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