Indications |
Oral Acute bacterial sinusitis Adult: 500 mg once daily for 10-14 days. Alternatively, 750 mg once daily for 5 days. Renal impairment: Haemodialysis/CAPD: Initially, 500 mg daily, then 250 mg every 48 hr. Alternatively: Initially, 750 mg daily, then 500 mg every 48 hr.
Oral Acute bacterial exacerbation of chronic bronchitis Adult: 500 mg once daily for 7 days. Renal impairment: Haemodialysis/CAPD: Initially, 500 mg daily, then 250 mg every 48 hr.
Oral Community-acquired pneumonia Adult: 500 mg once for 7-14 days. Alternatively, 750 mg once daily for 5 days. Renal impairment: Haemodialysis/CAPD: Initially, 500 mg daily, then 250 mg every 48 hr. Alternatively: Initially, 750 mg daily, then 500 mg every 48 hr.
Oral Nosocomial pneumonia Adult: 750 mg once daily for 7-14 days. Renal impairment: Haemodialysis/CAPD: Initially, 750 mg daily, then 500 mg every 48 hr.
Oral Complicated skin and skin structure infections Adult: 750 mg once daily for 7-14 days. Renal impairment: Haemodialysis/CAPD: Initially, 750 mg daily, then 500 mg every 48 hr.
Oral Uncomplicated urinary tract infections Adult: 250 mg once daily for 3 days. Oral Complicated urinary tract infections Adult: 250 mg once daily for 10 days.
Oral Acute pyelonephritis Adult: 250 mg once daily for 10 days.
Oral Uncomplicated skin and skin structure infections Adult: 500 mg once daily for 7-10 days. Renal impairment: Haemodialysis/CAPD: Initially, 500 mg daily, then 250 mg every 48 hr.
Oral Chronic bacterial prostatitis Adult: 500 mg once daily for 28 days. Renal impairment: Haemodialysis/CAPD: Initially, 500 mg daily, then 250 mg every 48 hr.
Oral Treatment and postexposure prophylaxis of inhalation anthrax Adult: 500 mg once daily for 60 days. Renal impairment: Haemodialysis/CAPD: Initially, 500 mg daily, then 250 mg every 48 hr.
Intravenous Acute bacterial sinusitis Adult: 500 mg once daily for 10-14 days. Alternatively, 750 mg once daily for 5 days. Infuse slowly over 60-90 min. Renal impairment: Haemodialysis/CAPD: Initially, 500 mg daily, then 250 mg every 48 hr. Alternatively: Initially, 750 mg daily, then 500 mg every 48 hr. Infuse slowly over 60-90 min.
Intravenous Acute bacterial exacerbation of chronic bronchitis Adult: 500 mg once daily for 7 days. Infuse slowly over 60 min. Renal impairment: Haemodialysis/CAPD: Initially, 500 mg daily, then 250 mg every 48 hr. Infuse slowly over 60-90 min.
Intravenous Community-acquired pneumonia Adult: 500 mg once for 7-14 days. Alternatively, 750 mg once daily for 5 days. Infuse slowly over 60-90 min. Renal impairment: Haemodialysis/CAPD: Initially, 500 mg daily, then 250 mg every 48 hr. Alternatively: Initially, 750 mg daily, then 500 mg every 48 hr. Infuse slowly over 60-90 min.
Intravenous Nosocomial pneumonia Adult: 750 mg once daily for 7-14 days. Infuse slowly over 60-90 min. Renal impairment: Haemodialysis/CAPD: Initially, 750 mg daily, then 500 mg every 48 hr. Infuse slowly over 60-90 min.
Intravenous Complicated skin and skin structure infections Adult: 750 mg once daily for 7-14 days. Infuse slowly over 60-90 min. Renal impairment: Haemodialysis/CAPD: Initially, 750 mg daily, then 500 mg every 48 hr. Infuse slowly over 60-90 min.
Intravenous Uncomplicated urinary tract infections Adult: 250 mg once daily for 3 days. Infuse slowly over 60-90 min. Intravenous Complicated urinary tract infections Adult: 250 mg once daily for 10 days. Infuse slowly over 60-90 min.
Intravenous Acute pyelonephritis Adult: 250 mg once daily for 10 days. Infuse slowly over 60-90 min.
Intravenous Uncomplicated skin and skin structure infections Adult: 500 mg once daily for 7-10 days. Infuse slowly over 60-90 min. Renal impairment: Haemodialysis/CAPD: Initially, 500 mg daily, then 250 mg every 48 hr. Infuse slowly over 60-90 min.
Intravenous Chronic bacterial prostatitis Adult: 500 mg once daily for 28 days. Infuse slowly over 60-90 min. Renal impairment: Haemodialysis/CAPD: Initially, 500 mg daily, then 250 mg every 48 hr. Infuse slowly over 60-90 min.
Intravenous Treatment and postexposure prophylaxis of inhalation anthrax Adult: 500 mg once daily for 60 days. Infuse slowly over 60-90 min. Renal impairment: Haemodialysis/CAPD: Initially, 500 mg daily, then 250 mg every 48 hr. Infuse slowly over 60-90 min.
Ophthalmic Ocular infections Adult: 1-2 drops of 0.5% solution every 2 hr while awake (up to 8 times daily) for 2 days, then 1-2 drops every 4 hr while awake (up to 4 times daily) for the next 5 days. Child: >1 yr: 1-2 drops of 0.5% solution every 2 hr while awake (up to 8 times daily) for 2 days, then 1-2 drops every 4 hr while awake (up to 4 times daily) for the next 5 days. Special Populations: For patients with CrCl of 20-49 mL/min, the initial dose of 500 mg is administered followed by 250 mg once daily. If CrCl is 10-19 mL/min, the initial dose of 500 mg is administered followed by 250 mg every 48 hours. Reduce dose in patients with renal impairment. |
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Contraindications |
Hypersensitivity to levofloxacin or other quinolones. Child <18 yr. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Warnings / Precautions |
Known or suspected CNS disorders (e.g. severe cerebral arteriosclerosis, epilepsy) or other risk factors that predispose to seizures. Avoid unnecessary exposure to sunlight or artificial UV light. History of prolonged QT interval, uncorrected electrolyte disturbances. DM (carefully monitor blood glucose levels). Periodically monitor renal, hepatic and haematopoietic functions during treatment. Pregnancy and lactation. Elderly. May impair ability to drive or operate machinery. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Adverse Reactions |
Oral/IV: Nausea, diarrhoea, constipation, headache, insomnia, inj site reactions (IV). Ophthalmic: Transient decrease in vision, ocular burning, ocular pain or discomfort, foreign body sensation, headache, fever, pharyngitis, photophobia. Potentially Fatal: Anaphylaxis. |
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Drug Interactions |
Increased concentration of ciclosporin or tacrolimus. Reduced absorption with didanosine, ferrous sulfate or dietary supplements containing zinc, calcium, magnesium or iron. May increase plasma levels of theophylline. Increased risk of tendon rupture with corticosteroids. Reduced absorption with sucralfate and antacids containing magnesium and aluminium; administer at least 2 hr before or 2 hr after antacids. Increased half-life and decreased clearance of procainamide. Altered glucose levels with antidiabetic agents (e.g. insulin, glyburide). Potentially Fatal: Increased risks of ventricular arrhythmias with QT prolonging drugs e.g. class IA (quinidine, procainamide) or class III (amiodarone, sotalol) antiarrhythmics, fluoxetine, imipramine. Increased risk of CNS stimulation and seizures with NSAIDs. Increased prothrombin time with warfarin. See Below for More levofloxacin Drug Interactions |
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Lab Interactions |
False-positive tests for opiates. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Mechanism of Actions |
Levofloxacin exerts antibacterial action by inhibiting bacterial topoisomerase IV and DNA gyrase, the enzymes required for DNA replication, transcription repair and recombination. It has in vitro activity against a wide range of gram-negative and gram-positive microorganisms. Absorption: Rapid and complete absorption from the GIT (oral); peak plasma concentrations within 1-2 hr. Distribution: Widely distributed in bronchial mucosa, lungs; CSF (relatively poor). Protein-binding: 30-40%. Metabolism: Limited. Excretion: Mainly via urine (largely as unchanged drug); 6-8 hr (elimination half-life). |
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Administration |
Tab: May be taken with or without food. (Ensure adequate fluid intake.) Oral soln: Should be taken on an empty stomach. (Take on an empty stomach 1 hr before or 2 hr after meals. Ensure adequate fluid intake.) |
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Storage Conditions |
Intravenous: Store below 25°C (77°F). Ophthalmic: Store at 15-25°C (59-77°F). Oral: Tablet: Store at 15-30°C (59-86°F). Oral solution: Store at 25°C (77°F). | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
ATC Classification |
J01MA12 - levofloxacin ; Belongs to the class of fluoroquinolones. Used in the systemic treatment of infections. S01AX19 - levofloxacin ; Belongs to the class of other antiinfectives. Used in the treatment of eye infections. |
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Storage |
Intravenous: Store below 25°C (77°F). Ophthalmic: Store at 15-25°C (59-77°F). Oral: Tablet: Store at 15-30°C (59-86°F). Oral solution: Store at 25°C (77°F). | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Available As |
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Levofloxacin
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Levofloxacin Containing Brands
Levofloxacin is used in following diseases
Drug - Drug Interactions of Levofloxacin
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