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Mouse Nerve Growth Factor for Injection

Function and Efficacy

Pharmacological action: The results of in vivo tests on rats showed that this product can improve the limb motor dysfunction caused by toxic peripheral neuropathy caused by hexadione and acrylamide in rats, shorten the latency of nerve-muscle action potential, and increase the amplitude of nerve-muscle action potential. The results of histopathological examination showed that this product can reduce the incidence of myelin swelling of the animal tibial nerve and reduce the number of degenerated tibial nerve fibers. The above results suggest that this product may promote the recovery of damaged nerves. Toxicological study: The results of repeated toxicological tests showed that: (1) Wister rats were injected intramuscularly with 30mu;g/Kg, 60mu;g/Kg and 120mu;g/Kg of this product for 12 weeks. Only the animals in the 120mu;g/Kg dose group showed decreased appetite, delayed weight gain, and reduced activity after 28 days of administration. (2) The highest dose of this product was 17.8mu;g/Kg injected intramuscularly in mixed dogs. After 60 days of continuous administration, no obvious toxic reactions were observed in the animals. The results of general reproductive toxicity, teratogenic sensitive period and perinatal toxicity tests on Shanghai mice showed that when the dose was as high as 200mu;g/Kg, it had no obvious effect on the fertility of animals, embryonic organ formation and the development of F1 generation mice.

Ingredients

The active ingredient of this product is the purified nerve growth factor (mNGF) extracted from the mouse submandibular gland. The finished product contains 5% mannitol and 0.1% human blood protein as protective agents.

Appearance

This product is a white lyophilized loose body. After adding the amount indicated on the bottle, the solution is a colorless clear liquid without foreign matter, turbidity or precipitation.

Indication

Hexane toxic peripheral neuropathy.

Usage and Dosage

This product is dissolved in 2 ml of injection water and injected intramuscularly. Once a day, one bottle (20g) each time. Four weeks is a course of treatment. Depending on the severity of the disease, multiple courses of continuous administration can be given as prescribed by the doctor.

Adverse Reactions

1. No serious adverse reactions. Clinical trials found that some patients had transient elevations in transaminase. 2. Pain at the injection site or lower limb pain on the injection side is common after medication (the incidence rates are 85% and 29%, respectively), which generally does not require treatment. For some patients with more severe symptoms, oral analgesics can relieve them. 3. Other symptoms (such as dizziness, insomnia, etc.) are occasionally seen, and the incidence rate is not significantly different from that of the placebo group.

Precautions

Do not use if you are allergic to this product.

Special Population Medication

Precautions for children: As there is no data on the use of this product in children, please follow the doctor's advice when using it for children. Precautions for pregnancy and lactation: This product promotes the growth and development of nerve cells. It is recommended that pregnant and lactating women use it with caution. Precautions for the elderly: Not yet clear.

Drug Interactions

Not yet clear.

Storage

Store at 2-8℃ away from light. Valid for 30 months.

Packaging Specification

20μg (not less than 9000AU)/2ml/bottle

Validity Period

30 months

Manufacturer

Wuhan Hiteck Biological Pharma Co., Ltd.

  • Founded in:

    1992-04-08
  • Address:

    Wuhan Economic and Technological Development Zone Haite Technology Park
  • Tax NO.:

    91420100724667038L
  • Registered Funds:

    130.894391 yuan
  • Website:

  • Email:

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