Product image of Moloxin (Moxifloxacin) supplied by GNH India

Moloxin

Active Ingredient:
Moxifloxacin
Origin:
EU

Moloxin (Moxifloxacin)

Moxifloxacin, the active ingredient in Moloxin, is a fluoroquinolone presented as an injection for intravenous use. It treats a broad spectrum of bacterial infections in adults and children when prescribed by a qualified healthcare professional.

GNH India supplies Moloxin as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable cold‑chain logistics for injectable products. Clients benefit from consistent batch release, regulatory support, and on‑time delivery across EU and global markets.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Moxifloxacin is indicated for several serious bacterial infections affecting the respiratory, skin, intra‑abdominal and ocular systems.

  • Community‑acquired pneumonia: effective eradication of susceptible pathogens in adult and pediatric patients.
  • Acute bacterial sinusitis: rapid symptom relief and bacterial clearance.
  • Acute bacterial exacerbation of chronic bronchitis: reduces bacterial load and improves lung function.
  • Skin and soft tissue infections: treats cellulitis, abscesses and other infections caused by susceptible organisms.
  • Intra‑abdominal infections: provides coverage for mixed aerobic and anaerobic bacteria in complicated cases.
  • Bacterial conjunctivitis: resolves ocular infection caused by susceptible strains.

How It Works

  • Moxifloxacin exerts its antibacterial activity by binding to bacterial DNA gyrase and topoisomerase IV, enzymes essential for DNA supercoiling and replication. Inhibition of these targets prevents DNA synthesis and transcription, leading to bacterial cell death. The drug shows concentration‑dependent killing against a broad range of Gram‑positive, Gram‑negative and atypical organisms.

Side Effects

Moxifloxacin may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Nausea
  • Diarrhea
  • Headache
  • Dizziness
  • Injection site pain
  • Transient elevation of liver enzymes

Serious or Rare Side Effects

  • Tendon rupture or tendinopathy
  • QT interval prolongation and arrhythmias
  • Severe allergic reactions including anaphylaxis
  • Clostridioides difficile‑associated diarrhea
  • Hepatic failure or severe liver injury
  • Stevens‑Johnson syndrome and toxic epidermal necrolysis

Precautions & Warnings

When using Moloxin, clinicians should consider several precautionary measures to minimize risk.

  • Renal impairment: assess renal function and adjust therapy as needed.
  • Hepatic impairment: monitor liver enzymes and use with caution.
  • QT prolongation risk: avoid in patients with known arrhythmias or concurrent QT‑prolonging drugs.
  • Pregnancy category C: prescribe only when the potential benefit justifies the potential fetal risk.
  • Concomitant fluoroquinolone use: avoid co‑administration to prevent additive toxicity.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Moxifloxacin can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Antacids containing aluminum or magnesium: reduce absorption of moxifloxacin.
  • Warfarin: may increase INR and bleeding risk.
  • Theophylline: can raise theophylline plasma concentrations, leading to toxicity.

Moderate Interactions (Monitor Closely)

  • Oral contraceptives: may reduce hormonal effectiveness; consider alternative contraception.
  • Diabetic agents: potential for hypoglycaemia; monitor blood glucose levels.

Frequently Asked Questions

Moloxin contains the fluoroquinolone moxifloxacin and is used to treat a range of serious bacterial infections, including community‑acquired pneumonia, acute bacterial sinusitis, exacerbations of chronic bronchitis, skin and soft‑tissue infections, intra‑abdominal infections, and bacterial conjunctivitis, when prescribed by a qualified clinician.

Moxifloxacin inhibits bacterial DNA gyrase and topoisomerase IV, enzymes required for DNA supercoiling, replication and transcription. By blocking these targets, the drug prevents bacterial DNA synthesis, leading to rapid bacterial cell death across many Gram‑positive, Gram‑negative and atypical pathogens.

The dose of Moloxin is determined by the prescribing clinician based on the specific infection, patient weight, renal and hepatic function, and local treatment guidelines. No fixed regimen is provided here; the prescriber sets the appropriate intravenous dosing schedule.

Moxifloxacin is classified as pregnancy category C, meaning it should be used only if the potential benefit justifies the potential risk to the fetus. Limited data are available for breastfeeding; it is generally advised to avoid use while nursing unless clearly needed and approved by a healthcare professional.

To order Moloxin, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details (including cold‑chain where required) and import documentation.

Moloxin (moxifloxacin) offers a broader spectrum against Gram‑positive and atypical organisms compared with many older fluoroquinolones, and it often allows once‑daily dosing. It has enhanced activity against Streptococcus pneumoniae and Haemophilus influenzae, but shares class‑related safety considerations such as tendon risk and QT prolongation.

Moloxin should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial. Keep it in the original packaging until use and ensure the cold‑chain is maintained during transport and storage in healthcare facilities.

Moloxin is given as an intravenous injection. The vial is reconstituted with the appropriate diluent according to the product label, then infused over the recommended period by a qualified healthcare professional. Administration should follow aseptic technique and institutional infusion protocols.

Serious risks include tendon rupture or tendinopathy, QT interval prolongation leading to arrhythmias, severe allergic

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GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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