Levofloxacin
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Last updated: June 2025
For educational purposes only
Clinical Reference
# Levofloxacin
## Overview
- **Classification**: Fluoroquinolone antibiotic.
- **Mechanism**: Inhibits bacterial DNA gyrase and topoisomerase IV, essential enzymes for DNA replication and repair, leading to bacterial cell death.
## Primary Indications
1. **Community-Acquired Pneumonia (CAP)** - Caused by susceptible organisms.
2. **Acute Bacterial Exacerbation of Chronic Bronchitis (ABECB)** - When other options are unsuitable.
3. **Acute Bacterial Sinusitis (ABS)** - When other options are unsuitable.
4. **Complicated Skin and Skin Structure Infections (cSSSI)** - Due to susceptible organisms.
5. **Complicated Urinary Tract Infections (cUTI) & Pyelonephritis** - Caused by susceptible organisms.
6. **Chronic Bacterial Prostatitis** - Caused by susceptible organisms.
## Adult Dosing
### Standard Dosing
**Community-Acquired Pneumonia (CAP)**
- **Dose**: **750 mg**
- **Frequency**: Once daily
- **Route**: PO/IV
- **Duration**: 5 days
**Acute Bacterial Exacerbation of Chronic Bronchitis (ABECB)**
- **Dose**: **500 mg**
- **Frequency**: Once daily
- **Route**: PO/IV
- **Duration**: 7 days
**Acute Bacterial Sinusitis (ABS)**
- **Dose**: **500 mg**
- **Frequency**: Once daily
- **Route**: PO/IV
- **Duration**: 10-14 days
**Complicated Skin and Skin Structure Infections (cSSSI)**
- **Dose**: **750 mg**
- **Frequency**: Once daily
- **Route**: PO/IV
- **Duration**: 7-14 days
**Complicated Urinary Tract Infections (cUTI) & Pyelonephritis**
- **Dose**: **750 mg**
- **Frequency**: Once daily
- **Route**: PO/IV
- **Duration**: 5 days
**Chronic Bacterial Prostatitis**
- **Dose**: **500 mg**
- **Frequency**: Once daily
- **Route**: PO/IV
- **Duration**: 28 days
### Dose Adjustments
- **Renal Impairment**: Adjust based on Creatinine Clearance (CrCl).
- **CrCl 20-49 mL/min**: Initial **750 mg**, then **250-500 mg** q24h.
- **CrCl 10-19 mL/min**: Initial **750 mg**, then **250 mg** q48h.
- **HD/CAPD**: Initial **750 mg**, then **250 mg** q48h post-dialysis.
- **Hepatic Impairment**: No dosage adjustment required.
- **Elderly Patients**: No specific adjustment; monitor renal function closely.
## Pediatric Dosing
**Note**: Use in pediatric patients (under 18 years) is generally avoided due to the risk of musculoskeletal adverse events. It is reserved for severe or life-threatening infections where benefits outweigh risks and alternative treatments are not feasible.
### Neonates (0-28 days)
- **Use**: Generally **NOT recommended**.
- **Indication (limited)**: Severe infections (e.g., resistant Gram-negative sepsis) where no alternatives exist.
- **Dose (if used)**: **5-8 mg/kg/dose**
- **Frequency**: Every 12 hours
- **Route**: IV/PO (oral solution may be used).
- **Maximum**: Not well-established.
- **Special Notes**: High risk of musculoskeletal toxicity. Close monitoring for arthropathy.
### Infants (1-12 months)
- **Use**: Generally **NOT recommended**.
- **Indication (limited)**: Severe, multi-drug resistant infections.
- **Dose (if used)**: **5-10 mg/kg/dose**
- **Frequency**: Every 12 hours
- **Route**: IV/PO (oral solution may be used).
- **Maximum**: **250 mg/dose** (approximate).
- **Special Notes**: Monitor for joint pain/swelling.
### Children (1-12 years)
- **Use**: Generally **NOT recommended for routine infections.**
- **Indication (specific)**: Post-exposure prophylaxis/treatment for inhalational anthrax, plague.
- **Dose (for anthrax/plague)**: **10 mg/kg/dose**
- **Frequency**: Every 12 hours
- **Route**: IV/PO (tablets/oral solution).
- **Maximum**: **500 mg/dose** (or **750 mg/dose** for anthrax treatment).
- **Special Notes**: Assess risk vs. benefit carefully.
### Adolescents (13-18 years)
- **Use**: Generally **NOT recommended for routine infections.**
- **Indication (specific)**: Severe, resistant infections where adult-level doses are appropriate.
- **Dose (if used)**: Approaches adult dosing, typically **500 mg** or **750 mg**.
- **Frequency**: Once daily
- **Route**: IV/PO
- **Maximum**: **750 mg/day**.
- **Special Notes**: Similar risks as adults, including tendon rupture.
## Safety Information
### Contraindications
- **Absolute**: Hypersensitivity to levofloxacin or other fluoroquinolones.
- **Absolute**: History of tendon disorders related to fluoroquinolone use.
- **Absolute**: Myasthenia Gravis (may exacerbate muscle weakness).
- **Absolute**: Co-administration with Tizanidine.
- **Relative**: Children and adolescents (<18 years) for non-life-threatening infections.
### Common Adverse Effects
- **Very Common (>10%)**: Nausea, diarrhea, headache.
- **Common (1-10%)**: Vomiting, constipation, abdominal pain, dizziness, insomnia, rash, photosensitivity.
- **Serious but Rare**: Tendon rupture/tendinitis, peripheral neuropathy, C. difficile infection, QT prolongation/arrhythmia, seizures, hypo/hyperglycemia, psychiatric effects.
### Key Drug Interactions
- **Antacids (Mg/Al), Sucralfate, Iron/Zinc supplements**: Decreased levofloxacin absorption.
- Administer levofloxacin at least **2 hours before or 2 hours after** these agents.
- **Warfarin**: Increased INR/bleeding risk.
- Monitor INR closely.
- **Corticosteroids**: Increased risk of tendon rupture.
- Avoid concomitant use if possible, especially in elderly.
- **NSAIDs**: Increased risk of CNS stimulation and seizures.
- Use with caution.
- **Antiarrhythmics (Class IA/III), TCAs, Macrolides**: Increased risk of QTc prolongation.
- Avoid co-administration if possible; monitor ECG.
- **Sulfonylureas/Insulin**: Risk of hypo- or hyperglycemia.
- Monitor blood glucose closely.
## Monitoring & Follow-up
- **Before Treatment**: Baseline renal function (CrCl), electrolytes (K, Mg).
- **During Treatment**: Monitor for tendon pain/swelling, peripheral neuropathy symptoms (tingling, numbness).
- **During Treatment**: Watch for signs of C. difficile infection (severe diarrhea).
- **Clinical Signs**: Monitor for allergic reactions, seizure activity, psychiatric changes, blood glucose fluctuations.
## Clinical Pearls
- 💡 **Black Box Warning**: Levofloxacin carries warnings for tendonitis/tendon rupture, peripheral neuropathy, CNS effects, and worsening of myasthenia gravis.
- 💡 **Photosensitivity**: Advise patients to use sun protection and avoid excessive sun exposure.
- 💡 **Hydration**: Encourage adequate hydration to prevent crystalluria (rare).
- 💡 **Complete Course**: Emphasize completing the entire prescribed course, even if feeling better.
- 💡 **Oral Admin**: Administer oral dose with a full glass of water.
- 💡 **IV Infusion**: Infuse IV doses (500mg/750mg) over **60-90 minutes** to minimize infusion-related reactions.
> **⚠️ Important**: This information is for educational purposes only. Always consult current prescribing information, local guidelines, and clinical judgment before prescribing.