Properties
What is it?
International Nonproprietary Name (Active Substance): thiamine, pyridoxine, cyanocobalamin Clinical-Pharmacological Group: Central Nervous System → Agents for Peripheral Nervous System Pathology Dosage Form: Film-coated tablets Description: Round, biconvex, pink, film-coated tablets. Composition Each film-coated tablet contains: Active substances: Vitamin B1 (thiamine hydrochloride) 250 mg Vitamin B6 (pyridoxine hydrochloride) 250 mg Vitamin B12 (cyanocobalamin) 1 mg Excipients: Mannitol, colloidal silicon dioxide, anhydrous, pregelatinized corn starch, polyvinylpyrrolidone, magnesium stearate. Coating composition: Acryl-EZE Pink 93O3405 (methacrylic acid copolymer, titanium dioxide, talc, triethyl citrate, colloidal silicon dioxide, anhydrous, sodium bicarbonate, carmine, sodium lauryl sulfate, indigo carmine aluminum lake). Pharmacotherapeutic Group: Vitamin B1 in combination with B6 and B12. Indications: As part of complex therapy, symptomatic treatment of nervous system diseases such as: - Neuritis, neuralgia (including trigeminal neuralgia), polyneuritis, polyneuropathy (including diabetic and alcoholic), herpes zoster, myalgias, radicular syndrome (caused by degenerative changes of the spine), retrobulbar neuritis, facial nerve palsy; - Systemic neurological diseases due to confirmed deficiency of vitamins B1, B6, and B12. In addition, the preparation is used in the following conditions: - Cardiomyopathy (associated with vitamin B1 deficiency); - Postoperative vomiting; - Radiation sickness; - Chronic intoxication observed in alcoholism. Dosage and Administration: NEURALON tablets should be taken orally, without chewing, with a sufficient amount of water. For prophylaxis, 1 tablet is prescribed daily. For treatment – 2-4 tablets daily. As symptoms subside, the dose can be reduced to 1 tablet per day. The course of treatment is at least 1 month. Contraindications: - Hypersensitivity to the components of the preparation. Side Effects: In isolated cases – sweating, acne-like rash, skin reactions (urticaria). Rarely – development of hypersensitivity reactions (skin rash, respiratory distress, anaphylactic shock, angioedema). Special Instructions: The issue of NEURALON administration in patients with acute and severe decompensated heart failure is decided individually, taking into account the patient's condition. Effect on Ability to Drive and Operate Machinery: There are no restrictions on the use of the preparation for driving vehicles and operating potentially hazardous machinery. Use During Pregnancy and Lactation: During pregnancy and lactation, the preparation can be used if necessary. Use in Pediatrics: There is no data on the efficacy and safety of NEURALON in children and adolescents.