Product image of Itorex (Cefuroxime Sodium) supplied by GNH India

Itorex

Active Ingredient:
Cefuroxime Sodium
Origin:
EU

Itorex (Cefuroxime Sodium)

Cefuroxime sodium, the active ingredient in Itorex, is a second‑generation cephalosporin presented as an injectable solution for intramuscular use. It treats a range of bacterial infections in adults and children as prescribed by a healthcare professional.

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

Manufacturer / TM Owner

Tecnopharma S.R.L.

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Indications & Clinical Uses

Cefuroxime sodium is a broad‑spectrum cephalosporin antibiotic used to treat infections of the respiratory, urinary, and skin systems.

  • Community‑acquired pneumonia: eliminates causative bacteria and improves respiratory symptoms.
  • Upper and lower respiratory tract infections: reduces bacterial load and accelerates recovery.
  • Urinary tract infections: eradicates common uropathogens and relieves urinary symptoms.
  • Skin and soft‑tissue infections: clears bacterial invasion of skin layers.
  • Acute otitis media: resolves middle‑ear infection and associated pain.
  • Sinusitis: treats bacterial sinus inflammation and restores normal drainage.

How It Works

  • Cefuroxime sodium inhibits bacterial cell‑wall synthesis by binding to penicillin‑binding proteins (PBPs) located on the inner surface of the bacterial membrane. This binding interferes with the cross‑linking of peptidoglycan strands, weakening the cell wall and leading to osmotic instability and bacterial lysis, particularly against Gram‑positive and some Gram‑negative organisms.

Side Effects

Cefuroxime sodium may cause a range of adverse reactions, most of which are mild and self‑limiting.

Common Side Effects

  • Injection site pain: mild discomfort at the intramuscular site.
  • Diarrhoea: loose stools occurring during therapy.
  • Nausea: feeling of queasiness without vomiting.
  • Vomiting: expulsion of stomach contents.
  • Rash: mild skin redness or itching.
  • Transient elevation of liver enzymes: temporary increase in hepatic markers.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction with breathing difficulty.
  • Clostridioides difficile‑associated diarrhoea: severe colitis after antibiotic use.
  • Stevens‑Johnson syndrome: rare, life‑threatening skin reaction.
  • Hemolytic anemia: destruction of red blood cells.
  • Thrombocytopenia: low platelet count increasing bleeding risk.
  • Acute renal impairment: sudden decrease in kidney function.

Precautions & Warnings

Before using Itorex, clinicians should consider several safety measures.

  • Assess allergy: verify no known hypersensitivity to cephalosporins or penicillins.
  • Evaluate renal function: adjust dose in patients with impaired kidney function.
  • Monitor hepatic enzymes: watch for significant liver enzyme elevations.
  • Caution in pregnancy: use only if the potential benefit outweighs risk.
  • Observe for superinfection: discontinue if signs of secondary infection appear.
  • Store at 2‑8 °C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Cefuroxime sodium can interact with other medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Probenecid: may increase cefuroxime plasma levels and risk toxicity.
  • Live bacterial vaccines: antibiotic may diminish vaccine effectiveness.
  • Warfarin: potential enhancement of anticoagulant effect leading to bleeding.

Moderate Interactions (Monitor Closely)

  • Aminoglycosides: additive nephrotoxic potential; monitor renal function.
  • Loop diuretics: may increase risk of renal impairment.
  • Oral contraceptives: possible reduction in contraceptive efficacy; advise alternative protection.

Frequently Asked Questions

Itorex, containing cefuroxime sodium, is prescribed for a variety of bacterial infections including community‑acquired pneumonia, upper and lower respiratory tract infections, urinary tract infections, skin and soft‑tissue infections, acute otitis media, and sinusitis. The specific indication depends on the clinician’s assessment of the infection type and severity.

Cefuroxime sodium works by binding to penicillin‑binding proteins on bacterial cell walls, blocking the cross‑linking of peptidoglycan strands. This inhibition weakens the cell wall, causing osmotic instability that leads to bacterial lysis and death, particularly against many Gram‑positive and some Gram‑negative organisms.

The dosage of Itorex is determined by the prescribing healthcare professional based on the infection being treated, patient age, weight, renal function, and severity of disease. Clinicians calculate the appropriate amount and frequency according to established clinical guidelines.

Safety data for cefuroxime sodium in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant. Healthcare providers should discuss individual risks and benefits with the patient.

To order Itorex, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide. After verification of trade or institutional credentials, the sales team will provide pricing, availability, shipping details (including cold‑chain if needed) and assist with import documentation.

Itorex (cefuroxime sodium) is a second‑generation cephalosporin offering broader Gram‑negative coverage than first‑generation agents while retaining activity against many Gram‑positive organisms. Compared with third‑generation cephalosporins, it has a more favorable safety profile and less impact on gut flora, but may have slightly narrower spectrum against resistant Gram‑negative bacteria.

Itorex should be stored at 2‑8 °C (refrigerated). Keep the vials in their original packaging, protect them from light, and avoid freezing or shaking the solution. Maintaining the cold chain preserves the drug’s stability and potency.

Itorex is supplied as an injectable solution for intramuscular injection. The healthcare professional prepares the dose according to the prescribed amount, selects an appropriate muscle site, and administers the medication using aseptic technique. The injection should be given slowly to minimize discomfort.

Serious risks include severe allergic reactions such as anaphylaxis, Clostridioides difficile‑associated colitis, Stevens‑Johnson syndrome, hemolytic anemia, thrombocytopenia, and acute renal impairment. Patients should be monitored for signs of these reactions, and treatment should be discontinued immediately if they occur.

Itorex should not be used in individuals with a known hypersensitivity to cefuroxime, other cephalosporins, or penicillins. Caution is also advised for patients with a history of severe allergic reactions, significant renal impairment, or those who have experienced previous severe adverse reactions to beta‑lactam antibiotics.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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