evaquin (generic name: levofloxacin; brand names include: Levotab / Levotas / Tavanic / Gatigol / Lebact / Terlev / Cravit / Levox/ Levores) is a third-generation fluoroquinolone antibiotic used for treating infections caused by certain bacteria.
Levaquin is a broad-spectrum antibiotic used to treat a variety of infections including pneumonia; chronic bronchitis; and sinus, urinary tract, kidney, and skin infections. It is currently the only respiratory quinolone antibiotic approved by the FDA for the treatment of nosocomial pneumonia. It may also be used to prevent or slow anthrax after exposure.
Levaquin works by killing bacteria that cause the infection.
Preparation of Intravenous Product Frequency not reported: Asthenia, fever, malaise, rigors, substernal chest pain, ascites, changed temperature sensation, ear disorder (unspecified), enlarged abdomen, hot flashes, gangrene, influenza-like symptoms, leg pain, multiple organ failure, earache, abscess, herpes simplex, bacterial infection, viral infection, otitis media, sepsis, pain, fatigue, face edema, flushing, back pain, aggravated condition, fungal infection a heart rhythm disorder, especially if you take amiodarone (Cordarone, Pacerone), dofetilide (Tikosyn), disopyramide (Norpace), ibutilide (Corvert), procainamide (Procan, Pronestyl), propafenone (Rythmol), quinidine (Quin-G), or sotalol (Betapace); Frequency not reported: Angina pectoris, arrhythmia, atrial fibrillation, bradycardia, cardiac failure, cerebrovascular disorder, circulatory failure, coronary thrombosis, heart block, hypertension, aggravated hypertension, hypotension, myocardial infarction, postural hypotension, purpura, supraventricular tachycardia, tachycardia, deep thrombophlebitis, vasculitis, ventricular fibrillation LEVAQUIN® is indicated for the treatment of nosocomial pneumonia due to methicillinsusceptible Staphylococcus aureus, Pseudomonas aeruginosa, Serratia marcescens, Escherichia coli, Klebsiella pneumoniae, Haemophilus influenzae, or Streptococcus pneumoniae. Adjunctive therapy should be used as clinically indicated. Where Pseudomonas aeruginosa is a documented or presumptive pathogen, combination therapy with an antipseudomonal β;-lactam is recommended [see Clinical Studies]. Food and LEVAQUIN® Tablets and Oral Solution Uncommon (0.1% to 1%): Arthralgia, myalgia, skeletal pain, tendinitis Storage And Handling http://edmedics.net/frblg/achat-clomid/#clomid-nausees
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bottles of 20 (NDC 50458-930-20) Preparation of Intravenous Product Frequency not reported: Asthenia, fever, malaise, rigors, substernal chest pain, ascites, changed temperature sensation, ear disorder (unspecified), enlarged abdomen, hot flashes, gangrene, influenza-like symptoms, leg pain, multiple organ failure, earache, abscess, herpes simplex, bacterial infection, viral infection, otitis media, sepsis, pain, fatigue, face edema, flushing, back pain, aggravated condition, fungal infection Excipients and Description of Dosage Forms narcotic medication such as methadone (Methadose, Diskets, Dolophine);
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Uncommon (0.1% to 1%): Urticaria joint problems; See also: Levaquin side effects (in more detail) Common (1% to 10%): Headache (6%), dizziness (3%) diarrhea that is watery or bloody; 500 mg (as expressed in the anhydrous form): hypromellose, crospovidone, microcrystalline cellulose, magnesium stearate, polyethylene glycol, titanium dioxide, polysorbate 80 and synthetic red and yellow iron oxides. Common (1% to 10%): Rash (2%), pruritus (1%)
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mild headache or dizziness; or LEVAQUIN® is indicated for inhalational anthrax (post-exposure) to reduce the incidence or progression of disease following exposure to aerosolized Bacillus anthracis. The effectiveness of LEVAQUIN® is based on plasma concentrations achieved in humans, a surrogate endpoint reasonably likely to predict clinical benefit. LEVAQUIN® has not been tested in humans for the post-exposure prevention of inhalation anthrax. The safety of LEVAQUIN® in adults for durations of therapy beyond 28 days or in pediatric patients for durations of therapy beyond 14 days has not been studied. Prolonged LEVAQUIN® therapy should only be used when the benefit outweighs the risk [see DOSAGE AND ADMINISTRATION and Clinical Studies]. FDA pregnancy category C: It is not known whether Levaquin is harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using Levaquin. Levofloxacin can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. Levaquin may cause swelling or tearing of a tendon (the fiber that connects bones to muscles in the body), especially in the Achilles' tendon of the heel. These effects may be more likely to occur if you are over 60, if you take steroid medication, or if you have had a kidney, heart, or lung transplant. Stop taking Levaquin and call your doctor at once if you have sudden pain, swelling, tenderness, stiffness, or movement problems in any of your joints. Rest the joint until you receive medical care or instructions. Do not share this medication with another person (especially a child), even if they have the same symptoms you have.
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Administration Instructions One survey reported 33 cases of peripheral neuropathy associated with levofloxacin (the active ingredient contained in Levaquin) ranging in severity from mild and reversible to severe and persistent. In one case, a 51-year-old female developed "electrical" sensations, numbness, allodynia, multiple severe tendinitis, partial tendon rupture, impaired memory, confusion, and impaired concentration, with some symptoms persisting after 1 year. Acute Bacterial Sinusitis: 5-day and 10–14 day Treatment Regimens Hypersensitivity Postmarketing reports: Psychosis, paranoia, suicide attempt (isolated reports), suicidal ideation (isolated reports) Levaquin (levofloxacin) is in a group of antibiotics called fluoroquinolones (flor-o-KWIN-o-lones). Levaquin fights bacteria in the body. A 74-year-old female developed hepatotoxicity and significant increases in AST (4962 units/L), ALT (7071 units/L), alkaline phosphatase (90 units/L), and total bilirubin (2.5 mg/dL) after starting levofloxacin therapy. Levels returned to normal within a week after discontinuation.
July 24 2025 13:35:58
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