Product image of Levofloxacina Generis Phar (Levofloxacin) supplied by GNH India

Levofloxacina Generis Phar

Active Ingredient:
Levofloxacin
Origin:
EU

Levofloxacina Generis Phar (Levofloxacin)

Levofloxacin, the active ingredient in Levofloxacina Generis Phar, is a Fluoroquinolone antibiotic presented as an oral dosage form for oral use. It treats a range of bacterial infections in adults and children when prescribed by a qualified health professional.

GNH India supplies Levofloxacina Generis Phar as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Generis Farmacêutica, S.A.

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Indications & Clinical Uses

Levofloxacin is a broad‑spectrum fluoroquinolone used to treat bacterial infections affecting several organ systems.

  • Respiratory tract infection: eradicates the causative bacteria and improves breathing symptoms.
  • Urinary tract infection: clears urinary pathogens and resolves dysuria and frequency.
  • Skin and soft tissue infection: eliminates skin‑resident bacteria and promotes wound healing.
  • Sinusitis: reduces sinus inflammation by targeting the infecting organisms.
  • Pharyngitis: treats bacterial throat infection and alleviates sore throat.

How It Works

  • Levofloxacin inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA replication, transcription, and repair. By stabilizing the enzyme–DNA complex, it prevents the resealing of DNA breaks, leading to bacterial cell death and a bactericidal effect against susceptible organisms.

Side Effects

Levofloxacin may cause a variety of adverse reactions, ranging from mild to severe.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhea: loose stools, sometimes watery.
  • Headache: transient cranial discomfort.
  • Dizziness: sensation of light‑headedness.
  • Insomnia: difficulty falling or staying asleep.
  • Photosensitivity: increased skin reaction to sunlight.

Serious or Rare Side Effects

  • Tendon rupture: sudden pain and loss of function, especially in the Achilles tendon.
  • QT interval prolongation: potential cardiac arrhythmias.
  • Severe allergic reactions: rash, swelling, or anaphylaxis.
  • Clostridioides difficile infection: severe colitis with watery diarrhea.
  • Peripheral neuropathy: tingling or numbness in extremities.
  • Hepatotoxicity: abnormal liver function tests or jaundice.

Precautions & Warnings

Levofloxacin should be used with caution in specific clinical situations.

  • Assess renal function: dose adjustment may be required in impaired kidneys.
  • Avoid in known hypersensitivity: discontinue if allergic reactions occur.
  • Monitor for tendon pain: stop the drug if tendon inflammation develops.
  • Use cautiously in patients with QT‑prolonging conditions: obtain ECG if risk is high.
  • Separate from antacids or supplements containing aluminum, magnesium, calcium, or iron: administer at least 2 hours apart.
  • Store at ambient temperature: keep below 25 °C, in the original packaging, protected from moisture.

Avoid Interactions

Levofloxacin can interact with several medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Antacids containing aluminum or magnesium: reduce levofloxacin absorption.
  • Warfarin: may increase INR and bleeding risk.
  • Theophylline: heightened risk of toxicity and seizures.

Moderate Interactions (Monitor Closely)

  • Other fluoroquinolones (e.g., ciprofloxacin): additive QT‑prolongation.
  • NSAIDs: increased chance of central nervous system effects.
  • Cyclosporine: elevated cyclosporine concentrations.

Frequently Asked Questions

Levofloxacina Generis Phar contains levofloxacin, a fluoroquinolone antibiotic indicated for bacterial respiratory tract infections, urinary tract infections, skin and soft‑tissue infections, sinusitis, and pharyngitis when prescribed by a qualified health professional.

Levofloxacin blocks bacterial DNA gyrase and topoisomerase IV, enzymes required for DNA replication and transcription. This inhibition prevents bacterial cells from repairing DNA breaks, leading to bacterial death and a bactericidal effect.

The specific dose and treatment duration are determined by the prescribing clinician based on the infection type, severity, patient age, weight, and renal function. Patients should follow the prescriber’s instructions precisely.

Levofloxacin’s safety in pregnancy and lactation is not well established. It should be used only if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by the treating physician.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any necessary import documentation.

Levofloxacin offers broad‑spectrum coverage against many Gram‑positive and Gram‑negative bacteria and has the convenience of once‑daily oral dosing. Compared with older agents like amoxicillin, it may be used when resistance is a concern, but it carries a higher risk of tendon and cardiac side effects, requiring careful patient selection.

Store the product at ambient temperature, below 25 °C, in its original container. Protect it from moisture and direct sunlight to maintain stability throughout its shelf life.

Levofloxacina Generis Phar is supplied as an oral formulation. It should be taken with a full glass of water, preferably on an empty stomach, and at least two hours apart from antacids or mineral supplements that could interfere with absorption.

Serious risks include tendon rupture (especially in the Achilles tendon), QT‑interval prolongation leading to arrhythmias, severe allergic reactions such as anaphylaxis, Clostridioides difficile‑associated colitis, and peripheral neuropathy. Patients should report any sudden pain, swelling, or cardiac symptoms immediately.

Levofloxacin is contraindicated in individuals with a known hypersensitivity to fluoroquinolones, those with a history of tendon disorders related to fluoroquinolone use, and patients with established prolonged QT interval unless benefits outweigh risks. It should also be avoided in patients receiving certain interacting medications without close monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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