Cefuroxime Injection powder for solution


Product Details
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Name Of Product(Genric Name) :

Cefuroxime Injection powder for solution

Dosage :

750mg/1.5mg

Product Description :

CEFUROXIME INJECTION 750 mg / 1.5 g
Sterile Powder for Solution for Intravenous or Intramuscular Administration

1. COMPOSITION
Each vial contains:
• Cefuroxime Sodium equivalent to Cefuroxime 750 mg / 1.5 g.
• Excipients: As applicable.

2. PHARMACEUTICAL FORM
Sterile, white to off-white powder for solution for intravenous or intramuscular administration.

3. THERAPEUTIC CLASS
Second-Generation Cephalosporin Antibiotic.

4. INDICATIONS
Cefuroxime Injection is indicated for the treatment of susceptible bacterial infections, including:
• Lower respiratory tract infections.
• Urinary tract infections.
• Skin and soft-tissue infections.
• Intra-abdominal infections.
• Bone and joint infections.
• Gynecological and obstetric infections.
• Septicemia and other serious bacterial infections.
• Perioperative antimicrobial prophylaxis where clinically appropriate.
Treatment should be guided by the susceptibility of the causative organism and applicable antimicrobial guidelines.

5. CONTRAINDICATIONS
• Hypersensitivity to cefuroxime, cephalosporins, or any component of the formulation.
• History of severe immediate hypersensitivity reactions to beta-lactam antibiotics.

6. DRUG INTERACTIONS
• Probenecid may reduce renal elimination of cefuroxime and increase its exposure.
• Concomitant nephrotoxic medicines may increase the risk of renal toxicity.
• Aminoglycosides may increase the risk of nephrotoxicity.
• Other medicines affecting renal function should be used with caution.
The treating physician should review all concomitant medications before administration.

7. ADMINISTRATION
For intravenous or intramuscular administration after reconstitution with a compatible diluent under aseptic conditions. Administer according to the approved product information and institutional protocol.

8. STORAGE
Store according to the storage conditions stated on the approved product label.