Clonazepam: Difference between revisions
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==Pharmacokinetics== | |||
{|class="wikitable" | |||
!style="text-align: left"| Oral bioavailability | |||
|Clonazepam is well absorbed after oral doses. | |||
|- | |||
!style="text-align: left"| Onset of action | |||
|Peak plasma concentrations occur between 1 and 4 hours of a dose. | |||
|- | |||
!style="text-align: left"| Metabolism | |||
|Clonazepam is metabolized in the liver | |||
|- | |||
!style="text-align: left"| Elimination half-life | |||
|Clonazepam is eliminated in the urine. | |||
Its elimination half-life ranges from about 20 to 40 hours, and occasionally more. | |||
|} | |||
Revision as of 02:15, 6 October 2020
Introduction
Clonazepam is a long-acting benzodiazepine with marked antiepileptic properties. It is used to prevent and treat seizures, panic disorder, and the movement disorder known as akathisia. It is taken by mouth. Effects begin within one hour and last between 6 and 12 hours.
Pronunciation
Clopidogrel 75mg
| Generic Name 藥名 | HA Code 藥物代碼 | Classification藥物分類 |
|---|---|---|
| Clonazepam Tablet 0.5 mg | CLON01 | DDA |
| Clonazepam Tablet 2 mg | CLON02 | DDA |
Mechanism of Action
- Clonazepam is a benzodiazepine.
- Gama-Aminobutyric acid (GABA) is an inhibitory neurotransmitter, acting on the GABA receptors in the central nervous system (CNS), thus inhibiting the nerve impulses.
- It acts on the benzodiazepine receptors in the brain and the spinal cord. Benzodiazepine receptors in the CNS are linked with GABA receptors as a complex.
- Clonazepam by binding to the benzodiazepine receptors results in activation of the GABA-benzodiazepine receptor complex, resulting in inhibition of nerve impulses, overall depression of brain and spinal cord.
- Thus Clonazepam use helps to promote muscle relaxation, reduce anxiety, control of convulsions and promote sleep.
Dosage
| Epilepsy and myoclonus | By mouth
ADULT:
ELDERLY:
ADMINISTRATION IN CHILDREN The following usual maintenance doses according to age:
|
|---|
Side Effects
Sedative drugs, including alprazolam, have been associated with an increased risk of death.
Possible side effects include:
| Very common (>10% of incidence)
or Common (1-10% of incidence) |
|
|---|---|
| Infrequent (0.1 -1% of incidence) |
|
| Rare (<0.1% of incidence) |
|
Overdosage can produce CNS depression and coma.
Paradoxical reactions
Although unusual, the following paradoxical reactions have been shown to occur:
- aggression
- mania, agitation, and restlessness
- rage
- twitches and tremor
Pharmacokinetics
| Oral bioavailability | Clonazepam is well absorbed after oral doses. |
|---|---|
| Onset of action | Peak plasma concentrations occur between 1 and 4 hours of a dose. |
| Metabolism | Clonazepam is metabolized in the liver |
| Elimination half-life | Clonazepam is eliminated in the urine.
Its elimination half-life ranges from about 20 to 40 hours, and occasionally more. |
