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Ataxia, discoordination, fatigue, drowsiness, weakness, dizziness, impaired memory and speech, visual disturbances, nervousness, weakening of the ability to learn, emotional lability, decreased libido, confusion, depression, symptoms of catarrhal inflammation of the upper respiratory tract, hypersalivation, constipation, abdominal pain, loss of appetite, muscle pain, menstrual disorders, urinary frequency, erythromycin, leukopenia and thrombocytopenia, increased blood concentrations of transaminases and alkaline phosphatase, paradoxical reactions - excitement, cutaneous allergic manifestations, insomnia (it requires drug withdrawal).

Description of the drug Klonopin
Klonopin (Clonazepam) is a benzodiazepine derivative that has an anticonvulsant, anxiolytic, muscular-relaxing, amnestic, sedative, and hypnotic effect. It reduces the excitability of the subcortical areas of the brain (limbic system, thalamus, and hypothalamus) and disturbs their interaction with the cortex. It oppresses polysynaptic spinal reflexes. It is quickly and completely absorbed in the digestive tract. After taken orally, Cmax is achieved in 1-2 hours. It is excreted mainly in urine. 1 tablet contains 0.5 or 2 mg of Clonazepam; one blister contains 30 pcs, one pack contains 1 blister.

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