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Tegafur Injection

Function and Efficacy

This product is a derivative of fluorouracil. It is activated by the liver in the body and gradually converted into fluorouracil to play an anti-tumor role. It can interfere with and block the synthesis of DNA, RNA and protein, and mainly acts on the S phase. It is a cell cycle-specific drug of the anti-pyrimidine class. Its mechanism of action, efficacy and anti-tumor spectrum are similar to those of fluorouracil, but it has a long-lasting effect, good absorption and low toxicity. The chemotherapy index is twice that of fluorouracil, and the toxicity is only 1/4 to 1/7 of that of fluorouracil. No severe bone marrow suppression was observed in the chronic toxicity test, and the effect on immunity was relatively mild.

Ingredients

The main ingredient of this product is Tegafur. Chemical name: 1-(tetrahydro-2-furanyl)-5-fluoro-2,4(1H,3H)-pyrimidinedione. Molecular formula: C8H9FN2O3 Molecular weight: 200.17 The auxiliary material is sodium hydroxide.

Name Description Content CAS NO. Manufacturer
TegafurIngredients

It is activated in the liver and gradually converted into fluorouracil to play an anti-tumor role. It can interfere with and block the synthesis of DNA, RNA and protein, and mainly acts in the S phase. It is a cell cycle-specific anti-pyrimidine drug. Its mechanism of action, efficacy and anti-tumor spectrum are similar to those of fluorouracil, but it has a long-lasting effect, good absorption and low toxicity. The chemotherapy index is twice that of fluorouracil, and the toxicity is only 1/4 to 1/7 of that of fluorouracil. No serious bone marrow suppression was observed in chronic toxicity tests, and the effect on immunity was relatively mild.

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17902-23-7 10

Appearance

This product is an almost colorless clear liquid.

Indication

It is mainly used to treat digestive tract tumors, such as gastric cancer, colorectal cancer, pancreatic cancer, liver cancer, and can also be used for breast cancer.

Usage and Dosage

The daily dose for adults is 800-1000 mg or 15-20 mg/kg per day based on body weight, dissolved in 500 ml of 5% glucose injection or 0.9% sodium chloride injection, and administered intravenously once a day, with a total of 20-40 g for one course of treatment. It can also be used in combination with other anti-tumor drugs.

Adverse Reactions

Bone marrow suppression reaction is mild, with a decrease in white blood cells and platelets. Neurotoxic reactions include headache, dizziness, ataxia, mental state changes, etc. A few patients experience nausea, vomiting, diarrhea, and changes in liver and kidney function. Local injection sites have phlebitis, swelling, and pain. Fever, skin itching, and pigmentation are occasionally seen.

Precautions

It is forbidden to use in pregnant and lactating women.

Drug Interactions

Tegafur is alkaline and contains carbonate. Avoid using it with drugs containing calcium or magnesium ions or with strong acidity.

Storage

Keep in a light-proof and airtight container.

Packaging Specification

5ml:0.2g

Manufacturer

Harbin Pharmaceutical Group Bioengineering Co., Ltd.

  • Founded in:

    1995-02-20
  • Address:

    No. 99, Zhuhai Road, Limin Development Zone, Hulan District, Harbin
  • Tax NO.:

    91230111128024298B
  • Registered Funds:

    186.0655 million yuan
  • Website:

  • Email:

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