Introduction

Delafloxacin is a broad-spectrum fluoroquinolone antibiotic used to treat various bacterial infections. It is effective against both Gram-positive and Gram-negative bacteria, including those resistant to other antibiotics. Delafloxacin is used to manage acute bacterial infections and offers an option for patients with infections that do not respond to other treatments.

Uses

Delafloxacin is indicated for the treatment of:

  • Acute bacterial skin and skin structure infections (ABSSSI)
  • Complicated urinary tract infections (cUTI)
  • Chronic bacterial infections that may not respond to first-line antibiotics
It is typically used when other antibiotics are ineffective or when a broad-spectrum agent is required.

Brand Name Delafloxacin
Type
Weight
Generic Delafloxacin
Manufacturer
Available in English বাংলা

Mechanism of Action

Delafloxacin works by inhibiting bacterial DNA gyrase and topoisomerase IV, essential enzymes for bacterial DNA replication and transcription. This inhibition prevents the bacteria from reproducing and repairing their DNA, leading to bacterial cell death.

How Long Does It Take to Work?

Patients may begin to see improvements in symptoms within 48-72 hours of starting delafloxacin. The full therapeutic effect may take up to a week, depending on the severity of the infection and individual patient response.

Absorption

Delafloxacin is well-absorbed after oral administration, with peak plasma concentrations typically occurring within 1-2 hours. The drug has good oral bioavailability, meaning a significant portion of the dose is absorbed into systemic circulation.

Route of Elimination

Delafloxacin is primarily metabolized in the liver, with a portion excreted unchanged in the urine. The drug is eliminated from the body mainly through the kidneys, with a smaller fraction eliminated in the feces.

Dosage

Route of administration: Intravenous (IV) Injection
 
Indications Dosage and Route of Administration Total Duration (days)
Acute Bacterial Skin and Skin Structure Infections (ABSSSI) 300 mg of Delafloxacin Injection every 12 hours over 60 minutes by intravenous infusion 5 to 14
Community-Acquired Bacterial Pneumonia (CABP) 5 to 10

Hepatic Impairment: No dosage adjustment is necessary for Delaflox (Delafloxacin) in patients with hepatic impairment.

Renal Impairment: Dosage adjustment is required for patients with severe renal impairment (eGFR 15-29 mL/min/1.73m2). In patients with severe renal impairment or ESRD (eGFR of < 15 mL/min/1.73 m2), accumulation of the intravenous vehicle, sulfobutylether-β-cyclodextrin (SBECD) occurs. Serum creatinine levels should be carefully monitored in patients in such case. If serum creatinine level increases, consider switching to oral Delafloxacin. Discontinue Delafloxacin if eGFR decreases to < 15 mL/min/1.73 m2.

The typical dosage for delafloxacin is:

  • For acute bacterial skin infections: 300 mg orally every 12 hours for 5-14 days, depending on the severity of the infection.
  • For complicated urinary tract infections: 450 mg orally every 12 hours for 7-14 days.
Dosage adjustments may be required based on patient-specific factors such as renal function and infection severity.

Administration

Delafloxacin should be taken orally, with or without food. Tablets should be swallowed whole with a glass of water. Consistent dosing times are important to maintain therapeutic drug levels.

Side Effects

Common side effects of delafloxacin include:

  • Nausea
  • Diarrhea
  • Headache
  • Dizziness
  • Abdominal pain
Serious side effects may include tendon rupture, severe allergic reactions, and Clostridium difficile-associated diarrhea.

Toxicity

In cases of overdose or severe adverse reactions, symptoms may include severe gastrointestinal distress, seizures, or cardiac issues. Immediate medical intervention is required to manage toxicity and provide supportive care.

Precautions

- Monitor patients for signs of tendonitis or tendon rupture, especially in those over 60 or on corticosteroids. - Use with caution in patients with a history of seizures or other central nervous system disorders. - Regularly monitor liver function in long-term or high-dose therapy.

Interaction

Delafloxacin may interact with other medications, including:

  • Antacids or products containing calcium, magnesium, or aluminum, which may reduce delafloxacin absorption.
  • Warfarin, which may increase the risk of bleeding.
  • Other drugs that affect liver enzymes, altering delafloxacin metabolism.

Disease Interaction

- Caution is advised in patients with liver disease, as delafloxacin is metabolized hepatically. - Adjustments may be needed for patients with renal impairment.

Drug Interaction

Delafloxacin may interact with medications that alter gastrointestinal pH or affect liver enzymes. It's essential to inform healthcare providers of all concurrent medications to avoid potential interactions.

Food Interactions

Food does not significantly affect the absorption of delafloxacin. The medication can be taken with or without food.

Pregnancy Use

Delafloxacin is classified as a Category C drug for pregnancy, meaning risk cannot be ruled out. It should be used during pregnancy only if the potential benefits outweigh the risks.

Lactation Use

It is not known whether delafloxacin is excreted in breast milk. Due to potential risks to the infant, breastfeeding is not recommended during treatment with delafloxacin.

Acute Overdose

Acute overdose may result in severe gastrointestinal symptoms, neurological effects, or cardiac issues. Immediate medical treatment is required to manage symptoms and provide appropriate care.

Contraindication

Delafloxacin is contraindicated in:

  • Patients with a known hypersensitivity to delafloxacin or other fluoroquinolones.
  • Pregnant or breastfeeding women due to potential risks to the fetus or infant.

Use Direction

Take the prescribed dose of delafloxacin orally, with or without food. Do not exceed the recommended dose. Follow the treatment regimen exactly as directed by your healthcare provider.

Storage Conditions

Store delafloxacin at room temperature, away from moisture and heat. Keep the medication in its original packaging to protect it from light and ensure it is out of reach of children.

Volume of Distribution

The volume of distribution for delafloxacin is approximately 40-50 L, indicating its extensive distribution throughout body tissues.

Half Life

The elimination half-life of delafloxacin is approximately 8-10 hours, allowing for twice-daily dosing.

Clearance

Delafloxacin is cleared primarily through renal excretion, with a clearance rate of approximately 20-30 L/h. This reflects its efficient elimination from the body through the kidneys.

See in details version Delafloxacin also Delafloxacin in bangla

Some Frequently Asked Questions About Delafloxacin

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