairay, 35133, Luitrรฉ, France

Pharmacodynamic properties

Pharmaceutical group: General anesthetics
ATC Code: N01AF03

This medicinal product is a thiobarbiturate with rapid onset for intravenous administration. Thiopental induces hypnosis and anesthesia, but not analgesia. Hypnosis is produced within 30 to 40 seconds. Recovery is within 30 minutes after adequate induction dose. Repeated injections give a prolonged anesthesia because of entry into fatty tissue.

Thiopental is a short-acting substituted barbiturate that is more lipid soluble than other groups of barbiturates. The drug reversibly depresses the activity of all excitable tissues. The CNS is particularly sensitive and normally a general anaesthesia can be achieved with thiopental sodium without significant effects on peripheral tissues.

Thiopental sodium acts through the CNS with particular activity in the mesencephalic reticular activating system. The barbiturates exert different effects on synaptic transmission, mostly those dependent on GABA. Autonomic ganglia of the peripheral nervous system are also depressed.

Pharmacokinetic properties

Following intravenous administration, unconsciousness occurs within 30 seconds and will be continued for 20 to 30 minutes after a single dose. Rapid uptake occurs to most vascular areas of the brain followed by redistribution into other tissues.

Thiopental is almost completely metabolized and only approximately 0.3% is excreted unchanged in the urine. Thiopental is extremely fat soluble and is largely metabolized in the liver but is slowly excreted from lipid depot and is very slowly transformed. During one hour 10-15% is metabolized, mainly in the liver. The half-life of the distribution phase after a single intravenous dose is 2-4 hours and the half-life of the elimination phase is 9-11 hours. The plasma protein binding is 80-90% at therapeutic concentration level.

Preclinical safety data

There are no preclinical data of relevance to the prescriber which are additional to that already included in other sections of the Summary of Product Characteristics.

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