Levofloxacin Tablets
Ingredients
Levofloxacin
| Name | Description | Content | CAS NO. | Manufacturer |
|---|---|---|---|---|
| LevofloxacinIngredients |
Extract from the above information More |
100986-85-4 | 33 |
Appearance
This product is a film-coated tablet, which appears white or light yellow after removing the coating.
Indication
This product is suitable for the following mild and moderate infections caused by sensitive bacteria: 1. Respiratory system infections: acute sinusitis, acute exacerbation of chronic bronchitis, community-acquired pneumonia; 2. Urinary system infections: acute pyelonephritis, complicated urinary tract infection, etc.; 3. Reproductive system infections: prostatitis, epididymitis, intrauterine infection, adnexitis, pelvic inflammatory disease (metronidazole can be used in combination when anaerobic infection is suspected); 4. Skin and soft tissue infections: infectious impetigo, cellulitis, lymphangiitis (adenitis), subcutaneous abscess, perianal abscess, etc.; 5. Intestinal infections: bacterial dysentery, infectious enteritis, salmonella enteritis, typhoid and paratyphoid, etc.; 6. Other infections: trauma, burns and postoperative wound infection, abdominal infection (use metronidazole in combination when necessary), mastitis, cholecystitis, cholangitis, bone and joint infection, and ENT infection, etc.
Usage and Dosage
The usual dose of levofloxacin oral tablets is 0.25g or 0.5g or 0.75gmg, taken orally once every 24 hours. See the instructions for details.
Adverse Reactions
1. Gastrointestinal reactions: abdominal discomfort or pain, diarrhea, nausea or vomiting. 2. Central nervous system reactions may include dizziness, headache, drowsiness or insomnia. 3. Allergic reactions: rash, itchy skin, occasionally exudative erythema multiforme and angioneurotic edema. Photosensitivity reactions are less common. 4. Occasionally, the following may occur: (1) epileptic seizures, mental abnormalities, irritability, confusion, hallucinations, tremors. (2) interstitial nephritis manifestations such as hematuria, fever, and rash. (3) phlebitis. (4) crystalluria, which is more common when high doses are used. (5) joint pain. 5. A small number of patients may experience elevated serum aminotransferase, elevated blood urea nitrogen, and decreased peripheral white blood cells, which are usually mild and transient.
Precautions
It is contraindicated for those who are allergic to any ingredient in this product.
Special Population Medication
Precautions for children: The safety of this product in infants and adolescents under 18 years of age has not been determined. However, this product can cause joint lesions when used in several young animals. Therefore, it should not be used in children and adolescents under 18 years of age. Precautions for pregnancy and lactation: Animal experiments have not confirmed that quinolones are teratogenic, but studies on the use of drugs in pregnant women have not yet reached a clear conclusion. Since this drug can cause joint lesions in underage animals, it is contraindicated for pregnant women, and lactating women should suspend breastfeeding when using this product. Precautions for the elderly: Elderly patients often have impaired renal function, and since this product is partially excreted through the kidneys, it needs to be used in reduced doses.
Storage
Keep in dark place and sealed
Packaging Specification
0.25 g
Validity Period
36 months
Manufacturer
Suzhou Yifan Pharmaceutical Co., Ltd.
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Founded in:
2013-03-21 -
Address:
North side of Jinjiang Road, Suzhou Economic Development Zone, Anhui Province -
Tax NO.:
91341300065208048B -
Registered Funds:
250 million yuan -
Email: