Clinical data | |
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Trade names | Klonopin, Rivotril, others |
AHFS/Drugs.com | Monograph |
MedlinePlus | a682279 |
License data |
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Pregnancy category |
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Dependence liability |
Moderate |
Routes of administration |
by mouth, intramuscular, intravenous, sublingual |
ATC code | |
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Pharmacokinetic data | |
Bioavailability | 90% |
Protein binding | ~85% |
Metabolism | Liver CYP3A4 |
Onset of action | Within an hour |
Biological half-life | 15–50 hours |
Duration of action | 6–12 hours |
Excretion | Kidney |
Identifiers | |
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CAS Number | |
PubChem CID | |
IUPHAR/BPS | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEBI | |
ChEMBL | |
ECHA InfoCard | 100.015.088 |
Chemical and physical data | |
Formula | C15H10ClN3O3 |
Molar mass | 315.715 |
3D model (Jmol) | |
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Clonazepam, sold under the brand name Klonopin among others, is a medication used to prevent and treat seizures, panic disorder, and for the movement disorder known as akathisia. It is a tranquilizer of the benzodiazepine class. It is taken by mouth. It begins having an effect within an hour and lasts between six and 12 hours.
Common side effects include sleepiness, poor coordination, and agitation. Long-term use may result in tolerance, dependence, and withdrawal symptoms if stopped abruptly. Dependence occurs in one-third of people who take clonazepam for longer than four weeks. It may increase risk of suicide in people who are depressed. If used during pregnancy it may result in harm to the baby. It binds to GABAA receptors and increases the effect of the neurotransmitter GABA.
Clonazepam was initially patented in 1964 and went on sale in the United States in 1975. It is available as a generic medication. The wholesale cost in the developing world is between US$0.01 and US$0.07 per pill. In the United States the pills are about 0.40 USD each. In many areas of the world it is commonly used as a recreational drug.
Clonazepam may be prescribed for epilepsy or anxiety disorders.
Clonazepam, like other benzodiazepines, while being a first-line treatment for acute seizures, is not suitable for the long-term treatment of seizures due to the development of tolerance to the anticonvulsant effects.
Clonazepam has been found effective in treating epilepsy in children, and the inhibition of seizure activity seemed to be achieved at low plasma levels of clonazepam. As a result, clonazepam is sometimes used for certain rare childhood epilepsies; however, it has been found to be ineffective in the control of infantile spasms. Clonazepam is mainly prescribed for the acute management of epilepsies. Clonazepam has been found to be effective in the acute control of non-convulsive status epilepticus; however, the benefits tended to be transient in many of the people, and the addition of phenytoin for lasting control was required in these patients.