

It has a protective effect on the normal intestinal microflora, thereby has increased gastrointestinal safety. Along with a powerful broad spectrum antibacterial effect, it has an immunomodulatory effect, which can be especially important in the treatment of chronic or recurrent diseases of infectious etiology.
Infectious and inflammatory diseases caused by microorganisms sensitive to the drug:
One tablet contains:
Active ingredient: levofloxacin hemihydrate (in terms of levofloxacin) 500 mg;
Excipients: lactulose, lactose monohydrate, low molecular weight povidone, croscarmellose sodium, sodium lauryl sulfate, talc, magnesium stearate, microcrystalline cellulose;
Shell auxiliary substances: hypromellose, talc, titanium dioxide, macrogol-4000.
Levofloxacin is marketed under different brands and generic names, and comes in different dosage forms:
Brand name | Manufacturer | Country | Dosage form |
---|---|---|---|
Levofloxacin | AVVA RUS | Russia | pills |
Levostar | Actavis Ltd | Iceland | pills |
Levofloxacin | Vertex | Russia | pills |
Floracid | Valenta | Russia | pills |
L-Optic® Rompharm | K.O.Romparm Company S.R.L | Romania | eye drops |
Signatum | Sentiss Pharma | India | eye drops |
Oftakviks | Santen | France | eye drops |
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Orally, before a meal or in a break between meals, without chewing, drinking a sufficient amount of liquid.
Acute sinusitis: 500 mg 1 time per day for 10-14 days;
Community-acquired pneumonia: 500 mg 1-2 times a day, 7-14 days;
Exacerbation of chronic bronchitis: 250-500 mg 1 time per day for 7-10 days;
Uncomplicated urinary tract infections - 250 mg 1 time per day for 3 days;
Complicated urinary tract infections (including pyelonephritis): 250 mg 1 time per day (for severe disease, the dose should be increased) for 7-10 days;
Chronic bacterial prostatitis - 500 mg 1 time per day, the course of treatment - 28 days;
Infections of the skin and soft tissues: 250-500 mg 1-2 times a day for 7-14 days;
Intraabdominal infection - 500 mg 1 time per day, treatment 7-14 days (in combination with antibacterial drugs acting on anaerobic microflora);
Combined therapy of drug-resistant forms of tuberculosis: 500 mg 1-2 times a day, the course of treatment is up to 3 months;
The duration of treatment depends on the type and severity of the disease.
After stopping the symptoms of acute inflammation and normalizing the temperature, it is recommended to continue therapy with levofloxacin for 48-72 hours.
Dosing of the drug in patients with impaired renal function (creatinine clearance less than 50 ml / min):
* including with hemodialysis and continuous ambulatory peritoneal dialysis
After hemodialysis or permanent ambulatory peritoneal dialysis, no additional doses are required.
Dose adjustment is not required in patients with impaired liver function.
On the part of the digestive system: nausea, vomiting, diarrhea (including blood), indigestion, loss of appetite, abdominal pain, pseudomembranous colitis; increased activity of liver enzymes, hyperbilirubinemia, hepatitis, dysbacteriosis.
Since the cardiovascular system: lower blood pressure, vascular collapse, tachycardia, prolongation of the QT interval, atrial fibrillation.
Nervous system disorders: headache, dizziness, weakness, drowsiness, insomnia, tremor, anxiety, paresthesias, fear, hallucinations, confusion, depression, movement disorders, convulsions.
From the senses: visual impairment, hearing, smell, taste and tactile sensitivity.
On the part of the musculoskeletal system: arthralgia, muscular weakness, myalgia, tendon rupture, tendonitis, rhabdomyolysis.
From the urinary system: hypercreatininemia, interstitial nephritis, acute renal failure.
From the side of blood-forming organs: eosinophilia, hemolytic anemia, leukopenia, neutropenia, agranulocytosis, thrombocytopenia, pancytopenia, hemorrhages.
Metabolism: hypoglycemia (increased appetite, increased sweating, tremors).
Allergic reactions include itching and redness of the skin, swelling of the skin and mucous membranes, urticaria, malignant exudative erythema (Stevens-Johnson syndrome), toxic epidermal necrolysis (Lyell's syndrome), bronchospasm, asthma, anaphylactic shock, allergic pneumonitis, vasculitis.
Other: asthenia, exacerbation of porphyria, photosensitization, persistent fever, development of superinfection.
Hypersensitivity to levofloxacin, other fluoroquinolones or components of the drug, epilepsy, tendon damage during previous treatment with quinolones, pregnancy, lactation, childhood and adolescence (under 18)
Lactose intolerance or lactase deficiency, as well as glucose-galactose malabsorption.
With care for the elderly, with a deficiency of glucose-6-phosphate dehydrogenase.
There are reports of a pronounced decrease in the convulsive readiness threshold with simultaneous use of quinolones and substances that lower the cerebral threshold of convulsive readiness. This also applies to the simultaneous administration of quinolones and theophylline, as well as non-steroidal anti-inflammatory drugs - propionic acid derivatives.
The effect of the drug is weakened when applied simultaneously with sucralfate, antacids containing magnesium or aluminum, and iron salts. Levofloxacin should be taken no less than 2 hours before taking these medicines.
With the simultaneous use of vitamin K antagonists, monitoring of blood coagulation parameters is necessary.
Renal clearance of levofloxacin is slightly slowed down by cimetidine and probenecid. Levofloxacin slightly increases the half-life of cyclosporine.
Taking glucocorticosteroids increases the risk of tendon rupture.
In the treatment of elderly patients should be borne in mind that they often suffer from impaired renal function.
Despite the fact that photosensitivity during treatment with levofloxacin is rarely observed, patients are not recommended to undergo strong solar or artificial ultraviolet radiation.
If pseudomembranous colitis is suspected, you should immediately cancel levofloxacin and begin appropriate treatment. In such cases, you can not use drugs that inhibit intestinal motility.
Patients with glucose-6-phosphate dehydrogenase deficiency (a hereditary metabolic disorder) can respond to fluoroquinolones by destroying red blood cells (hemolysis). In this regard, treatment with levofloxacin should be carried out with caution.
Side effects of levofloxacin, such as dizziness or drowsiness, as well as visual impairment (see the “Side Effects” section), can impair reactivity and hamper driving and maintaining machinery.
Symptoms of a drug overdose of levofloxacin appear at the level of the central nervous system (confusion, dizziness, impaired consciousness and convulsions). In addition, gastrointestinal disorders (eg, nausea, vomiting) and erosive lesions of the mucous membranes of the gastrointestinal tract may occur. In studies conducted with ultra-high doses of levofloxacin, prolongation of the QT interval has been shown.
Levofloxacin is not eliminated by hemodialysis or peritoneal dialysis. There is no specific antidote (opposing agent).
Treatment - gastric lavage and symptomatic therapy.
Studies and clinical trials of Levofloxacin (Click to expand)