Lomefloxacin Aspartate Sodium Chloride Injection
Function and Efficacy
Lomefloxacin is a synthetic quinolone broad-spectrum antibiotic. Its antibacterial mechanism is to inhibit the activity of bacterial DNA helicase, thereby inhibiting bacterial DNA transcription and replication. It has a bactericidal effect on a variety of Gram-positive and Gram-negative bacteria.
Ingredients
Lomefloxacin Aspartate
| Name | Description | Content | CAS NO. | Manufacturer |
|---|---|---|---|---|
| LOMEFLOXACIN, ASPARTATEIngredients |
Lomefloxacin is a synthetic quinolone broad-spectrum antibiotic. Its antibacterial mechanism is to inhibit the activity of bacterial DNA helicase, thereby inhibiting bacterial DNA transcription and replication. It has a bactericidal effect on a variety of Gram-positive and Gram-negative bacteria. More |
211690-33-4 | 7 |
Appearance
This product is a yellow-green clear liquid.
Indication
This product is suitable for the following infections caused by sensitive bacteria: 1. Respiratory tract infections: acute exacerbation of chronic bronchitis, bronchiectasis with infection, acute bronchitis and pneumonia, etc. 2. Urinary and reproductive system infections: acute cystitis, acute pyelonephritis, complicated urinary tract infection, acute exacerbation of chronic urinary tract infection, acute prostatitis, simple gonorrhea, etc. 3. Infections of the abdominal cavity, bile duct, intestines, typhoid fever, etc. 4. Skin and soft tissue infections. 5. Other infections: such as sinusitis, otitis media, blepharitis, etc.
Usage and Dosage
Intravenous drip, 0.2g (one bottle) each time for adults, twice a day, or as directed by a doctor.
Adverse Reactions
1. Abdominal discomfort or pain, diarrhea, nausea or vomiting. 2. Central nervous system reactions: dizziness, headache, drowsiness or insomnia. 3. Allergic reactions: rash, skin itching, occasionally exudative erythema multiforme and angioneurotic edema. Among them, photosensitivity reactions are more common than other commonly used quinolones. 4. A small number of patients may have increased serum aminotransferase and BUN values and decreased peripheral blood white blood cells, which are mostly mild and transient. 5. Occasionally occur: 1. Epileptic seizures, mental abnormalities, irritability, confusion, hallucinations, tremors. 2. Hematuria, fever, rash and other manifestations of interstitial nephritis. 3. Crystalluria, more common when used in high doses. 4. Joint pain. 5. Phlebitis.
Precautions
1. It is contraindicated for those who are allergic to this product or other quinolone drugs; 2. It is contraindicated for pregnant women, infants and patients under 18 years old.
Special Population Medication
Precautions for children: This product can cause permanent damage to the cartilage of the weight-bearing joints of dogs, resulting in lameness. It can also cause arthritis in several other underage animals, so it is contraindicated for infants and children under 18 years old. Precautions for pregnancy and lactation: This product can pass through the blood-placental barrier and is contraindicated for pregnant women. This product can also be secreted into breast milk, and its concentration is close to the blood drug concentration. Lactating women should stop breastfeeding when using this product. Precautions for the elderly: Elderly patients have decreased renal function, and the dosage should be reduced as appropriate.
Drug Interactions
1. This product has little effect on the liver metabolism and body clearance of theophylline drugs and caffeine. 2. Combination with fenbufen can cause central excitation and epileptic seizures. 3. Probenecid can delay the excretion of this product, increasing the average area under the curve (AUC) by 63%, extending the average time to peak (tmax) by 50%, and increasing the average peak concentration (Cmax) by 4%; therefore, when used in combination, toxicity may occur due to increased blood concentration of this product. 4. It can enhance the effects of oral anticoagulants such as warfarin, and prothrombin time and other items should be monitored. 5. Urine alkalinizers can reduce the solubility of this product in urine, leading to crystalluria and nephrotoxicity. 6. Combination with cyclosporine can increase the blood concentration of cyclosporine, and the blood concentration of cyclosporine must be monitored and the dosage adjusted.
Storage
Keep away from light and store in a cool dark place (keep away from light and do not exceed 20℃). Tentatively 24 months
Packaging Specification
100ml: Lomefloxacin 0.2g and sodium chloride 0.85g
Validity Period
Tentative 24 months
Manufacturer
Henan Yonghe Pharmaceutical Co., Ltd.
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Founded in:
1997-09-10 -
Address:
No. 28, Yinping Road, Zhengzhou High-tech Development Zone -
Tax NO.:
91410100268054747H -
Registered Funds:
35 million yuan -
Email: