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Cefotezol Sodium for Injection

Function and Efficacy

Ceftezole sodium is a semi-synthetic cephalosporin derivative, and its mechanism of action is to exert antibacterial activity by inhibiting the synthesis of bacterial cell walls. Ceftezole sodium has antibacterial activity against the following bacteria: 1. Aerobic Gram-positive bacteria: Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes. 2. Aerobic Gram-negative bacteria: Escherichia coli, Klebsiella pneumoniae, Proteus.

Ingredients

This product is a sterile powder of ceftezole sodium. Its chemical name is: sodium (6R, 7R)-3-[(1,3,4-thiadiazol-2-yl)thiomethyl]-8-oxo-7-[2-(1H-tetrazol-1-yl)acetylamino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate.

Name Description Content CAS NO. Manufacturer
Ceftezole sodiumIngredients

It exerts antibacterial activity by inhibiting the synthesis of bacterial cell walls and has antibacterial activity against aerobic Gram-positive bacteria (such as Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes) and aerobic Gram-negative bacteria (such as Escherichia coli, Klebsiella pneumoniae, Proteus)

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41136-22-5 25

Appearance

This product is white to light yellow crystalline powder, odorless and hygroscopic.

Indication

Respiratory tract infections, urinary tract infections, sepsis, peritonitis.

Usage and Dosage

Adults take 0.5g~2g (2~8 vials) at a time, twice a day, intravenously or intramuscularly. For severe infections, the dose can be appropriately increased as prescribed by the doctor. Preparation of injection: 1. Intravenous injection: Dissolve in water for injection, normal saline or 5% glucose injection, and inject slowly. 2. Intravenous drip: Dissolve in normal saline or 5% glucose injection. 3. Intramuscular injection: Dissolve in 0.5% lidocaine hydrochloride injection. If the injection becomes turbid due to temperature reasons when it is dissolved, it can be heated to clarify it before use. It is best to use it immediately after dissolution. If it needs to be stored, it should be stored in a cool place (below 15°C) to prevent precipitation, but it must be used within 72 hours.

Adverse Reactions

1. Shock: Shock rarely occurs, and close observation is required. If any symptoms related to the use of this product occur, such as discomfort, abnormal sensation in the mouth, asthma, dizziness, sudden abnormal bowel movements, tinnitus, sweating, etc., the drug should be stopped immediately and necessary treatment should be given. 2. A few have allergic reactions, such as rash, urticaria, skin redness, itching, fever, etc., which disappear when the drug is stopped. 3. Severe renal function abnormalities are rare, and blood creatinine is occasionally increased. If abnormalities are found, the drug should be stopped immediately and necessary treatment should be given. 4. Granulocytopenia, leukopenia, eosinophilia, thrombocytopenia, etc. are rare. When the above abnormalities are found, the drug should be stopped. 5. Increased GOT, GPT, and alkaline phosphatase are rare. When the above abnormalities occur, the drug should be stopped immediately. 6. Gastrointestinal reactions, such as nausea, vomiting, diarrhea, etc. are rare, and pseudomembranous colitis is rare. When abdominal pain and diarrhea occur, the drug should be stopped immediately. 7. Dysbacteriosis: Candida infection is rare. 8. Vitamin deficiency: Vitamin K deficiency and B vitamin deficiency are rare. 9. Interstitial pneumonia, toxic fever, cough, dyspnea, abnormal chest X-ray, eosinophilia are rare. When the above symptoms occur, the drug should be discontinued and appropriate treatment should be given. 10. Others: Headache, general malaise, fever, superficial glossitis are rare.

Precautions

1. Patients who are allergic to this product or other cephalosporin antibiotics are contraindicated. 2. Patients who have a history of allergy to lidocaine or acylanilide local anesthetics are contraindicated for intramuscular injection of this product. [Use in pregnant and lactating women] The safety of using the drug during pregnancy has not yet been determined. For pregnant women or women who may become pregnant, the pros and cons must be weighed, and the drug can only be used when the pros outweigh the cons. Therefore, pregnant and lactating women should use it with caution. [Use in children] Children should take 10 to 40 mg per kilogram of body weight once, twice a day, intravenously or intramuscularly (for the preparation of the injection, see: Dosage and Administration).

Special Population Medication

Precautions for children: 10-40 mg per kg of body weight for children, twice a day, intravenous or intramuscular administration (for the preparation of injection, see [Usage and Dosage]). Precautions for pregnancy and lactation: Women who may become pregnant, pregnant women and lactating women should use with caution. Precautions for the elderly: Not yet clear.

Drug Interactions

Not yet clear.

Storage

Keep in dark, airtight and cool place.

Packaging Specification

Calculated as C13H12N8O4S3 0.5g

Validity Period

24 months

Manufacturer

Harbin Pharmaceutical Group Co., Ltd. GENERAL Pharm. FACTORY

  • Founded in:

    1994-05-19
  • Address:

    No. 388, Hahei Highway, Hulan District (production base No. 109, Xuefu Road, Nangang District, No. 1, Junmin Street, Xiangfang District)
  • Tax NO.:

    912301008280277137
  • Registered Funds:

    -
  • Website:

  • Email:

Other Drugs of Harbin Pharmaceutical Group Co., Ltd. GENERAL Pharm. FACTORY

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