Product image of Labentrol (Ciprofloxacin Hydrochloride Monohydrate) supplied by GNH India

Labentrol

Active Ingredient:
Ciprofloxacin Hydrochloride Monohydrate
Origin:
EU

Labentrol (Ciprofloxacin Hydrochloride Monohydrate)

Ciprofloxacin Hydrochloride Monohydrate, the active ingredient in Labentrol, is a fluoroquinolone antibiotic presented as an oral tablet for oral use. It treats bacterial infections of the urinary, respiratory, skin and gastrointestinal tracts in adults and children as appropriate.

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

Manufacturer / TM Owner

Sja Pharm Ltd

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Indications & Clinical Uses

Labentrol (ciprofloxacin) is a fluoroquinolone antibiotic that targets a broad range of bacterial pathogens in several organ systems.

  • Urinary tract infections: eradicates common uropathogens and resolves symptoms.
  • Respiratory tract infections: treats community‑acquired pneumonia and bronchitis caused by susceptible bacteria.
  • Skin and soft tissue infections: clears bacterial cellulitis, abscesses and wound infections.
  • Gastrointestinal infections: manages bacterial gastroenteritis and travel‑related diarrhoea.

How It Works

  • Ciprofloxacin Hydrochloride Monohydrate inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA supercoiling and replication. By blocking these targets, the drug prevents bacterial DNA synthesis and transcription, leading to bactericidal activity against susceptible Gram‑negative and Gram‑positive organisms.

Side Effects

Ciprofloxacin may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Nausea: transient gastrointestinal upset.
  • Diarrhoea: may be mild to moderate.
  • Headache: occasional tension‑type headache.
  • Dizziness: transient light‑headedness.
  • Rash: mild skin erythema.
  • Abdominal pain: cramping or discomfort.

Serious or Rare Side Effects

  • Tendon rupture: especially Achilles tendon, often linked to activity.
  • Peripheral neuropathy: sensory disturbances that may be irreversible.
  • Clostridioides difficile‑associated diarrhoea: severe colitis.
  • Severe allergic reactions: anaphylaxis or angioedema.
  • QT interval prolongation: risk of cardiac arrhythmias.
  • Hepatic dysfunction: elevated liver enzymes or jaundice.

Precautions & Warnings

Before prescribing Labentrol, clinicians should consider several safety factors.

  • Renal function: adjust use in patients with severe renal impairment.
  • Age considerations: use caution in pediatric and elderly patients.
  • Photosensitivity: advise patients to avoid excessive sunlight exposure.
  • Drug resistance: limit use to confirmed bacterial infections to reduce resistance development.
  • Pregnancy and lactation: safety not established; weigh benefits against potential risks.
  • Store at ambient temperature: keep in original container, protect from moisture and heat.

Avoid Interactions

Ciprofloxacin interacts with several medicines; awareness helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Antacids containing magnesium or aluminum: reduce ciprofloxacin absorption.
  • Warfarin: may increase anticoagulant effect; monitor INR closely.
  • Theophylline: increased plasma levels can lead to toxicity.

Moderate Interactions (Monitor Closely)

  • Nonsteroidal anti‑inflammatory drugs (NSAIDs): may increase risk of central nervous system stimulation.
  • Corticosteroids: heightened risk of tendon rupture.
  • Diabetes medications (e.g., insulin, sulfonylureas): may affect glucose control.

Frequently Asked Questions

Labentrol contains ciprofloxacin, a broad‑spectrum fluoroquinolone antibiotic indicated for the treatment of urinary tract infections, respiratory tract infections, skin and soft‑tissue infections, and certain gastrointestinal infections caused by susceptible bacteria.

Ciprofloxacin inhibits bacterial DNA gyrase and topoisomerase IV, enzymes required for DNA replication and transcription. This blockade prevents bacterial DNA synthesis, leading to rapid bactericidal activity against a wide range of Gram‑negative and Gram‑positive organisms.

The dose of Labentrol is determined by the prescribing clinician based on the type and severity of infection, patient age, renal function and other clinical factors. Only a qualified healthcare professional should set the dosing regimen.

Safety data for ciprofloxacin in pregnancy and lactation are limited. It should be used only when the potential benefit justifies any potential risk to the fetus or infant, and the decision should be made by a qualified healthcare provider.

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

Labentrol (ciprofloxacin) shares the class‑wide mechanism of DNA‑gyrase inhibition but differs in spectrum and pharmacokinetics from alternatives such as levofloxacin or moxifloxacin. Ciprofloxacin generally offers strong activity against Gram‑negative pathogens and is often chosen for urinary and gastrointestinal infections.

Store Labentrol at ambient temperature below 25 °C, in the original packaging, protected from moisture and direct sunlight. Do not expose the tablets to excessive heat or humidity to maintain potency.

Labentrol is taken orally as a tablet with a full glass of water. It may be taken with or without food, but patients should follow any specific instructions from their prescriber regarding timing relative to meals.

Serious adverse events include tendon rupture (especially Achilles), peripheral neuropathy, Clostridioides difficile‑associated colitis, QT interval prolongation, severe allergic reactions such as anaphylaxis, and hepatic dysfunction. Patients should seek immediate medical attention if any of these occur.

Labentrol should be avoided in individuals with a known hypersensitivity to ciprofloxacin or other fluoroquinolones, those with a history of tendon disorders, patients receiving concomitant corticosteroids, and anyone for whom a safer alternative is available based on clinical judgment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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