Clonazepam

Cheap Clonazepam is an anticonvulsant primarily used in the treatment of seizure disorders. Clonazepam is a member of a class of drug known as benzodiazepines. This drug may also be used as an antianxiety, for the short-term relief of anxiety. Clonazepam may also be used to treat Touette's Syndrome, panic disorder, drug-induced mania, to help resistant depression, nocturnal myoclonus, relieve trigeminal neuralgia, bipolar affective disorder. Also to help control certain types of petit mal, atypical, akinetic, myoclonic, or absence seizures. Klonopin, a benzodiazepine, is available as scored tablets with a K-shaped perforation containing 0.5 mg, 1 mg or 2 mg clonazepam, and unscored tablets with a K-shaped perforation containing 1 mg or 2 mg of clonazepam. Each tablet also contains lactose, magnesium stearate, microcrystalline cellulose and corn starch, with the following colorants: 0.5 mg: FD&C yellow no. 6 lake; 1 mg: FD&C blue no. 1 lake and FD&C blue No. 2 lake. Chemically, clonazepam is 5-(o-Chlorophenyl)-1,3-dihydro-7-nitro- 2 H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has a molecular weight of 315.72. The molecular formula is C 15 H 10 ClN 3 O 3 The precise mechanism by which clonazepam exerts its antiseizure effects is unknown, although it is believed to be related to its ability to enhance the activity of gamma aminobutyric acid (GABA), the major inhibitory neurotransmitter in the central nervous system. Convulsions produced in rodents by pentylenetetrazol or, to a lesser extent, electrical stimulation are antagonized, as are convulsions produced by photic stimulation in susceptible baboons. A taming effect in aggressive primates, muscle weakness and hypnosis are also produced. In humans, clonazepam is capable of suppressing the spike and wave discharge in absence seizures (petit mal) and decreasing the frequency, amplitude, duration, and spread of discharge in minor motor seizures. Clonazepam is rapidly and completely absorbed after oral administration. The absolute bioavailability of clonazepam is about 90%. Maximum plasma concentrations of clonazepam are reached within 1 to 4 hours after oral administration. Cheap clonazepam is approximately 85% bound to plasma proteins. Clonazepam is highly metabolized, with less than 2% unchanged clonazepam being excreted in the urine. Biotransformation occurs mainly by reduction of the 7-nitro group to the 4-amino derivative. This derivative can be acetylated, hydroxylated, and glucuronidated. Cytochrome P-450, including CYP3A, may play an important role in clonazepam reduction and oxidation. The elimination half-life of clonazepam is typically 30 to 40 hours. Clonazepam pharmacokinetics are dose-independent throughout the dosing range. There is no evidence that cheap clonazepam induces its own metabolism or that of other drugs in humans. Contraindications Significant liver disease, narrow angle glaucoma, sensitivity to benzodiazepines