| Customization: | Available |
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| Dosage Form: | Infusion |
| Transport Package: | Carton |
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| Generic Name | Levofloxacin Hydrochloride and Sodium Chloride Injection 100ml |
| Strength | 100ml |
| Packing | 1bottle/box |
| Origin | China |
This product is suitable for the following moderate and severe infections caused by sensitive bacteria:
Respiratory infections: acute bronchitis, acute onset of chronic bronchitis, diffuse bronchitis, bronchiectasis with infection, pneumonia, tonsillitis (abscess around the tonsils).
Urinary system infection: pyelonephritis, complicated urinary tract infection, etc.
Reproductive system infection: acute prostatitis, acute epididymitis, uterine infection, uterine adnexitis, pelvic inflammation (suspected anaerobic bacteria infection can be combined with metronidazole).
Skin and soft tissue infection: infectious impetigo, cellulitis, lymphatic (nodal) inflammation, subcutaneous abscess, perianal abscess, etc.
Intestinal infections: bacillary dysentery, infectious enteritis, Salmonella enteritis, typhoid and paratyphoid.
Various infections in sepsis, granulocytopenia, and immunocompromised patients.
Other infections: mastitis, trauma, burn and postoperative wound infection, abdominal infection (metronidazole when necessary), cholecystitis, cholangitis, bone and joint infection and ent infection.
Intravenous infusion: Adults 400mg daily, divided into 2 times. For severely infected patients and pathogenic bacteria with poor sensitivity to this product (such as Pseudomonas aeruginosa), the maximum daily dose can be increased to 600mg, divided into 2 drops.
It can be increased or decreased according to the type of infection and symptoms.
1. This preparation is intended for intravenous infusion with an infusion time of at least 60 minutes per 100ml. This preparation should not be mixed with other drugs in the same bottle for intravenous drip, or in the same vein infusion tube for intravenous drip.
2. Patients with renal dysfunction should reduce the amount or use with caution.
3. Patients with a history of central nervous system disease and epilepsy should be used with caution.
4. Quinolones can also cause rare phototoxic reactions (incidence < 0.1%). Excessive sun exposure and artificial ultraviolet rays should be avoided when receiving treatment with this product. This product should be discontinued in case of photosensitivity reaction or skin damage. In addition, there are occasional reports of hamstring inflammation or hamstring fracture after medication, so if the above symptoms occur, it is necessary to immediately stop the drug and rest, and do not exercise until the symptoms disappear.
5. Check before use. If the bottle is found to have slight cracks, loose sealing, discoloration, turbidity or foreign matter, it cannot be used.
6. Strictly prohibited for food and feed processing.
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