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Antimicrobials

Moxifloxacin

Guidelines for use

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1. Spectrum of Activity

Active against:

  • Streptococcus (Streptococcus pneumoniae, Beta-hemolytic streptococci)
  • Most aerobic Gram negatives including Haemophilus influenza, Klebsiella pneumoniae, Moraxella catarrhalis
  • Atypical bacteria (Chlamydia pneumoniae, Mycoplasma pneumoniae, Legionella pneumophilia)
  • Select anaerobes, including Bacteroides fragilis (*note: ~30% resistance)

Not active against:

  • Methicillin-resistant S. aureus (MRSA)
  • Vancomycin-Resistant Enterococcus (VRE)
  • Pseudomonas aeruginosa

2. Clinical Use

Appropriate Uses:

  • Community-acquired pneumonia, in the setting of severe penicillin allergy (levofloxacin is the preferred respiratory fluoroquinolone for community-acquired pneumonia at SHSC)
  • Complicated intra-abdominal infections including polymicrobial infections and abscesses*
  • Skin and soft tissue infections including diabetic foot infections
  • *Note: combination therapy with metronidazole recommended in severe infections due to increasing resistance of B. fragilis to moxifloxacin (50% are not susceptible)

Inappropriate Uses:

  • Treatment of late onset hospital-acquired pneumonia (HAP) or ventilator-associated pneumonia (VAP)**
  • Treatment of UTI/urosepsis (achieves insufficient urinary concentrations)
  • **Note: during levofloxacin shortage, may consider moxifloxacin for early HAP onset < 5 days in the setting of a severe penicillin allergy where Pseudomonas is not a suspected pathogen

3. Precautions

  • Pregnancy: Limited human data; no evidence of significant risk for
  • Breastfeeding: Limited human data; likely excreted through human breast milk. Effects of exposure unknown

4. Adverse Effects

  • GI intolerance: abdominal pain, nausea, vomiting, diarrhea, dyspepsia
  • CNS (<1%): headache, dizziness, malaise, seizures (rare, <0.1% incidence)
  • Cardiac (<1%): QTc prolongation with risk for progression to Torsades de Pointes. Caution in patients with risk factors (concurrent QT prolonging medications, cardiac comorbidities, advanced age, etc)
  • Hypersensitivity reactions
  • Tendonopathy

5. Dosage

  • Usual: 400 mg PO/IV q24h
  • No dose reduction required in renal impairment or dialysis

6. Administration

  • Intermittent Infusion: Infuse over 60 minutes
  • Please refer to IV drug monograph on pharmacy intranet page for additional administration information.

Last updated: June 6, 2022