Product image of Moxifloxacina Hikma (Moxifloxacin) supplied by GNH India

Moxifloxacina Hikma

Active Ingredient:
Moxifloxacin
Origin:
EU

Moxifloxacina Hikma (Moxifloxacin)

Moxifloxacin, the active ingredient in Moxifloxacina Hikma, is a fluoroquinolone presented as an intravenous formulation for hospital use. It treats a range of serious bacterial infections in adult patients, including pneumonia, sinusitis, bronchitis exacerbations, skin infections, and intra‑abdominal infections.
GNH India supplies Moxifloxacina Hikma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Hikma Farmacêutica (Portugal), S.A.

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Indications & Clinical Uses

Moxifloxacina Hikma is a fluoroquinolone antibiotic used to treat infections caused by susceptible bacteria.

  • Community‑acquired bacterial pneumonia: achieves rapid bacterial clearance and clinical improvement.
  • Acute bacterial sinusitis: reduces sinus inflammation and resolves infection.
  • Acute bacterial exacerbation of chronic bronchitis: improves airflow and decreases bacterial load.
  • Skin and skin structure infections: eradicates pathogenic organisms in soft‑tissue infections.
  • Intra‑abdominal infections: provides broad‑spectrum coverage for mixed aerobic and anaerobic pathogens.

How It Works

  • Moxifloxacin inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA replication, transcription, and repair. By binding to these targets, the drug prevents the supercoiling and separation of bacterial DNA, leading to bactericidal activity against a wide range of Gram‑positive and Gram‑negative organisms.

Side Effects

Moxifloxacina Hikma may cause adverse reactions that vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: may be watery or loose.
  • Headache: transient and often resolves without intervention.
  • Dizziness: occasional light‑headed sensation.
  • Rash: mild skin erythema or pruritus.
  • Elevated liver enzymes: transient increase in hepatic transaminases.

Serious or Rare Side Effects

  • Tendon rupture: especially Achilles tendon, may occur without warning.
  • QT interval prolongation: risk of cardiac arrhythmias.
  • Severe allergic reactions: anaphylaxis, angioedema, or bronchospasm.
  • Clostridioides difficile‑associated diarrhea: potentially life‑threatening colitis.
  • Hepatic failure: rare but may present with jaundice and elevated bilirubin.
  • Stevens‑Johnson syndrome/toxic epidermal necrolysis: severe mucocutaneous reactions.

Precautions & Warnings

Before initiating therapy with Moxifloxacina Hikma, consider the following precautions.

  • Renal impairment: monitor renal function and adjust therapy as needed.
  • History of tendon disorders: avoid use in patients with prior tendon injury.
  • QT prolongation risk: obtain baseline ECG and avoid concurrent QT‑prolonging drugs.
  • Concurrent antacids containing aluminum or magnesium: separate administration by at least 2 hours.
  • Pregnancy and lactation: use only if potential benefits justify the risks.
  • Store at 2‑8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Moxifloxacina Hikma can interact with several medicines, requiring careful management.

Major Interactions (Avoid)

  • Antacids with aluminum or magnesium: reduce absorption; separate dosing.
  • Warfarin: may increase INR and bleeding risk.
  • QT‑prolonging agents (e.g., quinidine, amiodarone): heighten arrhythmia risk.
  • Systemic corticosteroids: increase tendon rupture potential.
  • Theophylline: may raise plasma theophylline concentrations.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may enhance central nervous system toxicity.
  • Oral contraceptives: possible reduction in contraceptive efficacy.
  • Cyclosporine: may increase cyclosporine levels.
  • Insulin or oral hypoglycemics: risk of hypoglycemia.
  • Digoxin: potential for elevated digoxin concentrations.

Frequently Asked Questions

Moxifloxacina Hikma is indicated for the treatment of community‑acquired bacterial pneumonia, acute bacterial sinusitis, acute bacterial exacerbations of chronic bronchitis, skin and skin‑structure infections, and intra‑abdominal infections caused by susceptible microorganisms.

Moxifloxacin blocks bacterial DNA gyrase and topoisomerase IV, enzymes required for DNA replication and transcription. This inhibition prevents bacterial DNA from unwinding and re‑winding, leading to bacterial cell death.

The specific dose and duration of Moxifloxacina Hikma are determined by the prescribing clinician based on the infection type, severity, patient weight, renal function, and local antimicrobial guidelines.

Safety in pregnancy and lactation has not been fully established. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and under close medical supervision.

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 (including any cold‑chain requirements), and necessary import documentation.

Moxifloxacina Hikma offers a broader spectrum against Gram‑positive organisms and better activity in respiratory infections compared with older fluoroquinolones such as ciprofloxacin. It also has a more favorable dosing schedule for intravenous use, though safety considerations like QT prolongation remain similar across the class.

The product should be stored at 2‑8 °C, protected from light, and must not be frozen. Keep the vial in its original packaging until use to maintain stability.

Moxifloxacina Hikma is given by intravenous infusion under the supervision of a healthcare professional. The infusion rate and duration are set by the prescriber, typically over a period of 60 minutes, and the solution should be administered using aseptic technique.

Serious risks include tendon rupture (especially Achilles), QT interval prolongation leading to arrhythmias, severe allergic reactions such as anaphylaxis, Clostridioides difficile‑associated colitis, and rare but life‑threatening skin reactions like Stevens‑Johnson syndrome.

Patients with a known hypersensitivity to moxifloxacin or other fluoroquinolones, those with a history of tendon disorders related to fluoroquinolone use, individuals with significant QT prolongation, and patients receiving concomitant medications that markedly increase the risk of tendon injury or cardiac arrhythmias should avoid this drug.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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