Tab Levoflox
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Last updated: June 2025
For educational purposes only
Clinical Reference
# Tab levoflox
## Overview
- **Classification**: Fluoroquinolone antibiotic
- **Mechanism**: Inhibits bacterial DNA gyrase and topoisomerase IV, enzymes essential for DNA replication, transcription, repair, and recombination.
## Primary Indications
1. **Community-Acquired Pneumonia (CAP)** - Caused by susceptible organisms
2. **Acute Bacterial Exacerbation of Chronic Bronchitis (ABECB)** - When other agents are not suitable
3. **Complicated Urinary Tract Infections (cUTI) & Pyelonephritis** - Caused by susceptible organisms
4. **Acute Bacterial Sinusitis (ABS)** - When other agents are not suitable
5. **Skin and Skin Structure Infections (SSSI)** - Uncomplicated and complicated
## Adult Dosing
### Standard Dosing
**Community-Acquired Pneumonia (CAP), Complicated UTI, Pyelonephritis, Acute Bacterial Sinusitis**
- **Dose**: **750 mg**
- **Frequency**: Once daily
- **Route**: Oral
- **Duration**: CAP (5 days), cUTI (5 days), Pyelonephritis (5 days), ABS (5 days)
**Acute Bacterial Exacerbation of Chronic Bronchitis (ABECB), Uncomplicated Skin and Skin Structure Infections**
- **Dose**: **500 mg**
- **Frequency**: Once daily
- **Route**: Oral
- **Duration**: ABECB (7 days), SSSI (7-14 days)
**Complicated Skin and Skin Structure Infections (cSSSI)**
- **Dose**: **750 mg**
- **Frequency**: Once daily
- **Route**: Oral
- **Duration**: 7-14 days
### Dose Adjustments
- **Renal Impairment**:
- **CrCl 20-49 mL/min**: Initial **750 mg**, then **250 mg** q24h for most indications. For **500 mg** initial dose, reduce to **250 mg** q24h.
- **CrCl 10-19 mL/min**: Initial **750 mg**, then **250 mg** q48h. For **500 mg** initial dose, reduce to **250 mg** q48h.
- **Hemodialysis/CAPD**: Initial **750 mg**, then **250 mg** q48h. Administer after dialysis.
- **Hepatic Impairment**: No dosage adjustment required.
- **Elderly Patients**: Adjust dose based on renal function; no specific age-related adjustment otherwise.
## Pediatric Dosing
**Note**: Use in pediatric patients is generally reserved for specific indications (e.g., anthrax, plague, MDR-TB, complicated UTI where alternatives are not feasible) due to risks of musculoskeletal adverse effects (arthropathy, tendon rupture).
### Neonates (0-28 days)
- **Use**: Not generally recommended due to safety concerns and lack of data.
- **Special Notes**: Consider only in life-threatening situations with no suitable alternatives, under expert guidance.
### Infants (1-12 months)
- **Use**: Not generally recommended due to safety concerns.
- **Special Notes**: Use only for specific, severe infections (e.g., anthrax, plague) where benefit outweighs risk and alternatives are unavailable.
### Children (6 months to 12 years)
**Complicated Urinary Tract Infection (cUTI) / Pyelonephritis (when alternatives not suitable)**
- **Dose**: **10 mg/kg/dose**
- **Frequency**: Every 12 hours
- **Maximum**: **250 mg/dose** for 6 months to <5 years; **500 mg/dose** for 5 to 12 years. Maximum daily **750 mg**.
- **Duration**: 10-14 days
**Anthrax (post-exposure), Plague**
- **Dose**: **8 mg/kg/dose** (for 6 months to <5 years) or **10 mg/kg/dose** (for 5-12 years)
- **Frequency**: Every 12 hours
- **Maximum**: **250 mg/dose** (6 months to <5 years); **500 mg/dose** (5-12 years). Max daily **1000 mg**.
- **Duration**: Anthrax (60 days), Plague (10-14 days)
### Adolescents (13-18 years)
- **Dose**: Generally follow adult dosing recommendations for the specific indication.
- **Maximum**: Adult maximum daily dose **750 mg** (or **1000 mg** for specific indications like anthrax).
- **Special Notes**: Continue to monitor for musculoskeletal adverse effects.
## Safety Information
### Contraindications
- **Absolute**: Hypersensitivity to levofloxacin or other fluoroquinolones.
- **Absolute**: History of tendinitis or tendon rupture associated with fluoroquinolone use.
- **Absolute**: Myasthenia Gravis (may exacerbate muscle weakness).
- **Relative**: Children <18 years, except for specific indications where benefit outweighs risk.
### Common Adverse Effects
- **Common (1-10%)**: Nausea, diarrhea, headache, insomnia, constipation, dizziness.
- **Serious but Rare**: Tendinitis and tendon rupture (Boxed Warning), Peripheral neuropathy (Boxed Warning), CNS effects (seizures, psychosis, suicidal thoughts - Boxed Warning), QT prolongation, Torsades de Pointes, Hypo/hyperglycemia, *Clostridioides difficile*-associated diarrhea (CDAD), Aortic aneurysm rupture/dissection (especially elderly, HTN, existing aneurysm).
### Key Drug Interactions
- **Corticosteroids**: Increased risk of tendon rupture. Avoid concomitant use if possible.
- **Antacids (Mg/Al), Sucralfate, Iron, Zinc, Calcium-containing products**: Decrease levofloxacin absorption. Administer levofloxacin at least 2 hours before or 2 hours after these agents.
- **Warfarin**: Enhanced anticoagulant effect, monitor INR closely.
- **QT-prolonging drugs (e.g., Class IA/III antiarrhythmics, tricyclic antidepressants)**: Increased risk of QT prolongation. Avoid co-administration if possible.
- **NSAIDs**: May increase risk of CNS stimulation and seizures.
## Monitoring & Follow-up
- **Before Treatment**: Obtain baseline renal function (CrCl). If risk factors for QT prolongation exist, consider baseline ECG.
- **During Treatment**: Monitor renal function in patients with impairment. Monitor blood glucose in diabetic patients.
- **Clinical Signs**: Educate patients to report tendon pain/swelling, muscle weakness, numbness/tingling, severe diarrhea, or signs of allergic reaction immediately.
## Clinical Pearls
- 💡 **Administration**: Can be taken with or without food. Ensure adequate hydration.
- 💡 **Timing**: Avoid taking with dairy products, antacids, or mineral supplements due to reduced absorption. Separate by at least 2 hours.
- 💡 **Adherence**: Complete the full course of therapy, even if symptoms improve, to prevent resistance.
- 💡 **Sun Sensitivity**: Advise patients on sun protection (sunscreen, protective clothing) due to photosensitivity risk.
> **⚠️ Important**: This information is for educational purposes only. Always consult current prescribing information, local guidelines, and clinical judgment before prescribing.