Tuinal: Difference between revisions
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File:Secobarbital_and_amobarbital.svg|Chemical structure of Secobarbital and Amobarbital | |||
File:Tuinal_DOJ.jpg|Tuinal capsules | |||
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Latest revision as of 01:59, 17 February 2025
Tuinal[edit]


Tuinal is a combination barbiturate medication that contains equal parts of two barbiturate salts: secobarbital and amobarbital. It was introduced in the late 1940s by Eli Lilly and Company as a sedative and hypnotic for the treatment of insomnia and other sleep disorders.
History[edit]
Tuinal was first introduced in 1946 and became widely used in the 1950s and 1960s. It was marketed as a prescription medication for patients who required a strong sedative. However, due to its potential for abuse and addiction, its use declined over the years.
Pharmacology[edit]
Tuinal acts as a central nervous system depressant. The combination of secobarbital and amobarbital enhances the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) in the brain, leading to sedative and hypnotic effects. The drug has a rapid onset of action and a relatively short duration of effect.
Medical Uses[edit]
Tuinal was primarily prescribed for the short-term treatment of severe insomnia. It was also used as a pre-anesthetic agent and for the treatment of certain types of seizures. Due to its high potential for dependence and overdose, it is no longer commonly prescribed.
Abuse and Dependence[edit]
Tuinal has a high potential for abuse and can lead to physical and psychological dependence. Overdose can result in severe respiratory depression, coma, and death. As a result, its use is now highly restricted.
Legal Status[edit]
Due to its potential for abuse, Tuinal is classified as a Schedule II controlled substance in the United States. This classification indicates that it has a high potential for abuse, with use potentially leading to severe psychological or physical dependence.
Related Pages[edit]
References[edit]
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Chemical structure of Secobarbital and Amobarbital
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Tuinal capsules