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Moxifloxacin

Moxifloxacin is a potent fluoroquinolone for respiratory, skin, and intra-abdominal infections. While effective, its use requires vigilance for QT prolongation, tendon injury, and drug interactions. Adherence to guidelines from the BNFLippincott Textbook of Pharmacology, and Lange Basic & Clinical Pharmacology ensures safe and effective therapy.

Moxifloxacin, a fourth-generation fluoroquinolone, exerts its bactericidal effect by inhibiting two critical bacterial enzymes: DNA gyrase (topoisomerase II) and topoisomerase IV. These enzymes are essential for DNA replication, transcription, repair, and chromosome segregation. By binding to these enzymes, moxifloxacin induces double-stranded DNA breaks, leading to rapid bacterial cell death.

Moxifloxacin has broad-spectrum activity against:

  • Gram-positive bacteriaStreptococcus pneumoniaeStaphylococcus aureus (methicillin-susceptible).
  • Gram-negative bacteriaHaemophilus influenzaeMoraxella catarrhalisEscherichia coli.
  • Atypical pathogensMycoplasma pneumoniaeChlamydia pneumoniaeLegionella pneumophila.
  • Anaerobic bacteriaBacteroides fragilis.

Moxifloxacin is indicated for:

  1. Respiratory Tract Infections:
    • Community-acquired pneumonia (CAP).
    • Acute bacterial sinusitis.
    • Acute exacerbations of chronic bronchitis (AECB).
  2. Skin and Soft Tissue Infections:
    • Uncomplicated cellulitis.
  3. Intra-Abdominal Infections:
    • Complicated infections (in combination with other agents).
  4. Ophthalmic Infections:
    • Bacterial conjunctivitis (0.5% ophthalmic solution).

Off-label uses include tuberculosis (as part of multidrug regimens) and pelvic inflammatory disease.

Adults:

  • Oral/IV: 400 mg once daily.
    • Duration: 5–14 days, depending on infection severity.
  • Ophthalmic: 1 drop to affected eye(s) 3 times daily for 7 days.

Special Populations:

  • Renal Impairment: No dose adjustment required (primarily hepatic metabolism).
  • Hepatic Impairment: Use with caution; avoid in severe cirrhosis (BNF).
  • Elderly: Monitor for tendonitis and CNS effects.
  • Common: Nausea, diarrhea, dizziness, headache.
  • Serious:
    • QT Prolongation: Risk of torsades de pointes (avoid in patients with baseline QT >450 ms).
    • Tendon Rupture: Risk increases with age >60, corticosteroid use, or renal failure.
    • Hepatotoxicity: Elevated transaminases (monitor LFTs).
    • CNS Effects: Insomnia, hallucinations, seizures (rare).
    • Hypersensitivity: Rash, anaphylaxis.
  1. Contraindications:
    • History of tendon disorders or QT prolongation.
    • Myasthenia gravis (may exacerbate muscle weakness).
  2. Pregnancy/Lactation:
    • Category C: Avoid unless benefits outweigh risks (teratogenic in animal studies).
    • Excreted in breast milk; discontinue breastfeeding.
  3. Hepatic/Renal Monitoring:
    • Monitor LFTs in liver disease; assess renal function in elderly.
  4. Photosensitivity: Advise sun protection.

Moxifloxacin interacts with:

  • QT-Prolonging Drugs:
    • Antiarrhythmics (e.g., amiodarone), antipsychotics (e.g., haloperidol) – additive risk of arrhythmias.
  • Antacids/Minerals:
    • Aluminum, magnesium, or iron supplements reduce absorption (administer 2–4 hours apart).
  • Corticosteroids:
    • Increased risk of tendon rupture.
  • Warfarin:
    • Enhanced anticoagulant effect (monitor INR).
  • Generic: Moxifloxacin (oral, IV, ophthalmic).
  • Brand Names: Avelox (oral/IV), Vigamox (ophthalmic).

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