Neuromidin solution 15mg / ml, No. 10
Expiration Date: 11/2025
Russian Pharmacy name:
Нейромидин раствор 15мг/мл, №10
diseases of the peripheral nervous system (mono- and polyneuropathy, polyradiculopathy, myasthenia gravis and myasthenic syndrome of various etiologies);
diseases of the central nervous system (bulbar paralysis and paresis; the recovery period of organic lesions of the central nervous system, accompanied by motor and / or cognitive impairment);
intestinal atony (treatment and prevention) (optional for tablets).
Inside, s / c or i / m. Doses and duration of treatment are determined individually, depending on the severity of the disease.
Pills
Diseases of the peripheral nervous system:
- mono- and polyneuropathy, polyradiculopathy, myasthenia gravis and myasthenic syndrome of various etiology - 10-20 mg (0.5-1 table) 1-3 times a day. The course of treatment is 1 to 2 months. If necessary, the course of treatment can be repeated several times with a break between courses of 1-2 months;
- to prevent myasthenic crises, in severe disorders of neuromuscular conduction, 1-2 ml (15-30 mg) of NeuromidinЃ 1.5% solution for injection is briefly parenterally injected, then treatment is continued with NeuromidinЃ tablets, the dose can be increased to 20-40 mg (table 1-2) 5 times a day.
Diseases of the central nervous system: bulbar paralysis and paresis, the recovery period of organic lesions of the central nervous system (traumatic, vascular and other genesis), accompanied by motor and / or cognitive impairments - 10-20 mg (0.5-1 table) 2-3 times day. The course of treatment is from 2 to 6 months. If necessary, repeat the course of treatment.
Treatment and prevention of intestinal atony - 20 mg (1 tab.) 2-3 times a day for 1-2 weeks.
Solution for intramuscular and subcutaneous administration
Diseases of the peripheral nervous system:
- mono- and polyneuropathy of various origins - s / c or i / m 5-15 mg 1-2 times a day, course - 10-15 days (in severe cases - up to 30 days); further treatment is continued with a tablet form of the drug;
- myasthenia gravis and myasthenic syndrome - s / c or i / m 15-30 mg 1-3 times a day with a further transition to the tablet form. The general course of treatment is 1-2 months. If necessary, the treatment can be repeated several times with a break between courses of 1-2 months.
Diseases of the central nervous system:
- bulbar paralysis and paresis - s / c or i / m 5-15 mg 1-2 times a day for 10-15 days; if possible, switch to a tablet form;
- rehabilitation for organic lesions of the central nervous system - i / m 10-15 mg 1-2 times a day, the course - up to 15 days, then, if possible, switch to the tablet form.
If the next dose was not taken on time, then it is not taken additionally.
The maximum daily dose is 200 mg.
Pills | 1 tab. |
active substance: | |
ipidacrine hydrochloride monohydrate | 20 mg |
(in terms of ipidacrine hydrochloride) | |
excipients: lactose monohydrate - 65 mg; potato starch - 14 mg; calcium stearate - 1 mg |
Solution for intramuscular and subcutaneous administration | 1 ml |
active substance: | |
ipidacrine hydrochloride monohydrate (calculated as ipidacrine hydrochloride) | 5 mg |
15 mg | |
auxiliary substances: concentrated hydrochloric acid - up to pH 3; water for injection - up to 1 ml |
hypersensitivity to any component of the drug;
epilepsy;
extrapyramidal diseases with hyperkinesis;
angina pectoris;
severe bradycardia;
bronchial asthma;
mechanical obstruction of the intestine or urinary tract;
vestibular disorders;
peptic ulcer of the stomach or duodenum in the acute stage;
pregnancy (the drug increases the tone of the uterus);
lactation period;
children under 18 years of age (there are no systematized data on the use).
With care: in case of gastric ulcer and duodenal ulcer, thyrotoxicosis, CVS diseases, as well as in patients with a history of obstructive respiratory system diseases or in acute respiratory tract diseases.
Additionally for tablets
With caution: with lactase deficiency, lactose intolerance, lactose / isomaltose malabsorption syndrome, because the preparation contains lactose.