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Cytisine has structure and system of action similar to those of nicotine and reduces its duration of interaction with the particular receptors. Thus, it prevents the appearance of abstinence syndrome. The outcome is progressive reduction of the common cigarette smokers' psychic and physical nicotine reliance and subsequent smoking cessation without undesirable effects.

PDF) An uncontrolled trial of cytisine (Tabex) for smoking cessation

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It does not impact the active motorists' attention and device operating. Daily, Mail Article about Tabex:.

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Tabex is an initial preparation of plant origin, meant for the treatment of tobacco smoking. The preparation is developed on the basis of the alkaloid Cystine, included in the plant Cytisus laborinum L. (Golden Rain acacia). The broad clinical research studies performed, show that the treatment with the preparation Tabex leads to giving up smoking cigarettes in more than 57% of the patients.

e. the specific substance cytisine "substitutes" nicotine, acting upon the exact same receptors, thus preventing the look of abstinence syndrome. This leads to a progressive decrease and suspension of the psychic and physical dependence to nicotine in smokers. Cytisine has a structure and system of action that are comparable to those of nicotine, but it has much lower toxicity.

Cytisus laborinum L the Tabex source plant aka Golder Rain acacia. Tabex is extremely well tolerated, and when applied in therapeutic doses, allows a progressive quiting of smoking cigarettes without any adverse effects. The total giving up of cigarette smoking needs to happen not behind the 5th day after the beginning of the treatment.

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5 mg Citysine can assist to stop cigarette smoking permanently.

Study Published In Peer Reviewed Journal, Nicotine And Tobacco Research Cost-efficient treatment has potential to advance smoking cessation internationally Based upon arise from effective TASC 740-patient pivotal trial recently released in the WILMINGTON, Del. & LONDON--(BUSINESS WIRE)-- Extab Corporation ("Extab") a scientific phase biopharmaceutical business with a concentrate on smoking cessation, today revealed the results of an expense effectiveness study released in the peer examined journal, Nicotine and Tobacco Research Study.

The primary endpoint of the TASC trial was the Russell Requirement criteria for cigarette smoking cessation determined at 12 months from the end of treatment. Given up benefits of quitting smoking were validated by exhaled carbon monoxide levels. The trial revealed a strongly statistically considerable outcome with a Risk Ratio of 3. 4 (p.