Monosialotetrahexosylganglioside sodium for injection

Monosialotetrahexosylganglioside can promote the functional recovery of central nervous system damage caused by various reasons. The mechanism of action is to promote neuroplasticity (including the survival of nerve cells, axon growth and synapse formation). Monosialotetrahexosylganglioside has a protective effect on secondary neurodegeneration after injury. The application of monosialotetrahexosylganglioside has a good effect on the improvement of cerebral hemodynamic parameters and the reduction of brain edema after injury. Monosialotetrahexosylganglioside reduces nerve cell edema by improving the activity of cell membrane enzymes. Animal experiments show that monosialotetrahexosylganglioside can improve behavioral disorders caused by Parkinson's disease. LD50 is 872mg/kg (i.v.) to 8g/kg (s.c.), depending on the animal species and route of administration. Subacute and chronic toxicity tests, teratogenicity tests, reproductive toxicity tests, perinatal toxicity tests and mutagenicity tests conducted on various animals did not show any toxic effects of this product.

The main ingredient of this product is monosialotetrahexosylganglioside sodium, its chemical name is: monosialotetrahexosylganglioside sodium, it is extracted from pig brain and has an effect on nerve cell function damage. Its structural formula is: Molecular formula: C73H130N3NaO31orC75H134N3NaO31 Molecular weight: 1568.84or1597.18.

This product is a clear, colorless or light yellow solution, sometimes with a slight opalescence.

Vascular or traumatic central nervous system injury; Parkinson's disease.

20-40 mg per day, once or divided into several intramuscular injections or slow intravenous drips as prescribed by the doctor. In the acute stage of the disease (especially acute trauma): 100 mg per day, intravenous drip; after 2-3 weeks, change to a maintenance dose of 20-40 mg per day, generally for 6 weeks. For Parkinson's disease, the first dose is 500-1000 mg, intravenous drip; from the second day onwards, 200 mg per day, subcutaneous, intramuscular or intravenous drip, generally for 18 weeks.

A small number of patients developed a rash reaction after using this product and should be advised to stop using it.

Allergy to this product has been confirmed; hereditary lipid metabolism disorders (ganglioside storage diseases, such as familial Tay-Sachs disease, retinal degeneration).

Precautions for children: So far, no adverse reactions have been reported in children using this product. Precautions for pregnancy and lactation: Experiments conducted on various animals have not shown any adverse reactions to the use of this product during pregnancy and lactation. Precautions for the elderly: So far, no adverse reactions have been reported in elderly patients using this product.

So far, no interaction between this product and other drugs has been found.

Keep away from light and store in sealed container.

40mg

24 months.

Qilu Pharmaceutical Co., Ltd.

• Founded in:

  1992-08-21

• Address:

  No. 317, Xinluo Street, High-tech Zone, Jinan City, Shandong Province

• Tax NO.:

  91370000614073351Q

• Registered Funds:

  600 million yuan

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