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Active substance: lidocaine; 1 ml of solution contains lidocaine hydrochloride monohydrate 10 mg; Excipients: sodium chloride, sodium hydroxide 1 M solution, water for injections.
Means for local anesthesia. ATX code N01B B02.
Hypersensitivity to the components of the drug, other amide local anesthetic agents, the presence in the anamnesis of epileptiform seizures on lidocaine, severe bradycardia, severe arterial hypotension, cardiogenic shock, severe forms of chronic heart failure (II-III degree), sinus node weakness syndrome, Wolff-Parkinson syndrome – White, Adams-Stokes syndrome, atrioventricular (AV) block II and III degree, hypovolemia, severe liver/kidney dysfunction, porphyria, myasthenia, retrobulbar injection in patients with glaucoma; contraindicated for patients in the first three months after a myocardial infarction with reduced cardiac output of the left ventricle (less than 35% of normal); blood coagulation disorders, anticoagulant therapy; infection at the injection site; non-contact patients are contraindicated; significant decrease in left ventricular function.
Administration of lidocaine requires a preliminary test to determine individual sensitivity to this medicinal product. For terminal anesthesia in adults, lubricate the mucous membranes with a drug in a dose of 2 mg/kg of lidocaine, the duration of anesthesia is 15-30 minutes. The maximum dose for adults is 20 ml.
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